期刊文献+

microRNA-21、PTEN、NF-κB、Caspase-9在结肠癌中的表达及意义 被引量:6

Expressions and significances of microRNA-21, PTEN, NF-κB and caspase-9 in colon carcinoma
原文传递
导出
摘要 目的研究microRNA-21(miR-21)、PTEN、NF-κB、Caspase-9在结肠癌中的表达及在肿瘤进展中的可能机制。方法检测结肠癌、结肠腺瘤及正常黏膜中上述指标的表达及凋亡细胞百分率。结果miR-21、PTEN、NF-κB、Caspase-9阳性表达率在正常黏膜中分别为0.39±0.02、50%、25%、50%,在结肠腺瘤中分别为0.62±0.06、50%、35%、55%,在结肠癌中分别为0.88±0.04、30%、75%、20%。凋亡细胞百分率分别为(24.64±7.66)%、(15.86±1.44)%、(6.20±2.57)%(均P〈0.05)。miR-21与TNM分期、浸润深度、分化程度及NF-κB表达呈正相关,与PTEN、Caspase-9表达及凋亡细胞百分率呈负相关(r=0.647、0.297、0.259、0.519、-0.299、-0.388、-0.931,P均〈0.05)。结论结肠癌中miR-21高表达可能通过下调PTEN、Caspase-9、上调NF-κB、从而抑制细胞凋亡参与肿瘤进展。 Objective To investigate expressions of microRNA-21 (miR-21), FFEN, NF-κB, and caspase-9 in colon carcinoma and their possible mechanisms in progression of tumor. Methods Expressions of above-mentioned indexes and percentage of apoptotic cells in colon carcinoma, colon adenoma, and normal tissue specimen were detected. Results Expressions of miR-21, PTEN, NF-κB, and caspase- 9 in normal tissue were 0. 39 ±0.02, 50% , 25% , and 50%. Expressions of them in colon adenoma were 0. 62 ±0. 06, 50%, 35% , and 55% , and those in colon carcinoma were 0. 88 ±0. 04, 30% , 75% , and 20%. Percentage of apoptotic cells were ( 24. 64 ± 7.66) %, ( 15.86± 1.44 ) % , and ( 6. 20± 2. 57 ) % , respectively. The above P-values were all less than 0.05. Expression of miR-21 was positively correlated with TNM stage, depth of infiltration, differentiated level and expression of NF-κB while inversely correlated with PTEN and caspase-9 expressions and percentage of apoptotic cells. The r-values were 0. 647, 0. 297, 0. 259, 0. 519, -0. 299, - O. 388, and - 0. 931, respectively. Conclusions Hyperexpression of miR- 21 participated in progression of colon carcinoma probably through down-regulating expressions of PTEN and caspase-9 and up-regulating expression of NF-κB and then suppressing cell apoptosis.
作者 蒋丽 张桂英
出处 《中国医师杂志》 CAS 2013年第1期39-41,共3页 Journal of Chinese Physician
关键词 微RNAs 代谢 基因 肿瘤抑制 NF-ΚB 代谢 半胱氨酸天冬氨酸蛋白酶9 代谢 结肠肿瘤 代谢 结肠肿瘤 病理学 MicroRNAs/metabolism Genes, tumor suppressor NF-kappa B/metabolism Caspase 9/metabolism Colonic neoplasms/metabolism Colonic neoplasms/pathology
  • 相关文献

参考文献13

二级参考文献73

共引文献34

同被引文献39

  • 1张谷月,张志勇,王晔,吴晨鹏,张林,刘丽云,李华,云翔,沈福海.PTEN在结肠癌组织中的表达及其临床意义[J].中国老年学杂志,2014,34(12):3270-3271. 被引量:5
  • 2Bae S, Ahn JH, Park CW, et al. Gene and microRNA expression signatures of human mesenchymal stromal ceils in comparison to fi- broblasts[J]. Cell Tissue Res, 2009, 335(3) : 565-573.
  • 3Calin GA, Crece CM. MicroRNA signatures in human cancers [J]. Nat Rev Cancer,2006, 6(11): 857-866.
  • 4Philippidou D, Schmitt M, Moser D, et al. Signatures of microR- NAs and selected microRNA target genes in human melanoma[ J]. Cancer Res, 2010, 70(10) : 4163-4173.
  • 5Chen GQ, Zhao ZW, Zhou HY, et al. Systematic analysis of mi- croRNA involved in resistance of the MCF-7 human breast cancer cell to doxorubicin[J]. Med Oncol, 2010, 27(2) : 406-415.
  • 6Eitan R, Kushnir M, Lithwick-Yanai G, et al. Tumor microRNA expression patterns associated with resistance to Platinum based chemotherapy and survival in ovarian cancer patients[ J]. Gynecol Oncol, 2009, 114(2) :253-259.
  • 7Boren T, Xiong Y, Hakam A, et al. MicroRNAs and their target messenger RNAs associated with ovarian cancer response to chemotherapy [J]. Gynecol Oncol, 2009, 113(20) :249-255.
  • 8Valadi H, Ekstrom K, Bossios A, et al. Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of ge- netic exchange between cells[J]. Nat Cell Biol, 2007, 9(6) : 654-659.
  • 9Therasse P, Arbuck SG, Eisenhauer EA, et al. New guidelines to evaluate the response to treatment in solid tumors. European Organization for Research and Treatment of Caneer, National Caneer Institute of the United States. National Cancer Institute of Canada [ J ]. JNatl Cancer Inst,2000, 92 ( 3 ) :205-216.
  • 10Sorrentino A, Liu CG, Addario A, et al. Role of microRNA in drngresistance ovarian cancer cells [ J ]. Gynecol Oncol, 2008, 111 (3) :478-486.

引证文献6

二级引证文献13

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