Department of Oncology and Central Laboratory, The Affiliated Hospital of Chengde Medical University, Chengde, China.
Department of Surgery (3), The Affiliated Hospital of Chengde Medical University, Chengde, China.
Histol Histopathol. 2024 Jan;39(1):117-130. doi: 10.14670/HH-18-618. Epub 2023 Apr 5.
Keratin 80 (KRT80) is a filament protein that participates in cell differentiation and the integrity of the epithelial barrier. Here, KRT80 expression was higher in gastric cancer compared with normal mucosa at both mRNA and protein levels by bioinformatic analysis, qRT-PCR and Western blot (p<0.05), however, the methylation of KRT80 was lower than in normal mucosa (p<0.05). There was a negative relationship between promoter methylation and expression level of KRT80 gene in gastric cancer (p<0.05). KRT80 mRNA and protein expression was positively correlated with the differentiation of gastric cancer (p<0.05), while KRT80 methylation was negatively associated with gastric cancer differentiation and p53 mutation (p<0.05). The expression of KRT80 mRNA was positively linked to the short survival time of gastric cancers (p<0.05). The differential genes of KRT80 mRNA were involved in ligand-receptor interaction, estrogen signal pathway, peptidase, filament and cytoskeleton, keratinocyte differentiation, vitamin D receptor, muscle contraction, and B cell-mediated immunity (p<0.05). KRT80-related genes were classified into cell adhesion and junction, cadherin binding, skin and epidermis development, and so forth (p<0.05). KRT80 knockdown suppressed proliferation, anti-apoptosis, anti-pyroptosis, migration, invasion and epithelial-mesenchymal transition in gastric cancer cells (p<0.05). These findings indicated that up-regulated expression of KRT80 played a crucial part in gastric carcinogenesis, and might be considered as a biological marker for aggressive behaviors and poor prognosis. Its silencing might be used as an approach of target therapy for gastric cancer patients.
角蛋白 80(KRT80)是一种参与细胞分化和上皮屏障完整性的丝氨酸蛋白。通过生物信息学分析、qRT-PCR 和 Western blot 发现,KRT80 在胃癌组织中的 mRNA 和蛋白水平均高于正常胃黏膜(p<0.05),但其启动子区甲基化水平低于正常胃黏膜(p<0.05)。胃癌组织中 KRT80 基因启动子区甲基化水平与表达水平呈负相关(p<0.05)。KRT80 mRNA 和蛋白表达与胃癌分化程度呈正相关(p<0.05),而 KRT80 甲基化与胃癌分化程度和 p53 突变呈负相关(p<0.05)。KRT80 mRNA 的表达与胃癌患者的短生存期呈正相关(p<0.05)。KRT80 mRNA 的差异基因参与配体-受体相互作用、雌激素信号通路、肽酶、丝氨酸、细胞骨架、角蛋白细胞分化、维生素 D 受体、肌肉收缩和 B 细胞介导的免疫反应等信号通路(p<0.05)。KRT80 相关基因参与细胞黏附与连接、钙黏蛋白结合、皮肤和表皮发育等生物学过程(p<0.05)。敲低 KRT80 表达抑制了胃癌细胞的增殖、抗凋亡、抗焦亡、迁移、侵袭和上皮-间充质转化(p<0.05)。这些发现表明,KRT80 的上调表达在胃癌发生中起着关键作用,可能成为侵袭性行为和不良预后的生物标志物。其沉默可能成为胃癌患者靶向治疗的一种方法。