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乳腺癌细胞系中线粒体和质膜乳酸转运体以及乳酸脱氢酶同工酶的表达。

Mitochondrial and plasma membrane lactate transporter and lactate dehydrogenase isoform expression in breast cancer cell lines.

机构信息

Exercise Physiology Laboratory, Department of Integrative Biology, University of California, Berkeley, California, USA.

出版信息

Physiol Genomics. 2011 Mar 16;43(5):255-64. doi: 10.1152/physiolgenomics.00177.2010. Epub 2010 Dec 21.

Abstract

We hypothesized that dysregulation of lactate/pyruvate (monocarboxylate) transporters (MCT) and lactate dehydrogenase (LDH) isoforms contribute to the Warburg effect in cancer. Therefore, we assayed for the expression levels and the localizations of MCT (1, 2, and 4), and LDH (A and B) isoforms in breast cancer cell lines MCF-7 and MDA-MB-231 and compared results with those from a control, untransformed primary breast cell line, HMEC 184. Remarkably, MCT1 is not expressed in MDA-MB-231, but MCT1 is expressed in MCF-7 cells, where its abundance is less than in control HMEC 184 cells. When present in HMEC 184 and MCF-7 cells, MCT1 is localized to the plasma membrane. MCT2 and MCT4 were expressed in all the cell lines studied. MCT4 expression was higher in MDA-MB-231 compared with MCF-7 and HMEC 184 cells, whereas MCT2 abundance was higher in MCF-7 compared with MDA-MB-231 and HMEC 184 cells. Unlike MCT1, MCT2 and MCT4 were localized in mitochondria in addition to the plasma membrane. LDHA and LDHB were expressed in all the cell-lines, but abundances were higher in the two cancer cell lines than in the control cells. MCF-7 cells expressed mainly LDHB, while MDA-MB-231 and control cells expressed mainly LDHA. LDH isoforms were localized in mitochondria in addition to the cytosol. These localization patterns were the same in cancerous and control cell lines. In conclusion, MCT and LDH isoforms have distinct expression patterns in two breast cancer cell lines. These differences may contribute to divergent lactate dynamics and oxidative capacities in these cells, and offer possibilities for targeting cancer cells.

摘要

我们假设乳酸/丙酮酸(单羧酸)转运体(MCT)和乳酸脱氢酶(LDH)同工型的失调导致癌症中的瓦伯格效应。因此,我们检测了乳腺癌细胞系 MCF-7 和 MDA-MB-231 中 MCT(1、2 和 4)和 LDH(A 和 B)同工型的表达水平和定位,并将结果与对照的未转化的原代乳腺细胞系 HMEC 184 进行了比较。值得注意的是,MCT1 在 MDA-MB-231 中不表达,但在 MCF-7 细胞中表达,其丰度低于对照 HMEC 184 细胞。当存在于 HMEC 184 和 MCF-7 细胞中时,MCT1 定位于质膜。MCT2 和 MCT4 在所有研究的细胞系中均有表达。与 MCF-7 和 HMEC 184 细胞相比,MCT4 在 MDA-MB-231 中的表达更高,而与 MDA-MB-231 和 HMEC 184 细胞相比,MCT2 的丰度在 MCF-7 中更高。与 MCT1 不同,MCT2 和 MCT4 除了定位于质膜外,还定位于线粒体。LDHA 和 LDHB 在所有细胞系中均有表达,但在两种癌细胞系中的丰度高于对照细胞。MCF-7 细胞主要表达 LDHB,而 MDA-MB-231 和对照细胞主要表达 LDHA。LDH 同工型除了定位于细胞质外,还定位于线粒体。这些定位模式在癌性和对照细胞系中是相同的。总之,MCT 和 LDH 同工型在两种乳腺癌细胞系中有不同的表达模式。这些差异可能导致这些细胞中乳酸动力学和氧化能力的不同,并为靶向癌细胞提供了可能性。

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