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在胃癌组织和细胞中的表达及其生物学行为。

expression in gastric cancer tissues and cells and its biological behavior.

作者信息

Sheng Wei-Zhong, Chen Yu-Sheng, Tu Chuan-Tao, He Juan, Zhang Bo, Gao Wei-Dong

机构信息

Wei-Zhong Sheng, Yu-Sheng Chen, Bo Zhang, Wei-Dong Gao, Department of General Surgery, Fudan University Affiliated Zhongshan Hospital, Shanghai 200032, China.

出版信息

World J Gastroenterol. 2016 Dec 21;22(47):10364-10370. doi: 10.3748/wjg.v22.i47.10364.

DOI:10.3748/wjg.v22.i47.10364
PMID:28058016
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5175248/
Abstract

AIM

To explore expression of angiopoietin-like protein 2 (ANGPTL2) and its effect on biological behavior such as proliferation and invasiveness in gastric cancer.

METHODS

Western blotting was used to detect expression of ANGPTL2 in 60 human normal gastric tissues, 60 human gastric cancer tissues and gastric cell lines including GES-1, N87, SGC7901, BGC823 and PAMC82. 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) and Transwell assay were used to detect the proliferation and invasive ability of gastric cancer cells.

RESULTS

Compared to normal tissues, ANGPTL2 protein levels were significantly upregulated in gastric tissues, and this level was closely correlated with gastric tumor grade, clinical stage and lymph node metastasis. Compared to GES-1 cells, ANGPTL2 mRNA and protein levels were significantly increased in gastric cancer cells including N87, SGC7901, BGC823 and PAMC82. The expression of ANGPTL2 in highly malignant gastric cancer cell lines BGC823 and PAMC82 was significantly higher than in low malignancy gastric cancer cell lines N87 and SGC7901. MTT and Transwell experiments indicated that the proliferation rate and invasive ability of stable overexpressed gastric cancer cells was faster than in cells transfected with Lv-NC and blank control cells, and the invasive ability of stable overexpressed gastric cancer cells was higher than that of cells transfected with Lv-NC and blank control cells.

CONCLUSION

ANGPTL2 contributed to proliferation and invasion of gastric cancer cells. In clinical treatment, ANGPTL2 may become a new target for treatment of gastric cancer.

摘要

目的

探讨血管生成素样蛋白2(ANGPTL2)在胃癌中的表达及其对增殖和侵袭等生物学行为的影响。

方法

采用蛋白质免疫印迹法检测60例人正常胃组织、60例人胃癌组织以及胃细胞系GES-1、N87、SGC7901、BGC823和PAMC82中ANGPTL2的表达。采用3-(4,5-二甲基噻唑-2)-2,5-二苯基四氮唑溴盐(MTT)法和Transwell实验检测胃癌细胞的增殖和侵袭能力。

结果

与正常组织相比,ANGPTL2蛋白水平在胃组织中显著上调,且该水平与胃肿瘤分级、临床分期及淋巴结转移密切相关。与GES-1细胞相比,ANGPTL2 mRNA和蛋白水平在N87、SGC7901、BGC823和PAMC82等胃癌细胞中显著升高。ANGPTL2在高恶性胃癌细胞系BGC823和PAMC82中的表达显著高于低恶性胃癌细胞系N87和SGC7901。MTT和Transwell实验表明,稳定过表达的胃癌细胞的增殖率和侵袭能力比转染Lv-NC的细胞及空白对照细胞更快,且稳定过表达的胃癌细胞的侵袭能力高于转染Lv-NC的细胞及空白对照细胞。

结论

ANGPTL2促进胃癌细胞的增殖和侵袭。在临床治疗中,ANGPTL2可能成为胃癌治疗的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/9e7c4420a0bd/WJG-22-10364-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/97be6809c5d7/WJG-22-10364-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/79254d61fc05/WJG-22-10364-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/9e7c4420a0bd/WJG-22-10364-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/97be6809c5d7/WJG-22-10364-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/79254d61fc05/WJG-22-10364-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40fa/5175248/9e7c4420a0bd/WJG-22-10364-g003.jpg

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