Abstract | OBJECTIVE: METHODS: We established an AIPC cell model LNCaP-AI by culturing the androgen-dependent LNCaP cell line in the hormone-deprived medium for over 3 months. The cell model was verified and the PTTG1 expression in the LNCaP cells was detected by Western blot and RT-PCR during hormone deprivation. RESULTS: The AIPC cell model LNCaP-AI was successfully established. The PTTG1 expression was gradually increased in the LNCaP cells with the prolonged time of hormone deprivation and the expressions of matrix metalloproteinases MMP-2 and -9 were elevated at the same time. CONCLUSIONS: The expression of PTTG1 is increased gradually in AIPC, which may be a target of gene therapy for advanced prostate cancer.
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Authors | Xi-Liang Cao, Xiao-Ming Song, Wen-Chao Yu, Yong-Qiang Chen, Yang-Yang Wei, Yong-Liang Liu, Ke-Quan Lu |
Journal | Zhonghua nan ke xue = National journal of andrology
(Zhonghua Nan Ke Xue)
Vol. 22
Issue 8
Pg. 686-691
(Aug 2016)
ISSN: 1009-3591 [Print] China |
PMID | 29019223
(Publication Type: Journal Article)
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Chemical References |
- Securin
- pituitary tumor-transforming protein 1, human
- Matrix Metalloproteinase 2
- Matrix Metalloproteinase 9
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Topics |
- Blotting, Western
- Cell Line, Tumor
- Gene Expression Regulation, Neoplastic
- Humans
- Male
- Matrix Metalloproteinase 2
(metabolism)
- Matrix Metalloproteinase 9
(metabolism)
- Neoplasms, Hormone-Dependent
- Prostatic Neoplasms
(enzymology, genetics)
- Securin
(genetics)
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