scholarly journals Ductal variant of prostate adenocarcinoma harbor Xenotropic murine leukemia virus related virus (XMRV) infection: a novel finding in subtype of prostate cancer

2017 ◽  
Vol 43 (3) ◽  
pp. 268-272 ◽  
Author(s):  
Faraz Ahmed Baig ◽  
Talat Mirza ◽  
Amna Hamid ◽  
Serajuddaula Syed ◽  
Qamar Jamal
Retrovirology ◽  
2009 ◽  
Vol 6 (1) ◽  
pp. 92 ◽  
Author(s):  
Oliver Hohn ◽  
Hans Krause ◽  
Pia Barbarotto ◽  
Lars Niederstadt ◽  
Nadine Beimforde ◽  
...  

2009 ◽  
Vol 84 (3) ◽  
pp. 1648-1651 ◽  
Author(s):  
Beihua Dong ◽  
Robert H. Silverman

ABSTRACT Xenotropic murine leukemia virus-related virus (XMRV) is a gammaretrovirus originally identified in a subset of prostate cancer patients. Because androgens stimulate prostate tumors and some retroviruses, we investigated the effects of dihydrotestosterone (DHT) on XMRV transcription and replication. Transcription from the XMRV U3 region was stimulated up to 2-fold by DHT, but only in cells containing a functional androgen receptor. Mutations in the glucocorticoid response element (GRE) of XMRV impaired basal transcription and androgen responsiveness. Furthermore, DHT stimulated XMRV replication 3-fold, whereas androgen inhibitors (casodex and flutamide) suppressed viral growth up to 3-fold. Findings suggest that integration of the XMRV long terminal repeat (LTR) into host DNA could impart androgen stimulation on cellular genes.


2016 ◽  
Vol 29 (4) ◽  
pp. 749-757 ◽  
Author(s):  
Andrew D. Johnson ◽  
Claudia S. Cohn

SUMMARYIn 2006, a new virus, xenotropic murine leukemia virus-related virus (XMRV), was discovered in a cohort of U.S. men with prostate cancer. Soon after this initial finding, XMRV was also detected in samples from patients with chronic fatigue syndrome (CFS). The blood community, which is highly sensitive to the threat of emerging infectious diseases since the HIV/AIDS crisis, recommended indefinite deferral of all blood donors with a history of CFS. As XMRV research progressed, conflicting results emerged regarding the importance of this virus in the pathophysiology of prostate cancer and/or CFS. Molecular biologists traced the development of XMRV to a recombination event in a laboratory mouse that likely occurred circa 1993. The virus was propagated via cell lines derived from a tumor present in this mouse and spread through contamination of laboratory samples. Well-controlled experiments showed that detection of XMRV was due to contaminated samples and was not a marker of or a causal factor in prostate cancer or CFS. This paper traces the development of XMRV in the prostate and CFS scientific communities and explores the effect it had on the blood community.


2015 ◽  
Vol 17 (12) ◽  
Author(s):  
Farhad Babaei ◽  
Ali Ahmadi ◽  
Farhad Rezaei ◽  
Somayeh Jalilvand ◽  
Nastaran Ghavami ◽  
...  

2009 ◽  
Vol 83 (14) ◽  
pp. 6995-7003 ◽  
Author(s):  
Seunghee Hong ◽  
Eric A. Klein ◽  
Jaydip Das Gupta ◽  
Kirsten Hanke ◽  
Christopher J. Weight ◽  
...  

ABSTRACT The xenotropic murine leukemia virus-related virus (XMRV) has recently been detected in prostate cancer tissues and may play a role in tumorigenesis. It is currently unclear how this virus is transmitted and which factors promote its spread in the prostate. We show that amyloidogenic fragments known as semen-derived enhancer of virus infection (SEVI) originating from prostatic acid phosphatase greatly increase XMRV infections of primary prostatic epithelial and stromal cells. Hybrid simian/human immunodeficiency chimeric virus particles pseudotyped with XMRV envelope protein were used to demonstrate that the enhancing effect of SEVI, or of human semen itself, was at the level of viral attachment and entry. SEVI enhanced XMRV infectivity but did not bypass the requirement for the xenotropic and polytropic retrovirus receptor 1. Furthermore, XMRV RNA was detected in prostatic secretions of some men with prostate cancer. The fact that the precursor of SEVI is produced in abundance by the prostate indicates that XMRV replication occurs in an environment that provides a natural enhancer of viral infection, and this may play a role in the spread of this virus in the human population.


2011 ◽  
Vol 8 (1) ◽  
pp. 531 ◽  
Author(s):  
Abhinav Dey ◽  
Chinmay Mantri ◽  
Jui Pandhare-Dash ◽  
Bindong Liu ◽  
Siddharth Pratap ◽  
...  

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