Division of Colon and Rectal Surgery, Department of Surgery, Soonchunhyang University College of Medicine, Soonchunhyang University Bucheon Hospital, Bucheon, South Korea.
Division of Colon and Rectal Surgery, Department of Surgery, Yonsei University College of Medicine, Yonsei University Severance Hospital, Seoul, South Korea.
Neoplasma. 2021 May;68(3):580-589. doi: 10.4149/neo_2021_201209N1333. Epub 2021 Feb 24.
G protein-coupled receptor 56 (GPR56) belongs to the adhesion G protein-coupled receptor subfamily, which plays a role in cell progression and survival. The aim of this study was to investigate the role of the GPR56 gene in a cell line study and the impact of its protein expression on the prognosis of colorectal cancer (CRC) patients. The effect of GPR56 on tumor cell proliferation (WST-1 assay), invasion (Transwell assay), migration (Transwell assay, wound healing assay), and colony-forming ability (semisolid agar colony-forming assay) was explored. The expression levels of GPR56 in tissue samples of 109 CRC patients were evaluated by immunohistochemistry. The prognostic value of GRP56 was analyzed using univariate and multivariate analyses. The downregulation of GPR56 in the CRC cell line reduced cell proliferation as compared with that in a control sample (48 h; p=0.042, 72 h; p=0.001). Downregulation of the GPR56 expression reduced cell invasion and migration abilities and inhibited colony-forming abilities (p<0.005). The 5-year overall survival rate was worse in the high-expression group as compared with that in the low-expression group (51.6% vs. 74.4%, p=0.008). High GPR56 expression was a significant prognostic factor for overall survival of CRC patients in the univariate (p=0.001) and multivariate (p<0.001) analyses. The expression level of GPR56 plays an important role in tumor progression in CRC, and it may serve as a prognostic indicator in CRC patients.
G 蛋白偶联受体 56(GPR56)属于黏附 G 蛋白偶联受体亚家族,在细胞增殖和存活中发挥作用。本研究旨在探讨 GPR56 基因在细胞系研究中的作用及其蛋白表达对结直肠癌(CRC)患者预后的影响。研究探讨了 GPR56 对肿瘤细胞增殖(WST-1 检测)、侵袭(Transwell 检测)、迁移(Transwell 检测、划痕愈合检测)和集落形成能力(半固体琼脂集落形成检测)的影响。采用免疫组织化学法检测 109 例 CRC 患者组织样本中 GPR56 的表达水平。采用单因素和多因素分析评估 GRP56 的预后价值。CRC 细胞系中 GPR56 的下调与对照组相比,细胞增殖减少(48 h:p=0.042,72 h:p=0.001)。下调 GPR56 的表达降低了细胞侵袭和迁移能力,并抑制了集落形成能力(p<0.005)。高表达组的 5 年总生存率低于低表达组(51.6%比 74.4%,p=0.008)。单因素(p=0.001)和多因素(p<0.001)分析均显示,GPR56 高表达是 CRC 患者总生存的显著预后因素。GPR56 的表达水平在 CRC 肿瘤进展中起重要作用,可能作为 CRC 患者的预后指标。