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肾癌缺氧微环境中的miRNA模式——PTEN的作用

miRNA Pattern in Hypoxic Microenvironment of Kidney Cancer-Role of PTEN.

作者信息

Majewska Aleksandra, Brodaczewska Klaudia, Filipiak-Duliban Aleksandra, Kajdasz Arkadiusz, Kieda Claudine

机构信息

Laboratory of Molecular Oncology and Innovative Therapies, Military Institute of Medicine, 128 Szaserow Street, 04-141 Warsaw, Poland.

Postgraduate School of Molecular Medicine (SMM), Warsaw Medical University, 61 Zwirki and Wigury Street, 02-091 Warsaw, Poland.

出版信息

Biomolecules. 2022 May 11;12(5):686. doi: 10.3390/biom12050686.

Abstract

MicroRNAs are post-transcriptional regulators of gene expression, and disturbances of their expression are the basis of many pathological states, including cancers. The miRNA pattern in the context of tumor microenvironment explains mechanisms related to cancer progression and provides a potential target of modern therapies. Here we show the miRNA pattern in renal cancer focusing on hypoxia as a characteristic feature of the tumor microenvironment and dysregulation of PTEN, being a major tumor suppressor. Methods comprised the CRSPR/Cas9 mediated PTEN knockout in the Renca kidney cancer cell line and global miRNA expression analysis in both in vivo and in vitro (in normoxic and hypoxic conditions). The results were validated on human cancer models with distinct PTEN status. The increase in miR-210-3p in hypoxia was universal; however, the hypoxia-induced decrease in PTEN was associated with an increase in miR-221-3p, the loss of PTEN affected the response to hypoxia differently by decreasing miR-10b-5p and increasing miR-206-3p. In turn, the complete loss of PTEN induces miR-155-5p, miR-100-5p. Upregulation of miR-342-3p in knockout PTEN occurred in the context of the whole tumor microenvironment. Thus, effective identification of miRNA patterns in cancers must consider the specificity of the tumor microenvironment together with the mutations of key suppressors.

摘要

微小RNA是基因表达的转录后调节因子,其表达紊乱是包括癌症在内的许多病理状态的基础。肿瘤微环境背景下的微小RNA模式解释了与癌症进展相关的机制,并提供了现代治疗的潜在靶点。在这里,我们展示了肾癌中的微小RNA模式,重点关注缺氧这一肿瘤微环境的特征以及主要肿瘤抑制因子PTEN的失调。方法包括在Renca肾癌细胞系中通过CRSPR/Cas9介导的PTEN基因敲除以及在体内和体外(常氧和缺氧条件下)进行全局微小RNA表达分析。结果在具有不同PTEN状态的人类癌症模型上得到了验证。缺氧条件下miR-210-3p的增加是普遍现象;然而,缺氧诱导的PTEN减少与miR-221-3p的增加相关,PTEN的缺失通过降低miR-10b-5p和增加miR-206-3p对缺氧的反应产生不同影响。反过来,PTEN的完全缺失会诱导miR-155-5p、miR-100-5p。在整个肿瘤微环境背景下,敲除PTEN后miR-342-3p上调。因此,有效识别癌症中的微小RNA模式必须考虑肿瘤微环境的特异性以及关键抑制因子的突变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e887/9138332/9c523f60c493/biomolecules-12-00686-g001.jpg

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