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Zhang Lab

Shaun Xiaoliu Zhang, M.D., Ph.D.

Director, Center for Nuclear Receptors and Cell Signaling; M.D. Anderson Professor
Department of Biology and Biochemistry

Office: SERC, 3005
Contact: shaunzhang@uh.edu - 832-842-8842

Center Director and M.D. Anderson Professor Shaun Xiaoliu Zhang brings a unique blend of academic and industrial research experience to the UH Center for Nuclear Receptors and Cell Signaling. Zhang joined the Center in 2009 to continue pursuing translational research in virology, oncology and immunotherapy. He is now focused on the clinical application of a virus which seeks and destroys cancer cells.

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“Our most promising project to date would be the development and patenting of FusOn-H2, a modified version of a type II herpes simplex virus,” says Zhang. “FusOn-H2 can selectively target and destroy tumor cells without consequence to normal, healthy cells and tissue.”

Contrary to traditional cancer treatments, virotherapy is focused on the modification of benign viruses for the purpose of attacking cancer cells. The killing activity on tumor cells by FusOn-H2 was also found to reenergize the body’s immune system. The unconventional approach is recognized as one of the more promising alternatives to traditional cancer treatments, such as surgery and chemotherapy.

The team currently is using preclinical tumor models to study the precise delivery of the oncolytic virus to tumor sites. The results may be beneficial in the treatment of a variety of cancers, such as breast cancer and prostate cancer. Zhang is specifically interested in pancreatic cancer due to its resistance to radiation and chemotherapy treatments. Future plans for the lab include the pursuit of nanoparticle-mediated drug delivery, another new approach to cancer treatment.

Recent News

Funding

NCI CPRIT

William & Ella Owens Medical Research

Shaun Xiaoliu Zhang

Shaun Xiaoliu Zhang, M.D., Ph.D.
Director, Center for Nuclear Receptors and Cell Signaling; M.D. Anderson Professor

Department of Biology and Biochemistry
University of Houston
Houston, Texas 77204-5001

Office: SERC 545, 3005
Phone: 832-842-8842
Email: shaunzhang@uh.edu

Xinping Fu

Xinping Fu
Research Associate Professor
Email: xfu3@uh.edu

Aiwu Jin

Aiwu Jin
Research Lab Manager
Email: ajin2@uh.edu

Lihua Tao

Lihua Tao
Research Technician
Email: ltao2@uh.edu

Jason Atkins

Jason Atkins
Graduate Student
Email: jlatkins2@uh.edu

Divya Ravirala

Divya Ravirala
Graduate Student
Email: dpravira@central.uh.edu

Drew Boagni

Drew Boagni
Undergraduate Intern
Email: daboagni@uh.edu

Megan Mai

Megan Mai
Undergraduate Intern
Email: mmai3@uh.edu

  1. Xinping Fu, Lihua Tao and Xiaoliu Zhang. Genetically coating oncolytic herpes simplex virus with CD47 allows efficient systemic delivery and prolongs virus persistence at tumor site. In press.
  2. Xinping Fu, Lihua Tao, Pin-Yi Wang, Timothy P. Cripe and Xiaoliu Zhang (2018). Comparison of infectivity and spread between HSV-1 and HSV-2 based oncolytic viruses on tumor cells with different receptor expression profiles. Oncotarget. 20;9(30):21348-21358.
  3. Mark A White, Efrosini Tsouko, Chenchu Lin, Kimal Rajapakshe, Jeffrey M Spencer, Sandi R Wilkenfeld, Sheiva S Vakili, Thomas L Pulliam, Dominik Awad, Fotis Nikolos, Rajasekhara Reddy Katreddy, Benny Abraham Kaipparettu, Arun Sreekumar, Xiaoliu Zhang, Edwin Cheung, Cristian Coarfa and Daniel E Frigo (2018). GLUT12 promotes prostate cancer cell growth and is regulated by androgens and CaMKK2 signaling. Endocrine-Related Cancer. 25 (4):453-469.
  4. Louiza Belkacemi, Jason Atkins, Lu Yang, Prajakta Gadgil, Amy Sater, Diana Chow, Rathindra N Bose and Shaun Xiaoliu Zhang (2018). Phosphaplatin Anti-tumor Effect Enhanced by Liposomes Partly via an Up-regulation of PEDF in Breast Cancer. Anticancer Res. 38(2): 623-646.
  5. Jeffrey M Spencer and Xiaoliu Zhang (2017). Deep mutational scanning of S. pyogenes Cas9 reveals important functional domains. Scientific Reports. 7(1): 16836.
  6. Louiza Belkacemi and Shaun Xiaoliu Zhang (2016). Anti-tumor effects of pigment epithelium-derived factor (PEDF): implication for cancer therapy. A mini-review. J Exp Clin Cancer Res. 35(1):4.
  7. Armando Rivera, Xinping Fu, Lihua Tao and Xiaoliu Zhang (2015). Expression of mouse CD47 on human cancer cells profoundly increases tumor metastasis in murine models
    BMC Cancer. 15(1): 964-974.
  8. Shaun Xiaoliu Zhang (2015). Turning killer into cure - the story of oncolytic herpes simplex viruses. Discovery Medicine. 20 (111): 303-309.
  9. Kwan Joong Joo, Hongtao Li, Xiaoliu Zhang and Seth P. Lerner (2015). Therapeutic Effect on Bladder Cancer with a Conditionally Replicating Oncolytic Virus Derived from Type II Herpes Simplex Virus. Bladder Cancer. 1(1): 81-90.
  10. X. Fu, L. A. Rivera, Tao and X. Zhang (2015). An HSV-2 based oncolytic virus can function as an attractant to guide migration of adoptively transferred T cells to tumor sites. Oncotarget. 6(2):902-914.
  11. Shana Williamson Loya and Xiaoliu Zhang (2015). Enhancing The Bystander Killing Effect Of An Oncolytic HSV By Arming It With A Secretable Apoptosis Activator. Gene Ther. 22, 237–246.
  12. Zhen Yang , Liangzi Deng , Yucheng Lan , Xiaoliu Zhang , Zhonghong Gao , Ching-Wu Chu, Dong Cai , Zhifeng Ren (2014). Molecular extraction in single live cells by sneaking in and out magnetic nanomaterials. PNAS. 111(30): 10966-71.
  13. Kim Anthony, Abhijit More and Xiaoliu Zhang (2014). Activation of silenced cytokine gene promoters by the synergistic effect of TBP-TALE and VP64-TALE activators. PLoS One. 22;9(4):e95790. doi: 10.1371/journal.pone.0095790. eCollection 2014.
  14. Chu J, Deng Y, Benson DM Jr, He S, Hughes T, Zhang J, Peng Y, Mao H, Yi L, Ghoshal K, He X, Devine SM, Zhang X, Caligiuri MA, Hofmeister CC, Yu J. (2013). CS1-specific chimeric antigen receptor (CAR)-engineered natural killer cells enhance In Vitro and In Vivo anti-tumor activity against human multiple myeloma. Leukemia. 2013 Sep 26. doi: 10.1038/leu.2013.279.
  15. Xinping Fu, Armando Rivera, Lihua Tao and Xiaoliu Zhang (2013). Genetically modified T cells targeting neovasculature efficiently destroy tumor blood vessels, shrink established solid tumors, and increase nanoparticle delivery. International Journal of Cancer. 133(10):2483-92. doi: 10.1002/ijc.28269.