天津医药
天津醫藥
천진의약
TIANJIN MEDICAL JOURNAL
2013年
8期
737-739
,共3页
高利飞%田延锋%赵增仁%张丽静%贺新奇%裴永彬
高利飛%田延鋒%趙增仁%張麗靜%賀新奇%裴永彬
고리비%전연봉%조증인%장려정%하신기%배영빈
结直肠肿瘤%癌%微RNAs%寡核苷酸序列分析%聚合酶链反应%miR-224%miR-378e
結直腸腫瘤%癌%微RNAs%寡覈苷痠序列分析%聚閤酶鏈反應%miR-224%miR-378e
결직장종류%암%미RNAs%과핵감산서렬분석%취합매련반응%miR-224%miR-378e
colorectal neoplasms%carcinoma%microRNAs%oligonucleotide array sequence analysis%polymerase chain reaction%miR-224%miR-378e
目的探讨miR-224和miR-378e在原位大肠癌癌组织和癌旁正常黏膜组织中的表达差异,并分析其临床意义。方法 miRNA表达谱芯片技术检测大肠癌癌组织和癌旁组织标本中表达差异的miRNA,运用荧光实时定量聚合酶链反应(real-time PCR)验证其结果,并分析其与临床病理资料之间的关系。结果 miRNA表达芯片分析发现,与正常黏膜组织比较,miR-224在大肠癌组织中表达显著上调,miR-378e在大肠癌组织中表达显著下调,并被real-time PCR所证实。miR-224在不同组织学类型癌组织中表达差异有统计学意义,miR-378e在不同浸润深度癌组织中表达差异有统计学意义,miR-224表达与组织学类型有关,miR-378e表达与大肠癌浸润深度有关。结论miR-224具有潜在的癌基因作用,miR-378e具有潜在的抑癌基因作用,miR-224和miR-378e可作为潜在的大肠癌分子标志物。
目的探討miR-224和miR-378e在原位大腸癌癌組織和癌徬正常黏膜組織中的錶達差異,併分析其臨床意義。方法 miRNA錶達譜芯片技術檢測大腸癌癌組織和癌徬組織標本中錶達差異的miRNA,運用熒光實時定量聚閤酶鏈反應(real-time PCR)驗證其結果,併分析其與臨床病理資料之間的關繫。結果 miRNA錶達芯片分析髮現,與正常黏膜組織比較,miR-224在大腸癌組織中錶達顯著上調,miR-378e在大腸癌組織中錶達顯著下調,併被real-time PCR所證實。miR-224在不同組織學類型癌組織中錶達差異有統計學意義,miR-378e在不同浸潤深度癌組織中錶達差異有統計學意義,miR-224錶達與組織學類型有關,miR-378e錶達與大腸癌浸潤深度有關。結論miR-224具有潛在的癌基因作用,miR-378e具有潛在的抑癌基因作用,miR-224和miR-378e可作為潛在的大腸癌分子標誌物。
목적탐토miR-224화miR-378e재원위대장암암조직화암방정상점막조직중적표체차이,병분석기림상의의。방법 miRNA표체보심편기술검측대장암암조직화암방조직표본중표체차이적miRNA,운용형광실시정량취합매련반응(real-time PCR)험증기결과,병분석기여림상병리자료지간적관계。결과 miRNA표체심편분석발현,여정상점막조직비교,miR-224재대장암조직중표체현저상조,miR-378e재대장암조직중표체현저하조,병피real-time PCR소증실。miR-224재불동조직학류형암조직중표체차이유통계학의의,miR-378e재불동침윤심도암조직중표체차이유통계학의의,miR-224표체여조직학류형유관,miR-378e표체여대장암침윤심도유관。결론miR-224구유잠재적암기인작용,miR-378e구유잠재적억암기인작용,miR-224화miR-378e가작위잠재적대장암분자표지물。
Objective To investigate the expression and clinical significance of microRNA-224 and microRNA-378e in colorectal cancer tissues and normal mucosa adjacent to tumor lesions. Methods The gene chip technology was used to detect the different expression of miRNA in colorectal carcinoma tissues and adjacent normal tissues, which was then confirmed by real-time PCR. The relationship between the pathology and clinical data was analyzed. Results The expres-sion level of miR-224 was significantly up-regulated in tumor tissue, while miR-378e was down-regulated in tumor tissue, which was confirmed by real-time PCR. The expression of miR-224 was strongly associated with histological types, while miR-378e was strongly associated with the infiltration depth of colorectal cancer. Conclusion miR-224 is a potent tumor promoter, while miR-378e is a potent tumor suppressor. Both miR-224 and miR-378e can be used as potential colorectal cancer molecular markers.