A world leader of research in molecular biology and biochemistry, Dr. Phillip A. Sharp is Institute Professor at the Massachusetts Institute of Technology’s David H. Koch Institute for Integrative Cancer Research. His research has centered on the molecular biology of gene expression relevant to cancer and the mechanisms of RNA splicing.

His discovery in 1977 provided the first indications of “discontinuous genes” in mammalian cells and fundamentally changed scientists’ understanding of gene structure, earning Dr. Sharp the 1993 Nobel Prize in Physiology or Medicine. Dr. Sharp co-founded Biogen (now Biogen Idec), Alnylam Pharmaceuticals, an early-stage therapeutics company and Magen Biosciences Inc., a biotechnology company developing agents to promote the health of human skin.

Dr. Elizabeth H. Blackburn is the Morris Herzstein Professor Emerita in the Department of Biochemistry and Biophysics at the University of California, San Francisco and President Emerita of the Salk Institute for Biological Studies. Dr. Blackburn earned a Bachelor of Science and a Master of Science at the University of Melbourne, Australia, and earned her Ph.D. from the University of Cambridge in England. She went on to do her postdoctoral study in molecular and cellular biology at Yale University, and in 1978 joined the faculty of the University of California, Berkeley in the Department of Molecular Biology. In 1990, she moved to the Department of Microbiology and Immunology at University of California, San Francisco (UCSF), where she served as Department Chair from 1993 to 1999.

For the majority of her career, Dr. Blackburn has been investigating the structure and roles of telomeres. Her pioneering and innovative research has included the development of an anti-cancer therapy that forces cells with active telomerase to make errors during telomere synthesis, effectively triggering cellular suicide. More recently, she has been applying her insights into telomere biology toward understanding the life experiences and social influences that affect human telomeres and associated disease risks, including cancer risks and progression. One goal is to modulate telomere biology in healthy and at-risk people to reduce such risks.

Throughout her career, Dr. Blackburn has been recognized with many prestigious awards, including the 2009 Nobel Prize in Physiology or Medicine, the Lasker Award, AACR-Pezcoller Foundation International Award for Cancer Research, General Motors Cancer Research Foundation Alfred P. Sloan Award, AACR-G.H.A. Clowes Memorial Award, American Cancer Society Medal of Honor, 26th Annual Bristol-Myers Squibb Award for Distinguished Achievement in Cancer Research, Albany Medical Center Prize in Medicine and Biomedical Research, the Eli Lilly Research Award for Microbiology and Immunology, the National Academy of Science Award in Molecular Biology, the Australia Prize, the Harvey Prize, the Keio Prize, E.B.Wilson Award of the American Society for Cell Biology, and the Dr. A.H. Heineken Prize for Medicine. She was named California Scientist of the Year in 1999, and one of TIME Magazine’s 100 Most Influential People in 2007. She has received honorary degrees from several major universities. She served as the 1998 President of the American Society for Cell Biology, and the 2010-11 President of the American Association for Cancer Research. Dr. Blackburn is an elected Fellow of the National Academy of Sciences, the Academy of Medicine, the American Academy of Arts and Sciences, the Royal Society of London, the American Academy of Microbiology, the American Philosophical Society and the American Association for the Advancement of Science.

Raymond N. DuBois, MD, PhD, is an internationally renowned expert for his studies on the molecular and genetic basis for colorectal cancer. His laboratory examines the molecular mechanisms by which inflammation and inflammatory mediators affect tumor development and serve as targets for cancer prevention.

Dr. DuBois was named Dean of the College of Medicine at the Medical University of South Carolina (MUSC) in March 2016. Prior to his role as Dean, Dr. DuBois served as the Executive Director of the Biodesign Institute at Arizona State University with a joint appointment as Professor of Medicine in the Mayo College of Medicine. Before that (2007-2012) he served as the Provost and Executive Vice President at The University of Texas MD Anderson Cancer Center in Houston. Previously he directed Vanderbilt’s Division of Gastroenterology, Hepatology and Nutrition, and served as Director of the Vanderbilt-Ingram Cancer Center.

Dr. DuBois is an internationally renowned cancer researcher and leader in the cancer community. He is known for elucidating a key role of prostaglandins (PGs) and other inflammatory mediators in colorectal cancer, which facilitated clinical trials targeting this pathway in humans for cancer prevention. His work also confirmed the existence of a novel tumor suppressor gene in the PG pathway (15-PGDH) in colon cancer which is responsible for inactivation of PGE2. His research revealed that prostaglandins in the tumor microenvironment increase immune tolerance and resistance to therapy.

Dr. DuBois a Fellow of the American Association for the Advancement of Science and the American Association for Cancer Research (AACR) Academy, Past President of the AACR, the Southern Society for Clinical Investigation, and the International Society for Gastrointestinal Cancer. He was also inducted as a member of the American Clinical and Climatological Association, the Royal College of Physicians in London, the Association of American Physicians and the American Society for Clinical Investigation. He also currently serves on the AACR Academy leadership council.

During his career as a physician-scientist, DuBois has published over 150 peer reviewed research articles, more than 60 review articles, 25 book chapters, and three books. His work has been cited over 55,000 times as of 2018 according to Google Scholar. He is a co-inventor of a method to identify and prevent cellular genes needed for viral growth and cellular genes that function as tumor suppressors in mammals. His research has been continuously funded from the NIH and other agencies/foundations for the past 25 years.

DuBois earned a bachelor’s degree from Texas A&M University and a doctoral degree from The University of Texas Southwestern Medical Center in Dallas. He obtained a medical degree from The University of Texas School of Medicine in San Antonio, followed by an Osler Medicine internship and residency, and a gastroenterology fellowship at the Johns Hopkins Hospital in Baltimore.

Lee J. Helman, MD, served as chief of the Pediatric Oncology Branch of the National Cancer Institute from 1997 to 2007 and as scientific director for clinical research at the Center for Cancer Research, NCI, from 2007 to 2016. He joined Children’s Hospital Los Angeles and the University of Southern California in 2017. Dr. Helman’s laboratory work focuses on the biology and treatment of rhabdomyosarcoma, Ewing’s sarcoma, osteosarcoma, and pediatric GIST tumors.

Major areas of research include the pathophysiologic consequences of IGF signaling, identification of the molecular/biochemical determinants of the biology of sarcomas, and the application of functional genomics to identify new treatment targets.

Arnold Levine is a leader in cancer research. In 1979, Levine was one of the co-discoverers of the p53 protein. The p53 gene and its protein are central players in our present day understanding of cancers. This discovery has generated more than 60,000 publications. In 1989, Dr. Levine’s group demonstrated that the wild type p53 gene and protein functioned as a tumor suppressor, preventing transformation by oncogenes. This observation changed the direction of the field.

The research paths of the Levine group provide clear evidence that the p53 pathway plays a central role in the prevention of human cancers and that polymorphic variations in components of the pathway can influence individual responses to environmental mutagens, age of cancer onset, sexual dimorphisms in cancers, response to therapy and survival times, all for a gene whose mutations cause the most common genetic alterations in cancers. This research helped to uncover the genetic origins of cancer and focus drug discovery on a rational path to treat cancers.

William G. Nelson, MD, PhD, is the Marion I. Knott Director and Professor of Oncology and Director of the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins University in Baltimore, MD. Dr. Nelson directs
a translational research laboratory focused on discovering new strategies for prostate cancer treatment and prevention and manages a clinical practice focused on developing these new treatment and prevention approaches in early “proof-of-principle” prostate clinical trials.

Dr. Nelson is a recognized leader in translational cancer research. He was one of three co-chairs of the National Cancer Institute’s Translational Research Working Group, which worked to re-engineer translational cancer science across the nation.

Dr. Adams has more than 30 years of experience in drug discovery and development with a strong focus on cancer research. In 2018 Dr. Adams joined Gamida Cell as CEO and Chairman, and serves Clal Biotechnology Industries as its Scientific Advisor. He was previously Chief Scientific Officer and President of Research and Development at Infinity Pharmaceuticals. Prior to joining Infinity in 2003, Dr. Adams was the senior vice president of drug discovery and development at Millennium Pharmaceuticals, where he headed multiple global drug discovery and development programs, including the successful Velcade® (bortezomib) program. Dr. Adams also held senior positions in research and development at LeukoSite (acquired by Millennium) and at ProScript, as well as in medicinal chemistry at Boehringer Ingelheim, where he is credited with discovering Viramune® (nevirapine) for HIV.

Julian has received many awards, including the 2012 Warren Alpert Foundation Prize for his role in the discovery and development of bortezomib, the 2012 C. Chester Stock Award Lectureship from Memorial Sloan-Kettering Cancer Center, and the 2001 Ribbon of Hope Award for Velcade® from the International Myeloma Foundation. He is an inventor on more than 40 patents and has authored over 100 papers and book chapters in peer-reviewed journals.

Dr. Adams received his B.S. from McGill University and his Ph.D. from the Massachusetts Institute of Technology. He also received a Doctor of Science, honoris causa, from McGill University in 2012.

Dr. Carlos L. Arteaga is the Director of the Harold C. Simmons Comprehensive Cancer Center and Associate Dean of Oncology Programs at UT Southwestern Medical Center.

Dr. Arteaga earned his medical degree at the University of Guayaquil in Ecuador. He trained in internal medicine and medical oncology at Emory University and the University of Texas Health Science Center at San Antonio. He joined Vanderbilt University Medical Center in 1989, where he held the Donna S. Hall Chair in Breast Cancer Research and served at the Vanderbilt-Ingram Cancer Center (VICC) as Director of the Center for Cancer Targeted Therapies, the Director of the Breast Cancer Program, and the Associate Director for Translational/Clinical Research until 2017, when he joined UT Southwestern.

Dr. Arteaga has more than 300 publications in the areas of oncogenes and breast tumor initiation and progression, development of targeted therapies and biomarkers of drug action and resistance, and investigator-initiated clinical trials in breast cancer. His research is or has been funded by the National Cancer Institute (NCI), CPRIT, the American Cancer Society, the Department of Defense Breast Cancer Research Program, Stand Up 2 Cancer (SU2C), and the Susan G. Komen for the Cure and Breast Cancer Research foundations.

During his career, Dr. Arteaga has received several awards, including the American Association for Cancer Research-Richard and Hinda Rosenthal Award, the American Cancer Society Clinical Research Professor Award, the Gianni Bonadonna Award from the American Society of Clinical Oncology, the Brinker Award for Scientific Distinction from the Susan G. Komen Foundation, the 2015 Prize for Scientific Excellence in Medicine from the American-Italian Cancer Foundation, and the Clinical Investigator Award from the U.S. Department of Veteran Affairs.

He is an elected Fellow of the American Association for the Advancement of Science, a Fellow of the American Association for Cancer Research Academy, an elected member of both the American Society for Clinical Investigation and the Association of American Physicians, and member of the Susan G. Komen Scientific Advisory Board. He also serves on the advisory boards.

Dr. Alan Bernstein is President of the Canadian Institute for Advanced Research (CIFAR), Canada’s global research institute. From 2008-2011, Dr. Bernstein was the executive director of the Global HIV Vaccine Enterprise, an international alliance of researchers and funders charged with accelerating the search for an HIV vaccine.

Previously, he served as the founding president of the Canadian Institutes of Health Research (2000-2007), Canada’s federal agency for the support of health research. In that capacity, he led the transformation of health research in Canada. After receiving his Ph.D. from the University of Toronto, and following postdoctoral work in London, Dr. Bernstein joined the Ontario Cancer Institute (1974-1985). In 1985, he joined the new Samuel Lunenfeld Research Institute in Toronto, was named Associate Director in 1988 and then Director of Research (1994-2000).

Internationally known for his contributions to our understanding of the molecular basis of cancer, Dr. Bernstein has made extensive contributions to the study of stem cells, hematopoiesis and cancer. He chairs or is a member of advisory and review boards in Canada, the US, UK and Italy. Dr. Bernstein has received numerous awards and honourary degrees for his contributions to science, including the 2008 Gairdner Wightman Award, induction into the Canadian Medical Hall of Fame, and the Henry G. Friesen International Prize in Health Research. He is a Senior Research Fellow of Massey College, received the Order of Ontario in 2018 and was appointed an Officer of the Order of Canada in 2002.

Richard B. Gaynor, MD, joined Eli Lilly and Company as vice president for cancer research and clinical investigation in August 2002. Currently, Dr. Gaynor is vice president, clinical development, and medical affairs at Lilly.

Gaynor received a doctor of medicine degree from the University Of Texas
Southwestern Medical School. He served his internship and residency in internal medicine at Parkland Memorial Hospital in Dallas, Texas. He completed a fellowship in hematology-oncology at the University of California at Los Angeles (UCLA) School of Medicine and then served on the faculty there. He received board certification in internal medicine, hematology, and medical oncology.

Prior to joining Lilly, Gaynor was a professor of medicine and microbiology at the University of Texas Southwestern Medical Center (UTSW) in Dallas and held several important leadership positions. He was chief of the Division of Hematology and Oncology at UTSW and director of the Harold C. Simmons Comprehensive Cancer Center there in addition to his work as the Lisa K. Simmons distinguished chair in comprehensive oncology. He served on numerous NIH advisory committees and was elected to both the American Society of Clinical Investigation and Association of American Physicians.

Gaynor is on the editorial board of several scientific journals and has an extensive publication record totaling more than 140 scientific articles. He serves on the board of the Damon Runyon Cancer Research Foundation and the Walther Cancer Institute and on several committees for the American Association of Cancer Research and other leading cancer organizations.

Nancy Goodman is Founder and Executive Director of Kids v Cancer, a nonprofit that was lead advocate and author of two Federal laws to incentivize and require pharmaceutical companies to develop drugs for children. The Creating Hope Act pediatric priority review voucher program, passed into law in 2012 as 12 U.S.C. 360ff, established a market-based incentive, a voucher, for companies to develop drugs expressly for children with pediatric rare diseases, including pediatric cancers. Over $1.2 billion in vouchers have been traded since the establishment of the program. The RACE for Children Act, which amends the Pediatric Research Equity Act (PREA), 21 U.S.C. 355c, was passed into law in 2017, authorizes the FDA to require companies developing cancer targeted therapies to undertake pediatric studies when the molecular targets of the drugs are substantially relevant to pediatric cancers.

Kids v Cancer was selected by Fast Company Magazine as top ten most innovative non-profits in 2016 and won the Peter Drucker Nonprofit Innovation Award in 2015. Nancy was awarded the Rare Disease Legislative Advocates Rare Disease Award and The One Hundred: top cancer leaders by Massachusetts General Hospital. She serves the National Cancer Institute Board of Scientific Counselors.

Nancy’s son, Jacob, died of a pediatric brain cancer when he was ten. Nancy is a graduate of the University of Chicago Law School, Harvard Kennedy School of Government and University of Pennsylvania.

Dr. William N. Hait is Global Head, Johnson & Johnson External Innovation, a unit that comprises Johnson & Johnson Innovation (Innovation Centers, J-Labs and the Johnson & Johnson Development Corporation), Johnson and Johnson Lung Cancer Initiative, and the World Without Disease Accelerator. In this role, he leads the mission to source innovation from wherever it originates, accelerate the filling of R&D pipelines in all of the J&J sectors, drive the creation of cross-sector R&D programs with a focus on prevention, interception and cures, and ensure the future by getting out ahead of potentially disruptive technologies.

Dr. Hait joined Johnson & Johnson in 2007 and was the Global Therapeutic Area Head, Oncology, from 2009 to 2011. He served as Global Head, Janssen R&D from 2011 through 2017.

Before joining J&J, he was the founding Director of The (Rutgers) Cancer Institute of New Jersey, which he led to receive the National Cancer Institute’s highest designation of Comprehensive Cancer Center in 2002. From 1993 to 2007 he was Professor of Medicine and Pharmacology and Associate Dean for Oncology Programs at the University of Medicine and Dentistry of New Jersey — Robert Wood Johnson Medical School.

After earning his B.A. from the University of Pennsylvania, Dr. Hait received his M.D. and Ph.D. (Pharmacology) cum laude from the Medical College of Pennsylvania, where he was elected to Alpha Omega Alpha. He joined the Yale University School of Medicine faculty in 1984 and became Associate Professor of Medicine and Pharmacology, Chief of the Division of Medical Oncology, Associate Director of the Yale University Comprehensive Cancer Center, Director of the Breast Cancer Unit and Co-Director of the Lung Cancer Unit. Dr. Hait is Board Certified in Internal Medicine and Medical Oncology.

Dr. Hait devoted his time to numerous advisory and editorial boards. He was Editor-in-Chief of Clinical Cancer Research and Associate Editor of Cancer Research, served as President of the American Association for Cancer Research from 2007 – 2008 and currently serves as Treasurer. He has served on various committees for the American Association of Cancer Research (Chair, Clinical Cancer Research Committee), the American Society of Clinical Oncology, the Association of American Cancer Institutes (Board of Directors), the National Cancer Institute Board of Scientific Advisors and was founding Chairman of the Executive Management Committee of Stand Up to Cancer. He currently is a member of the Rutgers Cancer Institute of New Jersey Director’s Advisory Board, Board of External Advisors for the Dana Farber/Harvard Cancer Center, the Stand Up to Cancer Scientific Advisory Board, The Board of Directors of Research America! and the Vanderbilt University Biomedical Science Advisory Board.

Dr. Waun Ki Hong is the Head of the Division of Cancer Medicine at the University of Texas M. D. Anderson Cancer Center. Dr. Hong received his bachelor of science and medical degree from the Yon Sei University College of Engineering Science in Seoul, Korea. He went on to do his residency at the Boston Veterans Affairs Medical Center and became a Medical Oncology Fellow at the Memorial Sloan-Kettering Cancer Center in New York City. He joined M. D. Anderson in 1984 as chief of the Section of Head and Neck Medical Oncology and became chair of the Department of Thoracic/Head and Neck Medical Oncology in 1993.

Dr. Hong’s research interest includes retinoids, genetic predisposition to disease, biological markers, and chemoprevention, particularly the area of translational aerodigestive cancer research. His major research focus is working to identify and develop effective novel personalized molecularly targeted preventive and therapeutic approaches in patients with aerodigestive cancers and/or identify high-risk individuals to reduce incidence and mortality through an integrated translational research team effort.

Dr. Hong was recently appointed to the National Cancer Advisory Board. In 1996, he became the first M. D. Anderson physician to receive an American Cancer Society Clinical Research Professorship, a lifetime honor presented in recognition of his distinguished career. In 2001-2002, he served as president of the American Association for Cancer Research. His many honors for outstanding achievements in clinical research and patient care include the AACR’s Joseph H. Burchenal and the Rosenthal Foundation Awards; and the American Society of Clinical Oncology’s most prestigious award, the David A. Karnofsky Award.

Dr. William G. Kaelin, Jr., is a Professor at the Dana-Farber Cancer Institute in Boston, MA. He received his medical degree from Duke University in 1982 and was a house officer in internal medicine at Johns Hopkins Hospital. He went on to become a medical oncology clinical fellow at the Dana-Farber Cancer Institute and a postdoctoral fellow in the laboratory of Dr. David Livingston, where he began his studies of tumor suppressor proteins. He became an independent investigator at Dana-Farber Cancer Institute in 1992 as a James S. McDonnell Scholar and became a Howard Hughes Medical Institute investigator in 1998. Dr. Kaelin is also a Professor in the Department of Medicine at Dana-Farber Cancer Institute and Brigham and Women’s Hospital, Senior Physician at Brigham and Women’s Hospital, and Associate Director for Basic Research at the Dana-Farber/Harvard Cancer Center.

Dr. Kaelin’s research interests have focused on tumor suppressor genes and the normal functions of the proteins they encode. The long-term goal of his work is to lay the foundation for the development of new anticancer therapies based on the functions of specific tumor suppressor proteins. His studies of tumor suppressor genes linked to hereditary forms of cancer have uncovered molecular pathways that are important in non-hereditary cancers and have accelerated the development of new treatments for kidney cancer.

Dr. Kaelin is an elected member of the Institute of Medicine and has served on numerous boards and committees, including the American Association for Cancer Research’s Board of Directors and the NCI Board of Scientific Advisors. He has received many awards for his work, including the AACR-Richard and Hinda Rosenthal Prize for Cancer Research and the Paul Marks Prize for Cancer Research from Memorial Sloan-Kettering Cancer.

Michael B. Kastan, MD, PhD, is the William and Jane Shingleton Professor of Pharmacology and Cancer Biology and Professor of Pediatrics at Duke University and serves as the Executive Director of the Duke Cancer Institute. He earned M.D. and Ph.D. degrees from the Washington University School of Medicine and did his clinical training in Pediatrics and Pediatric Hematology-Oncology at Johns Hopkins. He was a Professor of Oncology, Pediatrics, and Molecular Biology at Johns Hopkins prior to becoming Chair of the Hematology-Oncology Department and later Cancer Center Director at St. Jude Children’s Research Hospital, before moving to Duke in 2011. He is a Pediatric Oncologist and a cancer biologist; his laboratory research concentrates on DNA damage and repair, tumor suppressor genes, and causes of cancer related to genetic predisposition and environmental exposures. His discoveries have made a major impact on our understanding of both how cancers develop and how they respond to chemotherapy and radiation therapy and his publications reporting the roles of p53 and ATM in DNA damage signaling are among the most highly cited publications in the biomedical literature of the past two decades. He has received numerous honors for his highly cited work, including election to the National Academy of Sciences, National Academy of Medicine, the American Academy of Arts and Sciences, and receiving the AACR-G.H.A. Clowes Memorial Award for outstanding contributions to basic cancer research. He has served as Chairman of the Board of Scientific Counselors of the National Cancer Institute (NCI), on the Boards of Directors of the American Association for Cancer Research (AACR) and the American Association of Cancer Institutes (AACI), as Editor-in-Chief of the journal Molecular Cancer Research, and as Editor of the textbook Clinical Oncology. He also serves on the scientific advisory board of the V Foundation.

Dr. Guillermina (Gigi) Lozano is professor and chair of the department of genetics at The University of Texas MD Anderson Cancer Center. She received her Bachelor of Science degree magna cum laude in biology and mathematics from the University of Texas Pan American and her doctorate in biochemistry from Rutgers University and the University of Medicine and Dentistry of New Jersey. After a short postdoctoral fellowship at Princeton University, she became a faculty member at The University of Texas MD Anderson Cancer Center where she has risen through the ranks.

Dr. Lozano directs a research laboratory that studies the p53 tumor suppressor pathway. Her contributions include the identification of the tumor suppressor p53 as a transcriptional activator and the finding that p53 missense mutations commonly observed in cancers were transcriptionally inactive. Using animal models, she has characterized the physiological importance of Mdm2 and Mdm4 proteins as critical inhibitors of p53 and the significance of various p53 mutations on tumorigenesis in vivo.

Dr. Lozano was elected a fellow of the American Association for the Advancement of Science. She was honored with the Mattie Allen Fair Research Chair in 2004 from The University of Texas MD Anderson Cancer Center. In 2011, she received the Minorities in Cancer Research Jane Cooke Wright Lectureship from the American Association for Cancer Research. Dr. Lozano is also the recipient of distinguished alumni awards from both her undergraduate and graduate alma maters.

Dr. Tak W. Mak is the Director of the Campbell Family Institute for Breast Cancer Research at the Princess Margaret Hospital in Toronto. He received a bachelor’s of science in biochemistry in 1967 and a master of science in biophysics in 1968 from the University of Wisconsin.  He earned his Ph.D. in Biochemistry from the University of Alberta in 1971. He is also senior scientist in the division of Stem Cell and Developmental Biology, Ontario Cancer Institute. Since 1984, he has been a Professor in the Departments of Medical Biophysics and Immunology at the University of Toronto.

Dr. Mak co-discovered the t-cell receptor, a key component of the immune system. His research is concentrated on gaining fundamental knowledge of the biology of cells in normal and disease settings, and in particular on the mechanisms underlying immune responses and tumorigenesis. His lab has initiated several complementary programs, many of which have evolved from the production and analysis of genetically engineered mouse strains.

Dr. Mak has received several awards and honors for his work. He is a member of the Order of Ontario and was elected as a foreign associate to the National Academy of Sciences in the discipline of immunology in 2002. Dr. Mak has received the King Faisal Prize for Medicine, the Gairdner Foundation International Award, the Paul Ehrlich Prize, the Novartis Prize in Immunology, the Killam Prize by the Canada Council for the Arts, and the Sloan Prize of the General Motors Cancer Foundation, and the Robert L. Noble Prize by the National Cancer Institute of Canada.

Andre Nussenzweig, PhD BIO Dr. Nussenzweig is an NIH Distinguished Investigator, and chief of the Laboratory of Genome Integrity at the National Institute of Health’s National Cancer Institute. Dr. Nussenzweig is a leading contributor to the study of mechanisms that maintain genomic stability and prevent cancer. His laboratory has elucidated many fundamental features of DNA damage and repair proteins and revealed the critical role they play in both normal and pathogenic states. His studies have emphasized the importance of DNA repair pathways as drivers of specific hematological malignancies and as contributors to chemo-resistance/sensitivity in breast and ovarian cancers. The goal of his program is to use hypothesis-driven approaches to develop therapeutic strategies in the treatment of cancers. Dr. Nussenzweig serves on multiple editorial boards and scientific advisory committees, including Stand Up To Cancer.

Dr. Cecil B. Pickett is the former President of Research and Development at Biogen Idec, having retired in 2009. Dr. Pickett earned his B.S. in biology from California State University at Hayward and his Ph.D. in cell biology from University of California, Los Angeles. Previously, he served as Senior Vice President and President of Schering-Plough Research Institute, the pharmaceutical research arm of Schering-Plough Corporation. Dr. Pickett came to Schering-Plough Research Institute from Merck Research Laboratories, Montreal, Canada, and West Point, Pa., where he served as Senior Vice President of Basic Research. During his 15-years at Merck & Co., Dr. Pickett held various positions of increasing responsibility, including research fellow, biochemical regulation; associate director, department of molecular pharmacology and biochemistry; director, department of molecular pharmacology and biochemistry; executive director of research at the Merck Frosst Center for Therapeutic Research, Montreal; and vice president of the Center.

Dr. Pickett is an expert in drug development. During his career, he has overseen all aspects of the internal research and collaboration with partners aimed at developing, manufacturing, and marketing advanced drug therapies and has played an integral role in bringing several large and small molecule candidates into clinical development.

Dr. Pickett has published extensively in leading research journals and has been a frequent speaker at scientific symposia and conferences. He has received several major academic awards, appointments and fellowships and serves on a number of scientific committees and editorial boards of medical journals and research organizations. His awards and honors include the UCLA Alumni Association Award for Scholarly Achievement and Academic Distinction; the first Robert A. Scala Award and Lectureship in Toxicology of Rutgers University and the University of Medicine and Dentistry of New Jersey; and the CIIT Centers for Health Research Founders’ Award. Dr. Pickett served as a member of the U.S. Food and Drug Administration (FDA) Science Board, the Advisory Committee to the Director of the National Institutes of Health and The National Cancer Policy Board of the Institute of Medicine. He was elected to the Institute of Medicine of the National Academy of Sciences in 1993 and is also a member of The American Society for Cell Biology, American Society of Biochemistry & Molecular Biology, American Association for Cancer Research, and American Association for the Advancement of Science.

Arlene Sharpe, MD, PhD is the George Fabyan Professor of Comparative Pathology and Co-Chair of the Department of Microbiology and Immunobiology at Harvard Medical School. She is a member of the Department of Pathology at Brigham and Women’s Hospital, an Associate Member at the Broad Institute of MIT and Harvard, Leader of the Cancer Immunology Program at the Dana-Farber/Harvard Cancer Center, and Co-Director of the Evergrande Center for Immunologic Diseases at Harvard Medical School and Brigham and Women’s Hospital.

Dr. Sharpe earned her A.B. from Harvard University and her M.D. and Ph.D. degrees from Harvard Medical School. She completed residency training in Pathology at Brigham and Women’s Hospital and is board certified in Anatomic Pathology.

Dr. Sharpe is a leader in the field of T cell costimulation. Her laboratory has discovered and elucidated the functions of T cell costimulatory pathways, including the immunoinhibitory functions of the CTLA-4 and PD-1 pathways, which have become exceptionally promising targets for cancer immunotherapy. Her laboratory currently focuses on the roles of T cell costimulatory pathways in regulating T cell tolerance and effective antimicrobial and antitumor immunity, and translating fundamental understanding of T cell costimulation into new therapies for autoimmune diseases and cancer. Dr. Sharpe has published over 300 papers and was listed by Thomas Reuters as one of the most Highly Cited Researchers (top 1%) in 2014, 2015, 2017 and a 2016 Citation Laureate. She received the William B. Coley Award for Distinguished Research in Tumor immunology in 2014 and the Warren Alpert Foundation Prize in 2017 for her contributions to the discovery of PD-1 pathway.

Dr. Laura Shawver is chief executive officer of Cleave Biosciences focusing on the development of drugs against novel targets in protein homeostasis for difficult to treat cancers. She received her doctorate in pharmacology at the University of Iowa in 1984 and did postdoctoral training at the University of Virginia Cancer Center and the department of hematology and oncology at Washington University. Before joining Cleave, Shawver was CEO of Phenomix Corporation. Previously, she was president of SUGEN Inc. which focused on kinases and their function in cancer growth and survival. Her work in understanding the role of VEGF receptor in tumor angiogenesis led to the development of a new class of drugs including SutentTM currently marketed by Pfizer for kidney and stomach cancer. Prior to her employment at SUGEN Inc., Dr. Shawver was employed at Berlex Biosciences (formerly Triton Biosciences). Diagnosed with ovarian cancer in 2006, she founded the non-profit organization, The Clearity Foundation which provides access to molecular profiling for women with recurrent and refractory disease to help prioritize treatment options. Dr. Shawver is an active member in the American Association for Cancer Research currently serving on the Science Policy and Legislative Affairs Committee.

Ellen V. Sigal, PhD, is chairperson and founder of Friends of Cancer Research (Friends), a cancer research think tank and advocacy organization based in Washington, DC.

Friends is a leader in developing partnerships and advocating policies that will get treatments and therapies to patients in the safest and quickest way possible. Friends works with federal health agencies, Congressional leadership, academic research centers and private sector industry producing real results.

Dr. Sigal is vice chair of the inaugural board of directors of the Reagan-Udall Foundation, a partnership designed to modernize medical product development, accelerate innovation and enhance product safety in collaboration with the U.S. Food and Drug Administration. She serves on the Board of the Foundation for the National Institutes of Health where she chairs its Public/Private Partnerships Committee.

In 2010, Dr. Sigal was appointed to a six-year term on the Board of Governors of the Patient-Centered Outcomes Research Institute (PCORI) as a representative of patients and health consumers. PCORI is an independent organization created by Congress to initiate research that will help patients, physicians and caregivers make informed health care decisions and improve healthcare delivery.

She also holds leadership positions with a broad range of cancer advocacy, public policy organizations and academic health centers including the American Association for Cancer Research Foundation Board; Research!America Board; University of Texas MD Anderson Cancer Center External Advisory Board, the Duke University Cancer Center Board of Overseers and The Sidney Kimmel Comprehensive Cancer Center Advisory Council.

David Tuveson completed chemistry at M.I.T., an MD-PhD at Johns Hopkins, medical residency at Brigham and Women’s Hospital and a medical oncology fellowship at Dana-Farber/Harvard. While training, Dr. Tuveson co-developed KIT inhibitors with George Demetri for gastrointestinal stromal tumors, and Kras-dependent mouse cancer models with Tyler Jacks. At the University of Pennsylvania his lab generated the first mouse models of ductal pancreatic cancer, and at the University of Cambridge they identified new therapies. At Cold Spring Harbor Laboratory they developed organoid models of pancreatic cancer with Hans Clevers, enabling basic discoveries and clinical findings including signatures of “common responders” to chemotherapy. Dr. Tuveson is professor and director of Cold Spring Harbor Cancer Center, the chief scientist of Lustgarten Foundation for Pancreatic Cancer Research, Cancer Center Director and Roy J. Zuckerberg Professor at CSHL, and serves on the Board of Scientific Advisors of the NCI, the Scientific Advisory Committee of Stand Up To Cancer and the Board of Directors of AACR. Awards include the Rita Allen, Waldenstrom and Hamdan.

Dr. Alan Bernstein is President of the Canadian Institute for Advanced Research (CIFAR), Canada’s global research institute. From 2008-2011, Dr. Bernstein was the executive director of the Global HIV Vaccine Enterprise, an international alliance of researchers and funders charged with accelerating the search for an HIV vaccine.

Previously, he served as the founding president of the Canadian Institutes of Health Research (2000-2007), Canada’s federal agency for the support of health research. In that capacity, he led the transformation of health research in Canada. After receiving his Ph.D. from the University of Toronto, and following postdoctoral work in London, Dr. Bernstein joined the Ontario Cancer Institute (1974-1985). In 1985, he joined the new Samuel Lunenfeld Research Institute in Toronto, was named Associate Director in 1988 and then Director of Research (1994-2000).

Internationally known for his contributions to our understanding of the molecular basis of cancer, Dr. Bernstein has made extensive contributions to the study of stem cells, hematopoiesis and cancer. He chairs or is a member of advisory and review boards in Canada, the US, UK and Italy. Dr. Bernstein has received numerous awards and honourary degrees for his contributions to science, including the 2008 Gairdner Wightman Award, induction into the Canadian Medical Hall of Fame, and the Henry G. Friesen International Prize in Health Research. He is a Senior Research Fellow of Massey College, received the Order of Ontario in 2018 and was appointed an Officer of the Order of Canada in 2002.

A world leader of research in molecular biology and biochemistry, Dr. Phillip A. Sharp is Institute Professor at the Massachusetts Institute of Technology’s David H. Koch Institute for Integrative Cancer Research. His research has centered on the molecular biology of gene expression relevant to cancer and the mechanisms of RNA splicing.

His discovery in 1977 provided the first indications of “discontinuous genes” in mammalian cells and fundamentally changed scientists’ understanding of gene structure, earning Dr. Sharp the 1993 Nobel Prize in Physiology or Medicine. Dr. Sharp co-founded Biogen (now Biogen Idec), Alnylam Pharmaceuticals, an early-stage therapeutics company and Magen Biosciences Inc., a biotechnology company developing agents to promote the health of human skin.

Dr. Carlos L. Arteaga is the Director of the Harold C. Simmons Comprehensive Cancer Center and Associate Dean of Oncology Programs at UT Southwestern Medical Center.

Dr. Arteaga earned his medical degree at the University of Guayaquil in Ecuador. He trained in internal medicine and medical oncology at Emory University and the University of Texas Health Science Center at San Antonio. He joined Vanderbilt University Medical Center in 1989, where he held the Donna S. Hall Chair in Breast Cancer Research and served at the Vanderbilt-Ingram Cancer Center (VICC) as Director of the Center for Cancer Targeted Therapies, the Director of the Breast Cancer Program, and the Associate Director for Translational/Clinical Research until 2017, when he joined UT Southwestern.

Dr. Arteaga has more than 300 publications in the areas of oncogenes and breast tumor initiation and progression, development of targeted therapies and biomarkers of drug action and resistance, and investigator-initiated clinical trials in breast cancer. His research is or has been funded by the National Cancer Institute (NCI), CPRIT, the American Cancer Society, the Department of Defense Breast Cancer Research Program, Stand Up 2 Cancer (SU2C), and the Susan G. Komen for the Cure and Breast Cancer Research foundations.

During his career, Dr. Arteaga has received several awards, including the American Association for Cancer Research-Richard and Hinda Rosenthal Award, the American Cancer Society Clinical Research Professor Award, the Gianni Bonadonna Award from the American Society of Clinical Oncology, the Brinker Award for Scientific Distinction from the Susan G. Komen Foundation, the 2015 Prize for Scientific Excellence in Medicine from the American-Italian Cancer Foundation, and the Clinical Investigator Award from the U.S. Department of Veteran Affairs.

He is an elected Fellow of the American Association for the Advancement of Science, a Fellow of the American Association for Cancer Research Academy, an elected member of both the American Society for Clinical Investigation and the Association of American Physicians, and member of the Susan G. Komen Scientific Advisory Board. He also serves on the advisory boards.

Dr. Jenny C. Chang is Director of the Cancer Center at Houston Methodist Hospital in Houston, Texas, and Professor at Weill Cornell Medical School. She obtained her medical degree at Cambridge University in England, and then completed fellowship training in medical oncology at the Royal Marsden Hospital/Institute for Cancer Research in the United Kingdom. She was also awarded a research doctorate from the University of London. Her recent work has focused on the intrinsic therapy resistance of cancer stem cells (CSCs), which has led to several publications and international presentations. In addition, she has been awarded several federal grants to evaluate novel biologic agents, and holds patents on new technologic advances and therapeutic agents.

Dr. Chang has worked in the field of cancer stem cells for more than ten years. After her discovery that CSCs are chemo-resistant, and that targeting the EGFR/HER2 pathway can decrease this subpopulation, Dr. Chang has played a key role in demonstrating some of the limitations and mechanisms of CSCs (Creighton et al., 2009; Li et al., 2008). Her work is now focused on the mechanisms that regulate CSCs, as well as initiating and planning clinical trials that target this critical tumor initiating subpopulation. She is also interested in characterizing the cross-talk between these different pathways that may lead to mechanisms of resistance, and has identified some of the chief regulatory pathways, including inducible nitric oxide (iNOS) and JAK/STAT3 signaling involved in CSC self-renewal (Dave et al., 2014; Dave et al., 2017). She is a world-renown clinical investigator, credited as one of the first to describe intrinsic chemo-resistance of CSCs.

Carol Prives is the DaCosta Professor of Biological Sciences at Columbia University. She was educated in Canada, receiving her BSc and PhD from McGill University. After postdoctoral training at Albert Einstein College of Medicine and the Weizmann Institute, she became a faculty member at the Weizmann, after which she joined the Biological Sciences Department at Columbia University where she was appointed to a named professorship in 1995. Dr Prives served as Chair of that department between 2000 and 2004. Since the late 1980’s her work has focused on the p53 tumor suppressor protein, the product of the most frequently mutated gene in human cancers. Her work has focused on the structure and functional analysis of the p53 protein especially as it relates to its roles as a transcriptional activator. Similarly she has examined how cancer related mutant forms of p53 regulate tumorigenesis. Work from her group has also illuminated the functions of the p53 negative regulators, Mdm2 and MdmX.

Dr Prives has served as Chair of both the Experimental Virology and the Cell and Molecular Pathology Study Sections of the NIH and was a member of the NCI Intramural Scientific Advisory Board. She was also a member of the Advisory Boards of the Dana-Farber Cancer Center, the Memorial Sloan Kettering Cancer Center and the Massachusetts General Cancer Center as well as the American Association for Cancer Research. Dr Prives has received several honors including being named an American Cancer Society Research Professor, election to the American Academy of Arts and Sciences, the Institute of Medicine and the National Academy of Sciences. She has received awards and lectureships including the NCI Rosalind E Franklin Award for Women in Science and the AACR-Women in Cancer Research Charlotte Friend Memorial Lectureship Award. Most recently she was awarded an honorary doctorate from McGill University, her alma mater.

Patrick Sullivan is a passionate childhood cancer advocate, Chairman of the Board of Coast to Coast Against Cancer Foundation, the President and a founder of the Team Finn Foundation, and Co-Founder of Ac2orn. Patrick became an advocate after his twin son Finn was diagnosed with Rhabdomyosarcoma in 2007 and he heard the word “incurable” for the first time. His desire to make a change in cancer research is in part an effort to pay an un-payable debt to his son Finn and to change the stories of other Finn’s.

Patrick participates in several national and international initiatives that include member of the AACR Pediatric Cancer Working Group, lead Patient Advocate on the St. Baldrick’s – Stand-Up to Cancer Pediatric Cancer Dream Team, Patient Advocate on the SU2C Canada Cancer Stem Cell Dream Team, Director on the Canadian Cancer Research Alliance, Co-Lead of the Terry Fox Research Profyle initiative, member of the CTCG Lay Representative Committee and Chair of the Bio-CanRX Cancer Stakeholder Alliance.

By profession, Patrick is a securities and corporate-commercial litigator and one of the founding partners of Taylor Veinotte Sullivan. Patrick is the proud father of three remarkable children, Baird, Sarah and Finn and would do almost anything for the simple pleasure of holding Finn’s hand again.