|Grant Number:||5R01CA132874-05 Interpret this number|
|Primary Investigator:||Chinnaiyan, Arul|
|Organization:||University Of Michigan|
|Project Title:||Molecuar Sub-Typing of Prostate Cancer Based on Recurrent Gene Fusions|
DESCRIPTION (provided by applicant): Employing a bioinformatics approach to analyze prostate cancer gene expression profiles, we identified recurrent gene fusions/translocations in the majority of prostate cancers (Tomlins et al, Science 2005). Specifically, we identified the androgen regulatory elements of TMPRSS2 fused to the members of the ETS family of transcription factors including ERG, ETV1, ETV4 and ETV5. Analogous to hematological malignancies, gene fusions/translocations identified in prostate cancer may represent pathognomonic biomarkers and molecular sub-types of disease. In this application, we plan to focus our efforts on characterizing this new class of gene fusion biomarkers. Preliminary work done by our group and others suggest that molecular subtypes as well as transcript variants of gene fusions may be associated with clinical sub-types of prostate cancer. The central hypothesis of this application is that molecular sub-types based on gene fusions and variants will be useful predictors of the aggressive potential of clinically localized prostate cancer and thus guide treatment. Given this, we propose the following Aims: Specific Aim 1: Discovery and nomination of novel molecular sub-types of prostate cancer. Specific Aim 2: Characterize associations of molecular sub-types of prostate cancer with clinical outcome and/or aggressiveness of disease in a radical prostatectomy cohort. Specific Aim 3. Characterize associations of molecular sub-types of prostate cancer with clinical outcome and/or aggressiveness of disease using prostate needle biopsy samples.
Novel RNA hybridization method for the in situ detection of ETV1, ETV4, and ETV5 gene fusions in prostate cancer.
Authors: Kunju LP, Carskadon S, Siddiqui J, Tomlins SA, Chinnaiyan AM, Palanisamy N
Source: Appl Immunohistochem Mol Morphol, 2014 Sep;22(8), p. e32-40.
The lncRNA PCAT29 inhibits oncogenic phenotypes in prostate cancer.
Authors: Malik R, Patel L, Prensner JR, Shi Y, Iyer MK, Subramaniyan S, Carley A, Niknafs YS, Sahu A, Han S, Ma T, Liu M, Asangani IA, Jing X, Cao X, Dhanasekaran SM, Robinson DR, Feng FY, Chinnaiyan AM
Source: Mol Cancer Res, 2014 Aug;12(8), p. 1081-7.
EPub date: 2014 Jul 16.
Molecular pathways: targeting ETS gene fusions in cancer.
Authors: Feng FY, Brenner JC, Hussain M, Chinnaiyan AM
Source: Clin Cancer Res, 2014 Sep 1;20(17), p. 4442-8.
EPub date: 2014 Jun 23.
HOXB13 G84E-related familial prostate cancers: a clinical, histologic, and molecular survey.
Authors: Smith SC, Palanisamy N, Zuhlke KA, Johnson AM, Siddiqui J, Chinnaiyan AM, Kunju LP, Cooney KA, Tomlins SA
Source: Am J Surg Pathol, 2014 May;38(5), p. 615-26.
PCAT-1, a long noncoding RNA, regulates BRCA2 and controls homologous recombination in cancer.
Authors: Prensner JR, Chen W, Iyer MK, Cao Q, Ma T, Han S, Sahu A, Malik R, Wilder-Romans K, Navone N, Logothetis CJ, Araujo JC, Pisters LL, Tewari AK, Canman CE, Knudsen KE, Kitabayashi N, Rubin MA, Demichelis F, Lawrence TS, Chinnaiyan AM, Feng FY
Source: Cancer Res, 2014 Mar 15;74(6), p. 1651-60.
EPub date: 2014 Jan 28.
The central role of EED in the orchestration of polycomb group complexes.
Authors: Cao Q, Wang X, Zhao M, Yang R, Malik R, Qiao Y, Poliakov A, Yocum AK, Li Y, Chen W, Cao X, Jiang X, Dahiya A, Harris C, Feng FY, Kalantry S, Qin ZS, Dhanasekaran SM, Chinnaiyan AM
Source: Nat Commun, 2014;5, p. 3127.
The long noncoding RNA SChLAP1 promotes aggressive prostate cancer and antagonizes the SWI/SNF complex.
Authors: Prensner JR, Iyer MK, Sahu A, Asangani IA, Cao Q, Patel L, Vergara IA, Davicioni E, Erho N, Ghadessi M, Jenkins RB, Triche TJ, Malik R, Bedenis R, McGregor N, Ma T, Chen W, Han S, Jing X, Cao X, Wang X, Chandler B, Yan W, Siddiqui J, Kunju LP, Dhanasekaran SM, Pienta KJ, Feng FY, Chinnaiyan AM
Source: Nat Genet, 2013 Nov;45(11), p. 1392-8.
EPub date: 2013 Sep 29.
Evaluation of tissue PCA3 expression in prostate cancer by RNA in situ hybridization--a correlative study with urine PCA3 and TMPRSS2-ERG.
Authors: Warrick JI, Tomlins SA, Carskadon SL, Young AM, Siddiqui J, Wei JT, Chinnaiyan AM, Kunju LP, Palanisamy N
Source: Mod Pathol, 2014 Apr;27(4), p. 609-20.
EPub date: 2013 Sep 27.
The role of sarcosine metabolism in prostate cancer progression.
Authors: Khan AP, Rajendiran TM, Ateeq B, Asangani IA, Athanikar JN, Yocum AK, Mehra R, Siddiqui J, Palapattu G, Wei JT, Michailidis G, Sreekumar A, Chinnaiyan AM
Source: Neoplasia, 2013 May;15(5), p. 491-501.
Advancing precision medicine for prostate cancer through genomics.
Authors: Roychowdhury S, Chinnaiyan AM
Source: J Clin Oncol, 2013 May 20;31(15), p. 1866-73.
EPub date: 2013 Apr 15.
Identification of targetable FGFR gene fusions in diverse cancers.
Authors: Wu YM, Su F, Kalyana-Sundaram S, Khazanov N, Ateeq B, Cao X, Lonigro RJ, Vats P, Wang R, Lin SF, Cheng AJ, Kunju LP, Siddiqui J, Tomlins SA, Wyngaard P, Sadis S, Roychowdhury S, Hussain MH, Feng FY, Zalupski MM, Talpaz M, Pienta KJ, Rhodes DR, Robinson DR, Chinnaiyan AM
Source: Cancer Discov, 2013 Jun;3(6), p. 636-47.
EPub date: 2013 Apr 4.
Novel dual-color immunohistochemical methods for detecting ERG-PTEN and ERG-SPINK1 status in prostate carcinoma.
Authors: Bhalla R, Kunju LP, Tomlins SA, Christopherson K, Cortez C, Carskadon S, Siddiqui J, Park K, Mosquera JM, Pestano GA, Rubin MA, Chinnaiyan AM, Palanisamy N
Source: Mod Pathol, 2013 Jun;26(6), p. 835-48.
EPub date: 2013 Jan 25.
Gene Fusion Markup Language: a prototype for exchanging gene fusion data.
Authors: Kalyana-Sundaram S, Shanmugam A, Chinnaiyan AM
Source: BMC Bioinformatics, 2012 Oct 16;13, p. 269.
EPub date: 2012 Oct 16.
SLC45A3-ELK4 chimera in prostate cancer: spotlight on cis-splicing.
Authors: Kumar-Sinha C, Kalyana-Sundaram S, Chinnaiyan AM
Source: Cancer Discov, 2012 Jul;2(7), p. 582-5.
Expressed pseudogenes in the transcriptional landscape of human cancers.
Authors: Kalyana-Sundaram S, Kumar-Sinha C, Shankar S, Robinson DR, Wu YM, Cao X, Asangani IA, Kothari V, Prensner JR, Lonigro RJ, Iyer MK, Barrette T, Shanmugam A, Dhanasekaran SM, Palanisamy N, Chinnaiyan AM
Source: Cell, 2012 Jun 22;149(7), p. 1622-34.
The mutational landscape of lethal castration-resistant prostate cancer.
Authors: Grasso CS, Wu YM, Robinson DR, Cao X, Dhanasekaran SM, Khan AP, Quist MJ, Jing X, Lonigro RJ, Brenner JC, Asangani IA, Ateeq B, Chun SY, Siddiqui J, Sam L, Anstett M, Mehra R, Prensner JR, Palanisamy N, Ryslik GA, Vandin F, Raphael BJ, Kunju LP, Rhodes DR, Pienta KJ, Chinnaiyan AM, Tomlins SA
Source: Nature, 2012 Jul 12;487(7406), p. 239-43.
From sequence to molecular pathology, and a mechanism driving the neuroendocrine phenotype in prostate cancer.
Authors: Lapuk AV, Wu C, Wyatt AW, McPherson A, McConeghy BJ, Brahmbhatt S, Mo F, Zoubeidi A, Anderson S, Bell RH, Haegert A, Shukin R, Wang Y, Fazli L, Hurtado-Coll A, Jones EC, Hach F, Hormozdiari F, Hajirasouliha I, Boutros PC, Bristow RG, Zhao Y, Marra MA, Fanjul A, Maher CA, Chinnaiyan AM, Rubin MA, Beltran H, Sahinalp SC, Gleave ME, Volik SV, Collins CC
Source: J Pathol, 2012 Jul;227(3), p. 286-97.