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微小RNA-223通过靶向RhoB促进胃癌肿瘤进展。

MiR-223 Promotes Tumor Progression via Targeting RhoB in Gastric Cancer.

作者信息

Hu You, Yi Bin, Chen Xin, Xu Lu, Zhou Xiaojun, Zhu Xinguo

机构信息

Department of Gastroenterology, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, China.

出版信息

J Oncol. 2022 Jan 6;2022:6708871. doi: 10.1155/2022/6708871. eCollection 2022.

Abstract

Gastric cancer (GC) is among the most prevalent causes of cancer-related death globally. MiR-223 has been implicated in a variety of cellular mechanisms linked to cancer progression. However, the miR-223 expressions and its function in GC are unknown. We discovered that miR-223 expression was raised in GC tissues in comparison with nearby normal tissues in this investigation. Additionally, multiplied miR-223 expression was strongly linked with TNM stage (=0.022), live metastasis (=0.004),lymph node metastasis (=0.004),and Borrmann type and was associated with an unfavorable prognostic for patients with GC. Furthermore, suppressing miR-223 significantly increased cell death and prevented cell migration and invasion in vitro. Additionally, miR-223 silencing decreased tumor development in vivo. Additionally, we discovered that miR-223 enhanced GC development by specifically targeting RhoB. In summary, our findings reveal that miR-223 increases tumor progression in GC by targeting RhoB, suggesting that it could serve to be a potential biomarker for the prediction of the disease.

摘要

胃癌(GC)是全球癌症相关死亡的最常见原因之一。MiR-223与多种与癌症进展相关的细胞机制有关。然而,miR-223在GC中的表达及其功能尚不清楚。在本研究中,我们发现与邻近正常组织相比,GC组织中miR-223表达升高。此外,miR-223表达倍增与TNM分期(=0.022)、远处转移(=0.004)、淋巴结转移(=0.004)和Borrmann分型密切相关,且与GC患者的不良预后相关。此外,抑制miR-223可显著增加细胞死亡,并在体外阻止细胞迁移和侵袭。此外,miR-223沉默可减少体内肿瘤生长。此外,我们发现miR-223通过特异性靶向RhoB促进GC进展。总之,我们的研究结果表明,miR-223通过靶向RhoB促进GC肿瘤进展,提示其可能作为预测该疾病的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40c1/8758265/0f443dddb662/JO2022-6708871.001.jpg

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