Rugang Zhang, Ph.D.

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Wistar Institute Associate Professor of Genetics
Department: Genetics
Graduate Group Affiliations

Contact information
The Wistar Institute
3601 Spruce Street
Room 308
Philadelphia, PA 19104
Office: 215-495-6840
Anhui Normal University, Anhui, China, 1997.
Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China, 2002.
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Description of Research Expertise

Research Interests:

To understand the basic mechanisms underlying oncogene-induced senescence, an important tumor suppression mechanism.

To identify novel intervention strategies for epithelial ovarian cancer (EOC), the most lethal gynecological malignancy in the developed world.

Key Words:

Cellular Senescence, Tumor Suppression, Chromatin Structure, Cancer Metabolism, Epithelial Ovarian Cancer, Epigenetic Cancer Therapy, Targeted Cancer Therapy Resistance, Immunological Vulnerability, EZH2, SWI/SNF, ARID1A, ARID2

Research Details:

It is well known that cancer is a disease caused by oncogene activation and inactivation of tumor suppressor genes. Paradoxically, activation of oncogenes or inactivation of tumor suppressor genes alone in primary mammalian cells often triggers a state of stable cell growth arrest, known as cellular senescence. Overcoming the senescence-associated cell growth arrest is a necessary step during cell transformation. It is therefore critical to understand the mechanistic basis of oncogenic signaling in the context of senescence induction and bypass. This biological process represents an ideal paradigm to examine the role of DNA damage response, epigenetically determined chromatin structure, and metabolic reprogramming during cancer initiation and progression.

A major discovery in recent cancer genome-wide sequencing is the identification of significant genetic changes in chromatin-modifying genes. However, despite great strides in identifying the various epigenetic enzymes/factors involved in cancer, the translational application of these findings in cancer intervention remains to be explored. Zhang lab will pursue these issues in the coming years by focusing on the epigenetic SWI/SNF and PRC2 complexes as proof of principles in the context of ovarian cancer and melanoma.

Zhang lab will continue to use its strengths in biochemical, molecular and cellular cancer biology to decipher the mechanistic basis of cancer. Simultaneously, the lab will increase its focus on the utilization of model organisms, including genetic mouse models, and carefully chosen clinically relevant pre-clinical cancer models to explore the translational application of the mechanistic findings. His laboratory primarily focuses on ovarian cancer, which ranks first as the cause of death for gynecological cancers in the developed world.

Rotation Projects for 2015-2018

1. Chromatin basis of senescence-associated secretory phenotype.
2. Targeting senescence-associated metabolic vulnerability to develop cancer therapeutics.
3. Targeting senescence-associated immunological vulnerability to develop cancer therapeutics.
4. Epigenetic approaches to therapy resistance in ovarian cancer.
5. Epigenetic approaches to immunological therapeutic targets in ovarian cancer.
6. Developing mechanism guided therapeutic strategies for loss of function mutations in the SWI/SNF complex subunits such as ARID1A and ARID2 in ovarian cancer and melanoma.
7. PARP inhibitors resistance mechanism in "BRCAness" ovarian cancer.

Lab personnel:

Benjamin Bitler, Ph.D., Postdoctoral Fellow (Supported by NIH/NCI K99/R00 Award)
Katherine Aird, Ph.D., Postdoctoral Fellow (Supported by NIH/NCI K99/R00 Award)
Hengrui Zhu, Ph.D., Postdoctoral Associate
Yuki Yokoyama, Ph.D., Postdoctoral Associate
Sergey Karakashev, Ph.D., Postdoctoral Associate
Linh Le, B.S., Predoctoral Student, CB/CAMB (Supported by T32GM007229 Fellowship)
Nail Fatkhutdinov, M.S., Predoctoral Student
Pyoung Hwa (Peace) Park, B.S., Technician

Selected Publications

Zhu H, Ren S, Bitler BG, Aird KM, Tu Z, Skordalakes E, Zhu Y, Yan J, Sun Y, Zhang R. : SPOP E3 Ubiquitin Ligase Adaptor Epigenetically Promotes Cellular Senescence by Degrading the SENP7 deSUMOylase. Cell Reports 2015 Notes: In Press.

Bitler BG, Garipov A, Amatangelo M, Kossenkov A, Schultz DC, Shih IM, Conejo-Garcia JR, Speicher DW, Zhang R. : Synthetic lethality by targeting EZH2 methyltransferase activity in ARID1A-mutated cancers. Nature Medicine 21(3): 231-238, 2015.

Zhao B, Zhang WD, Lu YQ, Cun YX, Li CH, Guo K, Nie WH, Li L, Zhang R, Zheng P. : ESC-specific protein Filia is a master regulator of DNA damage response and safeguards genomic stability of mouse ESCs. Cell Stem Cell 16(6): 684-98, 2015.

Rutkowski MR, Stephen TL, Svoronos N, Allegrezza MJ, Perales-Puchalt A, Tesone AJ, Escovar-Fadul X, Nguyen JM, Cadungog MG, Zhang R, Salatino M, Rabinovich GA, Tchou J, Conejo-Garcia JR. : Microbially driven TLR-dependent signalling governs distal malignant progression through tumor-promoting inflammation. Cancer Cell 27: 27-40, 2015.

Aird KM, Worth AJ, Snyder NW, Lee JV, Sivanand S, Liu Q, Blair IA, Wellen KE, Zhang R.: ATM couples replication stress and metabolic reprogramming during cellular senescence. Cell Reports 11(6): 893-901, 2015.

Aird KM, Zhang G, Li H, Tu Z, Bitler BG, Garipov A, Wu H, Wei Z, Wagner SN, Herlyn M, Zhang R.: Suppression of Nucleotide Metabolism Underlies the Establishment and Maintenance of Oncogene-Induced Senescence. Cell Reports 3: 1252-1265, 2013.

Tu Z, Zhuang X, Yao YG, Zhang R.: BRG1 is required for formation of senescence-associated heterochromatin foci (SAHF) induced by oncogenic RAS or BRCA1 loss. Molecular and Cellular Biology 33: 1819-1829, 2013.

Tu, Z., Aird, K. M., Bitler, B. G., Nicodemus, J. P., Beeharry, N., Xia, B., Yen, T. J., Zhang, R.: Oncogenic RAS regulates BRIP1 expression to induce dissociation of BRCA1 from chromatin, inhibit DNA repair, and promote senescence. Developmental Cell 21(6): 1077-91, 2011.

Bitler, B. G., Nicodemus, J. P., Li, H., Cai, Q., Wu, H., Hua, X., Li, T., Birrer, M. J., Godwin, A. K., Cairns, P., Zhang, R.: Wnt5a suppresses epithelial ovarian cancer by promoting cellular senescence. Cancer Research 71(19): 6184-94, 2011.

Kennedy, A. L., Morton, J. P., Manoharan, I., Nelson, D. M., Jamieson, N. B., Pawlikowski, J. S., McBryan, T., Doyle, B., McKay, C., Oien, K. A., Enders, G. H., Zhang, R., Sansom, O. J., Adams, P. D.: Activation of the PIK3CA/AKT pathway suppresses senescence induced by an activated RAS oncogene to promote tumorigenesis. Molecular Cell 42(1): 36-49, 2011.

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Last updated: 09/29/2015
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