Recombinant adenovirus vector expressing wildtype p53 is a potent inhibitor of prostate cancer cell proliferation

Shiv Srivastava, Dai Katayose, Yue Ao Tong, Caroline R. Craig, David G. McLeod, Judd W. Moul, Kenneth H. Cowan, Prem Seth

Research output: Contribution to journalArticle

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Abstract

Objectives: A recombinant adenovirus vector (AdWTp53) expressing wild-type p53 was evaluated for its cell growth inhibitory effects on metastatic human prostate cancer cells. Methods: Human prostate cancer cells LNCaP, DU145, PC3, 1LN, and DUPro-1 were infected with AdWTp53 vector and expression of exogenous p53 in these cells was analyzed by immunoprecipitation and western blot assays. The cell growth inhibitory effects of AdWTp53 were determined by counting cell number on a hemocytometer or by crystal violet staining of cells after infection with AdWTp53. The p53-regulated gene WAF1 and DNA fragmentation were also analyzed in prostate cancer cells infected with AdWTp53. Results: High levels of the AdWTp53 vector-derived p53 protein were present in metastatic prostate cancer cells, and the p53-regulated gene WAF1 was induced in these cells. Infection of these tumor cell lines with AdWTp53 vector resulted in severe growth inhibition and cell death in comparison to untreated or control adenovirus vector-infected cells. Furthermore, fragmentation of genomic DNA, a property associated with apoptosis, was also observed in prostate cancer cells infected with AdWTp53. Conclusions: AdWTp53 vector exhibited a potent inhibitory effect on the growth of all of human metastatic prostate cancer cells, and both cytostatic and cytotoxic effects of AdWTp53 were observed. The induction of p53-regulated gene WAF1 in AdWTp53-infected prostate cancer cells suggests the involvement of cellular p53 pathway in the cell growth inhibition. These results provide a molecular basis for further evaluation of antitumorigenic effects of AdWTp53 vector in animal models of prostate cancer.

Original languageEnglish (US)
Pages (from-to)843-848
Number of pages6
JournalUrology
Volume46
Issue number6
DOIs
StatePublished - Dec 1995

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Adenoviridae
Prostatic Neoplasms
Cell Proliferation
p53 Genes
Growth
DNA Fragmentation
Gentian Violet
Cytostatic Agents
Infection
Tumor Cell Line
Immunoprecipitation
Cell Death
Animal Models
Cell Count
Western Blotting
Apoptosis
Staining and Labeling

ASJC Scopus subject areas

  • Urology

Cite this

Srivastava, S., Katayose, D., Tong, Y. A., Craig, C. R., McLeod, D. G., Moul, J. W., ... Seth, P. (1995). Recombinant adenovirus vector expressing wildtype p53 is a potent inhibitor of prostate cancer cell proliferation. Urology, 46(6), 843-848. https://doi.org/10.1016/S0090-4295(99)80355-0

Recombinant adenovirus vector expressing wildtype p53 is a potent inhibitor of prostate cancer cell proliferation. / Srivastava, Shiv; Katayose, Dai; Tong, Yue Ao; Craig, Caroline R.; McLeod, David G.; Moul, Judd W.; Cowan, Kenneth H.; Seth, Prem.

In: Urology, Vol. 46, No. 6, 12.1995, p. 843-848.

Research output: Contribution to journalArticle

Srivastava, S, Katayose, D, Tong, YA, Craig, CR, McLeod, DG, Moul, JW, Cowan, KH & Seth, P 1995, 'Recombinant adenovirus vector expressing wildtype p53 is a potent inhibitor of prostate cancer cell proliferation', Urology, vol. 46, no. 6, pp. 843-848. https://doi.org/10.1016/S0090-4295(99)80355-0
Srivastava, Shiv ; Katayose, Dai ; Tong, Yue Ao ; Craig, Caroline R. ; McLeod, David G. ; Moul, Judd W. ; Cowan, Kenneth H. ; Seth, Prem. / Recombinant adenovirus vector expressing wildtype p53 is a potent inhibitor of prostate cancer cell proliferation. In: Urology. 1995 ; Vol. 46, No. 6. pp. 843-848.
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abstract = "Objectives: A recombinant adenovirus vector (AdWTp53) expressing wild-type p53 was evaluated for its cell growth inhibitory effects on metastatic human prostate cancer cells. Methods: Human prostate cancer cells LNCaP, DU145, PC3, 1LN, and DUPro-1 were infected with AdWTp53 vector and expression of exogenous p53 in these cells was analyzed by immunoprecipitation and western blot assays. The cell growth inhibitory effects of AdWTp53 were determined by counting cell number on a hemocytometer or by crystal violet staining of cells after infection with AdWTp53. The p53-regulated gene WAF1 and DNA fragmentation were also analyzed in prostate cancer cells infected with AdWTp53. Results: High levels of the AdWTp53 vector-derived p53 protein were present in metastatic prostate cancer cells, and the p53-regulated gene WAF1 was induced in these cells. Infection of these tumor cell lines with AdWTp53 vector resulted in severe growth inhibition and cell death in comparison to untreated or control adenovirus vector-infected cells. Furthermore, fragmentation of genomic DNA, a property associated with apoptosis, was also observed in prostate cancer cells infected with AdWTp53. Conclusions: AdWTp53 vector exhibited a potent inhibitory effect on the growth of all of human metastatic prostate cancer cells, and both cytostatic and cytotoxic effects of AdWTp53 were observed. The induction of p53-regulated gene WAF1 in AdWTp53-infected prostate cancer cells suggests the involvement of cellular p53 pathway in the cell growth inhibition. These results provide a molecular basis for further evaluation of antitumorigenic effects of AdWTp53 vector in animal models of prostate cancer.",
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AU - Moul, Judd W.

AU - Cowan, Kenneth H.

AU - Seth, Prem

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