RETRACTED: Effects of cisplatin on the LSD1-mediated invasion and metastasis of prostate cancer cells (Retracted article. See vol. 28, pg. 140, 2023)

被引:6
作者
Chen, Zhi-Yuan [1 ]
Chen, Hui [1 ]
Qiu, Tao [1 ]
Weng, Xiao-Dong [1 ]
Guo, Jia [1 ]
Wang, Lei [1 ]
Liu, Xiu-Heng [1 ]
机构
[1] Wuhan Univ, Dept Urol, Renmin Hosp, 238 Jiefang Rd, Wuhan 430060, Hubei, Peoples R China
关键词
lysine-specific demethylase 1; DDP; prostate cancer; proliferation; invasion; PREDICT RISK; TGF-BETA; GROWTH; ANGIOGENESIS; ERK; EXPRESSION; APOPTOSIS; VEGF;
D O I
10.3892/mmr.2016.5571
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Prostate cancer poses a major public health problem in men. Metastatic prostate cancer is incurable, and ultimately threatens the life of patients. Lysine-specific demethylase 1 (LSD1) is an androgen receptor-interacting protein that exerts a key role in regulating gene expression and is involved in numerous biological processes associated with prostate cancer. Cisplatin, also known as cis-diamminedichloroplatinum or DDP, is a standard chemotherapeutic agent used to treat prostate cancer; however, it has the disadvantage of various serious side effects. The present study aimed to investigate the effects of LSD1 knockdown, and the interplay between LSD1 and DDP, on prostate cancer cell proliferation, apoptosis and invasion, and, therefore, the potential of LSD1 as a target for prostate cancer therapy. Flow cytometric analysis, Cell Counting kit 8 assay, Transwell assay and western blotting results revealed that LSD1 knockdown, in combination with DDP treatment, exerted antiproliferative, proapoptotic and anti-invasive effects on PC3 prostate cancer cells. In addition, knockdown of LSD1 acted synergistically with DDP, thereby enhancing the induction of apoptosis, and the inhibition of proliferation and invasion in prostate cancer cells. These results indicated that LSD1 may serve as a potential therapeutic target, and may enhance the sensitivity of PC3 cells to DDP.
引用
收藏
页码:2511 / 2517
页数:7
相关论文
共 42 条
[1]   Impact of Age at Diagnosis on Prostate Cancer Treatment and Survival [J].
Bechis, Seth K. ;
Carroll, Peter R. ;
Cooperberg, Matthew R. .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (02) :235-241
[2]   E-cadherin-integrin crosstalk in cancer invasion and metastasis [J].
Canel, Marta ;
Serrels, Alan ;
Frame, Margaret C. ;
Brunton, Valerie G. .
JOURNAL OF CELL SCIENCE, 2013, 126 (02) :393-401
[3]   International Variation in Prostate Cancer Incidence and Mortality Rates [J].
Center, Melissa M. ;
Jemal, Ahmedin ;
Lortet-Tieulent, Joannie ;
Ward, Elizabeth ;
Ferlay, Jacques ;
Brawley, Otis ;
Bray, Freddie .
EUROPEAN UROLOGY, 2012, 61 (06) :1079-1092
[4]   Molecular determinants of resistance to antiandrogen therapy [J].
Chen, CD ;
Welsbie, DS ;
Tran, C ;
Baek, SH ;
Chen, R ;
Vessella, R ;
Rosenfeld, MG ;
Sawyers, CL .
NATURE MEDICINE, 2004, 10 (01) :33-39
[5]   Functions and regulation of transforming growth factor-beta (TGF-β) in the prostate [J].
Danielpour, D .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (06) :846-857
[6]   The RAS/RAF/MEK/ERK and the PI3K/AKT signalling pathways: role in cancer pathogenesis and implications for therapeutic approaches [J].
De Luca, Antonella ;
Maiello, Monica R. ;
D'Alessio, Amelia ;
Pergameno, Maria ;
Normanno, Nicola .
EXPERT OPINION ON THERAPEUTIC TARGETS, 2012, 16 :S17-S27
[7]   A history of prostate cancer treatment [J].
Denmeade, SR ;
Isaacs, JT .
NATURE REVIEWS CANCER, 2002, 2 (05) :389-396
[8]   T Cell Surveillance of Oncogene-Induced Prostate Cancer Is Impeded by T Cell-Derived TGF-β1 Cytokine [J].
Donkor, Moses K. ;
Sarkar, Abira ;
Savage, Peter A. ;
Franklin, Ruth A. ;
Johnson, Linda K. ;
Jungbluth, Achim A. ;
Allison, James P. ;
Li, Ming O. .
IMMUNITY, 2011, 35 (01) :123-134
[9]   The biology of VEGF and its receptors [J].
Ferrara, N ;
Gerber, HP ;
LeCouter, J .
NATURE MEDICINE, 2003, 9 (06) :669-676
[10]  
Florea Ana-Maria, 2011, Cancers (Basel), V3, P1351, DOI 10.3390/cancers3011351