Positions
- Professor
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University of Washington
- Adjunct Professor
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Baylor College of Medicine
Addresses
- N326 (Office)
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Mailstop 358056
Seattle, WA, 98109
United States
Phone: (206) 543-6551
xin18@uw.edu
Education
- Post-Doctoral Fellowship at University of California, Los Angeles
- 07/2008 - Los Angeles, CA, United States
- PhD from Shanghai Institute of Biochemistry and Cellular Biology, Chinese Academy of Sciences
- 07/2001 - Shanghai, China
- BS from Nanjing University
- 07/1996 - Nanjing, Jiangsu, China
Professional Interests
- Prostate stem cells, development and carcinogenesis.
Professional Statement
My lab is interested in using the prostate as a tissue model to study the molecular and cellular mechanisms that regulate development, tissue homeostasis and carcinogenesis. Currently, there are two major research focuses in the lab. The first research focus is to characterize the prostate epithelial lineage hierarchy. We seek to investigate how individual prostate epithelial lineages are maintained in adults by prostate stem cells or progenitors, and to identify master regulators that control adult prostate homeostasis. The second focus of the lab is to investigate the molecular and cellular basis of aggressive prostate cancer. We are interested in determining the function of disease-associated genes in prostate cancer initiation and progression, and characterizing the identity of the cells of origin for prostate cancer. The major approaches that we utilize are cell culture-based prostate stem cell assays, genetically engineered mouse models, and a prostate regeneration method.
I have relocated my laboratory to the University of Washington at Seattle since August 1, 2018. https://www.washington.edu/urology/people/li-xin-ph-d/.
I have relocated my laboratory to the University of Washington at Seattle since August 1, 2018. https://www.washington.edu/urology/people/li-xin-ph-d/.
Websites
Selected Publications
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Valdez JM, Zhang L, Su Q, Dakhova O, Zhang Y, Shahi P, Spencer DM, Creighton CJ, Ittmann MM, Xin L. " Notch and TGFß Form a Reciprocal Positive Regulatory Loop that Suppresses Murine Prostate Basal Stem/Progenitor Cell Activity. " Cell Stem Cell. 2012 Nov 2; 11 (5) : 676-88.
Pubmed PMID: 23122291. -
Choi N, Zhang B, Zhang L, Ittmann M, Xin L. " Adult Murine Prostate Basal and Luminal Cells Are Self-Sustained Lineages that Can Both Serve as Targets for Prostate Cancer Initiation. " Cancer Cell. 2012 Feb 14; 21 (2) : 253-65.
Pubmed PMID: 22340597. -
Kwon O, Zhang L, Ittmann and Xin L. " Prostatic inflammation enhances basal-to-luminal differentiation and accelerates initiation of prostate cancer with a basal cell origin. " Proc Natl Acad Sci U S A. 2014 Feb 4; 111 (5) : E592-600.
Pubmed PMID: 24367088. -
Kwon OJ, Valdez JM, Zhang L, Zhang B, Wei X, Su Q, Ittmann MM, Creighton CJ, Xin L. " Increased Notch signalling inhibits anoikis and stimulates proliferation of prostate luminal epithelial cells. " Nature Communications. 2014 Jul 22; 5 : 4416.
Pubmed PMID: 25048699.
Memberships
- American Association of Cancer Research
- Society of Basic Urological Research
- International Society for Stem Cell Research
Funding
-
The prostate epithelial cell lineage hierarchy
#R01DK092202 - Grant funding from NIH/NIDDK
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The Notch signaling in prostate homeostasis and carcinogenesis
#R01CA190378 - Grant funding from NIH/NCI
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