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:: Volume 13, Issue 6 (Feb & March 2009) ::
pajoohande 2009, 13(6): 469-474 Back to browse issues page
Probing the Relation between Gene Promoters Hypermethylation of RARB and p16 among Patients with Prostatic Cancer of Different Prognosis
Ameri A , Alidousti A , Mojir Sheibani Kh , Ghanbari Motlagh A , Valaei N , Emranpour MH * , Abbaszadegan MR , Hosseini Y , Parvin M
, mohammadhassanemranpour @ gmail.com
Abstract:   (13751 Views)
Background: With regard to the increasing prevalence and mortality rate of prostate cancer and several related reports studying the role of promoter Hypermethylation of RARB and p16 in predicting the prognosis, this research is carried out on 3 groups of subjects with poor prognostic factors (case), good prognostic factors (control-2) and healthy person (control-1), at three general hospitals of Imam Hossein, Modarres and Labbafineyhad, between 2007-2009. Materials and Methods: The research has case-control Design. All three goup of participants (21 subjects in each group) were analyzed for hypermethylation of RARB- p16. All groups were matched for age, tumor stage, grade & PSA. The technique was methylation specific polymerase chain reaction (MSPCR). Results: In control-1, no methylation of RARB were observed. In control-2, RARB was positive in 33%. In case group, the RARB was positive for 71.4%. For control 2 and case groups, the RAR positivity was higher than control-1 (P< 0.001), however, that of case group was higher than control-2(p
Keywords: RARB, MSPCR, p16, Prostate cancer, Poor prognosis
Full-Text [PDF 88 kb]   (2083 Downloads)    
Type of Study: Original | Subject: Medicine
Received: 2017 | Accepted: 2017 | Published: 2017
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Ameri A, Alidousti A, Mojir Sheibani Kh, Ghanbari Motlagh A, Valaei N, Emranpour MH, et al . Probing the Relation between Gene Promoters Hypermethylation of RARB and p16 among Patients with Prostatic Cancer of Different Prognosis. pajoohande 2009; 13 (6) :469-474
URL: http://pajoohande.sbmu.ac.ir/article-1-716-en.html


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Volume 13, Issue 6 (Feb & March 2009) Back to browse issues page
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