Clinical Medical Research Center, Henan Provincial People's Hospital and Zhengzhou University People's Hospital, Zheng Zhou, China.
Department of Hypertension, Henan Provincial People's Hospital and Zhengzhou University People's Hospital, Zheng Zhou, China.
Pathol Oncol Res. 2021 Sep 27;27:1609914. doi: 10.3389/pore.2021.1609914. eCollection 2021.
The angiopoietin-like protein (ANGPTL) family members, except for the novel atypical member ANGPTL8/betatrophin, have been reported to participate in angiogenesis, inflammation and cancer. ANGPTL8/betatrophin is a metabolic regulator that is involved in lipid metabolism and glucose homeostasis. However, little is known about the expression and prognostic value of ANGPTL8/betatrophin in human cancers. In this study, we first conducted detailed analyses of ANGPTL8/betatrophin expression in cancer/normal samples the Human Protein Atlas (HPA), Gene Expression Profiling Interactive Analysis (GEPIA), DriverDBv3, ENCORI and UALCAN databases. ANGPTL8/betatrophin showed high tissue specificity (enriched in the liver) and cell-type specificity (enriched in HepG2 and MCF7 cell lines). More than one databases demonstrated that the gene expression of ANGPTL8/betatrophin was significantly lower in cholangiocarcinoma (CHOL), breast invasive carcinoma (BRCA), lung adenocarcinoma (LUAD), lung squamous cell carcinoma (LUSC), uterine corpus endometrial carcinoma (UCEC), and significantly higher in kidney renal clear cell carcinoma (KIRC) compared with that in normal samples. However, the protein expression of ANGPTL8/betatrophin displayed opposite results in clear cell renal cell carcinoma (ccRCC)/KIRC. Based on the expression profiles, the prognostic value was evaluated with the GEPIA, DriverDBv3, Kaplan Meier plotter and ENCORI databases. Two or more databases demonstrated that ANGPTL8/betatrophin significantly affected the survival of KIRC, uterine corpus endometrial carcinoma (UCEC), pheochromocytoma and paraganglioma (PCPG) and sarcoma (SARC); patients with PCPG and SARC may benifit from high ANGPTL8/betatrophin expression while high ANGPTL8/betatrophin expression was associated with poor prognosis in KIRC and UCEC. Functional analyses with the GeneMANIA, Metascape and STRING databases suggested that ANGPTL8/betatrophin was mainly involved in lipid homeostasis, especially triglyceride and cholesterol metabolism; glucose homeostasis, especially insulin resistance; AMPK signaling pathway; PI3K/Akt signaling pathway; PPAR signaling pathway; mTOR signaling pathway; HIF-1 signaling pathway; autophagy; regulation of inflammatory response. ANGPTL8/betatrophin may be a promising prognostic biomarker and therapeutic target, thus providing evidence to support further exploration of its role in defined human cancers.
血管生成素样蛋白 (ANGPTL) 家族成员,除了新型非典型成员 ANGPTL8/β-细胞素,已被报道参与血管生成、炎症和癌症。ANGPTL8/β-细胞素是一种代谢调节剂,参与脂质代谢和葡萄糖稳态。然而,关于 ANGPTL8/β-细胞素在人类癌症中的表达和预后价值知之甚少。在这项研究中,我们首先在癌症/正常样本中进行了 ANGPTL8/β-细胞素表达的详细分析——人类蛋白质图谱 (HPA)、基因表达谱交互式分析 (GEPIA)、DriverDBv3、ENCORI 和 UALCAN 数据库。ANGPTL8/β-细胞素表现出高度的组织特异性(富含肝脏)和细胞类型特异性(富含 HepG2 和 MCF7 细胞系)。多个数据库表明,在胆管癌 (CHOL)、乳腺癌浸润性癌 (BRCA)、肺腺癌 (LUAD)、肺鳞状细胞癌 (LUSC)、子宫体子宫内膜癌 (UCEC) 中,ANGPTL8/β-细胞素的基因表达明显低于正常样本,而在肾透明细胞癌 (KIRC) 中则明显高于正常样本。然而,在透明细胞肾细胞癌 (ccRCC)/KIRC 中,ANGPTL8/β-细胞素的蛋白表达显示出相反的结果。基于表达谱,使用 GEPIA、DriverDBv3、Kaplan Meier plotter 和 ENCORI 数据库评估预后价值。两个或更多的数据库表明,ANGPTL8/β-细胞素显著影响 KIRC、子宫体子宫内膜癌 (UCEC)、嗜铬细胞瘤和副神经节瘤 (PCPG) 和肉瘤 (SARC) 的生存;PCPG 和 SARC 患者可能受益于高 ANGPTL8/β-细胞素表达,而高 ANGPTL8/β-细胞素表达与 KIRC 和 UCEC 的预后不良相关。使用 GeneMANIA、Metascape 和 STRING 数据库进行的功能分析表明,ANGPTL8/β-细胞素主要参与脂质稳态,特别是甘油三酯和胆固醇代谢;葡萄糖稳态,特别是胰岛素抵抗;AMPK 信号通路;PI3K/Akt 信号通路;PPAR 信号通路;mTOR 信号通路;HIF-1 信号通路;自噬;炎症反应的调节。ANGPTL8/β-细胞素可能是一种有前途的预后生物标志物和治疗靶点,因此为进一步探索其在特定人类癌症中的作用提供了证据支持。