DEPARTMENT OF PATHOLOGY

Gen-Sheng Feng, Ph.D.

Gen-Sheng Feng, M.D.

  • Professor
  • Ph.D. - Indiana University, 1990
  • Postdoctoral fellowship at the University of Toronto

Tel: (858) 822-5441   |   E-mail: gfeng@ucsd.edu

Research Interests

Molecular Signaling in Liver Cancer, Stem Cells and Metabolism

At the heart of cancer research is the elucidation of oncogenes and tumor suppressor genes (or anti-oncogenes), which has been a driving force in the cancer field for several decades. Most recent studies in this and other labs have revealed dual roles of genes in promoting and suppressing hepatocellular carcinoma (HCC). Deciphering the “paradoxical” effects of these genes may provide a fresh view on the fundamental mechanisms of carcinogenesis, which can lead to development of mechanism-based therapeutics for HCC. Our current focuses are on delineating genetic and epigenetic interactions and cell-cell communications that drive hepatocarcinogenesis. We are very interested in isolating and characterizing cancer stem cells, CSCs (or tumor-initiating cells, TICs) in the liver, and in dissecting the dynamic interplay between tumors and the hepatic microenvironment. Efforts are also being devoted to elucidation of metabolic changes in tumor cells and to search of biomarkers for early diagnosis of liver cancers.

We are also interested in deciphering the common and distinct biochemical pathways in self-renewal of hematopoietic stem cells (HSCs) and leukemia stem cells (LSCs), with the objective of understanding how an HSC pool is maintained throughout life, and with the ultimate goal of identifying novel targets for elimination of LSCs.

Another focus is on dissecting the signaling events involved in metabolic disorders such as obesity and diabetes. Ongoing experiments are aimed at understanding the intertwining of leptin and estrogen signaling cascades, to illustrate why estrogen has a leptin-like effect in control of metabolism, why postmenopausal women have the tendency to develop obesity, and why obesity promotes breast cancer. Whereas obesity has become a serious health problem in developed countries worldwide, one ongoing project in the lab is to investigate an indispensable physiological role of adipogenesis and adipose tissue in mammals, as revealed by the most recent data obtained in this lab.

Most Recent Publications

  1. Zhu HH, X Luo, K Zhang, J Cui, H Zhao, Z Ji, Z Zhou, J Yao, L Zeng, K Ji, WQ Gao, ZY Zhang, and GS Feng (2015). Shp2 and Pten have antagonistic roles in myeloproliferation but cooperate to promote erythropoiesis in mammals. Proc Natl Acad Sci USA112, 13342-7.
  2. Deng Z, S Ma, H Zhou, Aiping Zang, Y Fang, T Li, H Shi, M Liu, M Du, PR Taylor, HH Zhu, J Chen, G Meng, F Li, C Chen, Y Zhang, X Zhang, E Pearlman, X Li, GS Feng and H Xiao (2015). Tyrosine phosphatase SHP2 mediates Dectin-induced SYK activation and anti-fungal TH17 response. Nature Immunol. 16, 642-52.
  3. Li S, DDF Hsu, B Li, X Luo, N Alderson, L Qiao, L Ma, HH Zhu, Z He, K Suino-Powell, K Ji, J Li, J Shao, HE Xu, T Li, and GS Feng (2014). Cytoplasmic tyrosine phosphatase Shp2 coordinates hepatic regulation of bile acid and FGF15/19 signaling to repress bile acid synthesis. Cell Metabolism 20, 320-332 (recommended by Faculty 1000, Previewed, Cell Metabolism 20, 203-204.
  4. He Z, HH Zhu, TJ Bauler, J Wang, T Ciaraldi, N Alderson, S Li, MA Raquil, K Ji, S Wang, J Shao, R Henry, PD King, and GS Feng (2013). Non-receptor tyrosine phosphatase Shp2 promotes adipogenesis through inhibition of p38 MAP kinase. Proc Natl Acad Sci USA. 110, E79-88.
  5. He Z, SS Zhang, Q Meng, S Li, HH Zhu, MA Raquil, N Alderson, H Zhang, J Wu, L Rui, D Cai, and GS Feng (2012). Shp2 controls female body weight and energy balance by integrating leptin and estrogen signals. Mol Cell Biol 32, 1867-1878, 2012. PMCID 3347413
  6. Feng GS (2012).Conflicting roles of moleculesin hepatocarcinogenesis: paradigm or   paradox (Invited Review). Cancer Cell 21, 150-154.
  7. Bard-Chapeau EA, S Li, J Ding, SS Zhang, HH Zhu, F Princen, DD Fang, T Han, B Bailly-Maitre, V Poli, NM Varki, H Wang and GS Feng (2011). PTPN11/Shp2 acts as a tumor suppressor in hepatocellular carcinogenesis. Cancer Cell 19, 629-639.

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Selected Publications

  1. Feng GS, CC Hui, and T Pawson. SH2-containing phosphotyrosine phosphatase as a target of protein-tyrosine kinases. Science 259, 1607-1611, 1993.
  2. Feng GS, and T Pawson. Phosphotyrosine phosphatases with SH2 domains: regulators of signal transduction (review article). Trends in Genetics10, 54-58, 1994.
  3. You M, LM Flick, DH Yu, and GS Feng. Modulation of the nuclear factor-kappaB pathway by Shp-2 tyrosine phosphatase in interleukin (IL)-6 induction by IL-1 or tumor necrosis factor. J Exp Med193, 101-109, 2001.
  4. Zhang EE, E Chapeau, K Hagihara and GS Feng. Neuronal Shp2 tyrosine phosphatase controls energy balance and metabolism. Proc Natl Acad Sci USA 101, 16064-16069, 2004.
  5. Chapeau E, AL Hevener, S Long, EE Zhang, JM Olefsky and GS Feng. Deletion of Gab1 in the liver leads to enhanced glucose tolerance and improved hepatic insulin action. Nature Medicine 11, 567-571, 2005.
  6. Bard-Chapeau, EA, J Yuan, N Droin, S Long, EE Zhang, TV Nguyen, and GS Feng. Concerted functions of Gab1 and Shp2 in liver regeneration and hepatoprotection. Mol Cell Biol 26, 4664-4674, 2006.
  7. Ke Y, D Wu, F Princen, T Nguyen, Y Pang, J Lesperance, WJ Muller, RG Oshima, and GS Feng. Role of Gab2 in mammary tumorigenesis and metastasis. Oncogene26, 4951-4960, 2007.
  8. Ke K, EE Zhang, K Hagihara, D Wu, YH Pang, R Klein, T Curran, B Ranscht, and GS Feng. Deletion of Shp2 in the brain leads to defective proliferation and differentiation in neural stem cells and early postnatal lethality. Mol Cell Biol 27, 6706-6717, 2007.
  9. Zhang SS, E Hao, J Yu, W Liu, J Wang, F Levine, and GS Feng. Coordinated regulation by Shp2 tyrosine phosphatase of signaling events controlling insulin biosynthesis in pancreatic beta-cells. Proc Natl Acad Sci USA 106, 7531-7536, 2009. PMCID 2678606

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