期刊文献+

外阴鳞癌组织中p14^(ARF)表达与人乳头状瘤病毒感染状态关系的研究 被引量:2

Expression of p14^(ARF) and HPV status in vulvar squamous cell carcinomas
下载PDF
导出
摘要 目的:探讨p14ARF表达与不同HPV感染状态的外阴鳞癌发生和发展的关系。方法:采用RT-PCR和蛋白印迹技术检测42例外阴鳞癌组织、10例正常外阴组织中p14ARF基因mRNA及蛋白表达水平,PCR技术检测其HPV-DNA,分析HPV阳性组和阴性组外阴鳞癌组织中,p14ARF基因mRNA及蛋白表达与其临床病理特性的关系。结果:外阴鳞癌组p14ARF基因mRNA及蛋白表达强度为0.92±0.24和1.09±0.11;正常外阴组分别为0.93±0.06和1.02±0.38,两组比较差异无统计学意义,P>0.05;低、中和高分化鳞癌组p14ARF基因mRNA表达分别为0.98±0.11、0.94±0.15和0.91±0.07;p14ARF基因蛋白表达低、中和高分化分别为1.14±0.24、1.11±0.27和1.07±0.29,3组间比较差异均无统计学意义,P>0.05。p14ARF基因mRNA及蛋白在HPV阳性组表达强度分别为0.99±0.04和1.11±0.02,HPV阴性组表达强度分别为0.61±0.07和0.76±0.06,两组比较差异有统计学意义,P<0.05。结论:p14ARF可能参与了外阴鳞癌的发生发展过程,并可能成为HPV感染的外阴鳞癌发生进展相关的基因。 OBJECTIVE: To investigate the relationship between the expression of p14^ARF and the development and progression of vulvar squamous cell carcinoma (VSCC) with different HPV infection status. METHODS: Forty-two cases of VSCC and 10 cases of normal vulvar tissues were surveyed for p14^ARF mRNA and protein by RT-PCR and Western-blot, respectively. HPV-DNA was tested by PCR technology, and then the relationship between the expression of mRNA and protein of p14^ARF and its clinical pathological characters in the HPV positive and negative groups of VSCC was investigated. RESULTS: The relative expression content of p14^ARF mRNA and protein were 0. 92±0. 24 and 1.09 ± 0. 11 respectively in VSCC, and 0.93 ± 0.06 and 1.02±0.38 in normal vulvar tissues. There was no significant difference between VSCC and normal vulvar tissue groups (P〉0.05). There was no significant difference among the poorly differentiated (0.98 ± 0.11, 1.14 ± 0.24), moderately differentiated (0.94 ± 0. 15, 1.11 ± 0.27) and well differentiated (0.91 ± 0.07, 1.07±0.29) groups (P〉0.05). The expression of mRNA and protein of p14^ARF in the HPV positive group and HPV negative group were 0. 99±0. 04, 1.11±0. 02 and 0. 61±0.07, 0.76±0. 06 respectively, and there was a significant difference between the two groups (P〈0. 05). CONCLUSION: p14^ARF may take part in the development and progression of VSCC, and it is also a gene involved in the development and progression of HPV-positive VSCC probably.
出处 《中华肿瘤防治杂志》 CAS 2008年第5期325-328,共4页 Chinese Journal of Cancer Prevention and Treatment
基金 辽宁省自然科学基金资助项目(20042067) 辽宁省教育厅攻关计划项目(2004D178)
关键词 鳞状细胞/病理学 外阴肿瘤/病理学 p14^ARF蛋白 乳头状瘤病毒 肿瘤病毒感染 印迹法 蛋白质 carcinoma, squamous cell/pathology vulvar neoplasms/pathology p14^ARF protein papillomavirus, hu-man tumor virus infections blotting, western
  • 相关文献

参考文献8

  • 1乐杰.妇产科学[M].6版.北京:人民卫生出版社,2003:154—158. 被引量:245
  • 2欧阳玲,张淑兰,王欣.外阴鳞状细胞癌组织中染色体变异与人乳头状瘤病毒感染状态的关系[J].中华妇产科杂志,2006,41(10):701-705. 被引量:6
  • 3欧阳玲,林蓓,张淑兰,张冰.外阴鳞癌组织MDM2 mRNA和p53蛋白表达及其意义[J].肿瘤防治杂志,2003,10(7):727-729. 被引量:6
  • 4Kanao H, Enomoto T, Ueda Y, et al. Correlation between P14ARF/P16INK4a expression and HPV infection in uterine cervical cancer[J]. Cancer Letter, 2004,213 (1) : 31 - 37. 被引量:1
  • 5Sano T, Masuda N, Oyama T, et al. Overexpression of p16 and P14ARF is associated with human papillomavirus infection in cervical squamous cell carcinoma and dysplasia[J]. Pathology Int, 2002, 52(5-6) :375-383. 被引量:1
  • 6Tsuda H, Hashibuchi Y, Nishimura S, et al. Relationship between HPV typing and abnormality of G1 cell cycle regulators in cervical neoplasm[J]. Gynecologic Oncology, 2003, 91 (3):476-485. 被引量:1
  • 7Stott F J, Bates S, James M C, et al. The alternative product from the human CDKN2A locus, pl4ARF, participates in a regulatory feedback loop with p53 and mdm2[J]. Eur Mol Biol Org J, 1998, 17(17):5001-5014. 被引量:1
  • 8Sano T, Hikino T, Xue Q, et al. Immunohistochemical inactivation of pl4ARF concomitant with MDM2 overexpression inversely correlates with p53 overexpresion in oral sqarnous cell carcinorna[J]. Pathol Int, 2000, 50 (9) : 709-716. 被引量:1

二级参考文献16

  • 1乐杰.妇产科学(第5版)[M].北京:人民卫生出版社,2003.15. 被引量:22
  • 2Flowers LC,Wistuba II,Scurry J,et al.Genetic changes during the multistage pathogenesis of human papillomavirus positive and negative vulvar carcinomas.J Soc Gynecol Investig,1999,6:213-221. 被引量:1
  • 3Jee KJ,Kim YT,Kim KR,et al.Loss in 3p and 4p and gain of 3q are concomitant aberrations in quamous cell carcinoma of the vulva.Mod Pathol,2001,14:377-381. 被引量:1
  • 4Al-Ghamdi A,Freedman D,Miller D,et al.Vulvar squamous cell carcinoma in young women:a clinicopathologic study of 21 cases.Gynecol Oncol,2002,84:94-101. 被引量:1
  • 5Scurry J,Flowers L,Wistuba I,et al.Human papillomavirus presence and survival.Int J Gynecol Cancer,1999,9:173-174. 被引量:1
  • 6Bryndorf T,Kirchhoff M,Larsen J,et al.The most common chromosome aberration detected by high-resolution comparative genomic hybridization in vulvar intraepithelial neoplasia is not seen in vulvar squamous cell carcinoma.Cytogenet Genome Res,2004,106:43-48. 被引量:1
  • 7Allen DG,Hutchins AM,Hammet F,et al.Genetic aberrations detected by comparative genomic hybridisation in vulvar cancers.Br J Cancer,2002,86:924-928. 被引量:1
  • 8Huang FY,Kwok YK,Lau ET,et al.Genetic abnormalities and HPV status in cervical and vulvar squamous cell carcinomas.Cancer Genet Cytogenet,2005,157:42-48. 被引量:1
  • 9Yen CC,Chen YJ,Chen JT,et al.Comparative genomic hybridization of esophageal squamous cell carcinoma:correlations between chromosomal aberrations and disease progression/prognosis.Cancer,2001,92:2769-2777. 被引量:1
  • 10Raitanen M,Worsham MJ,Lakkala T,et al.Characterization of 10 vulvar carcinoma cell lines by karyotyping,comparative genomic hybridization and flow cytometry.Gynecol Oncol,2004,93:155-163. 被引量:1

共引文献253

同被引文献27

  • 1王淑珍,孙建衡.外阴癌的诊断与治疗[J].中华肿瘤防治杂志,2006,13(9). 被引量:11
  • 2Jha AK,Nikbakht M,Jain V,et al. p16INK4a and p15INK4b gene pro- moter methylation in cervical cancer patients [ J ]. Oncol Lett,2012, 30(6) :1331 - 1335. 被引量:1
  • 3Ozenne P ,Eymin B, Brambilla E, et at. l lae Alxr tumor supplul ; Structure,fuuefions and status in cancer [ J ]. Int J Cancer,2010, 127 ( 10 ) :2239 - 2247. 被引量:1
  • 4Zeng Y,Kotake Y, Pei XH, et al. p53 binds to and Is required for the repression of arf tumor suppressor by HDAC and polycomb[ J]. Cancer Res,2011,71 (7) :2781 - 2792. 被引量:1
  • 5Pollice A, Vivo M, La Mantia G. The promiscuity of ARF interac- tions with the proteasome [ J ]. FEBS Lett, 2008,582 ( 23 - 24 ) : 3257 - 3262. 被引量:1
  • 6Shen J,Zhang S,Li Y,et al. p14ARF inhibits the functions of adeno- virus E1A oncoprotein[ J]. Biochem J,2011,434(2) :275 - 285. 被引量:1
  • 7Chen D, Shah J, Zhu WG. Transcription - independent ARF regula- tion in oncogenic stress - mediated p53 responses [ J]. Nature, 2010,464 (7288) :624 - 627. 被引量:1
  • 8Kim YT, Zhao M. Aberrant cell cycle regulation in cervical carcino- ma[ J]. Yonsei Med J,2005,46 (5) :597 - 613. 被引量:1
  • 9Di Tommaso A, Hagen J, Tompkins V, et al. Residues in the alter- native reading frame tumor suppressor that influence its stability and p53 - independent activities [ J ]. Exp Cell Res, 2009,315(7) :1326 - 1335. 被引量:1
  • 10Freedberg DE, Rigas SH, Russak J, et al. Frequent p16 - Inde- pendent Inactivation of p14ARt in human melanoma [ J]. J Natl Cancer Inst,2008,100( 11 ) :784 -795. 被引量:1

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部