期刊文献+

非小细胞肺癌Stathmin mRNA的表达及临床意义

Expression of stathmin mRNA in non-small cell lung carcinoma and its clinical signification
下载PDF
导出
摘要 目的 探讨Stathmin mRNA在非小细胞肺癌中的表达及临床意义.方法 成对收集非小细胞肺癌手术切除的癌和癌旁组织,抽提总RNA,利用半定量RT-PCR技术检测Stathmin mRNA的表达,对其与临床病理指标的关系进行统计学分析.结果 共收集癌和癌旁组织43对,癌组织中Stathmin mRNA表达的阳性率为76.7%,癌旁组织中为60.5%,癌组织的Stathmin相对表达量明显高于癌旁组织(Z=5.359,P=0.000);无论是癌还是癌旁组织,男性中Stathmin的相对表达量明显高于女性(χ^2=5.059、5.799,P=0.024、0.016).癌组织中,鳞癌中Stathmin的相对表达量高于腺癌(χ^2=5.821,P=0.016)、中央型明显高于周围型(χ^2=4.308,P=0.038).结论 非小细胞肺癌中Stathmin mRNA的表达具有较高的阳性率,其中鳞癌、中央型肺癌和男性患者中增高最明显. Objective To investigate the expression of stathmin mRNA in non-small cell lung carcinoma (NSCLC)and its clinical significance. Methods Two-steps RT-PCR was employed to detect the levels of Stathmin mRNA in cancer tissue and corresponding pericancerous tissue from 43 NSCLC patients. Results Among 43 patients stathmin mRNA was detected in 76.7% of cancer samples and 60.5% of pericancerous tissue samples. The relative expression levels of stathmin mRNA in cancer tissue were significantly higher than those in corresponding pericancerous tissues (Z=5.359, P=0.000 ). In both cancer and pericancerous tis- sues male patients showed higher levels than females (χ^2=5.059,5.799,P=0.024,0.016). The expression of stathmin mRNA in squamous cell carcinoma and central bronchogenic carcinoma was significantly higher than that in adenocarcinoma(χ^2=5.821, P=-0.016)and peripheral lung cancer(χ^2=4.308,P=0.038 ), respectively. Conclusion Stathmin mRNA was expressed positively in most NSCLC patients, especially in male patients and patients with squamous cell carcinoma or central bronchogenic carcinoma.
出处 《浙江医学》 CAS 2011年第9期1285-1288,共4页 Zhejiang Medical Journal
基金 基金项目:浙江省医药卫生科学研究基金(2008A160)
关键词 非小细胞肺癌 STATHMIN MRNA Non-small-cell lung cancer Stathmin RNA Messenger
  • 相关文献

参考文献9

  • 1Dumontet C,Jordan M A.Microtubule-binding agents:a dynamic field of cancer therapeutics[J].Nat Rev Drug Discov,2010,9(10):790-803.
  • 2Mistry S J,Bank A,Atweh G F.Synergistic antiangiogenic effects of stathmin inhibition and taxol exposure[J].Mol Cancer Res,2007,5(8):773-782.
  • 3Alli E,Yang J M,Ford J M,et al.Reversal of stathmin-mediated resistance to paclitaxel and vinblastine in human breast carcinoma cells[J].Mol Pharmacol,2007,71(5):1233-1240.
  • 4Gavet O,Ozon S,Manceau V,et al.The stathmin phosphoprotein family:intracellular localization and effects on the microtubule network[J].J Cell Sci,1998,111 (Pt 22):3333-3346.
  • 5Honnappa S,Jahnke W,Seelig J,et al.Control of intrinsically disordered stathmin by multisite phosphorylation[J].J Biol Chem,2006,281(23):16078 -16083.
  • 6Rubin C I,Atweh G F.The role of stathmin in the regulation of the cell cycle[J].J Cell Biochem,2004,93(2):242-250.
  • 7甘淋,刘银坤.Stathmin蛋白:一个潜在的肿瘤标志物[J].肿瘤,2010,30(1):73-76. 被引量:8
  • 8李文涛,梁栋,闫培,张斌,尤伟.Stathmin基因在乳腺癌组织中的表达及其临床意义[J].中华实验外科杂志,2009,26(1):45-46. 被引量:4
  • 9丛光东,李建喆,杜亚明,王中彬.在非小细胞肺癌组织中stathmin蛋白的表达及与含紫杉方案化疗敏感性的关系[J].中国医药指南,2010,8(21):55-57. 被引量:2

二级参考文献51

  • 1井晓荣,刘丽,赵辉,张惠中.Stathmin基因表达与肿瘤化疗药物敏感性的关系[J].第四军医大学学报,2005,26(9):784-788. 被引量:8
  • 2张水军,李文涛,周闯,赵龙拴,范正军.抑癌基因TSLC1在肝癌组织中的表达及临床意义[J].中华实验外科杂志,2007,24(2):185-186. 被引量:9
  • 3Rubin CI, Atweh GF. The role of Stathmin in the regulation of the cell cycle. J Cell Biochem,2004,93:242-250.
  • 4Charbaut E, Curmi PA, Ozon S, et al. Stathmin family proteins display specific molecular and tubulin binding properties. J Biol Chem,2001, 276 : 16146-16154.
  • 5Chen Y, Lin MC, Yao H, et al. Lentivirus-mediated RNA interference targeting enhancer of zeste homolog 2 inhibits hepatocellular carcinoma growth through down-regulation of Stathmin. Hepatology, 2007,46: 200-208.
  • 6Rana S, Maples PB, Senzer N, et al. Stathmin 1 : a novel therapeutic target for anticancer activity. Expert Review of Anticancer Therapy, 2008,8 : 1461-1470.
  • 7Wu CC, Peng PH, Chang YT, et al. Identification of potential serum markers for nasopharyngeal carcinoma from a xenografted mouse model using Cy-dye labeling combined with three-dimensional fractionation. Proteomics, 2007,8 : 3605-3620.
  • 8Mistry SJ, Benham CJ, Atweh GF. Development of ribozymes that target Stathmin, a major regulator of the mitotic spindle. Antisense Nucleic Acid Drug Dev,2001,11:41-49.
  • 9Larsson N, Melander H, Marklund U, et al. G2/M transition requires multisite phosphorylation of oncoprotein 18 by two distinct protein kinase systems. J Biol Chem, 1995,270:14175-14183.
  • 10CHARBAUT E, CURMI P A, OZON S, et al. Stathmin family proteins display specific molecular and tubulin binding properties [ J ]. J Biol Chem, 2001,276 (19) : 16146-16154.

共引文献10

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