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紧密连接蛋白6通过抑制TAZ介导的c-MYC有氧糖酵解来抑制乳腺癌增殖。

CLDN6 Suppresses c-MYC-Mediated Aerobic Glycolysis to Inhibit Proliferation by TAZ in Breast Cancer.

作者信息

Qu Huinan, Qi Da, Wang Xinqi, Dong Yuan, Jin Qiu, Wei Junyuan, Quan Chengshi

机构信息

The Key Laboratory of Pathobiology, Ministry of Education, College of Basic Medical Sciences, Jilin University, 126 Xinmin Avenue, Changchun 130021, China.

出版信息

Int J Mol Sci. 2021 Dec 23;23(1):129. doi: 10.3390/ijms23010129.

Abstract

Claudin 6 (CLDN6) was found to be a breast cancer suppressor gene, which is lowly expressed in breast cancer and inhibits breast cancer cell proliferation upon overexpression. However, the mechanism by which CLDN6 inhibits breast cancer proliferation is unclear. Here, we investigated this issue and elucidated the molecular mechanisms by which CLDN6 inhibits breast cancer proliferation. First, we verified that CLDN6 was lowly expressed in breast cancer tissues and that patients with lower CLDN6 expression had a worse prognosis. Next, we confirmed that CLDN6 inhibited breast cancer proliferation through in vitro and in vivo experiments. As for the mechanism, we found that CLDN6 inhibited c-MYC-mediated aerobic glycolysis based on a metabolomic analysis of CLDN6 affecting cellular lactate levels. CLDN6 interacted with a transcriptional co-activator with PDZ-binding motif (TAZ) and reduced the level of TAZ, thereby suppressing c-MYC transcription, which led to a reduction in glucose uptake and lactate production. Considered together, our results suggested that CLDN6 suppressed c-MYC-mediated aerobic glycolysis to inhibit the proliferation of breast cancer by TAZ, which indicated that CLDN6 acted as a novel regulator of aerobic glycolysis and provided a theoretical basis for CLDN6 as a biomarker of progression in breast cancer.

摘要

Claudin 6(CLDN6)被发现是一种乳腺癌抑制基因,在乳腺癌中低表达,过表达时可抑制乳腺癌细胞增殖。然而,CLDN6抑制乳腺癌增殖的机制尚不清楚。在此,我们对这一问题进行了研究,并阐明了CLDN6抑制乳腺癌增殖的分子机制。首先,我们证实CLDN6在乳腺癌组织中低表达,且CLDN6表达较低的患者预后较差。接下来,我们通过体外和体内实验证实CLDN6抑制乳腺癌增殖。至于其机制,基于对CLDN6影响细胞乳酸水平的代谢组学分析,我们发现CLDN6抑制c-MYC介导的有氧糖酵解。CLDN6与具有PDZ结合基序的转录共激活因子(TAZ)相互作用,并降低TAZ水平,从而抑制c-MYC转录,导致葡萄糖摄取和乳酸生成减少。综合来看,我们的结果表明CLDN6通过TAZ抑制c-MYC介导的有氧糖酵解来抑制乳腺癌增殖,这表明CLDN6作为有氧糖酵解的新型调节因子,为CLDN6作为乳腺癌进展的生物标志物提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5039/8745066/26ba6e8c19c6/ijms-23-00129-g001.jpg

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