期刊文献+

变异性分化抗原簇44(CD44v17)对宫颈癌的临床诊断意义 被引量:1

Clinical Diagnosis Value of CD44V17 in Cervical Cancer
原文传递
导出
摘要 目的:探讨CD44v17对宫颈癌的临床诊断意义。方法:将CD44v17si RNA、CD44v17、生理盐水转染至传代后的人宫颈癌细胞。检测细胞转染后存活率;检测细胞凋亡率。在裸鼠左肩背部注入人宫颈癌细胞悬液,随机分为CD44v17组、CD44v17si RNA组、对照组。在CD44v17组、CD44v17si RNA组裸鼠瘤体内分别注入CD44v17病毒颗粒、CD44v17si RNA病毒颗粒。检测瘤体的质量与体积。选取疑有宫颈病变患者阴道镜下活检组织80例,正常宫颈组织15例、宫颈上皮内瘤变(CIN)I级组织l5例、CIN II级15例、CIN III级组织15例和宫颈癌组织20例。检测CD44v17在不同组织中的表达量。结果:CD44v17si RNA转染的宫颈癌细胞凋亡率(19.20±2.14%)高于CD44v17转染的宫颈癌细胞凋亡率(6.13±1.08%)(P<0.05)。CD44v17组裸鼠瘤体质量(15.9±3.4)g高于对照组裸鼠瘤体质量(11.8±2.7)g(P<0.05)。CD44v17在不同组织中的表达量,按正常宫颈、CINⅠ级、CINⅡ级、CINⅢ级、宫颈癌发展过程呈递增趋势(P<0.05)。结论:CD44v17能抑制宫颈癌细胞凋亡,促进宫颈癌细胞的生长、增殖。通过降低CD44v17表达量可能是遏制CIN向宫颈癌发展的一个手段。 Objective: To explore the clinical diagnosis value of CD44V17 in cervical cancer. Methods: CD44v17 si RNA, CD44v17,physiological saline was transfected into cultured human cervical cancer cells. The cell viability was detected. The rate of apoptosis was detected. Human cervical cancer cell was suspensioned the left shoulder of nude mice. The nude mice were randomly divided into CD44v17 group, CD44v17 si RNA group and control group. The nude mice of CD44v17 group and CD44v17 si RNA group were injected with CD44v17 virus particles and CD44v17 si RNA virus particles, respectively. The quality and volume of tumor were detected. The biopsy tissues of totally 80 patients with cervical lesions were selected. According to pathological classification, there were 15 cases of normal cervical tissues, cervical intraepithelial neoplasia(CIN) I grade 15 cases, II grade CIN 15 cases, III grade CIN 15 cases and 20 cases of cervical cancer tissues. The expression of CD44v17 in different tissues was detected. Results: The rate of apoptosis of cervical cancer cells transfected with CD44v17 si RNA(19.20±2.14 %) was higher than that of CD44v17 transfected cervical cancer cell(6.13±1.08 %)(P 〈0.05). The quality of tumor(15.9±3.4) g in CD44v17 group was higher than that in control group(11.8 ±2.7) g(P〈0.05).The expression of CD44v17 in normal cervix, cervical intraepithelial neoplasia grade, grade II CIN, cervical intraepithelial neoplasia grade, cervical cancer was progressively increased with statistical significance(P〈0.05). Conclusions: CD44v17 can inhibit the apoptosis of cervical cancer cells and promote the growth and proliferation of cervical cancer cells. By reducing the expression of CD44v17 may be a effective method to curb the development of CIN to cervical cancer.
出处 《现代生物医学进展》 CAS 2016年第19期3625-3628,3609,共5页 Progress in Modern Biomedicine
基金 上海市卫生局科研基金项目(03.02.12.003)
关键词 变异性分化抗原簇44 宫颈上皮内瘤变 宫颈癌 CD44V17 Cervical intraepithelial neoplasia Cervical cancer
  • 相关文献

参考文献18

二级参考文献94

  • 1王临虹,邱琇,郑睿敏,狄江丽.我国宫颈癌流行病学状况及防治策略的回顾与展望[J].中国妇幼卫生杂志,2010,1(3):146-149. 被引量:76
  • 2章必成,王俊,陈正堂.肿瘤相关巨噬细胞的研究进展[J].临床肿瘤学杂志,2007,12(3):228-231. 被引量:10
  • 3Schiffman M, Castle PE, Jeronimo J, et al. Human papillomavirus and cervical cancer[ J]. Lancet, 2007, 370 : 890 - 907.
  • 4Bosch FX,Lorinezc A, Munoz N, et al. The causal relation between human papomavirus and cervieal cancer[ J]. J Clin Pathol, 2002, 55 (4) : 244 -265.
  • 5Li N, Franceschi S, Howell -Jones R, et al. Clifford GM. Human papillomavirus type distribution in 30, 848 invasive cervical cancers worldwide: variation by geographical region, histological type and year of publication[J]. Int J Cancer, 2011, 128 : 927 -935.
  • 6Kalantari M, Villa LL, Calleja - Macias IE, et al. Human papilloma- virus - 16 and - 18 in penile carcinomas: DNA methylation, chromo- somal recombination and genomic variation[ J. Int J Cancer, 2008, 123 (8): 1832-1840.
  • 7Spitzer M. In vitro conventional cytology historical strengths and cur- rent limitations [ J ]. Obstet Gynecol Clin North Am, 2002, 29 (4) : 673 - 683.
  • 8Trottier H, Mahmud S, Costa MC, et al. Human papillomavirus in- fections with multiple typesand risk of cervical neoplasia. Cancer Epi- demiol. Biomark[J]. Prey, 2006, 15 (7): 1274-1280.
  • 9Kinney W, Stoler MH, Castle PE. Special commentary: patient safe- ty and the next generation of HPV DNA tests [ J ]. Am J Clin Pathol, 2010, 134:193-199.
  • 10Fernandez AF, EsteUer M. Viral epigenomes in human tumorigenesis [J]. Oncogene, 2010, 29: 1405-1420.

共引文献123

同被引文献6

引证文献1

二级引证文献5

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