中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2013年
8期
1730-1733
,共4页
贺东强%李玉民%刘涛%王小军
賀東彊%李玉民%劉濤%王小軍
하동강%리옥민%류도%왕소군
胃癌%白细胞介素-8%DNA甲基化
胃癌%白細胞介素-8%DNA甲基化
위암%백세포개소-8%DNA갑기화
Gastric carcinoma%Interleukin-8%DNA methylation
目的 观察胃癌患者癌组织及与其配对的正常胃黏膜组织中白细胞介素-8(IL-8)基因启动子甲基化及其mRNA表达,探讨IL-8基因甲基化与胃癌的关系.方法 收集经病理确诊并行外科手术切除的胃癌组织及配对的正常胃黏膜组织各52例,用实时荧光定量聚合酶链反应(FQ-PCR)分别检测癌组织及正常组织中IL-8基因mRNA表达;用甲基化特异性PCR(MSP)检测上述两种组织中IL-8基因甲基化状态.结果 胃癌组织中IL-8基因mRNA的表达量是正常组织中的1.94倍(P<0.01).胃癌组织中IL-8基因甲基化率为32.7%,而正常组织中的甲基化率为73.1%(P<0.01);胃癌组织中IL-8基因mRNA表达及启动子的去甲基化与性别、年龄、肿瘤大小无明显相关(P>0.05),而与肿瘤的分化程度、Borrmann分型、浸润程度及有无淋巴结转移均具有明显相关(P<0.05);去甲基化的胃癌组织中IL-8 mRNA表达是甲基化胃癌组织的2.13倍(P <0.001).结论 IL-8基因mRNA在胃癌组织中过表达;胃癌组织中IL-8基因启动子区呈低甲基化状态;IL-8基因启动子区去甲基化促进了其在胃癌组织中高表达.
目的 觀察胃癌患者癌組織及與其配對的正常胃黏膜組織中白細胞介素-8(IL-8)基因啟動子甲基化及其mRNA錶達,探討IL-8基因甲基化與胃癌的關繫.方法 收集經病理確診併行外科手術切除的胃癌組織及配對的正常胃黏膜組織各52例,用實時熒光定量聚閤酶鏈反應(FQ-PCR)分彆檢測癌組織及正常組織中IL-8基因mRNA錶達;用甲基化特異性PCR(MSP)檢測上述兩種組織中IL-8基因甲基化狀態.結果 胃癌組織中IL-8基因mRNA的錶達量是正常組織中的1.94倍(P<0.01).胃癌組織中IL-8基因甲基化率為32.7%,而正常組織中的甲基化率為73.1%(P<0.01);胃癌組織中IL-8基因mRNA錶達及啟動子的去甲基化與性彆、年齡、腫瘤大小無明顯相關(P>0.05),而與腫瘤的分化程度、Borrmann分型、浸潤程度及有無淋巴結轉移均具有明顯相關(P<0.05);去甲基化的胃癌組織中IL-8 mRNA錶達是甲基化胃癌組織的2.13倍(P <0.001).結論 IL-8基因mRNA在胃癌組織中過錶達;胃癌組織中IL-8基因啟動子區呈低甲基化狀態;IL-8基因啟動子區去甲基化促進瞭其在胃癌組織中高錶達.
목적 관찰위암환자암조직급여기배대적정상위점막조직중백세포개소-8(IL-8)기인계동자갑기화급기mRNA표체,탐토IL-8기인갑기화여위암적관계.방법 수집경병리학진병행외과수술절제적위암조직급배대적정상위점막조직각52례,용실시형광정량취합매련반응(FQ-PCR)분별검측암조직급정상조직중IL-8기인mRNA표체;용갑기화특이성PCR(MSP)검측상술량충조직중IL-8기인갑기화상태.결과 위암조직중IL-8기인mRNA적표체량시정상조직중적1.94배(P<0.01).위암조직중IL-8기인갑기화솔위32.7%,이정상조직중적갑기화솔위73.1%(P<0.01);위암조직중IL-8기인mRNA표체급계동자적거갑기화여성별、년령、종류대소무명현상관(P>0.05),이여종류적분화정도、Borrmann분형、침윤정도급유무림파결전이균구유명현상관(P<0.05);거갑기화적위암조직중IL-8 mRNA표체시갑기화위암조직적2.13배(P <0.001).결론 IL-8기인mRNA재위암조직중과표체;위암조직중IL-8기인계동자구정저갑기화상태;IL-8기인계동자구거갑기화촉진료기재위암조직중고표체.
Objective To investigate the promoter methylation status and mRNA expression of interleukin-8 (IL-8) in gastric cancer tissue and paired normal tissue,and to explore the relationship between IL-8 promoter methylation and gastric cancer.Methods The gastric cancer tissues (n =52) and paried normal tissues (n =52) confirmed pathologically and resected surgically were collected,and the mRNA expression of IL-8 was detected by using real-time fluorescent quantitative polymerase chain reaction (FQ-PCR) and methylation status of the IL-8 gene by methylation-specific PCR (MSP).Results There was significant difference in IL-8 gene mRNA expression and methylation status between normal gastric mucosa and gastric cancer (P < 0.01).The IL-8 gene mRNA expression and methylation status in gastric cancer were not significantly correlated with gender,age and tumor size (P > 0.05),but significantly with degree of differentiation,Borrmann type,degree of infiltration and lymph node metastasis (P < 0.05).There was also significant difference in the IL-8 mRNA expression between methylated gastric cancer tissue and unmethylated gastric cancer tissue (P < 0.01).Conclusion The hypomethylation of IL-8 gene promoter promotes the over-expression of IL-8 mRNA in gastric cancer.