Health Management Center, Jiangxi Provincial People's Hospital (The First Affiliated Hospital of Nanchang Medical College), Nanchang, China.
Department of Urology, The First Affiliated Hospital, Harbin Medical University, Harbin, China.
J Clin Lab Anal. 2022 Sep;36(9):e24648. doi: 10.1002/jcla.24648. Epub 2022 Aug 10.
The objective of the study was to investigate the expression of LAMTOR3 in kidney renal clear cell carcinoma (KIRC) and its clinical significance.
The expression of LAMTOR3 in KIRC and its relationship with clinical features were analyzed using the UALCAN online database. The results were verified using KIRC gene chip data and clinical specimens. The prognosis of KIRC patients was analyzed with the GEPIA2 database. GO, KEGG, and GSEA analyses were conducted to analyze the possible molecular mechanism of LAMTOR3 in KIRC. Immunohistochemical (IHC) and hematoxylin and eosin (H&E) staining were used for histopathological detection.
UALCAN database analysis showed that LAMTOR3 expression in KIRC was significantly lower than in normal kidney tissues and correlated with the clinical stage, pathological grade, and tumor genotype (p < .05). GSE53757 dataset analysis consistently showed that the expression of LAMTOR3 in KIRC was significantly lower than in normal kidney tissues (p < .01). GEPIA2 database analysis indicated that patients with low LAMTOR3 expression had poor overall and disease-free survival rates. GSEA analysis suggested that LAMTOR3 positively regulated the citrate cycle and drug metabolism cytochrome P450 and negatively regulated folate biosynthesis and olfactory transduction. The expression of LAMTOR3 in KIRC was also significantly correlated with immune cell infiltration. Finally, IHC showed that LAMTOR3 expression in the KIRC tissues was lower than in the adjacent normal tissues.
LAMTOR3 expression is significantly lower in KIRC. LAMTOR3 may be a potential marker for KIRC diagnosis and therapy.
研究的目的是探讨 LAMTOR3 在肾透明细胞癌(KIRC)中的表达及其临床意义。
利用 UALCAN 在线数据库分析 LAMTOR3 在 KIRC 中的表达及其与临床特征的关系。利用 KIRC 基因芯片数据和临床标本验证结果。利用 GEPIA2 数据库分析 KIRC 患者的预后。进行 GO、KEGG 和 GSEA 分析,以分析 LAMTOR3 在 KIRC 中的可能分子机制。采用免疫组织化学(IHC)和苏木精和伊红(H&E)染色进行组织病理学检测。
UALCAN 数据库分析表明,LAMTOR3 在 KIRC 中的表达明显低于正常肾组织,且与临床分期、病理分级和肿瘤基因型相关(p<0.05)。GSE53757 数据集分析一致表明,LAMTOR3 在 KIRC 中的表达明显低于正常肾组织(p<0.01)。GEPIA2 数据库分析表明,LAMTOR3 低表达的患者总生存率和无病生存率较差。GSEA 分析表明,LAMTOR3 正向调节柠檬酸循环和药物代谢细胞色素 P450,负向调节叶酸生物合成和嗅觉转导。LAMTOR3 在 KIRC 中的表达也与免疫细胞浸润明显相关。最后,IHC 显示,KIRC 组织中 LAMTOR3 的表达低于相邻正常组织。
LAMTOR3 在 KIRC 中的表达明显降低。LAMTOR3 可能是 KIRC 诊断和治疗的潜在标志物。