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微小 RNA-135b 通过作为结肠癌致癌途径的下游效应物促进癌症进展。

MicroRNA-135b promotes cancer progression by acting as a downstream effector of oncogenic pathways in colon cancer.

机构信息

Institute of Cancer Sciences, University of Glasgow, Glasgow G61 1BD, UK.

Institute of Cancer Sciences, University of Glasgow, Glasgow G61 1BD, UK.

出版信息

Cancer Cell. 2014 Apr 14;25(4):469-83. doi: 10.1016/j.ccr.2014.03.006.

Abstract

MicroRNA deregulation is frequent in human colorectal cancers (CRCs), but little is known as to whether it represents a bystander event or actually drives tumor progression in vivo. We show that miR-135b overexpression is triggered in mice and humans by APC loss, PTEN/PI3K pathway deregulation, and SRC overexpression and promotes tumor transformation and progression. We show that miR-135b upregulation is common in sporadic and inflammatory bowel disease-associated human CRCs and correlates with tumor stage and poor clinical outcome. Inhibition of miR-135b in CRC mouse models reduces tumor growth by controlling genes involved in proliferation, invasion, and apoptosis. We identify miR-135b as a key downsteam effector of oncogenic pathways and a potential target for CRC treatment.

摘要

microRNA 失调在人类结直肠癌(CRC)中很常见,但尚不清楚它是否代表旁观者事件,还是实际上在体内驱动肿瘤进展。我们表明,miR-135b 的过表达是由 APC 缺失、PTEN/PI3K 通路失调和 SRC 过表达在小鼠和人类中触发的,并促进肿瘤转化和进展。我们表明,miR-135b 的上调在散发性和炎症性肠病相关的人类 CRC 中很常见,并且与肿瘤分期和不良临床结局相关。在 CRC 小鼠模型中抑制 miR-135b 通过控制参与增殖、侵袭和凋亡的基因来减少肿瘤生长。我们将 miR-135b 鉴定为致癌途径的关键下游效应因子和 CRC 治疗的潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6d3/3995091/fcf3642b5d6d/gr1.jpg

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