The p53 tumor suppressor gene frequently is altered in gynecologic cancers.

作者: Andrew Berchuck , Matthew F. Kohler , Jeffrey R. Marks , Roger Wiseman , Jeff Boyd

DOI: 10.1016/S0002-9378(94)70414-7

关键词: OvaryHSPA1LCervixBiologyCancer researchMutantMutationEndometriumTumor suppressor geneGene

摘要: Mutation of the p53 tumor suppressor gene, often accompanied by overexpression mutant protein, is most frequent molecular genetic event described thus far in human cancers. In adenocarcinomas ovary and endometrium, seen approximately 10% to 15% early 40% 50% advanced Similar many other types cancers, ovarian endometrial cancers that overexpress protein contain mutations conserved regions gene. These are predominantly transitions, which suggests they arise spontaneously rather than being caused carcinogen exposure. Alteration gene does not appear be a feature hyperplasias or benign borderline tumors. Although mutation rarely occur cervix, vulva, vagina, it has been shown papillomavirus E6 oncoproteins bind inactivate protein. Studies have begun provide insight into pathogenesis gynecologic

参考文章(57)
A. Berchuck, B. J.M. Kerns, Robert C Bast, J. R. Marks, M. F. Kohler, P. A. Humphrey, Mutation and overexpression of p53 in early-stage epithelial ovarian cancer. Obstetrics & Gynecology. ,vol. 81, pp. 643- 650 ,(1993)
Wrede D, Vousden Kh, Crook T, p53 point mutation in HPV negative human cervical carcinoma cell lines. Oncogene. ,vol. 6, pp. 873- ,(1991)
D. D. Koeberl, R. P. Ketterling, C. D. K. Bottema, S. S. Sommer, D. P. Lillicrap, P. J. Bridge, Mutations causing hemophilia B: direct estimate of the underlying rates of spontaneous germ-line transitions, transversions, and deletions in a human gene. American Journal of Human Genetics. ,vol. 47, pp. 202- 217 ,(1990)
U. Pastorino, S. Pilotti, C. T. Cariani, R. Donghi, M. Miozzo, G. Sozzi, G. Della Porta, M. A. Pierotti, Deletions of 17p and p53 mutations in preneoplastic lesions of the lung. Cancer Research. ,vol. 52, pp. 6079- 6082 ,(1992)
Osamu Tanizawa, Takayuki Enomoto, Masami Fujita, Seiichi Iwamoto, Masaki Inoue, Alterations of the p53 gene in human primary cervical carcinoma with and without human papillomavirus infection. Cancer Research. ,vol. 52, pp. 5323- 5328 ,(1992)
Paula M. Fishbaugh, Robert C. Knapp, Chi-Ho Mok, Ching C. Lau, Sai-Wah Tsao, Unifocal origin of advanced human epithelial ovarian cancers. Cancer Research. ,vol. 52, pp. 5119- 5122 ,(1992)
Benjamin F. Trump, Inca Kusters, William P. Bennett, Curtis C. Harris, Si-min Zhu, David P. Lane, Judith A. Welsh, Monica C. Hollstein, A. He, James H. Resau, Robert A. Metcalf, p53 mutation and protein accumulation during multistage human esophageal carcinogenesis. Cancer Research. ,vol. 52, pp. 6092- 6097 ,(1992)
Malcolm C. Pike, Susan Preston-Martin, Brian E. Henderson, Peter A. Jones, Ronald K. Ross, INCREASED CELL DIVISION AS A CAUSE OF HUMAN CANCER Cancer Research. ,vol. 50, pp. 7415- 7421 ,(1990)
R. P. Ketterling, S. S. Sommer, Hong-Sup Yoon, C. D. K. Bottema, The pattern of factor IX germ-line mutation in Asians is similar to that of Caucasians. American Journal of Human Genetics. ,vol. 47, pp. 835- 841 ,(1990)
A. Berchuck, D. L. Clarke-Pearson, Billie-Jo M. Kerns, Andrew M. Davidoff, Robert C. Bast Jr., Jeffrey R. Marks, Jeffrey C. Pence, R. K. Dodge, James Dirk Iglehart, P. A. Humphrey, Overexpression and Mutation of p53 in Epithelial Ovarian Cancer Cancer Research. ,vol. 51, pp. 2979- 2984 ,(1991)