Qihong Huang, M.D., Ph.D.
Qihong Huang, M.D., Ph.D.
- Associate Professor, Tumor Microenvironment and Metastasis Program
- 215-495-6835, Office
The laboratory of Qihong Huang develops and applies screening technologies to functional genomics and cancer research. These advanced screening techniques are often called “high-throughput” due to their ability to rapidly screen large volumes of genetic information quickly. Huang uses these methods to systemically screen the entire human genome to find molecules related to tumor development. His goal is to study tumor metastasis, identify novel chemotherapy drug targets, and improve the efficacy of current cancer treatments.
Huang joined The Wistar Institute as an assistant professor in 2005. He received his medical degree at Shanghai Medical University, before becoming a researcher at the Shanghai Institute of Biochemistry of Chinese Academy of Sciences. He then came to the University of California, Davis, where he received a doctorate in microbiology in 2000. Huang began his work on genomic screening technologies at The Scripps Research Institute, where he was a postdoctoral fellow. There, he developed array-format high-throughput technology to discover new regulators of the gene p53, a tumor suppressor believed to be mutated in more than half of all human cancers.
At Wistar, a major focus of Huang’s research program is to discover new genes and signaling pathways that allow advanced cancer to metastasize, a poorly understood process that is the forerunner of most cancer-related deaths. His work has also grown to encompass the role of non-coding RNAs in cancer. Non-coding RNAs—RNA molecules are encoded much like genes in our DNA but do not code for proteins—are part of an emerging body of science that has demonstrated how RNA can, among other activities within a cell, regulate gene activity. The Huang laboratory uses screening technology to scan for new non-coding RNAs that have a role in promoting cancer metastasis. Ultimately, the Huang laboratory seeks to systemically identify molecules and signaling pathways that, when disrupted, will kill tumor cells but have no effect on normal cells.
With this selection of potential targets at hand, the Huang laboratory also uses screening technologies to find new potential therapeutics that will specifically inhibit the mechanisms that support tumor development. The small molecules found in these screens may also be more selective than conventional chemotherapy drugs and have fewer side effects. The laboratory also looks to use the principal of RNA interference—knocking out RNA before it can be transcribed into protein or effect gene regulation—as a means to create new cancer therapies. According to Huang, these studies will lead to new drug targets and chemotherapies that may be effective in the treatment of a broad spectrum of tumors.
1 - Li, N., Kaur, S. , Greshock, J., Lassus, H., Zhang, X., Wang, Y., Leminen, A., Shao, Z., Hu, X., Shun, L., Katsaros, D., Huang, Q., Bützow, R., Weber, B. L., Coukos, G., Zhang, L. (2012) A combined array-based comparative genomic hybridization and functional library screening approach identified mir-30d as an oncomir in cancer. Cancer Research 72:154-164.
2 - Sundarum, P., Hultine, S., Smith, L. M., Dews, M., Fox, J., Biyashev, D., Schelter, J. M., Huang, Q., Cleary, M. A., Volpert, O., Thomas-Tikhonenko, A. (2011) p53-responsive miR-194 inhibits thrombospondin-1 and promotes angiogenesis in colon cancer. Cancer Research 71:7490-7501.
3 - Chen, J., Sprouffske, K., Huang, Q., Maley, C. (2011) Solving the puzzle of metastasis: The evolution of cell migration in neoplasms. PLoS ONE 6(4):e17933.
4 - Zhong, X., Li, N., Liang, S., Huang, Q., Coukos, G., Zhang, L. (2010) Identification of microRNAs regulating reprogramming factor LIN28 in embryonic stem cells and cancer cells. Journal of Biological Chemistry 285:41961-41971.
5 - Ørom, U. A., Derrien, T., Beringer, M., Gumireddy, K., Gardini, A., Bussotti, G., Lai, F., Zytinicki, M, Notredame, C., Huang, Q., Guigo, R., Shiekhattar, R. (2010) Long noncoding RNAs with enhancer-like function in human cells. Cell 143(1):46-58. Comment in: Dev. Cell. 2010 Oct 19;19(4):P485-6.; Nat Methods. 2010 Dec;7(12):947.
6 - Megraw, M., Sethupathy, P., Gumireddy, K., Jensen, S. T., Huang, Q.*, Hatzigeorgiou, A. G. * (2010) Isoform specific gene auto-regulation via miRNAs: a case study on miR-128b and ARPP-21. Theoretical Chemistry Accounts 125:593-598.
7 - Gumireddy, K., Huang, Q. (2010) Identification of metastasis genes by a functional genomics approach. Cell Cycle 9(3):423-423.
8 - Gumireddy, K., Li, A., Gimotty, P. A., Klein-Szanto, A. J., Showe, L. C., Katsaros, D., Coukos, G., Zhang, L., Huang, Q. (2009) KLF17 is a negative regulator of epithelial-mesenchymal transition and metastasis in breast cancer. Nature Cell Biology 11(11):1297-1304.
9 - Huang, Q. *, Gumireddy, K., Schrier, M., le Sage, C., Nagel, R., Nair, S., Egan, D. A., Li, A., Huang, G., Klein-Szanto, A. J., Gimotty, P. A., Katsaros, D., Coukos, G., Zhang, L., Puré, E., Agami, R. * (2008) The microRNAs miR-373 and miR-520c Promote Tumor Invasion and Metastasis. Nature Cell Biology 10(2):202-210.
(Highlighted in Cell 132(5):717)
10 - Gumireddy, K., Young, D. D., Xiong, D., Hogenesch, J. B., Huang, Q.*, Deiters, A. * (2008) Small Molecule Inhibitors of MicroRNA miR-21 Function. Angewandte Chemie International Edition 47(39):7482-7484.
11 - Gumireddy, K., Sun, F., Klein-Szanto, A. J., Gibbins, G. M., Gimotty, P. A., Saunders, A. J., Schultz, P. G., Huang, Q. (2007) An in vivo Selection for Metastasis Promoting Genes in the Mouse. Proceedings of National Academy of Sciences USA 104(16): 6696-6701.
12 - Huang, Q., Raya, A., DeJesus, P., Chao, J., Quon, K. C., Caldwell, J. S., Chanda, S. K., Izpisua-Belmonte, J. C., and Schultz, P. G. (2004) Identification of p53 Regulators by Genome-wide Functional Analysis. Proceedings of National Academy of Sciences USA 101(10):3456-3461.
13 - Huang, Q., Deveraux, Q. L., Maeda, S., Stennicke, H. R., Hammock, B. D., and Reed, J. C. (2001) Cloning and Characterization of a Novel Inhibitor of Apoptosis Protein from Bombyx mori. Biochimica et Biophysica Acta 1499(3):191-198.
14 - Huang, Q., Deveraux, Q. L., Maeda, S., Salvesen, G. S., Stennicke, H. R., Hammock, B. D., and Reed, J. C. (2000) Evolutionary Conservation of Apoptosis Mechanism: Lepidopteran and Baculoviral IAPs are Inhibitors of Mammalian Caspase-9. Proceedings of National Academy of Sciences USA 97(4):1427-1432.
15 - Zhang, H. *, Huang, Q.*, Ke, N., Matsuyama, S., Hammock, B. D., Godzik, A., and Reed, J. C. (2000) Drosophila Pro-apoptotic Bcl-2/Bax Homologue Reveals Evolutionary Conservation of Cell Death Mechanism. Journal of Biological Chemistry 275(35):27303-27306.