Lin Lumin, He Yanbin, Ni Zhuona, Zhang Min, Liu Jie, Mao Qianqian, Huang Bin, Lin Jiumao
Department of Spleen and Stomach Diseases, The Second Affiliated Hospital of Fujian University of Traditional Chinese Medicine, Fuzhou 350003, China.
Academy of Integrative Medicine, Fujian Key Laboratory of Integrative Medicine on Geriatrics, Fujian University of Traditional Chinese Medicine, Fuzhou, Fujian, 350122, China.
Open Med (Wars). 2022 Feb 14;17(1):304-316. doi: 10.1515/med-2022-0421. eCollection 2022.
Glypican-2 (GPC2) has been reported to promote tumor progression through metabolic pathways. However, the role of GPC2 in colon adenocarcinoma (COAD) remains to be further investigated. This study was designed to evaluate the role of GPC2 in COAD. Based on patients with complete clinical information and GPC2 expression from the Cancer Genome Atlas-COAD database, we found that GPC2 mRNA was highly expressed in COAD tissues, which was associated with poor prognosis and tumornode-metastasis (TNM) stage. The predicted survival probability based on GPC2 mRNA expression and TNM stage was in good agreement with the observed survival probability. Furthermore, the genes coexpressed with GPC2 in COAD tissues were significantly enriched in basal cell carcinoma, Notch signaling pathway, and Hedgehog signaling pathway. After GPC2 was decreased through transfecting short hairpin RNA of GPC2 into HCT-8 and SW620 cells, cell cycle was arrested in G0/G1 phase, proliferation was decreased, apoptosis was increased, and migration and invasion were repressed. In conclusion, decreasing GPC2 significantly inhibited proliferation, migration, and invasion, and enhanced apoptosis, which implied that GPC2 can be considered a promising therapeutic target of COAD in the future.
据报道,磷脂酰肌醇蛋白聚糖-2(GPC2)可通过代谢途径促进肿瘤进展。然而,GPC2在结肠腺癌(COAD)中的作用仍有待进一步研究。本研究旨在评估GPC2在COAD中的作用。基于癌症基因组图谱-COAD数据库中具有完整临床信息和GPC2表达的患者,我们发现GPC2 mRNA在COAD组织中高表达,这与预后不良及肿瘤-淋巴结-转移(TNM)分期相关。基于GPC2 mRNA表达和TNM分期预测的生存概率与观察到的生存概率高度一致。此外,在COAD组织中与GPC2共表达的基因在基底细胞癌、Notch信号通路和Hedgehog信号通路中显著富集。将GPC2的短发夹RNA转染到HCT-8和SW620细胞中使GPC2表达降低后,细胞周期停滞于G0/G1期,增殖减少,凋亡增加,迁移和侵袭受到抑制。总之,降低GPC2可显著抑制增殖、迁移和侵袭,并增强凋亡,这意味着GPC2未来可被视为COAD有前景的治疗靶点。