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P16 methylation of the colorectal cancer and association with dukes stages

  • Clinical Observation
  • Published:
Chinese Journal of Cancer Research

Abstract

Objective: To explore whether methylation of the CpG island in the promoter of the p16 tumor suppressor gene was associated with clinicopathological characteristics of the colorectal cancer patients. Methods: Methylation-specific PCR (MSP) was used to detect p16 methylation of the colorectal cancer patients. Results: In 58 sporadic colorectal cancer, 43.1% of the tumors had detectable p16 methylation. Dukes’ stage was associated with p16 methylation status. Dukes C, D patients (75%) were more likely to contain methylated p16 compared with Dukes A, B patients (13.3%). Conclusion: p16 methylation plays a role in the carcinogenesis of a subset of colorectal cancer. P16 methylation might be considered as a prognostic indicator.

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References

  1. Serrano M, Hannon GJ, Beach D. A new regulatory motif in cell cycle control causing specific inhibition of cyclinD/CDK4[J]. Nature 1993; 366: 704.

    Article  PubMed  CAS  Google Scholar 

  2. Kamb A, Gruis N, Weaver FJ, et al. A cell cycle regulator potentially involved in genesis of many tumor types[J]. Science 1994; 264: 436.

    Article  PubMed  CAS  Google Scholar 

  3. Margarida R, Gordon P. The p16INK4a/CDKN2A tumor suppressor and its relatives[J]. Biochimica et Biophysica Acta 1998; 1378: 115.

    Google Scholar 

  4. Herman JG, Merlo A, mao L. Inactivetion of the CDKN2/p16/MTS1 gene is frequently associated with aberrant DNA methylation in all common human cancers[J]. Cancer Res 1995; 55: 4525.

    PubMed  CAS  Google Scholar 

  5. Jen J, Harper W, Bigner SH, et al. Delection of p16 and p15 genes in brain tumors[J]. Cancer Res 1994; 54: 6353.

    PubMed  CAS  Google Scholar 

  6. Wiencke JK, zheng S, Lafuente A, et al. Aberrant methylation of p16INK4a in anatomic and gender-specific subtypes of sporadic colorectal cancer[J]. Cancer Epidemiol Biomarker Prev 1999; 8: 501.

    CAS  Google Scholar 

  7. Peter W Laird, Rudolf Jaenisch. The role of DNA methylation in cancer genetics and epigenetics[J]. Annu Res Genet 1996; 30: 441.

    Article  CAS  Google Scholar 

  8. Baylin SB, Herman JG, Graff JR, et al. Alterations in DNA methylaion: A fundamental aspect of neoplasia[J]. Adv Cancer Res 1998; 72: 141.

    Article  PubMed  CAS  Google Scholar 

  9. Merlo A, herman JG, Mao L, et al. 5’CpG island methylation is associated with transcriptional silencing of the tumor suppressor p16/CDKN2/MTS1 in human cancers[J]. Natl Med 1995; 1: 686.

    Article  CAS  Google Scholar 

  10. Gonzalez ZM, Bender CM, Yang AS, et al. Methylation of the 5′CpG island of the p16/CDKN2 tumor suppressor gene in normal and transformed human tissues correlates with gene silencing[J]. Cancer Res 1995; 55: 4531.

    Google Scholar 

  11. Herman JG, Jeremy RG, Sanna M, et al. Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands[J]. Proc Natl Acad Sci USA 1996; 93: 9821.

    Article  PubMed  CAS  Google Scholar 

  12. Guan RJ, Fu YN, Holt PR, et al. Association of K-ras mutations with p16 methylation in human colon cancer[J]. Gastroenterology 1999; 116: 1063.

    Article  PubMed  CAS  Google Scholar 

  13. Liang JT, chang KJ, Chen JC, et al. Hypermethylation of the p16 gene in sporadic T3N0M0 stage colorectal cancers: association with DNA replication error and shorter survival[J]. Oncology 1999; 57: 149.

    Article  PubMed  CAS  Google Scholar 

  14. Esteller M, Tortola S, Toyota M, et al. Hypermethylation-associated inactivation of p14(ARF) is independent of p16(INK4a) methylation and p53 mutational status[J]. Cancer Res 2000; 60: 129.

    PubMed  CAS  Google Scholar 

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Correspondence to Wang Zhi-wei.

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Foundation item: This work was supported by a grant from Ministry of Public Health of China (No. 98-1-303) and The Education Committee of Shanghai(No. 1 2000B02).

Biography: WANG Zhi-wei(1970–), master of medicine, Department of Cell Biology, Shanghai Second Medical University, majors in cell biology of cancer.

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Wang, Zw., Yi, J., Cang, H. et al. P16 methylation of the colorectal cancer and association with dukes stages. Chin. J. Cancer Res. 13, 288–290 (2001). https://doi.org/10.1007/s11670-001-0050-8

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  • DOI: https://doi.org/10.1007/s11670-001-0050-8

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