Yeh Elizabeth S, Williams Christina J, Williams Carly Bess, Bonilla Ingrid V, Klauber-DeMore Nancy, Phillips Stephanie L
Department of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, SC, USA.
Department of Surgery, Medical University of South Carolina, Charleston, SC, USA.
Oncotarget. 2017 Nov 25;8(65):109358-109369. doi: 10.18632/oncotarget.22678. eCollection 2017 Dec 12.
Connexin 43 (Cx43) is a gap junction protein whose function in the development of breast cancer and in breast cancer progression remains unclear. Evidence suggests that Cx43 () mRNA and protein expression is altered in breast tumors. However, reports indicate both increased and decreased Cx43 levels in human breast cancer samples. Studies also suggest that loss of Cx43 regulated gap junction intercellular communication is a common feature of breast malignancies that potentially correlates with histological stage. Further evidence suggests that Cx43 () mRNA expression is negatively correlated with HER2 positivity but a relationship between Cx43 and HER2 in breast cancer is not well defined. Therefore, in this study, we sought to evaluate the relationship between Cx43 activity, HER2, and drug resistance. Using HER2+ breast cancer cell lines that are sensitive or resistant to HER2 inhibitor, we evaluated Cx43 gap junction function. We found that Cx43 gap junction activity is completely lost in drug resistant HER2-positive (HER2+) breast cancer cells, whereas Cx43 gap junction activity can be restored by Cx43 overexpression in drug sensitive HER2+ cells. Moreover, the dysregulation of Cx43 resulted in increased tumorigenic and migratory capacity of the HER2+ drug resistant breast cancer cells.
连接蛋白43(Cx43)是一种间隙连接蛋白,其在乳腺癌发生发展过程中的功能尚不清楚。有证据表明,乳腺肿瘤中Cx43()的mRNA和蛋白表达发生了改变。然而,报告显示人类乳腺癌样本中Cx43水平既有升高也有降低。研究还表明,Cx43调控的间隙连接细胞间通讯的丧失是乳腺恶性肿瘤的一个共同特征,这可能与组织学分期相关。进一步的证据表明,Cx43()的mRNA表达与HER2阳性呈负相关,但Cx43与乳腺癌中HER2之间的关系尚未明确。因此,在本研究中,我们试图评估Cx43活性、HER2与耐药性之间的关系。使用对HER2抑制剂敏感或耐药的HER2 +乳腺癌细胞系,我们评估了Cx43间隙连接功能。我们发现,耐药的HER2阳性(HER2 +)乳腺癌细胞中Cx43间隙连接活性完全丧失,而在药物敏感的HER2 +细胞中,Cx43过表达可恢复Cx43间隙连接活性。此外,Cx43的失调导致HER2 +耐药乳腺癌细胞的致瘤能力和迁移能力增强。