Speaker Biographies
Molecular Epidemiology of Cancer Incidence and Progression with an Eye Toward Translation of Findings into Strategies for Prevention and Treatment

Elizabeth A. Platz, ScD, MPH
View Abstract & Bio
Abstract: In this talk, Dr. Platz will showcase examples of molecular epidemiology research on cancer incidence and progression that leverage large scale -omics platforms and complex tissue-based measurements. Across these examples, Dr. Platz will illustrate challenges related to samples, measurement, classification based on measurements, external cohort confirmation, and inferences when implementing emerging technologies in large observational studies. Dr. Platz will also highlight the critical need for collaboration with basic scientists to achieve meaningful “back translation” to strengthen causal inference and thus advance the development of strategies for cancer prevention and treatment.
Biography: Elizabeth A. Platz, ScD, MPH, is a Professor and the Martin D. Abeloff, MD Scholar in Cancer Prevention in the Department of Epidemiology at the Johns Hopkins Bloomberg School of Public Health. Dr. Platz holds joint appointments in the Departments of Oncology and Urology at the Johns Hopkins University School of Medicine and is the Associate Director for Population Sciences at the Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins. Her research, conducted in large cohort studies, focuses on the molecular epidemiology of cancer incidence and progression with an eye toward translation of findings into strategies for prevention and treatment. Dr. Platz is the editor-in-chief of the American Association for Cancer Research’s journal Cancer Epidemiology, Biomarkers and Prevention and is an elected Fellow of the American Association for the Advancement of Science.
Moderators:
Rajeev Agarwal, PhD, NIH Office of the Director | David Miller, PhD, NCI Division of Cancer Prevention
Talk 1: Scalable Multimodal AI for Cancer Microbiome Epidemiology

Himel Mallick, PhD
View Abstract & Bio
Abstract: Rapid advances in microbiome and multi-omics profiling have created new opportunities to improve cancer risk prediction, yet translation to large-scale population studies remains limited by data heterogeneity, batch effects, missing modalities, and a lack of uncertainty-aware modeling. In this talk, Dr. Mallick will discuss emerging multimodal AI frameworks for integrating and harmonizing microbiome multi-omics data across studies, assays, and populations, with a focus on feasibility for epidemiological research.
Biography: Himel Mallick, PhD, is a tenure-track Assistant Professor of Population Health Sciences and an adjunct faculty member of Statistics and Data Science and Gastroenterology and Hepatology at Cornell University. Prior to joining Cornell, Dr. Mallick was an Associate Director at Merck Research Laboratories and a postdoctoral fellow at Harvard University and the Broad Institute. He previously served as the primary statistician for the Integrated Human Microbiome Project (iHMP), published in Nature in 2019. He is the developer of several bioBakery tools, including MelonnPan and MaAsLin2, which are widely used in microbiome data analysis. Dr. Mallick has authored multiple book chapters on microbiome multi-omics integration, including Metagenomics for Microbiology, and co-authored Orchestrating Microbiome Analysis, a widely adopted community resource outlining best practices for microbiome research. He is the recipient of multiple early-career awards in statistics and data science and is a Fellow of the American Statistical Association and an Elected Member of the International Statistical Institute.
Talk 2: Artificial Intelligence for Dynamic Cancer Risk Prediction and Personalized Survivorship Care

Yufen Lin, PhD
View Abstract & Bio
Abstract: Emerging artificial intelligence (AI) technologies offer unprecedented opportunities to enhance cancer epidemiology by enabling dynamic, scalable risk prediction and personalized survivorship care across large populations. Dr. Lin will present an integrated AI framework, spanning pre-treatment risk stratification to post-diagnosis survivorship management.
In head and neck cancer (HNC) patients undergoing radiotherapy, Dr. Lin’s research team developed and validated an AI system to predict post-radiotherapy epigenetic aging acceleration (EAA) using only pre-treatment sociodemographic, clinical, symptom, and immune biomarker data. Deep learning approaches, particularly TabNet, outperformed conventional algorithms (average RMSE 4.08 ± 0.32), with strongest performance immediately post-treatment (Time 2 RMSE 4.87). Baseline immune markers, including absolute eosinophil count and hemoglobin levels, consistently predicted longitudinal EAA trajectories. Importantly, this approach enables identification of high-risk patients without costly epigenetic assays, demonstrating feasibility for large-scale population implementation.
Building on this predictive infrastructure, Dr. Lin’s research team is developing AI-enabled digital survivorship platforms (e.g., CancerCompanion, DietAI24) that leverage large language models, reinforcement learning, and just-in-time adaptive interventions (JITAI) to dynamically monitor diet, physical activity, and symptoms in real time. These platforms function not only as interventions but also as scalable digital cohort infrastructures, generating high-frequency longitudinal data that continuously refine risk prediction models and enable adaptive, personalized care.
Collectively, this integrated AI paradigm supports a shift from static risk estimation to dynamic, population-scale cancer trajectory modeling. By combining pre-treatment biological risk prediction with post-treatment digital phenotyping and intervention, AI has the potential to enhance precision cancer epidemiology, improve early identification of vulnerable populations, and facilitate cost-effective, equitable implementation across diverse clinical settings.
Biography: Yufen Lin, PhD, is an Assistant Professor at Emory University's Nell Hodgson Woodruff School of Nursing and a member of the Cancer Prevention and Control Research Program at the Winship Cancer Institute. She completed her postdoctoral fellowship at Emory School of Nursing and earned her PhD in Nursing from Duke University. Her research interests focus on cancer symptom science and management, innovative interventions, -omics science, and health equity. Her current research program centers on two main themes: (i) developing and evaluating technology- and AI-based interventions to improve health outcomes for cancer patients and their family caregivers through a lens of health equity; and (ii) investigating the biological mechanisms underlying cancer-related aging outcomes using AI-powered multi-omics approaches. Dr. Lin’s research has been supported by multiple organizations, including the National Institutes of Health, the American Cancer Society, the Oncology Nursing Foundation, and intramural funding sources. Her honors include the Distinguished Dissertation Award from Duke University, the Early-Stage Investigator Fellowship from NRG Oncology, and the Rising Star Award from Sigma Theta Tau International Honor Society of Nursing.
Talk 3: Generative AI for Predicting Cancer Outcomes Using Multi-omic Data

Anai N. Kothari, MD, MS
View Abstract & Bio
Abstract: Advances in multi-omics have provided new sources of data to characterize tumor biology, but translating these data into accurate, population-scale outcome predictions is a major challenge. Generative artificial intelligence (AI) offers a promising paradigm shift. By learning latent representations across heterogeneous data modalities (including genomic, transcriptomic, and clinical data), emerging models may better capture complex disease patterns to enhance prognostic modeling beyond traditional approaches. This presentation will provide an overview of the role of generative AI in predicting cancer outcomes, including reviewing key considerations for scaling and implementation, such as harmonizing multi-omic data, computational infrastructure requirements, interpretability, and governance needed for responsible implementation. Drawing on real-world efforts to integrate molecular and clinical data at scale, this talk will highlight practical pathways and current limitations.
Biography: Anai N. Kothari, MD, MS, is an Assistant Professor in the Division of Surgical Oncology, Department of Surgery, at the Medical College of Wisconsin. He holds additional faculty appointments in the Clinical & Translational Science Institute of Southeast WI (CTSI) and the MCW Data Science Institute. Dr. Kothari grew up in Manitowoc, Wisc., and received his BS and MD at the University of Wisconsin-Madison. Dr. Kothari completed his General Surgery training at Loyola University Medical Center, where he also earned a master’s degree in Epidemiology, followed by a fellowship in Complex General Surgical Oncology at the University of Texas MD Anderson Cancer Center. Dr. Kothari’s clinical expertise is the surgical treatment of upper gastrointestinal tract and advanced cancers of the GI tract, including the use of advanced techniques such as minimally invasive and robot-assisted surgery.
Moderators:
Ramona Gianina Dumitrescu, PhD, NIH Center for Scientific Review | Neeraj Saxena, PhD, NCI Division of Cancer Prevention
Talk 4: 3’ End Modification: A Personalized Index of MicroRNA Dynamics

Seyedtaghi (Shervin) Takyar, PhD
View Abstract & Bio
Abstract: MicroRNAs (miRNAs) control gene expression through robust regulatory networks. The mode of regulation through miRNAs, their cross talk with other noncoding RNAs, and their utility as biomarkers of specific cellular functions have been well described. However, the regulatory processes controlling the fate of microRNAs themselves are not well known.
MiRNAs are produced through several biogenesis steps and loaded onto Argonaut (Ago) proteins to form miRNA-induced silencing complexes (miRISC). Each of these steps can be regulated by feedback loops. However, mature miRNAs, the final effective form of miRNAs, are also under strict regulatory control. A group of cellular enzymes modify and degrade the 3’ end of the mature miRNAs in miRISC, fine-tuning miRNAs at their site of action. This process produces tell-tale 3’ miRNA isoforms (isomiRs) that can be quantified and used to monitor the activity of specific molecular pathways within the cells.
Dr. Takyar’s research team has recently shown that VEGF specifically degrades mature miR-1 in the lung endothelial cells. This degradation is necessary and sufficient for angiogenic activation in lung adenocarcinoma (LUAD). They have now found that MiR-1 degradation is mediated by unique 3’ modification enzymes and produces specific 3’ isomiRs. The level of these enzymes and their catalytic products (3’ isomiRs) can be quantified in tumors and used as a personalized measure of miRNA status and angiogenic activation in LUAD patients.
Biography: The overall goal of the research program of Seyedtaghi (Shervin) Takyar, PhD, is to determine the role of endothelial gene regulation in lung pathologies, with an emphasis on cancer. Dr. Takyar’s background is in basic molecular biology and RNA biochemistry. Through Dr. Takyar’s PhD and postdoctoral training, he took part in a wide variety of molecular investigations, from cloning and optimization of gene therapy vectors to mechanistic aspects of hepatitis C virus propagation, and finally the structural basis of ribosomal translation. During his residency and clinical fellowship, he became interested in the molecular aspects of lung inflammation. However, he chose to focus on the less explored role of endothelium in the inflammatory cascade. These investigations led to his work on VEGF-mediated microRNA regulation and angiogenic activation. Together with his group at Yale, Dr. Takyar devised models and methods to specifically probe the endothelial miRNAs. At the same time, he started collaborative projects to investigate the translational aspects of these regulations in lung cancer patients.
Dr. Takyar’s team is now exploring the modes of non-coding RNA regulation in the lung, with a specific focus on smoking and lung adenocarcinoma. In their miRNA studies, they are dissecting the molecular machinery that tailors the prevalence of miRNAs to the activation status of the endothelial cells.
Talk 5: Rhythmic QTLs Link Circadian Regulation to Cancer Risk

Dongyin Guan, PhD
View Abstract & Bio
Abstract: The circadian system regulates 24-hour physiological rhythms that shape metabolism and influence disease risk. Genetic and lifestyle-driven variation in circadian rhythms contributes to cancer development and progression, creating opportunities for circadian medicine to optimize disease diagnosis and treatment timing. By incorporating time-dependent strategies into clinical practice, circadian medicine has the potential to reduce medication burden, enhance therapeutic efficacy, and improve diagnostic accuracy and specificity. However, how individual genetic variation modulates 24-hour rhythmic processes and contributes to cancer risk remains largely unexplored. In this presentation, Dr. Guan will describe approaches for studying circadian rhythms in human peripheral tissues and introduce a newly defined class of molecular quantitative trait loci, termed rhythmic QTLs, which regulate interindividual variation in rhythmic gene expression. Dr. Guan will further discuss the underlying molecular mechanisms, their contributions to human disease risk and complex traits, and the potential applications of rhythmic QTLs in cancer diagnosis, prognosis, and precision medicine.
Biography: Dr. Dongyin Guan received his PhD from Case Western Reserve University and completed his postdoctoral training in Dr. Mitchell A. Lazar’s laboratory at the University of Pennsylvania. During this time, he employed genome-wide circadian enhancer mapping to identify transcriptional regulatory networks that control circadian rhythm remodeling in response to overnutrition. He demonstrated that targeting the key regulatory transcription factor PPARα at specific times of day improves drug efficacy, providing a preclinical proof of concept for circadian medicine. He also adapted single-cell RNA sequencing approaches and performed the first single-nucleus RNA-seq study in the liver, leading to the discovery of intrahepatic clock communication.
Dr. Guan is currently an Assistant Professor of Medicine at Baylor College of Medicine. His laboratory recently defined, for the first time, how genetic variants influence circadian rhythms across human tissues and elucidated how interactions between genetic variation and overnutrition regulate circadian rhythms. The overarching goal of his research program is to dissect gene-environment interactions that govern circadian physiology and to leverage this knowledge to develop circadian medicine strategies and personalized nutritional interventions based on individual genetic backgrounds. His research has been supported by an NIH R37 MERIT Award, CPRIT, and V Scholar Awards. He is also active in the scientific community, serving as a reviewer for journals including Science, Cell Metabolism, and Nature Metabolism, as well as on NIH study sections.
Talk 6: The Role of NIST Reference Materials in Harmonizing Large-Scale Metabolomics Studies

Sandra Da Silva, PhD
View Abstract & Bio
Abstract: As gut metabolomics transitions into large-scale population studies, the field faces significant challenges regarding data reproducibility and the lack of an established "ground truth." In this presentation, Dr. Da Silva will discuss the crucial role of the new NIST Human Fecal Material (RM 8048) and the Fecal Metabolites Calibrant Solution (RGTM 10212) in addressing the reproducibility challenges in gut metabolomics. She will share insights from recent interlaboratory studies and demonstrate how these standards contribute to the harmonization of molecular technologies for large-scale population studies. Additionally, Dr. Da Silva will present 13-month stability data at -80 °C and homogeneity assessments to confirm that these materials are fit-for-purpose for long-term research studies. By identifying sources of measurement variability and bias, these standards provide a collaborative framework to advance global data comparability.
Biography: Sandra M. Da Silva, PhD, is a Research Chemist at NIST within the Material Measurement Laboratory, where she leads the NIST RM 8048 Metabolomics Efforts. RM 8048 is a human fecal reference material designed to aid the gut metagenomics and metabolomics communities. Dr. Da Silva’s work focuses on developing methods and reference materials for microbial characterization to support stakeholders in various fields where microbes are significant, such as live biotherapeutics and human health. The goal of her research is to enhance measurement confidence in microbial metrology by developing standardized measurement tools and facilitating large-scale interlaboratory studies to improve data harmonization across different analytical platforms.
Moderators:
Anil Wali, PhD, NCI Center to Reduce Cancer Health Disparities | Gabriela Riscuta, PhD, NCI Division of Cancer Prevention
Talk 7: Use of Aging Measures in Hematological Malignancy Research

Vijaya Raj Bhatt, MBBS, MS
View Abstact & Bio
Abstract: This talk will discuss measures of aging that can be applied in clinical research in patients with hematological malignancies. The measures expand from traditional functional and frailty measures to newer measures of cognitive impairment, such as event-related potentials, and blood-based biological measures of aging. The goal of this presentation is to provide real examples of application of such tools in clinical research.
Biography: Vijaya Raj Bhatt, MBBS, MS, is a Professor, Section Leader of the Malignant Hematology Section, and Medical Director of the Leukemia Program in the UNMC Division of Hematology, Department of Internal Medicine. Dr. Bhatt is board certified in Internal Medicine, Hematology, and Oncology. He has also completed a Master of Science in Clinical and Translational Research. Dr. Bhatt manages patients with acute leukemia, myeloid malignancies and other hematologic disorders, and those who have undergone hematopoietic stem cell transplants. He finds great joy in interacting with his patients and working in a multidisciplinary team to support patients through the course of their treatment. Dr. Bhatt has authored or co-authored more than 240 articles and has presented widely at several national meetings of professional societies.
Talk 8: Bridging the Efficacy-Effectiveness Gap: Cancer Control Research Through the Lens of Economics in an AI-Powered Era

Yilu (Bill) Dong, PhD
View Abstract & Bio
Abstract: While breakthrough innovations continue to emerge in cancer care, significant economic and logistical barriers often prevent the success of clinical trials from achieving their intended impact in real-world settings. Dr. Dong offers an economic perspective on cancer control research, focusing on the frictions of transitioning innovative but expensive treatments from controlled trials to the real world—a shift that often creates a gap between trial efficacy and real-world effectiveness. He will highlight the research implications of this transition, including the incorporation of long-term value evaluations and the necessity of using advanced quasi-experimental designs to mitigate confounding bias in observational research. Finally, he will discuss additional opportunities to improve cancer control, such as leveraging AI-powered clinical data infrastructure to advance precision oncology and addressing the discordance in treatment preferences between stakeholders that can affect optimal treatment selection and the long-term trajectory of disease management.
Biography: Dr. Yilu Dong earned his PhD in Economics from the University of South Florida in 2020, specializing in Health Economics, Behavioral Economics, and Industrial Organization. Currently, he is a faculty member at the Medical College of Wisconsin. Dr. Dong’s research leverages advanced quasi-experimental designs to rigorously evaluate the effectiveness and value of care in real-world clinical settings. Furthermore, he utilizes discrete choice experiments to elicit the preferences and trade-offs driving patient and provider decision-making under uncertainty. His work also extends to systemwide clinical data capture and management.
Talk 9: GeoAI-Based Zoning Strategies to Enhance Sub-County Cancer Surveillance

Gabriel A. Benavidez, PhD, MPH
View Abstract & Bio
Abstract: County boundaries remain the dominant unit for cancer surveillance in the United States, but they often fail to reflect meaningful geographic variation in cancer burden; particularly, in a state as large and heterogeneous as Texas. In rural counties, small populations and low case counts frequently trigger data suppression, limiting visibility into local trends. In large urban counties, aggregated reporting can conceal high-burden neighborhoods within a single county estimate. Together, these limitations constrain the ability of public health agencies to identify, monitor, and respond to inequities in cancer outcomes. This challenge is especially consequential for breast, colorectal, and lung cancers, which together account for a substantial share of cancer incidence and mortality in Texas.
Biography: Gabriel Benavidez, MPH, PhD, is an epidemiologist and Assistant Professor in the Department of Public Health at Baylor University. He received his MPH from Baylor in 2019 and his PhD from the Arnold School of Public Health at the University of South Carolina in 2023. Dr. Benavidez is also an alumnus of the Robert Wood Johnson Foundation-funded Health Policy Research Scholars fellowship. He joined Baylor University in 2023.
Dr. Benavidez’s research examines disparities in access to health care services among socially disadvantaged populations (i.e., racial and ethnic minorities, persons of low socioeconomic status, and rural populations). Specifically, his work employs traditional and spatial epidemiologic methods to identify specific populations or geographic areas lacking access to critical health care services. Additionally, his work aims to examine how lack of access to health care services impacts the burden of cancer morbidity and mortality among socially disadvantaged populations.