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Updated: Jun 2, 2026

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Expression and sequence analysis of the SDI1/WAF1/CIP1/p21 tumor suppressor gene in prostate cancer cell lines
C Papandreou1, T Bogenrieder, H Scher
1MEM SLOAN KETTERING CANC CTR,GENITOURINARY ONCOL RES LAB,NEW YORK,NY 10021. MEM SLOAN KETTERING CANC CTR,LAB MAMMALIAN CELL TRANSFORMAT,NEW YORK,NY 10021. MEM SLOAN KETTERING CANC CTR,DEPT MED,DIV SOLID TUMOR ONCOL,GENITOURINARY ONCOL SERV,NEW YORK,NY 10021. CORNELL UNIV,MED CTR,NEW YORK,NY 10021.
Abstract:
The SDI1/WAF1/CIP1 gene encodes a M(r) 21,000 protein (p21) that can arrest cell growth by associating with and inhibiting cyclin-dependent kinase complexes necessary for cells to exit G(1). It is a critical downstream effector in the p53 growth control pathway and can be transcriptionally upregulated by increasing levels of wild-type p53 protein. Somatic mutations in the p21 gene have been detected in 17% of primary prostate cancers. In the current study, we examined four prostate cancer cell lines for expression of and mutations in the p21 gene. Transcripts for p21 mRNA were present in all PC cell lines; p21 protein was detected in androgen-dependent LNCaP cells, as well as in androgen-independent DU-145 and TSU-Pr1 cells but not in androgen-independent PC-3 cells. Examination of the entire coding region of the p21 gene by SSCP analysis and direct DNA sequencing did not detect mutations in the coding domains of the p21 gene. These data indicate that mutations of the SDI1/WAF1/CIP1/p21 gene are not present in cultured PC cells and suggest that defects in the p21 gene are infrequent in prostate cancers.
Insights
Prostate cancer cell lines express p21 mRNA and protein, but lack mutations in the SDI1/WAF1/CIP1/p21 gene. This suggests p21 gene defects are uncommon in prostate cancers.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- The SDI1/WAF1/CIP1 gene encodes p21, a protein that inhibits cyclin-dependent kinases to arrest cell growth.
- p21 is a key downstream effector in the p53 pathway and is upregulated by wild-type p53.
- Somatic mutations in the p21 gene occur in 17% of primary prostate cancers.
Purpose of the Study:
- To investigate the expression and mutation status of the p21 gene in prostate cancer cell lines.
- To determine if mutations in the p21 gene are present in cultured prostate cancer cells.
Main Methods:
- Analysis of p21 mRNA and protein expression in four prostate cancer cell lines.
- Mutation screening of the entire coding region of the p21 gene using SSCP analysis and direct DNA sequencing.
Main Results:
- p21 mRNA was detected in all examined prostate cancer cell lines.
- p21 protein was found in LNCaP, DU-145, and TSU-Pr1 cells, but not in PC-3 cells.
- No mutations were identified in the coding domains of the p21 gene across the tested cell lines.
Conclusions:
- Mutations in the SDI1/WAF1/CIP1/p21 gene are absent in the studied prostate cancer cell lines.
- These findings suggest that defects in the p21 gene are infrequent in prostate cancers.
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