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催产素受体在结肠腺癌中的预后作用。

Prognostic role of oxytocin receptor in colon adenocarcinoma.

作者信息

Sun Junjie, Xu Zhenyu, Mao Yong, Zhang Ting, Qin Yan, Hua Dong

机构信息

Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, 215004, Jiangsu, P. R. China.

Department of Oncology, The Affiliated Hospital of Jiangnan University, No. 200, Huihe Road, Wuxi, 214000, Jiangsu, P. R. China.

出版信息

Open Med (Wars). 2021 Nov 22;16(1):1762-1776. doi: 10.1515/med-2021-0387. eCollection 2021.

Abstract

The oxytocin receptor (OXTR) is directly involved in the pathological mechanisms of multiple cancers, including breast cancer, prostate cancer, and ovarian cancer; however, the role of OXTR in the modulation of colon adenocarcinoma (COAD) growth, metastasis, and clinical prognosis remains to be elucidated. This study used systematic bioinformatics analysis to explore the effects of OXTR on modulating COAD growth and prognosis in patients with COAD. Compared with normal tissues, OXTR mRNA level was higher in COAD tissues, which was associated with tumor progression. Elevated mRNA level of OXTR also indicated a poor prognosis in COAD patients. Furthermore, high mRNA level of OXTR was significantly associated with pathways involved in cell cycle regulation and signal transduction pathways, including the hedgehog, mTOR, TGF-β, and Wnt signaling pathways. OXTR expression was significantly correlated with the infiltration level of type 2T helper cell, central memory CD8 T cell, CD56 bright natural killer cell, activated CD8 T cell, activated B cell, and Type 1T helper cell. Moreover, silencing OXTR inhibited cell proliferation, migration, and invasion, and arrested the cell cycle. In conclusion, high mRNA level of OXTR indicates poor prognosis.

摘要

催产素受体(OXTR)直接参与多种癌症的病理机制,包括乳腺癌、前列腺癌和卵巢癌;然而,OXTR在调节结肠腺癌(COAD)生长、转移及临床预后中的作用仍有待阐明。本研究采用系统生物信息学分析方法,探讨OXTR对COAD患者COAD生长及预后的影响。与正常组织相比,COAD组织中OXTR mRNA水平较高,这与肿瘤进展相关。OXTR mRNA水平升高也提示COAD患者预后不良。此外,OXTR的高mRNA水平与细胞周期调控及信号转导通路相关,包括刺猬信号通路、mTOR、TGF-β和Wnt信号通路。OXTR表达与2型辅助性T细胞、中央记忆CD8 T细胞、CD56bright自然杀伤细胞、活化CD8 T细胞、活化B细胞和1型辅助性T细胞的浸润水平显著相关。此外,沉默OXTR可抑制细胞增殖、迁移和侵袭,并使细胞周期停滞。总之,OXTR的高mRNA水平提示预后不良。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1d8e/8610102/b07b14f74826/j_med-2021-0387-fig001.jpg

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