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[KAI1基因对乳腺癌细胞体外生长的抑制作用]

[Inhibitory effect of KAI1 gene on breast cancer cell growth in vitro].

作者信息

Lu Dan, Wang Wen-xiu, Xu Yu-qing, Jiang Qiu-ying, Yang Yu

机构信息

Department of Oncology, the Second Affiliated Hospital of Harbin Medical University, Harbin, 150086, China.

出版信息

Zhonghua Zhong Liu Za Zhi. 2007 Aug;29(8):580-3.

Abstract

OBJECTIVE

To explore the inhibitory effect of KAI1 gene on breast cancer cell growth in vitro.

METHODS

Highly metastatic human breast cancer cell line MDA-MB-231 was transfected with pCMV-KAI1 or mock transfected plasmid pCMV with lipofectamine. Western blot was used to determine the expression of target protein of KAI1. The proliferative ability of cells was tested by MTT assay and colony-forming test. The cell cycle pattern was assayed by flow cytometry. The metastatic ability was investigated by cell adhesion and invasion assays.

RESULTS

A stable cell clone transfected with KAI1 gene was obtained and over-expression of KAI1 protein was observed. There was a significant decline in cell proliferative ability of pCMV-KAI1 transfected MDA-MB-231 cells in comparison with the mock-transfected ones and non-transfected ones, revealed by MTT assay and colony-forming test (P < 0.05). The ability of adherence and invasion of pCMV-KAI1 transfected cells was significantly reduced in comparison with the other two groups (P < 0.05). Also, flow cytometry analysis revealed that in KAI1 transfected cell group the number of cells in G0/G1 phase increased markedly from 36.78% +/- 0.61% to 64.00% +/- 7.56%, while the number of cells in G2/M phase decreased from 17.88% +/- 0.76% to 7.63% +/- 0.60%, comparing with the non-transfected ones.

CONCLUSION

KAI1 gene suppresses the invasive ability of human breast cancer cells in vitro and may inhibit the proliferative ability by changing the cell cycle pattern.

摘要

目的

探讨KAI1基因对体外乳腺癌细胞生长的抑制作用。

方法

采用脂质体介导,将pCMV-KAI1或空载质粒pCMV转染高转移人乳腺癌细胞系MDA-MB-231。运用蛋白质免疫印迹法检测KAI1靶蛋白的表达。通过MTT法和集落形成试验检测细胞的增殖能力。采用流式细胞术分析细胞周期模式。通过细胞黏附试验和侵袭试验研究细胞的转移能力。

结果

获得了转染KAI1基因的稳定细胞克隆,观察到KAI1蛋白的过表达。MTT法和集落形成试验显示,与空载质粒转染组和未转染组相比,pCMV-KAI1转染的MDA-MB-231细胞的增殖能力显著下降(P<0.05)。与其他两组相比,pCMV-KAI1转染细胞的黏附能力和侵袭能力显著降低(P<0.05)。此外,流式细胞术分析显示,与未转染组相比,KAI1转染细胞组G0/G1期细胞数量从36.78%±0.61%显著增加至64.00%±7.56%,而G2/M期细胞数量从17.88%±0.76%降至7.63%±0.60%。

结论

KAI1基因可抑制体外人乳腺癌细胞的侵袭能力,并可能通过改变细胞周期模式抑制其增殖能力。

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