P
Peter S. Nelson
Researcher at Fred Hutchinson Cancer Research Center
Publications - 497
Citations - 57568
Peter S. Nelson is an academic researcher from Fred Hutchinson Cancer Research Center. The author has contributed to research in topics: Prostate cancer & Cancer. The author has an hindex of 96, co-authored 425 publications receiving 47923 citations. Previous affiliations of Peter S. Nelson include University of Washington & National Institutes of Health.
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Journal ArticleDOI
EZH2 cooperates with gain‐of‐function p53 mutants to promote cancer growth and metastasis
Yu Zhao,Liya Ding,Dejie Wang,Zhenqing Ye,Yundong He,Linlin Ma,Runzhi Zhu,Yunqian Pan,Qiang Wu,Qiang Wu,Kun Pang,Kun Pang,Xiaonan Hou,Saravut J. Weroha,Conghui Han,Roger Coleman,Ilsa Coleman,R. Jeffery Karnes,Jun Zhang,Peter S. Nelson,Liguo Wang,Haojie Huang +21 more
TL;DR: A non‐methyltransferase function of EZH2 that controls protein translation of p53 GOF mutants, inhibition of which causes synthetic lethality in cancer cells expressing p53 GoF mutants is revealed.
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Role of androgen receptor splice variant-7 (AR-V7) in prostate cancer resistance to 2nd-generation androgen receptor signaling inhibitors.
Yezi Zhu,Susan L. Dalrymple,Ilsa Coleman,S. Lilly Zheng,Jianfeng Xu,Jody E. Hooper,Emmanuel S. Antonarakis,Angelo M. De Marzo,Alan K. Meeker,Peter S. Nelson,Peter S. Nelson,William B. Isaacs,Samuel R. Denmeade,Jun Luo,W. Nathaniel Brennen,John T. Isaacs +15 more
TL;DR: In vitro and in vivo growth responses of Abi-/Enza-resistant LNCaP-95 cells in which CRISPR-Cas9 was used to knockout AR-FL or AR-V7 alone or in combination were evaluated, and RNAseq analysis demonstrates that both AR- FL- and AR- V7-dependent transcriptional complementation are needed for Abi/ Enza resistance.
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PPP2R2C loss promotes castration-resistance and is associated with increased prostate cancer-specific mortality
Eric G. Bluemn,Elysia Sophie Spencer,Brigham H Mecham,Brigham H Mecham,Ryan R. Gordon,Ilsa Coleman,Daniel J Lewinshtein,Daniel J Lewinshtein,Elahe A. Mostaghel,Elahe A. Mostaghel,Xiaotun Zhang,James Annis,James Annis,Carla Grandori,Carla Grandori,Carla Grandori,Christopher R. Porter,Peter S. Nelson,Peter S. Nelson +18 more
TL;DR: In vitro high-throughput RNA interference screen identifies pathways in androgen-dependent prostate cancer cell lines whose loss-of-function promotes androgen ligand-independent growth and shows that loss of PPP2R2C promotes androgens ligand depletion-resistant prostate cancer growth without altering AR expression or canonical AR-regulated gene expression.
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Characterizing the molecular features of ERG-positive tumors in primary and castration resistant prostate cancer.
Martine Roudier,Brian Winters,Ilsa Coleman,Hung-Ming Lam,Hung-Ming Lam,Xiaotun Zhang,Roger Coleman,Lisly Chéry,Lawrence D. True,Celestia S. Higano,Bruce Montgomery,Paul H. Lange,Paul H. Lange,Linda A. Snyder,Shiv Srivastava,Eva Corey,Robert L. Vessella,Robert L. Vessella,Peter S. Nelson,Peter S. Nelson,Aykut Üren,Colm Morrissey +21 more
TL;DR: The TMPRSS2‐ERG gene fusion is detected in approximately half of primary prostate cancers (PCa) yet the prognostic significance remains unclear, and it is hypothesized that ERG promotes the expression of common genes in primary PCa and metastatic castration‐resistant PCa.
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Estradiol suppresses tissue androgens and prostate cancer growth in castration resistant prostate cancer.
TL;DR: 17β-estradiol significantly suppressed tumor T and DHT and inhibits growth of CRPC in an estrogen receptor independent manner and the ability to manipulate tumoral androgens will be critical in the development and testing of agents targeting CRPC through tissue steroidogenesis.