Identification of the Interaction between P-Glycoprotein and Anxa2 in Multidrug-resistant Human Breast Cancer Cells

被引:0
作者
Haichang Zhang [1 ,2 ]
Fei Zhang [1 ,2 ]
Bing Wu [1 ,2 ]
Jinghua Han [1 ,2 ]
Wei Ji [1 ,2 ]
Yan Zhou [1 ,2 ]
Ruifang Niu [1 ,2 ]
机构
[1] Public Laboratory,Key Laboratory of Breast Cancer Prevention and Therapy,Tianjin Medical University,Ministry of Education
[2] Tianjin Medical University Cancer Institute and Hospital
关键词
P-glycoprotein; Anxa2; drug resistance; multiple; neoplasm metastasis; breast neoplasm;
D O I
暂无
中图分类号
R737.9 [乳腺肿瘤];
学科分类号
100214 ;
摘要
<正>Objective To explore the interaction of Anxa2 with P-Glycoprotein(P-gp) in the migration and invasion of the multidrug-resistant (MDR) human breast cancer cell line MCF-7/ADR. Methods A pair of short hairpin RNA(shRNA) targeting P-gp was transfected into MCF-7/ADR cells,and monoclonal cell strains were screened.The expression of P-gp was detected by Western blot.Transwell chambers were used to observe the cell migration capacity and invasion ability.The interaction between P-gp and Anxa2 was examined by immunoprecipitation and immunofluorescence confocal microscopy analyses. Results P-gp expression was significantly knocked down,and there were notable decreasing trends in the migration and invasion capability of MDR breast cancer cells(P<0.05).There was a close interaction between Anxa2 and P-gp. Conclusions MCF-7/ADR is an MDR human breast cancer cell line with high migration and invasion abilities.The knockdown of P-gp notably impaired the migration and invasion abilities of the tumor cells.The interaction of Anxa2 with P-pg may play an important role in the enhanced invasiveness of MDR human breast cancer cells.
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页码:99 / 104
页数:6
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[1]  
Distinctive alterations of invasiveness, drug resistance and cell–cell organization in 3D-cultures of MCF-7, a human breast cancer cell line, and its multidrug resistant variant[J] . Muriel Affoué dit Faute,Luc Laurent,Dominique Ploton,Marie-France Poupon,Jean-Claude Jardillier,Hélène Bobichon.Clinical and Experimental Metastasis . 2002 (2)