Silencing phosphatase of regenerating liver cell-3 gene regulates proliferation and apoptosis of LNCaP cells
Pengfei Zhou, Dawen Wang, Cunjin Nan, Tielin Wu, Sen Yang, Yinghe Chen
Abstract
Pengfei Zhou, Dawen Wang, Cunjin Nan, Tielin Wu, Sen Yang, Yinghe Chen
Abstract
Objective To study the effects of small interfering RNA (siRNA) silencing phosphatase of regenerating liver cell 3 (PRL-3) on proliferation and apoptosis of human prostate cancer LNCaP cells.Methods After prostate cancer LNCaP cells were transfected by PRL-3 siRNA,the mRNA and protein of PRL-3 were detected by reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting,respectively.The growth of LNCaP cells was exmined by cell counting kit-8 (CCK-8).Flow cytometry was used to detect apoptosis.Results The siRNA could downregulate the mRNA and protein expression level of PRL-3 in a dose-dependent manner (P < 0.05).Low doses of PRL-3 siRNA did not affect the proliferation of LNCaP cells,but 100 nmol/L PRL-3 siRNA could effectively inhibit the proliferation of LNCaP cells after 48 h in vitro (P < 0.05).Apoptosis rate of LNCaP cells with low,middle and high PRL3 siRNA interventions in vitro was (28.1 ± 3.8) %,(25.2 ± 2.5) %,and (27.1 ± 0.7) % respectively (P < 0.05).Conclusion Downregulating PRL-3 could inhibit proliferation of LNCaP cells and promote apoptosis of LNCaP cells.PRL-3 gene might play an important role in proliferation and apoptosis of LNCaP cells. Key words: Prostate cancer; Phosphatase of regenerating liver cell 3 ; RNA interference
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Objective To study the effects of small interfering RNA (siRNA) silencing phosphatase of regenerating liver cell 3 (PRL-3) on proliferation and apoptosis of human prostate cancer LNCaP cells.Methods After prostate cancer LNCaP cells were transfected by PRL-3 siRNA,the mRNA and protein of PRL-3 were detected by reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blotting,respectively.The growth of LNCaP cells was exmined by cell counting kit-8 (CCK-8).Flow cytometry was used to detect apoptosis.Results The siRNA could downregulate the mRNA and protein expression level of PRL-3 in a dose-dependent manner (P < 0.05).Low doses of PRL-3 siRNA did not affect the proliferation of LNCaP cells,but 100 nmol/L PRL-3 siRNA could effectively inhibit the proliferation of LNCaP cells after 48 h in vitro (P < 0.05).Apoptosis rate of LNCaP cells with low,middle and high PRL3 siRNA interventions in vitro was (28.1 ± 3.8) %,(25.2 ± 2.5) %,and (27.1 ± 0.7) % respectively (P < 0.05).Conclusion Downregulating PRL-3 could inhibit proliferation of LNCaP cells and promote apoptosis of LNCaP cells.PRL-3 gene might play an important role in proliferation and apoptosis of LNCaP cells. Key words: Prostate cancer; Phosphatase of regenerating liver cell 3 ; RNA interference
Key concepts: LNCaP, Gene silencing, Cell growth, Small interfering RNA, Transfection, Apoptosis, Biology, Flow cytometry