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Rong Li Chair, Department of Biochemistry & Molecular Medicine Ross Professor of Basic Science Research Professor
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Breast cancer susceptibility gene BRCA1; Tumor microenvironment; mechanisms of anti-cancer therapies. Lab Website: https://lilab.smhs.gwu.edu/publications Office Location: Ross Hall 433 Email: rli69 [at] gwu [dot] edu (rli69[at]gwu[dot]edu)
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- Research Interest:
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At the Horvath Lab, We develop computational methods to analyze genetic and regulatory variation at single-cell resolution. Using short- and long-read single-cell RNA sequencing, we quantify expressed mutations, isoform diversity, and allele-specific expression to reveal coordinated, state-dependent regulatory programs within individual cells. We build software platforms-including scExecute, scReadCounts, and scSNViz and develop isoform- and variant-aware machine learning models that link genetic variation to cellular identity, evolution, and therapeutic response. Our work provides a systems-level framework for understanding tumor heterogeneity and advancing precision medicine. Lab Website: https://horvathlab.smhs.gwu.edu Office location: Ross Hall 731B Email:horvatha [at] gwu [dot] edu (horvatha[at]gwu[dot]edu)
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Jiyoung Lee
Assistant Professor Co-Director of Cancer Biology PhD Program, Integrated Biomedical Sciences
- Research Interest:
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Cancer metastasis and metabolism, Molecular signaling of breast and head and neck cancer. Lab Website: https://leelab.smhs.gwu.eduOffice location: Ross Hall 437A Email: jiyounglee [at] gwu [dot] edu (jiyounglee[at]gwu[dot]edu)
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- Research Interest:
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The Mazumder Research Group develops high-performance computational tools for bioinformatics research and communication. The group builds and maintains the HIVE platform in collaboration with the FDA and develops standards for bioinformatics communication through BioCompute Objects. Its work also includes the creation and curation of knowledge bases for glycoinformatics (GlyGen), cancer research (BiomarkerKB, OncoMX, BioMuta, BioXpress), and microbiome analysis. The group leverages knowledge graphs and machine learning and artificial intelligence technologies, including large language models, to harmonize, map, and extract insights from clinical data, omics datasets, knowledgebases, and scientific publications.
Lab Website: https://hivelab.smhs.gwu.edu/ Email: mazumder [at] gwu [dot] edu (mazumder[at]gwu[dot]edu) Office location: Ross Hall, Room 431
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Luis Rodriguez Assistant Professor
- Research Interest:
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The lab has a deep interest in understanding the fundamental biology that underlies the pulmonary wound response throughout our lifespan. We ask this question using mouse injury models, innovative in-vitro models, primary human samples, and through collaborations across the country with labs that have unique and complementary models of injury. Our focus starts with the alveolar epithelium as the site of gas exchange and a point of vulnerability for recurring injury. We also consider a number of factors such as intrinsic epithelial dysfunction, external stressors, and aging, which may disrupt the normal wound healing process. Modeling these factors in our murine models allows us to capitalize on powerful genetic tools developed to study lung disease. We then perform careful reductionist biology using our in-vitro models to interrogate mechanisms. Finally, we take the hypotheses and mechanisms generated in our models and test them in human-derived systems, including organoid platforms or collaboratively with groups that have complementary human models such as precision cut lung slices or induced pluripotent stem cell-derived epithelial cells. Our goal is to help understand the pathology that occurs in human pulmonary disease to identify new therapeutic targets for acute lung injury and chronic pulmonary disease. Lab Website: https://rodriguezlab.smhs.gwu.edu Office location: Ross Hall 447 Email: luis [dot] rodriguez [at] email [dot] gwu [dot] edu (luis[dot]rodriguez[at]email[dot]gwu[dot]edu)
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Edward Seto Professor King Fahd Professor of Cancer Biology
- Research Interest:
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The Seto Lab has a long-standing interest in gene regulation and histone deacetylases (HDACs). Early on, we discovered and cloned HDAC2 and HDAC3 enzymes and performed detailed analyses of these proteins. Over the last 25 years, we have been actively studying many different aspects of histone deacetylation, including the dissection of all 18 human HDACs. Our work has led to seminal discoveries regarding regulation of histone deacetylation and identification of key non-histone targets of the HDAC enzymes. More recently, our work has extended to the analysis of how the activities/functions of histone acetyltransferases (HATs) and HDACs are interrelated, elucidating the role of HDACs in anti-tumor immunity, and identifying HDAC-specific inhibitors for disease treatments.
Lab Website: https://setolab.smhs.gwu.edu Office location: SEH 8800 Email: seto [at] gwu [dot] edu (seto[at]gwu[dot]edu)
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Brett Shook Associate Professor
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Altered immune responses are central to tissue dysfunction and impaired healing. The Shook Lab combines modern wet- and dry-lab technologies to investigate mechanisms that regulate the immune response during skin wound healing. In particular, we are interested in cellular communication between stromal and immune cells. By investigating the intersection of inflammation and tissue repair using animal and human models, we aim to give translational value to basic science discoveries. Lab Website: https://shooklab.smhs.gwu.edu Office location: Ross Hall 437A Email: brettshook [at] gwu [dot] edu (brettshook[at]gwu[dot]edu)
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Ray-Chang Wu Professor
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My reseach focuses on understanding the biological functions of transcriptional co-regulators AT-rich interaction protein 4B (ARID4B, also known as retinoblastoma binding protein 1-like 1, RBPL1). Using integrative, synergistic approaches, novel conditional Arid4b knockout and ARID4B knockin mouse models and other genetically modified mouse models, the objective and long-term goal of my research program are to: (1) dissect the emerging oncogenic function of ARID4B in the development and progression of breast and prostate cancers, (2) conform the role of ARID4B in therapy resistance, (3) elucidate the underlying molecular mechanism by which ARID4B drives cancer development ad progression to therapy resistance, (4) validate ARID4B pathway is a new therapeutic target in cancers, and (5) develop the first-in-class small molecule inhibitors of the ARID4B pathway toward pharmacological inhibition of ARID4B for treatment of cancers. Identification of ARID4B as a new component critical oncogenic signaling, coupled with comprehensive understanding into its functional mechanism, and development of the first-in-class ARID4B inhibitors will pave the way for better treatment for cancers. Our study has the potential to revolutionize treatment of cancers, impact treatment outcomes and the lives of cancer patients.
Lab location: Ross Hall 556 Office Location: Ross Hall 542 Lab Website: https://smhs.gwu.edu/faculty-research/ray-chang-wu-phd Email: rwu [at] email [dot] gwu [dot] edu (rwu[at]email[dot]gwu[dot]edu)
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Wenge Zhu Professor
- Research Interest:
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The Zhu lab focuses on DNA replication and DNA repair mechanisms, anti-cancer drug resistance, and therapeutic drug discovery across multiple cancer types, including breast, ovarian, skin, and colon cancers Lab Website: https://zhulab.smhs.gwu.edu Office location: SEH Suite 8870 Email: wz6812 [at] gwu [dot] edu (wz6812[at]gwu[dot]edu)
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