CD147 mediates chemoresistance in breast cancer via ABCG2 by affecting its cellular localization and dimerization.

CD147 mediates chemoresistance in breast cancer via ABCG2 by affecting its cellular localization and dimerization.
复制标题

CD147 通过 ABCG2 通过影响其细胞定位和二聚化来介导乳腺癌的化疗耐药性。

DOI:
10.1016/j.canlet.2013.04.025
复制
发表时间:
2013-09
期刊:
影响因子:
9.7
通讯作者:
Kuang, Yehong
Kuang, Yehong
中科院分区:
医学1区
文献类型:
--
作者:
Li, Jie;Liao, Liqiu;Chen, Chen;Zeng, Weiqi;Liu, Shuang;Su, Juan;Zhao, Shuang;Chen, Mingliang;Kuang, Yehong

文献摘要

参考文献

相似文献

CD 147和ABCG 2均被报道介导乳腺癌的多药耐药(MDR)。最近的研究表明,原发性渗出性淋巴瘤中CD 147可与ABCG 2在细胞膜上形成复合物。然而,这两种分子是否在乳腺癌中相互调节并导致MDR尚不清楚。我们建立了4株转染CD 147和/或ABCG 2的MCF-7细胞系,发现CD 147可以增加ABCG 2的表达和二聚化,影响其细胞定位,调节其药物转运功能。来自细胞的发现随后在化疗敏感/耐药乳腺癌的临床样本中得到了证实。
CD147 and ABCG2 both have been reported to mediate Multidrug resistance (MDR) in breast cancer. Recent study demonstrates that CD147 could form a complex with ABCG2 on the cell membrane in primary effusion lymphoma. However, whether these two molecules regulate each other in breast cancer and result in MDR is not clear. We established four MCF-7 cell lines transfected with CD147 and/or ABCG2 and found that CD147 could increase the expression and dimerization of ABCG2, affect its cellular localization and regulate its drug transporter function. The findings derived from cells were confirmed subsequently in clinic samples of chemotherapy-sensitive/resistant breast cancer.
DOI: 10.1016/j.canlet.2008.11.010
发表时间: 2009-04-18
期刊: CANCER LETTERS
影响因子: 9.7
作者:
Kuang, Ye-Hong;Chen, Xiang;Kanekura, Takuro
通讯作者: Kanekura, Takuro
DOI: 10.1038/leu.2011.144
发表时间: 2011-10
期刊: Leukemia
影响因子: 11.4
作者:
通讯作者: --
DOI: 10.1371/journal.pone.0016007
发表时间: 2011-01-24
期刊: PloS one
影响因子: 3.7
作者:
Goler-Baron V;Assaraf YG
通讯作者: Assaraf YG
DOI: 10.1111/j.1349-7006.2001.tb01115.x
发表时间: 2001-04
期刊: Japanese journal of cancer research : Gann
影响因子: --
作者:
Kanzaki A;Toi M;Nakayama K;Bando H;Mutoh M;Uchida T;Fukumoto M;Takebayashi Y
通讯作者: Takebayashi Y
DOI: 10.1016/j.ejca.2008.10.026
发表时间: 2009-01-01
影响因子: 8.4
作者:
Eisenhauer, E. A.;Therasse, P.;Verweij, J.
通讯作者: Verweij, J.