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Asian J Androl ; 19(4): 453-457, 2017.
Article in English | MEDLINE | ID: mdl-27232851

ABSTRACT

To determine whether PlncRNA-1 induces apoptosis in prostate cancer cells through the Her-2 pathway. The expression of PlncRNA-1, Her-2, and related cyclin proteins in 23 cases of prostate cancer and adjacent normal tissues was analyzed and compared. LNCaP cells were divided into a control group and an LNCaP-PlncRNA-1-siRNA experimental group. Normal prostate RWPE-1 cells were divided into an RWPE-1 control group and an RWPE-1-PlncRNA-1 experimental group. After PlncRNA-1 silencing and overexpression, changes in Her-2 and cyclinD1 expression levels were detected both in vivo and in vitro. In prostate cancer tissues, Her-2 and PlncRNA-1 were highly expressed and significantly correlated. In LNCaP cells, the expression of Her-2 and cyclinD1 decreased following the downregulation of PlncRNA-1 as assessed by real-time PCR and Western blotting. In RWPE-1 cells, the expression of Her-2 and cyclinD1 increased following PlncRNA-1 overexpression. Flow cytometry revealed that the proportion of LNCaP cells in G2/M phase was significantly increased after PlncRNA-1 silencing and that the proportion of RWPE-1 cells in G2/M phase was significantly decreased after PlncRNA-1 overexpression. Furthermore, animal experiments validated these results. In conclusion, in prostate cancer, PlncRNA-1 regulates the cell cycle and cyclinD1 levels and can also regulate proliferation and apoptosis in prostate cancer cells through the Her-2 pathway.


Subject(s)
Genetic Therapy/methods , Prostatic Neoplasms/genetics , Prostatic Neoplasms/therapy , RNA, Long Noncoding/genetics , RNA, Small Interfering/therapeutic use , Receptor, ErbB-2/drug effects , Animals , Apoptosis/drug effects , Cell Cycle/drug effects , Cell Proliferation/drug effects , Cyclin D1/biosynthesis , Cyclin D1/genetics , Gene Expression Regulation, Neoplastic , Gene Knockdown Techniques , Gene Silencing/drug effects , Humans , Male , Mice , Mice, Nude , Neoplasm Transplantation , RNA, Small Interfering/genetics
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