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αvβ6整合素对顺铂诱导的卵巢癌细胞凋亡的影响
引用本文:Wu XH,Li DX,Li L,Guo YH,Yang B,Shan BE. αvβ6整合素对顺铂诱导的卵巢癌细胞凋亡的影响[J]. 中华妇产科杂志, 2004, 39(2): 112-115
作者姓名:Wu XH  Li DX  Li L  Guo YH  Yang B  Shan BE
作者单位:1. 050011,石家庄,河北医科大学第四医院妇产科
2. 050011,石家庄,河北医科大学第四医院科研中心
3. 石家庄妇产医院生殖医学中心
基金项目:河北省自然科学基金资助项目 (3 0 13 91)
摘    要:目的 探讨αvβ6整合素介导的细胞与细胞外基质的黏附 ,及其对顺铂诱导的卵巢癌细胞凋亡的影响。方法 采用流式细胞仪测定卵巢癌细胞株SKOV3、AO、3AO细胞表面αvβ6整合素的表达 ,并利用酶联免疫吸附实验、吖啶橙 溴化乙锭双荧光染色法分析顺铂诱导的细胞凋亡及αvβ6整合素对细胞凋亡的影响。结果 SKOV3、AO、3AO细胞均表达αvβ6整合素 ,其相对荧光指数 (FI)均为 1 0 3± 0 0 1。顺铂可以诱导SKOV3、AO、3AO细胞凋亡 ,经顺铂 (10 μg/ml)作用 4 8h后 ,酶联免疫吸附实验结果显示 ,生长于αvβ6整合素配体———纤维粘连蛋白 (FN)上的细胞的富集系数 (EF)分别为 2 11± 0 0 4、2 15± 0 0 6、2 11± 0 0 4 ,明显低于生长于非整合素配体———多聚赖氨酸 (polylisin)上的细胞 (分别为 3 5 1± 0 0 3、3 5 5± 0 0 4、3 6 6± 0 0 4 ,P <0 0 1) ;吖啶橙 溴化乙锭双荧光染色法结果显示 ,生长于FN上的细胞凋亡率分别为 (5 0± 0 7) %、(5 0± 0 7) %、(6 0± 0 7) % ,明显低于生长于polylisin上的细胞凋亡率[分别为 (2 8 0± 0 7) %、(2 8 0± 0 7) %、(2 9 0± 0 7) % ,P <0 0 0 1],用αvβ6整合素的特异性阻断抗体封闭过的细胞再次生长于FN上时 ,细胞凋亡率 [分别为 (15 0± 0

关 键 词:αvβ6整合素 顺铂 诱导 卵巢癌 细胞凋亡
修稿时间:2003-07-23

Alphavbeta 6 integrin inhibits cisplatin-induced apoptosis in ovarian cancer cell lines
Wu Xiao-hua,Li Dong-xiu,Li Li,Guo Yan-hong,Yang Bo,Shan Bao-en. Alphavbeta 6 integrin inhibits cisplatin-induced apoptosis in ovarian cancer cell lines[J]. Chinese Journal of Obstetrics and Gynecology, 2004, 39(2): 112-115
Authors:Wu Xiao-hua  Li Dong-xiu  Li Li  Guo Yan-hong  Yang Bo  Shan Bao-en
Affiliation:Department of Obstetrics and Gynecology, Fourth Hospital of Hebei Medical University, Shijiazhuang 050011, China.
Abstract:OBJECTIVE: To investigate the effects of alphavbeta6 integrin-mediated cell adhesion on cisplatin (DDP) induced apoptosis in ovarian cancer cell lines. METHODS: The expression of integrin alphavbeta6 in ovarian cancer cell lines SKOV3, AO, and 3AO was analyzed by flow cytometry, and the apoptosis induced by DDP was measured by enzyme-linked immunosorbent assay (ELISA) method and acridine orange-ethidium bromide (AO-EB) double fluorescent dye staining. RESULTS: Ovarian cancer cell lines SKOV3, AO and 3AO all expressed integrin alphavbeta6. Treated by different concentrations of DDP, SKOV3, AO and 3AO displayed significant apoptosis status compared with the control. However, after cultured in medium containing 10 micro g/ml DDP for 48 hours, SKOV3, AO and 3AO planted on fibronectin (FN)-ligand of alphavbeta6 integrin, had lower enrichment factor (EF), compared with those planted on non-integrin ligand polylisin measured by ELISA method (2.11 +/- 0.04 vs 3.51 +/- 0.03, 2.15 +/- 0.06 vs 3.55 +/- 0.04, 2.11 +/- 0.04 vs 3.66 +/- 0.04, P < 0.01). Similarly, by AO-EB double fluorescent dye staining, lower percentages of apoptosis were found in cells planted on FN (5.0 +/- 0.7)%, (5.0 +/- 0.7)%, (6.0 +/- 0.7)%, than on polylisin (28.0 +/- 0.7)%, (28.0 +/- 0.7)%, (29.0 +/- 0.7)% (P < 0.001). When cells preincubated with integrin alphavbeta6 blocking antibody were planted on FN, the percentages of apoptosis rose again, (15.0 +/- 0.7)%, (16.0 +/- 0.7)%, (15.0 +/- 0.7)% (P < 0.01). CONCLUSIONS: The de novo expression of alphavbeta6 integrin occurs in ovarian cancer cell lines SKOV3, AO, and 3AO. alphavbeta6 integrin-mediated cell adhesion to FN can inhibit the effect of cisplatin-induced apoptosis. These results suggest that inhibiting apoptotic cell adhesion may improve drug resistance in ovarian cancer cell lines.
Keywords:Antigens neoplasm  Integrins  Ovarian neoplasms  Cisplatin  Apoptosis  Drug resistance   neoplasm
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