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BRAF-MAPK信号通路对人类黑色素瘤细胞的癌症免疫逃逸至关重要。

The BRAF-MAPK signaling pathway is essential for cancer-immune evasion in human melanoma cells.

作者信息

Sumimoto Hidetoshi, Imabayashi Fumie, Iwata Tomoko, Kawakami Yutaka

机构信息

Division of Cellular Signaling, Institute for Advanced Medical Research, Keio University School of Medicine, Tokyo 160-8582, Japan.

出版信息

J Exp Med. 2006 Jul 10;203(7):1651-6. doi: 10.1084/jem.20051848. Epub 2006 Jun 26.

Abstract

The mitogen-activated protein kinase (MAPK) pathway is frequently activated in human cancers, leading to malignant phenotypes such as autonomous cellular proliferation. Here, we demonstrate a novel role of the activated MAPK pathway in immune evasion by melanoma cells with the mutation of BRAF, which encodes a MAPKKs, (BRAF(V600E)). MEK inhibitor U0126 or RNA interference (RNAi) for BRAF(V600E) decreased production of the immunosuppressive soluble factors interleukin (IL)-10, VEGF, or IL-6 from melanoma cells to levels comparable to those after signal transducer and activator of transcription (STAT)3 inactivation. The suppressive activity of the culture supernatants from the melanoma cells on the production of inflammatory cytokines IL-12 and tumor necrosis factor alpha by dendritic cells upon lipopolysaccharide stimulation was markedly reduced after transduction with BRAF(V600E) RNAi, comparable to the effects observed with STAT3 RNAi transduction. No additive or synergistic effects were observed by the simultaneous transduction of RNAi for both BRAF(V600E) and STAT3. Furthermore, specific DNA binding and transcriptional activity of STAT3 were not affected by down-regulation of the MAPK signaling with the BRAF RNAi. These results indicate that the MAPK signal, along with the STAT3 signal, is essential for immune evasion by human melanomas that have constitutively active MAPK signaling and is a potential molecular target for overcoming melanoma cell evasion of the immune system.

摘要

丝裂原活化蛋白激酶(MAPK)通路在人类癌症中经常被激活,导致恶性表型,如细胞自主增殖。在此,我们证明了激活的MAPK通路在具有BRAF突变(BRAF(V600E),BRAF编码一种MAPKKs)的黑色素瘤细胞免疫逃逸中的新作用。MEK抑制剂U0126或针对BRAF(V600E)的RNA干扰(RNAi)可将黑色素瘤细胞中免疫抑制性可溶性因子白细胞介素(IL)-10、血管内皮生长因子(VEGF)或IL-6的产生降低至与信号转导和转录激活因子(STAT)3失活后相当的水平。在用BRAF(V600E) RNAi转导后,黑色素瘤细胞培养上清液对脂多糖刺激下树突状细胞产生炎性细胞因子IL-12和肿瘤坏死因子α的抑制活性显著降低,与STAT3 RNAi转导所观察到的效果相当。同时转导针对BRAF(V600E)和STAT3的RNAi未观察到相加或协同效应。此外,BRAF RNAi下调MAPK信号传导并不影响STAT3的特异性DNA结合和转录活性。这些结果表明,MAPK信号与STAT3信号一起,对于具有组成性激活MAPK信号传导的人类黑色素瘤的免疫逃逸至关重要,并且是克服黑色素瘤细胞免疫逃逸的潜在分子靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/25ae/2118331/c950fdf18756/jem2031651f01.jpg

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