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miR-125b-5p, 一个潜在的转录靶点,为 CD44 促进乳腺癌进展提供了基础。

, a Potential Transcriptional Target Underpinning CD44-Promoted Breast Cancer Progression.

机构信息

Biological Sciences Program, Department of Biological and Environmental Sciences, College of Arts and Sciences, Qatar University, Doha P.O. Box 2713, Qatar.

Department of Basic Medical Science, College of Medicine, QU Health, Qatar University, Doha P.O. Box 2713, Qatar.

出版信息

Molecules. 2022 Jan 26;27(3):811. doi: 10.3390/molecules27030811.

Abstract

CD44, a cell-adhesion molecule has a dual role in tumor growth and progression; it acts as a tumor suppressor as well as a tumor promoter. In our previous work, we developed a tetracycline-off regulated expression of CD44's gene in the breast cancer (BC) cell line MCF-7 (B5 clone). Using cDNA oligo gene expression microarray, we identified (superoxide dismutase 2) as a potential CD44-downstream transcriptional target involved in BC metastasis. gene belongs to the family of iron/manganese superoxide dismutase family and encodes a mitochondrial protein. plays a role in cell proliferation and cell invasion via activation of different signaling pathways regulating angiogenic abilities of breast tumor cells. This review will focus on the findings supporting the underlying mechanisms associated with the oncogenic potential of in the onset and progression of cancer, especially in BC and the potential clinical relevance of its various inhibitors.

摘要

CD44 是一种细胞黏附分子,在肿瘤生长和进展中具有双重作用;它既是肿瘤抑制因子,也是肿瘤促进因子。在我们之前的工作中,我们在乳腺癌 (BC) 细胞系 MCF-7(B5 克隆)中开发了四环素调控的 CD44 基因表达。使用 cDNA 寡基因表达微阵列,我们鉴定出(超氧化物歧化酶 2)作为参与 BC 转移的潜在 CD44 下游转录靶标。该基因属于铁/锰超氧化物歧化酶家族,编码一种线粒体蛋白。通过激活不同的信号通路调节乳腺肿瘤细胞的血管生成能力,在细胞增殖和细胞侵袭中发挥作用。这篇综述将重点介绍支持与该基因在癌症发生和进展中的致癌潜力相关的潜在机制的研究结果,特别是在乳腺癌中,以及其各种抑制剂的潜在临床相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0900/8839817/895d1d6934fb/molecules-27-00811-g001.jpg

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