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张瑜,高一萌,李文燕,彭慧娟,刘斌,王辉,令狐华.鸟嘌呤核苷交换因子Dock180与Elmo1在卵巢癌细胞中的共表达[J].陆军军医大学学报(原第三军医大学学报),2012,34(13):1277-1280.
Zhang Yu,Gao Yimeng,Li Wenyan,Peng Huijuan,Liu Bin,Wang Hui,Linghu Hua.Co-expression of guanine-nucleotide exchange factor DOCK180 and ELMO1 in ovarian cancer cells[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(13):1277-1280.
张瑜,高一萌,李文燕,彭慧娟,刘斌,王辉,令狐华.鸟嘌呤核苷交换因子Dock180与Elmo1在卵巢癌细胞中的共表达[J].陆军军医大学学报(原第三军医大学学报),2012,34(13):1277-1280. DOI:
Zhang Yu,Gao Yimeng,Li Wenyan,Peng Huijuan,Liu Bin,Wang Hui,Linghu Hua.Co-expression of guanine-nucleotide exchange factor DOCK180 and ELMO1 in ovarian cancer cells[J].J Amry Med Univ (J Third Mil Med Univ),2012,34(13):1277-1280. DOI:
目的 寻找卵巢癌细胞中鸟嘌呤核苷交换因子Dock180与Elmo1呈相互协同作用的依据。 方法 采用 Western blot检测人卵巢癌组织、良性肿瘤组织及正常卵巢组织中的Dock180与Elmo1的表达水平;免疫组化检测卵巢癌组织中Dock180与Elmo1的分布;免疫荧光检测Dock180与Elmo1在卵巢癌细胞SKOV3中的定位分布;检测Dock180表达缺失的SKOV3细胞中内源性Elmo1的表达水平。 结果 Dock180与Elmo1在人卵巢癌组织中的表达水平呈明显正相关(r=0.829,P0.05),在卵巢癌组织中二者的表达水平显著高于卵巢良性肿瘤组织组和卵巢正常组织组(P0.05)[Dock180:(1.054±0.114)、(0.518±0.126)、(0.425±0.072);Elmo1: (0.864±0.114)、(0.374±0.076)、(0.300±0.105)]。免疫组化及细胞化学染色均显示二者在人卵巢癌组织和细胞内的分布具有一致性。而且在Dock180表达缺失细胞中,Elmo1的表达水平也同时降低。 结论 Dock180与Elmo1在促进卵巢癌的癌变过程中可能具有相互协同作用。
Objective To seek evidence to support the synergic effect of guanine-nucleotide exchange factor (GEF) downstream of crk with moleculer weight of 180kDa of human (Dock180) and engulfment and cell motility1 (Elmo1) in ovarian cancer cells. Methods Dock180 and Elmo1 expression were detected by Western blotting in ovarian cancer tissues (EOC
n=29)
benign ovarian tumors (BOT
n=14) and normal ovary tissues (Normal
n=10). Immunohistochemistry was performed to detect the distribution of Dock180 and Elmo1 in the ovarian cancer tissues. Immunofluorescence staining was utilized to detect the location and distribution of Dock180 and Elmo1 in ovarian cancer cell SKOV3. And finally
endogenous Elmo1 expression was assayed in Dock180 knockdown cells
which was established previously. Results Both Dock180 and Elmo1 expression presented at higher levels in EOC than those in benign and normal ovarian tissues (P0.05)
and no significant difference was found between BOT and normal group either for Dock180 or Elmo1 expression(Dock180: 1.054±0.114
0.518±0.126
0.425±0.072; Elmo1: 0.864±0.114
0.374±0.076
0.300±0.105
P0.05).Dock180 expression displayed a consistence with that of Elmo1 in EOC tissues(r=0.829
P0.05).Their co-expression was also observed through immunohistochemical staining in EOC tissues. Moreover
consistent distribution of these two molecules was shown in SKOV3 cells through immunofluorescence staining. Finally
Dock180-knockdown SKOV3 cells presented with evidently decreased expression of Elmo1
as compared with wild-type
negative and mock controls. Conclusion Co-expression of Dock180 and Elmo1 in EOC tissues and their consistent distribution in ovarian cancer cells support their synergistic effect in the pathogenesis of EOC.
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