Department of Gynecology and Obstetrics, The People's Hospital of China Three Gorges University/The First People's Hospital of Yichang, Yichang 443000, China.
Crit Rev Eukaryot Gene Expr. 2023;33(4):63-83. doi: 10.1615/CritRevEukaryotGeneExpr.2023044081.
Runt-related transcription factor 3 (RUNX3) plays a pivotal role in tumor microenvironment and immune infiltration. However, the prognostic and immunological roles of RUNX3 in pancancer remain unclear. In the current study, we explored the expression profiles, prognostic landscape, and immune infiltration of RUNX3 in pancancer through a variety of online platforms, including HPA, ONCOMINE, UALCAN, GEPIA, PrognoScan, TCGA, TIMER, R2, and Reactome databases. In general, RUNX3 was widely expressed in tonsil, gallbladder, skin, spleen, lymph node, and bone marrow, and RUNX3 was frequently higher expression in tumor tissues compared to normal tissues. In prognostic analysis, the RUNX3 expression level was significantly correlated with the clinical outcomes of bladder cancer, blood cancer, brain cancer, breast cancer, colorectal cancer, lung cancer, and ovarian cancer. In mutation analysis, a total 72 mutation sites were located within amino acids 1 to 415 of RUNX3, including 65 missense sites and seven truncating sites, whereas the mutation frequency of skin cutaneous melanoma and uterine corpus endometrial carcinoma (UCEC) is relatively high (> 3%). In immune infiltration analysis, the RUNX3 expression level was significantly related to recognized markers and the immune infiltration levels of various types of immune cells in colon adenocarcinoma (COAD) and brain lower grade glioma (LGG). After that, 453 RUNX3 co-expressed genes were recognized in COAD, lymphoid neoplasm diffuse large B-cell lymphoma, LGG, and ovarian serous cystadenocarcinoma (OV). Pathway enrichment analysis revealed that RUNX3 co-expressed genes were remarkably enriched in immune system and tumor progression pathways. RUNX3 expression is associated with clinical prognosis, immune infiltration, and identified RUNX3 related pathways in a variety of tumors, which may serve as targets of promising prognostic markers and novel therapeutic targets for various human cancers.
Runt 相关转录因子 3(RUNX3)在肿瘤微环境和免疫浸润中发挥着关键作用。然而,RUNX3 在泛癌症中的预后和免疫作用仍不清楚。在本研究中,我们通过 HPA、ONCOMINE、UALCAN、GEPIA、PrognoScan、TCGA、TIMER、R2 和 Reactome 数据库等多种在线平台,探讨了 RUNX3 在泛癌症中的表达谱、预后景观和免疫浸润。总的来说,RUNX3 在扁桃体、胆囊、皮肤、脾脏、淋巴结和骨髓中广泛表达,并且在肿瘤组织中比正常组织中更常高表达。在预后分析中,RUNX3 的表达水平与膀胱癌、血液癌、脑癌、乳腺癌、结直肠癌、肺癌和卵巢癌的临床结局显著相关。在突变分析中,RUNX3 内的 72 个突变位点位于氨基酸 1 至 415 内,包括 65 个错义位点和 7 个截断位点,而皮肤黑色素瘤和子宫体子宫内膜癌(UCEC)的突变频率相对较高(>3%)。在免疫浸润分析中,RUNX3 的表达水平与结肠腺癌(COAD)和脑低级别胶质瘤(LGG)中各种类型免疫细胞的公认标志物和免疫浸润水平显著相关。之后,在 COAD、弥漫性大 B 细胞淋巴瘤、LGG 和卵巢浆液性囊腺癌(OV)中识别出 453 个 RUNX3 共表达基因。通路富集分析表明,RUNX3 共表达基因在免疫系统和肿瘤进展途径中显著富集。RUNX3 的表达与多种肿瘤的临床预后、免疫浸润和鉴定的 RUNX3 相关途径相关,可能成为有前途的预后标志物和各种人类癌症的新治疗靶点。