泛癌分析发现ARHGAP23是胰腺腺癌的潜在生物标志物

IF 1.4 Q4 ONCOLOGY Molecular and clinical oncology Pub Date : 2023-11-03 DOI:10.3892/mco.2023.2696
Xiaolong Liu, Xin Li, Ling Wang, Kaihua Yu, Dean Wu, Pengxian Tao, Yulan Li
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引用次数: 0

摘要

已知Rho - GTPASE激活蛋白23 (ARHGAP23)可激活Rho - GTPASE,在肿瘤的浸润和转移中具有重要作用。尽管先前的研究表明它与某些人类癌症有关,但它在泛癌症中的作用仍不清楚。本研究通过Human Protein Atlas、Tumor IMmune Estimation Resource、Gene Set Co - expression Analysis、Gene expression profile Interactive Analysis、cBio cancer Genomics Portal、Tumor - IMmune System Interactions Database (TISIDB)等公共数据库对ARHGAP23在泛癌中的表达、预后和潜在功能进行评估。通过这些数据结合多种生物信息分析方法,本研究探讨了ARHGAP23作为致癌基因的潜在作用。本研究分析显示,ARHGAP23在10例肿瘤中表达异常,并与预后差异有关。此外,本研究结果表明,ARHGAP23与这些肿瘤的DNA甲基化和多种免疫细胞浸润有关。ARHGAP23表达与临床预后、DNA甲基化和免疫浸润有关。这些发现支持了ARHGAP23作为预后生物标志物和癌症治疗分子靶点的潜力。
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Pan‑cancer analysis identified ARHGAP23 as a potential biomarker for pancreatic adenocarcinoma
Rho GTPASE‑activating protein 23 (ARHGAP23) is known to activate RHO‑GTPase and has an important role in the infiltration and metastasis of tumors. Although previous studies suggested its involvement in certain human cancers, its role in pan‑cancer remains unclear. In the present study, the expression, prognosis and potential functions of ARHGAP23 in pan‑cancer were evaluated through various public databases such as Human Protein Atlas, Tumor IMmune Estimation Resource, Gene Set Co‑Expression Analysis, Gene Expression Profiling Interactive Analysis, cBio Cancer Genomics Portal, Tumor‑Immune System Interactions Database (TISIDB) and others. Through these data combined with a variety of biological information analysis methods, the potential role of ARHGAP23 as a carcinogenic gene was explored in the present study. The present analysis revealed that ARHGAP23 expressed abnormalities in >10 tumors, which was associated with differences in prognosis. Furthermore, the findings of the present study indicated that ARHGAP23 is associated with DNA methylation and multiple immune cell infiltrations in these tumors. ARHGAP23 expression was related to clinical prognosis, DNA methylation and immune infiltration. These findings support the potential of ARHGAP23 as a prognostic biomarker and a molecular target for cancer treatment.
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