中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2014年
3期
489-491
,共3页
樊清波%刘红山%秦秉玉%王存真%刘晗%郑鹏远
樊清波%劉紅山%秦秉玉%王存真%劉晗%鄭鵬遠
번청파%류홍산%진병옥%왕존진%류함%정붕원
Kiss1%胃癌%增殖%转移
Kiss1%胃癌%增殖%轉移
Kiss1%위암%증식%전이
Kiss1%Gastric cancer%Proliferation%Metastasis
目的 检测Kiss1在人胃腺癌及癌旁组织中的表达,探讨Kiss1对胃癌细胞增殖和转移的作用及其分子机制.方法 免疫组织化学法检测Kiss1在40例人胃腺癌及其癌旁组织中的表达.利用慢病毒载体建立Kiss1过表达胃癌SGC-7901细胞株,Western blot检测Kiss1、增殖细胞核抗原(PCNA)及基质金属蛋白酶-2(MMP-2)的蛋白表达水平;噻唑蓝(MTT)法和Transwell侵袭实验检测Kiss1过表达对胃癌细胞增殖和转移的影响.结果 Kiss1蛋白在胃腺癌及癌旁组织的阳性表达率分别为40.0%和67.5%,差异有统计学意义(x2=4.302,P<0.05);与癌旁组织(1.00)比较,Kiss1 mRNA在胃腺癌组织中的相对表达量(0.52 ±0.13)明显降低(P<0.01);与对照组和空载组比较,Kiss1蛋白在转染组表达明显升高,而PCNA和MMP-2蛋白的表达下降,差异均有统计学意义(P<0.01).结论 Kiss1可能作为抑癌基因参与胃癌细胞增殖和转移.
目的 檢測Kiss1在人胃腺癌及癌徬組織中的錶達,探討Kiss1對胃癌細胞增殖和轉移的作用及其分子機製.方法 免疫組織化學法檢測Kiss1在40例人胃腺癌及其癌徬組織中的錶達.利用慢病毒載體建立Kiss1過錶達胃癌SGC-7901細胞株,Western blot檢測Kiss1、增殖細胞覈抗原(PCNA)及基質金屬蛋白酶-2(MMP-2)的蛋白錶達水平;噻唑藍(MTT)法和Transwell侵襲實驗檢測Kiss1過錶達對胃癌細胞增殖和轉移的影響.結果 Kiss1蛋白在胃腺癌及癌徬組織的暘性錶達率分彆為40.0%和67.5%,差異有統計學意義(x2=4.302,P<0.05);與癌徬組織(1.00)比較,Kiss1 mRNA在胃腺癌組織中的相對錶達量(0.52 ±0.13)明顯降低(P<0.01);與對照組和空載組比較,Kiss1蛋白在轉染組錶達明顯升高,而PCNA和MMP-2蛋白的錶達下降,差異均有統計學意義(P<0.01).結論 Kiss1可能作為抑癌基因參與胃癌細胞增殖和轉移.
목적 검측Kiss1재인위선암급암방조직중적표체,탐토Kiss1대위암세포증식화전이적작용급기분자궤제.방법 면역조직화학법검측Kiss1재40례인위선암급기암방조직중적표체.이용만병독재체건립Kiss1과표체위암SGC-7901세포주,Western blot검측Kiss1、증식세포핵항원(PCNA)급기질금속단백매-2(MMP-2)적단백표체수평;새서람(MTT)법화Transwell침습실험검측Kiss1과표체대위암세포증식화전이적영향.결과 Kiss1단백재위선암급암방조직적양성표체솔분별위40.0%화67.5%,차이유통계학의의(x2=4.302,P<0.05);여암방조직(1.00)비교,Kiss1 mRNA재위선암조직중적상대표체량(0.52 ±0.13)명현강저(P<0.01);여대조조화공재조비교,Kiss1단백재전염조표체명현승고,이PCNA화MMP-2단백적표체하강,차이균유통계학의의(P<0.01).결론 Kiss1가능작위억암기인삼여위암세포증식화전이.
Objective To examine the expression of Kiss1 in human gastric adenocarcinomas and corresponding adjacent non-cancerous tissues (ANCT),and further explore the effects and molecular mechanisms of Kiss1 in proliferation and metastasis of gastric cancer cells.Methods The expression of Kiss1 in 40 cases of gastric adenocarcinomas tissues and ANCT was detected by using immunohistochemistry.Human gastric cancer SGC-7901 cells in vitro were stably transfected with lentivirus-mediated overexpression of Kiss1 (Lv-Kiss1),and the expression levels of Kiss1,proliferating cell nuclear antigen (PCNA) and metalloproteinase-2 (MMP-2) were detected by using Western blotting.The proliferative activity and metastatic capability of gastric cancer cells were assessed by methyl thiazol tetrazolium (MTT)and Transwell assays.Results The expression of Kissl protein was observed in 40.0% gastric adenocarcinoma tissues compared with that in 67.5% ANCT (P < 0.01),and its mRNA level (0.52 ± 0.13) was also decreased in gastric adenocarcinoma tissues compared with thaat in ANCT (1.00).Overexpression of Kissl by Lv-Kiss1 could down-regulate the expression of PCNA and MMP-2,and inhibit proliferative activities and metastatic potential of gastric cancer cells.Conclusion Kissl may function as a tumor suppressor involved in gastric cancer cell proliferation and metastasis,suggesting a promising therapeutic target for the treatment of cancer.