Up‐regulation of miR‐582‐5p regulates cellular proliferation of prostate cancer cells under androgen‐deprived conditions. Issue 16 (29th August 2014)
- Record Type:
- Journal Article
- Title:
- Up‐regulation of miR‐582‐5p regulates cellular proliferation of prostate cancer cells under androgen‐deprived conditions. Issue 16 (29th August 2014)
- Main Title:
- Up‐regulation of miR‐582‐5p regulates cellular proliferation of prostate cancer cells under androgen‐deprived conditions
- Authors:
- Maeno, Atsushi
Terada, Naoki
Uegaki, Masayuki
Goto, Takayuki
Okada, Yoshiyuki
Kobayashi, Takashi
Kamba, Tomomi
Ogawa, Osamu
Inoue, Takahiro - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pros22877-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>MicroRNAs are noncoding small RNA that negatively regulate target gene expression by binding to the 3′‐UTR of mRNA. Previous studies have shown that several microRNAs play a pivotal role in prostate cancer by acting as oncogenes or tumor suppressors. This study was aimed at identifying microRNAs that contribute to the progression to castration resistant prostate cancer.</p> </sec> <sec id="pros22877-sec-0002" sec-type="section"> <title>METHODS</title> <p>MicroRNAs expression profiles of a xenograft model and cell lines were examined by microarray analysis and real‐time PCR. Functional analysis of miR‐582‐5p in cellular proliferation was examined by cell counting. Furthermore, in order to investigate a candidate target of miR‐582‐5p, microarray analysis and analysis in silico were utilized.</p> </sec> <sec id="pros22877-sec-0003" sec-type="section"> <title>RESULTS</title> <p>MiR‐582‐5p was identified to be up‐regulated at the castration resistant stage of a xenograft model, KUCaP2 and in castration resistant cell line, AILNCaP#1. Overexpression of miR‐582‐5p increased the number and the percentage of S phase of LNCaP cells under androgen deprived condition. Moreover, suppression of miR‐582‐5p decreased the number and the percentage of S phase of AILNCaP#1 cells. Furthermore, we identified that miR‐582‐5p<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <sec id="pros22877-sec-0001" sec-type="section"> <title>BACKGROUND</title> <p>MicroRNAs are noncoding small RNA that negatively regulate target gene expression by binding to the 3′‐UTR of mRNA. Previous studies have shown that several microRNAs play a pivotal role in prostate cancer by acting as oncogenes or tumor suppressors. This study was aimed at identifying microRNAs that contribute to the progression to castration resistant prostate cancer.</p> </sec> <sec id="pros22877-sec-0002" sec-type="section"> <title>METHODS</title> <p>MicroRNAs expression profiles of a xenograft model and cell lines were examined by microarray analysis and real‐time PCR. Functional analysis of miR‐582‐5p in cellular proliferation was examined by cell counting. Furthermore, in order to investigate a candidate target of miR‐582‐5p, microarray analysis and analysis in silico were utilized.</p> </sec> <sec id="pros22877-sec-0003" sec-type="section"> <title>RESULTS</title> <p>MiR‐582‐5p was identified to be up‐regulated at the castration resistant stage of a xenograft model, KUCaP2 and in castration resistant cell line, AILNCaP#1. Overexpression of miR‐582‐5p increased the number and the percentage of S phase of LNCaP cells under androgen deprived condition. Moreover, suppression of miR‐582‐5p decreased the number and the percentage of S phase of AILNCaP#1 cells. Furthermore, we identified that miR‐582‐5p down‐regulates EFNB2 expression, which is down‐regulated at the castration resistant stage of a xenograft model, KUCaP2 and in castration resistant cell line, AILNCaP#1.</p> </sec> <sec id="pros22877-sec-0004" sec-type="section"> <title>CONCLUSIONS</title> <p>Our results suggest that up‐regulation of miR‐582‐5p contributes to an increase in the proliferation of prostate cancer cells under androgen deprived conditions. <italic>Prostate 74: 1604–1612, 2014</italic>. © 2014 Wiley Periodicals, Inc.</p> </sec> </abstract> … (more)
- Is Part Of:
- Prostate. Volume 74:Issue 16(2014)
- Journal:
- Prostate
- Issue:
- Volume 74:Issue 16(2014)
- Issue Display:
- Volume 74, Issue 16 (2014)
- Year:
- 2014
- Volume:
- 74
- Issue:
- 16
- Issue Sort Value:
- 2014-0074-0016-0000
- Page Start:
- 1604
- Page End:
- 1612
- Publication Date:
- 2014-08-29
- Subjects:
- Prostate -- Diseases -- Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-0045 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/pros.22877 ↗
- Languages:
- English
- ISSNs:
- 0270-4137
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6935.194000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 3787.xml