Cancer Biology Faculty
Mark G. Alexandrow, PhD – Associate Member
The Alexandrow Lab studies the mechanisms involved in the assembly and activation of the replicative CMG helicase, how deregulation of this process promotes tumorigenesis, and how the CMG helicase offers innovative targeting for chemotherapeutic drug development.
Srikumar P. Chellappan, PhD – Department Chair, Senior Member
The major research interest is to understand the mechanisms by which extra-cellular signals regulate the cell cycle machinery and how a loss of this regulation leads to oncogenesis. We focus on regulatory pathways that promote tumor growth, angiogenesis and metastasis and how they can be targeted for drug discovery.
Jiandong Chen, PhD – Senior Member
The Chen Lab investigates the function, regulation, and therapeutic targeting of the p53 tumor suppressor pathway.
Y. Ann Chen, PhD - Associate Member
Dr. Chen’s research has been focused on developing statistical methods and computational tools to incorporate multiple omics sources, select biologically relevant markers, and predict clinical outcomes in a unified framework. Her work on Bayesian methodological development of data integration for regulatory network inference and pathway and gene selection for cancer survival prediction facilitates the identification of deregulated pathways with therapeutic relevance in subsets of human cancer.
John L. Cleveland, PhD – Division Chair, Senior Member
Major research interest in the molecular pathogenesis of cancer, interrogating the regulation and role of oncogenes and tumor suppressors in controlling cancer cell growth and survival, and in defining new targets that play essential roles in the development and maintenance of cancer.
W. Douglas Cress, PhD – Senior Member
The Cress Lab is interested in the molecular biology of lung adenocarcinoma.
Gina M. DeNicola, PhD - Assistant Member
Dr. DeNicola's research is focused on understanding how cells meet energetic and anabolic needs for growth and proliferation, and the mechanisms governing the regulation of tumor metabolism in vivo. The DeNicola laboratory investigates the influence of both genomic alterations and the microenvironment on cellular metabolism in vivo.
Elsa R. Flores, PhD – Department Chair and Senior Member
The Flores Lab utilizes mouse models to identify therapeutic vulnerabilities of the p53 pathway in cancer.
Robert J. Gillies, PhD – Department Chair
The work of Dr. Gillies focuses on: Define & characterize deregulated pathways with therapeutic relevance in subsets of human cancers. Work in this area has examined two different pathways: 1) cell surface proteins that can be targeted by imaging or therapy, and 2) energy metabolic pathways and their sequelae.
Anna R. Giuliano, PhD - Senior Member
Her work focuses on the relationship between human papillomavirus (HPV) infections and cervical cancer in women, which has evolved over the past several decades to encompass HPV and penile, anal, and oral cancers in men. Research includes the rate at which HPV infections are acquired and cleared, the proportion that progress to disease, and also to HPV vaccine protection against multiple diseases in women and men.
Eric B. Haura, MD – Senior Member
Our lab uses proteomic tools to characterize kinase pathways and networks in cancer cells to discover novel therapeutic strategies using kinase inhibitors.
Florian A. Karreth, PhD – Assistant Member
The Karreth Lab creates mouse models to elucidate the functions of cancer-associated proteins and non-coding RNAs in melanoma and ovarian cancer.
Eric K. Lau, PhD – Assistant Member
The Lau laboratory studies how the modification of cellular proteins by the dietary sugar L-fucose (a.k.a., fucosylation) regulates signaling and cell:cell interactions. Active investigations currently include how specific fucosylated proteins regulate (i) RNA biology and (ii) tumor:immune cell interactions and efficacy of immunotherapies in melanoma, and (iii) integrin signaling in breast cancer. Ultimately, our goal is to use our newfound knowledge to improve patient stratification and efficacy of therapeutic modalities.
Alan F. List, MD – Senior Member
Dr. List’s research purpose as a translational physician scientist and clinical investigator is to understand the biology and advance the development of novel therapeutics for acute myeloid leukemia (AML) and myelodysplastic syndromes (MDS).
Conor Lynch, PhD - Associate Member
The goal of our laboratory is to understand how metastatic prostate cancer cells interact with the bone microenvironment to establish and grow as secondary cancers using in vivo and in vitro techniques. The lab has made major inroads into defining how matrix metalloproteinases (MMPs) contribute the prostate cancer progression in bone.
Karen M. Mann, PhD – Assistant Member
The Karen Mann Lab aims to define and characterize cooperating molecular events driving cancer progression, metastasis and drug resistance, with a focus on pancreatic cancer and myeloid leukemia.
Michael B. Mann, PhD – Assistant Member
The Michael Mann Lab's research program is dedicated to discovering the genetic events that drive skin cancer evolution.
Andriy Marusyk, PhD - Assistant Member
Our mission is to understand the development of therapy resistance from eco-evolutionary angle, considering both changes occurring in tumor cells, as well as influences of tumor microenvironment. Then, we aim use this knowledge to design new therapeutic approaches, aimed at forestalling the ability of tumors to evolve resistance.
Alvaro Monteiro, PhD - Senior Member
The main theme of the Monteiro lab is the integration of epidemiological, genomic, and proteomics datasets to explore the role of genetic variation on cancer predisposition, development, and treatment.
Eric Padron, MD - Assistant Member
Our research interests focus on understanding the molecular and genetic pathway of chronic myelomonocytic leukemia to better design targeted agents for study in the clinic.
Jong Park, PhD – Senior Member
Dr. Park and his laboratory team are interested in genetic and epigenetic variations associated with prostate cancer recurrence. In addition, Dr. Park is also interested in health disparity on risk for prostate cancer, among African American men.
Gary W. Reuther, PhD – Associate Member
The Reuther Lab utilizes molecular, cellular, and genetic approaches to identify novel therapies that could improve the lives of patients with myeloproliferative neoplasms.
Kenneth H. Shain, MD, PhD - Assistant Member
Dr. Shain’s translational research has focused on the mechanisms by which components of the bone marrow microenvironment influence myeloma biology, survival, and drug response.
Keiran S. Smalley, PhD - Senior Member
The focus of the Smalley lab is upon melanoma, the deadliest form of skin cancer. We use advanced proteomics, single cell RNA-seq and mouse models to develop novel melanoma therapies which we then translate into the clinic. Current projects in the lab are focused upon immunotherapy/targeted therapy sequencing, melanoma brain metastases, acral melanoma and uveal melanoma.
Daniel Sullivan, MD – Senior Member
Dr. Sullivan’s laboratory is focused on defining the role of alterations in DNA topoisomerase I and II in drug resistance to inhibitors of these enzymes, more recently focusing on microenvironmental factors that modulate topoisomerase intracellular location in human myeloma and hence drug sensitivity.
Jamie Teer, PhD– Associate Member
Dr. Teer's research interests are focused on developing methods to analyze, interpret and visualize massively-parallel sequencing information in cancer genetics. This includes developing and applying computational methods and graphical tools to better detect genetic variations from sequencing data, understand the functional context of sequence changes, and visualize the results of large-scale genomics studies.
Kenneth Y. Tsai, MD, PhD – Associate Member
The Tsai Lab has the collective goals of identifying, testing, and validating novel targets for the targeted chemoprevention and treatment of skin cancer.
Lixin Wan, PhD – Assistant Member
The Wan Lab is dedicated to understanding how cancer cells hijack protein post-translational modification machinery to rewire the central signaling pathways for proliferation advantage and drug resistance.