Early Career Investigators
Rebecca C. Arend, MD
Assistant Professor, Gynecologic Oncology, UAB Comprehensive Cancer Center
Education: MD, Albert Einstein, New York, NY
OBGYN residency: Columbia Presbyterian, New York, NY
Gynecologic oncology fellowship: University of Alabama, Birmingham, AL
More information: https://providerdirectory.uabmedicine.org/provider/Rebecca++Arend/573564
The overarching goals of my research are to understand tumor immune response to alterations in specific molecular pathways both in the tumor and in the tumor microenvironment. My basic and clinical research interests are focused on development of novel combination therapeutic approaches using targeted therapy, immunotherapy, and chemotherapy for treatment of patients with ovarian cancer. Specifically, I’m focusing on overcoming immune evasion by targeting the WNT pathway and ways to prime the immune systemic to change a “cold” tumor into a “hot” tumor so that they are more responsive to immunotherapy. Using syngeneic ovarian cancer mouse models, I am exploring sequencing and timing of therapy and investigating the specific effects on the microenvironment and specific subsets of immune cells. In addition, I am using human samples and genomics to better understand the relationship between Tumor Infiltrating Lymphocytes (TILs) to T regulatory cell ratios and gene expression in Homologous Recombination Deficiency and other conical cancer pathways.
Salvatore Condello, PhD
Assistant Professor, Department of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IN
Education: Ph.D., Cellular and Molecular Biology, University of Messina, Italy
Postdoc: Department of Obstetrics and Gynecology, Indiana University School of Medicine, Indianapolis, IN
My ongoing research aims at understanding the intersection between tissue transglutaminase, a multifunctional protein highly expressed in ovarian tumors, and the oncogenic Wnt/beta-catenin pathway in promoting the cancer stem cell phenotype, which has been associated with the clinically relevant problem of platinum resistance in ovarian cancer. My research program interrogates several ovarian cancer cell lines, primary cells, cancer stem-like cells, and animal models to address the importance of various signaling pathways and metabolic pattern alterations in this inherently heterogeneous disease with the ultimate goal to find new functional target genes and test novel therapeutics.
Juan R. Cubillos-Ruiz, PhD
Assistant Professor of Immunology in Obstetrics & Gynecology
Member, Sandra and Edward Meyer Cancer Center
Weill Cornell Medical College
Education: Ph.D.: Tumor Immunology, Geisel School of Medicine at Dartmouth.
Post-doc: Harvard School of Public Health and Weill Cornell Medical College.
More information: http://vivo.med.cornell.edu/display/cwid-jur2016
My research integrates immunology, cancer biology, genetics and nanotechnology to understand and disable the mechanisms that ovarian cancers use to paralyze and manipulate the protective function of immune cells. We currently focus on characterizing the role of abnormal stress responses in tumor-infiltrating immune cells, and we seek to exploit this knowledge for devising the next generation of targeted immunotherapies for ovarian cancer.
Sophia HL George, PhD
Assistant Professor, Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Sylvester Comprehensive Cancer Center, Miller School of Medicine, University of Miami
Education: PhD, Molecular Genetics, University of Toronto, Ontario, Canada
Postdoc: Princess Margaret Cancer Center, Ontario, Canada and Duke University, Durham, NC
The George lab studies Hereditary Breast and Ovarian Cancer syndrome, with the goal of understanding the effects of inherited genetic mutations on the fallopian tube epithelia and their involvement in the development of high-grade serous ovarian cancer. We hope to characterize the functional interplay between DNA damage response genes and antioxidant systems in early events in the fallopian tube epithelia as it is important to both prevention and chemotherapy resistance. Understanding the mechanisms that preneoplastic fallopian tube epithelia and ovarian cancer cells employ to circumvent oxidative stress and drive tumorigenesis will improve our ability to prevent and supplement treatment modalities.
Neil Johnson, PhD
Assistant Professor Fox Chase Cancer Center
Education: BSc, Genetics and Biochemistry, Newcastle University, Newcastle upon Tyne, UK, 2002
PhD, Cancer Biology and Therapeutics, Newcastle University, Newcastle upon Tyne, UK, 2006
Postdoctoral training, Dana-Farber Cancer Institute, Geoffrey Shapiro mentor, 2006-20013
More information: https://www.foxchase.org/neil-johnson
Our research involves investigating factors that enable cancer cells containing BRCA mutations to carry out homologous recombination DNA repair and survive DNA damaging agent chemotherapy. Several factors may contribute to homologous recombination DNA repair proficiency in BRCA mutant tumors. We are examining the ability of mutant BRCA1 proteins to contribute to homologous recombination in cancer cells.
John B. Liao, MD, PhD
Associated Professor. Division of Gynecologic Oncology, Department of Obstetrics and Gynecology. University of Washington School of Medicine, Seattle, WA
Education: PhD, Yale university, MD, George Washington University, Fellowship in Gynecologic Oncology, University of Pennsylvania
More information: https://www.uwmedicine.org/bios/john-liao
Clinical trials of immune therapies, translational research and modeling of immune responses to ovarian cancer
Karen McLean, MD, PhD
Assistant Professor, Gynecologic Oncology, University of Michigan Medical Center
Education: MD and PhD, Cellular and Molecular Biology, University of Michigan Medical Center, Ann Arbor, MI; Residency in Obstetrics and Gynecology and Fellowship in Gynecologic Oncology, University of Michigan Medical Center, Ann Arbor, MI.
More information: https://www.uofmhealth.org/profile/2581/karen-mclean-md-phd
My research laboratory performs translational research characterizing the role of the tumor microenvironment on ovarian cancer growth, with the goal of identifying new targets for treatment for women with this disease. Specific areas of focus include defining and inhibiting growth-promoting signals from microenvironment mesenchymal stem cells to the cancer cells as well as the interaction between these signals and estrogen signaling.
Geeta Mehta, PhD
Assistant Professor, Department of Materials Science and Engineering, Department of Biomedical Engineering, University of Michigan
Education: PhD, Biomedical Engineering, University of Michigan, Ann Arbor, MI
Postdoc, Biological Engineering, MIT, Cambridge, MA
More information: https://macro.engin.umich.edu/profile/geeta-mehta/
The ultimate goal the research being conducted in my lab is to develop novel therapeutics to increase cancer cure rates for ovarian cancers and decrease patient suffering. My lab is dedicated to understanding how intercellular interactions and mechanical stimulation within the tumor microenvironment, impact cellular phenotypes in carcinogenesis, by creating and utilizing specific engineered microenvironments To enable this goal, we have created a 3D physiologically relevant high throughput multicellular spheroid model of ovarian cancers. Our in vitro and in vivo models not only advance fundamental biological studies, such as, recurrence of tumor after primary chemotherapy, but are also applied towards finding novel and more efficient drugs against ovarian cancer.
Anirban K. Mitra, PhD
Assistant Professor of Medical and Molecular Genetics, Medical Sciences Program Indiana University School of Medicine
Associate Member Indiana University Melvin and Bren Simon Cancer Center
Education: Post-Doctoral Fellowship University of Chicago, Chicago, IL
Ph.D. University of Mumbai, Mumbai, India
My laboratory seeks to understand the paracrine and juxtacrine interactions between cancer cells and their microenvironment that regulate metastatic colonization in ovarian cancer. We are using in vitro organotypic 3D culture models, live 3D time-lapse microscopy and mouse xenograft models of metastasis along with cell and molecular biological approaches to study the reciprocal interactions between the metastasizing cancer cells with their microenvironment at the site of metastasis. We are specifically interested in the regulation of key microRNAs and transcription factors by these paracrine/juxtacrine interactions and the mechanism by which they drive metastatic colonization in ovarian cancer.
David Pépin, PhD
Assistant Professor, department Surgery, Massachusetts General Hospital, Harvard Medical School, Pediatric Surgical Research Laboratories.
Education: Post-doctoral fellowship: Massachusetts General Hospital, Harvard Medical School, Boston.
Doctorate: University of Ottawa, Canada.
My laboratory studies the role of Mullerian Inhibiting Substance in female reproductive development and its application in the treatment of ovarian cancer. We are pursuing translational aspects of those discoveries such as single-cell transcriptomics and gene editing screens to identify synthetic lethality in chemoresistant ovarian cancer, and rapid target validation using viral and nanoparticle-based gene therapies in patient-derived xenografts.
Erinn Rankin, PhD
Assistant Professor, Department of Radiation Oncology, Department of Obstetrics and Gynecology, Stanford University
Education: PhD, Cellular and Molecular Biology, University of Pennsylvania, Philadelphia, PA
Postdoc, Radiation Oncology, Stanford University, Stanford, CA
More information: https://profiles.stanford.edu/erinn-rankin
The tumor microenvironment plays a key role in promoting tumor progression, metastasis, and resistance to therapy. Hypoxia, or low oxygen tensions, is a hallmark feature of the tumor microenvironment that plays a central role in tumor initiation and progression. Clinically, hypoxia and activation of hypoxic signaling is associated with poor patient survival, metastasis, and drug resistance. The Rankin Lab studies the cellular and molecular mechanisms by which hypoxia promotes tumor progression, metastasis and drug resistance with the goal of developing novel therapeutic strategies for the treatment of cancer.
Jogender Tushir-Singh, PhD
Assistant Professor of Biochemistry and Molecular Genetics, Member, Emily Couric Cancer Center, University of Virginia School of Medicine, Charlottesville VA
Education: Ph.D. Cell and Molecular Biology, University Notre Dame, Notre Dame IN
Post Doctoral Studies: University of Massachusetts Medical School, Worcester MA
More information: https://med.virginia.edu/faculty/faculty-listing/js2yr/
I am a rare early stage academic investigator who knows what it takes to translate research into the clinic due to both basic and industrial training. The overarching goals of my research are to investigate molecular mechanism of ovarian cancer and rationally apply antibody engineering based strategies for therapeutic targeting. We are particularly interested in dual-specificity antibodies, antibody conjugates and chimeric receptors. Current projects in my laboratory are focused on Bispecific Anchored Cytotoxic Activator strategy and CAR-NK cells against ovarian cancer overexpressed receptors. We currently focus on characterizing, comparing and combining both immune-dependent (Cancer Immunotherapy) and immune-independent strategies for effective ovarian cancer targeting. Additional projects are planned towards combinatorial ways to overcome clinical resistance to ovarian cancer therapies.
Rachel I. Vogel, PhD
Assistant Professor, Department of Obstetrics, Gynecology, and Women's Health, Medical School
University of Minnesota
Education: M.S.: Biostatistics and Ph.D., Epidemiology. University of Minnesota School of Public Health
More information: https://med.umn.edu/bio/obgyn-faculty/rachel-isaksson%20vogel
My research focuses on cancer survivors with the end goal of maximizing survivors' quality of life and outcomes. As the number of cancer survivors increases, the long-term effects of the disease and treatment have become a substantial public health concern. The goal of this funded research is to determine whether CMV (cytomegalovirus) reactivation in the presence of high inflammation contributes to patient-reported fatigue and negatively affects cancer prognosis among women with ovarian cancer.
Wa Xian, PhD
Assistant Professor, Center for Stem Cell Biology and Regenerative Medicine, Institute of Molecular Medicine, University of Texas Health Sciences Center, Houston, TX
Education: PhD, MD Anderson Cancer Center/ University of Texas (Molecular Genetics), Postdoctoral training at the Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA
My laboratory addresses the problem of intratumor heterogeneity and chemotherapy resistance in high-grade ovarian cancer by developing technologies for generating patient-specific libraries of cancer stem cells (CSCs). Individual CSCs share 80% of the copy number variation with all other clones in the library, and each can generate tumors in immunodeficient mice with histology identical to the patient’s resected tumor. Our findings to date show that these libraries contain clones that are highly resistant to standard of care chemotherapeutics. We are examining the possibility that these resistant clones mirror those responsible for recurrent disease and that these clones are reliable surrogates for identifying appropriate therapeutics for their elimination.
Yang Yang-Hartwich, PhD
Assistant Professor, Department of Obstetrics, Gynecology, and Reproductive Sciences School of Medicine Yale University
Education: Ph.D., Microbiology, Nankai University, China.
Postdoctoral training, Tumor Biology, Yale University.
More information: https://medicine.yale.edu/profile/yang_yang/
My research interest focuses on the origin of ovarian cancer. We use cell and animal models to investigate the molecular mechanisms underlying the initiation of ovarian cancer. Currently my lab is working on understanding the influence of ovulation-associated factors at the early stage of ovarian cancer initiation. Furthermore, we also investigate the role of menopause in the development of ovarian cancer at cellular and molecular levels. Our goal is to discover new early detection markers and therapeutic targets in order to improve the survival rate of ovarian cancer patients.
Dmitriy Zamarin, MD, PhD
Assistant Attending Physician, Gynecologic Medical Oncology and Immunotherapeutics, Memorial Sloan Kettering Cancer Center
Education: MD/PhD, Mount Sinai School of Medicine, New York, NY
Internal medicine residency: Mount Sinai Hospital, New York, NY
Medical oncology fellowship: Memorial Sloan Kettering Cancer Center, New York, NY
My basic and clinical research interests are focused on development of novel immunotherapies using locoregional and systemic approaches for treatment of patients with ovarian cancer. Specifically, I’m focusing on oncolytic viruses, a novel class of immune therapeutics that can activate anti-tumor immunity through multiple mechanisms. By studying the interaction of genetically engineered oncolytic viruses with the tumor microenvironment in mouse tumor models, the goals of my research are to identify pathways of immune response and adaptive immune resistance and to develop novel therapeutic combinations targeting these pathways directly within the tumor and systemically.