钙外排泵,PMCA2,在哺乳变化的人乳腺组织中作为乳腺癌的治疗靶点

Amelia A. Peters, Wei C. Lee, Eloise Dray, Chanel E. Smart, Lynne Reid, Leonard da Silva, Sunil R. Lakhani, Sarah J. Roberts-Thomson, Gregory R. Monteith
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引用次数: 0

摘要

钙泵和钙通道通过调节细胞内钙(Ca2+)来调节细胞增殖和凋亡。质膜Ca2+ atp酶异构体PMCA2是一种钙外排机制,它将Ca2+从细胞质溶胶中挤出到细胞外空间。PMCA2表达受限,包括在耳蜗毛细胞和小脑浦肯野细胞中表达。哺乳期间,PMCA2在小鼠乳腺中的表达增加,在Ca2+排泄到乳汁中起主要作用;然而,PMCA2在哺乳期变化的人类乳腺组织中的表达尚未被评估。我们之前的研究表明,PMCA2 mRNA水平在一些乳腺癌细胞系中升高,泛pmca反义减弱MCF-7乳腺癌细胞的增殖。然而,在乳腺癌细胞中沉默PMCA2的后果仍然没有得到很好的理解。我们的研究评估了PMCA2在乳腺组织中表现出哺乳变化和人类恶性乳腺组织样本中的表达。PMCA2在乳腺癌细胞增殖中的作用也被评估。兔抗PMCA2抗体免疫组化显示乳腺组织腔上皮中膜性PMCA2表达表现出哺乳变化。在组装成组织微阵列的人乳腺肿瘤样本中评估PMCA2表达。96个乳腺肿瘤中有9个(9.4%)显示膜性PMCA2染色。PMCA2表达与乳腺癌病理标志物、雌激素、孕激素或HER2受体状态无显著相关性。高含量成像表明,MDA-MB-231乳腺癌细胞中的PMCA2沉默与细胞数量减少和s期阳性细胞百分比的抑制有关。在MDA-MB-231细胞中,使用动态成像系统(IncuCyte)评估PMCA2沉默联合各种细胞毒(顺铂、阿霉素或丝裂霉素C)对细胞增殖的影响。结果表明,PMCA2沉默促进了一些细胞毒素的作用。这些发现表明,PMCA2蛋白表达在人类哺乳期和一些乳腺癌中升高。PMCA2抑制剂可能代表了一些乳腺癌的一种新的治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Calcium efflux pump, PMCA2, in human breast tissue with lactational change and as a therapeutic target in breast cancer

Calcium pumps and channels modulate cell proliferation and apoptosis by regulating intracellular calcium (Ca2+). The plasma membrane Ca2+ ATPase isoform, PMCA2, is a calcium efflux mechanism that extrudes Ca2+ from the cytosol into the extracellular space. PMCA2 has a restricted expression, including expression in cochlear hair cells and cerebellar Purkinje cells. PMCA2 expression is increased in mouse mammary glands during lactation where it plays a major role in the excretion of Ca2+ into milk; however, PMCA2 expression has not been assessed in human breast tissue exhibiting lactational changes. Our previous studies have shown that PMCA2 mRNA levels are elevated in some breast cancer cell lines and that pan-PMCA antisense attenuates the proliferation of MCF-7 breast cancer cells. However, the consequences of silencing PMCA2 in breast cancer cells are still not well understood. Our study assessed PMCA2 expression in breast tissue exhibiting lactational change and in human malignant breast tissue samples. The role of PMCA2 in the proliferation of breast cancer cells was also evaluated. Immunohistochemistry using a rabbit anti-PMCA2 antibody showed membranous PMCA2 expression in the luminal epithelium of breast tissue exhibiting lactational change. PMCA2 expression was assessed in human breast tumor samples assembled into tissue microarrays. Nine of 96 breast tumours (9.4%) showed membranous PMCA2 staining. PMCA2 expression did not significantly correlate with the breast cancer pathological markers, estrogen, progesterone or HER2 receptor status. High-content imaging demonstrated that PMCA2 silencing in MDA-MB-231 breast cancer cells is associated with a reduction in cell number and an inhibition of the percentage of S-phase positive cells. The effect of PMCA2 silencing combined with various cytotoxics (cisplatin, doxorubicin or mitomycin C) on cell proliferation was assessed in MDA-MB-231 cells using a kinetic imaging system (IncuCyte). The results showed that PMCA2 silencing promotes the effects of some cytotoxics. These findings indicate that PMCA2 protein expression is elevated during human lactation and in some breast cancers. Inhibitors of PMCA2 may represent a novel therapeutic strategy for some breast cancers.

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