STAT3相互作用组预测了口腔鳞状细胞癌中调节免疫系统的蛋白质的存在。

IF 2.6 Q1 DENTISTRY, ORAL SURGERY & MEDICINE
Rajdeep Chakraborty, Pallavi Khodlan, Aidan Tay, Fei Liu
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引用次数: 0

摘要

目的:信号转导和转录激活因子 3(STAT3)是与增殖机制相关的关键蛋白之一,有助于口腔鳞状细胞癌(OSCC)的进展。STAT3 的免疫逃避是由 JAK2/STAT3/PDL1 信号轴介导的。基于之前的研究结果,我们假设 STAT3 结合伙伴参与了 OSCC 抗肿瘤活性的抑制:方法:我们利用口腔癌细胞系 SCC4、SCC9、SCC25 和 CAL27 以及正常口腔细胞系 OKF6 构建了三维癌症-免疫共培养模型。细胞与自然杀伤细胞(NK-92)和Jurkat细胞共培养。根据 SWATH 数据选择了目标蛋白 STAT3,并进行了基于共免疫沉淀(Co-IP)的蛋白质组学研究。对共沉淀 LC-MS/MS 产物进行分析,以确定蛋白质相互作用网络、基因本体、通路分析和蛋白质集群注释:结果:口腔癌细胞系中的 STAT3 与表皮生长因子受体(EGFR)及其他参与增殖和免疫机制的蛋白质相互作用。蛋白质组分析表明,本研究发现的一些 STAT3 结合蛋白是已知的免疫系统调节因子:总之,STAT3 交互蛋白可调节口腔鳞状细胞癌细胞的免疫系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
STAT3 interactome predicts presence of proteins that regulates immune system in oral squamous cell carcinoma.

Objectives: Signal transducer and activator of transcription 3 (STAT3) is one of the key proliferation mechanism-related proteins that helps in oral squamous cell carcinoma (OSCC) progression. Immune evasion by STAT3 is mediated by the JAK2/STAT3/PDL1 signaling axis. Based on previous findings, we hypothesized that STAT3-binding partners participate in the inhibition of anti-tumor activity in OSCC.

Methods: A 3D cancer-immune co-culture model was constructed using oral cancer cell lines SCC4, SCC9, SCC25, and CAL27 and normal oral cell line OKF6. The cells were co-cultured with natural killer (NK-92) and Jurkat cells. The target protein STAT3 was chosen based on SWATH data, and co-immunoprecipitation (Co-IP)-based proteomics was conducted. The Co-IP LC-MS/MS output was analyzed to determine the protein interaction network, gene ontology, pathway analysis, and protein cluster annotation.

Results: STAT3 in oral cancer cell lines interacts with the epidermal growth factor receptor (EGFR) and other proteins that participate in proliferation and immune mechanisms. Proteome analysis showed that some STAT3-binding proteins found in this study are known immune system regulators.

Conclusion: Overall, STAT3 interactive proteins regulate the immune system in oral squamous cell carcinoma cells.

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来源期刊
Journal of Oral Biosciences
Journal of Oral Biosciences DENTISTRY, ORAL SURGERY & MEDICINE-
CiteScore
4.40
自引率
12.50%
发文量
57
审稿时长
37 days
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