NXPH4 可用作泛癌症的生物标记物,并促进结肠癌的进展

Zhipeng Zhang, Pengfei Wang, Siwen Chen, Dezhi Xiang, Jinzhen Chen, Wanchang Huang, Xiao Liu, Tongwen Yi, Dawei Wang, Yunfei Pu, Longfu He, Hao Zhang
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摘要

NXPH4 可促进癌症的增殖和侵袭。然而,它在癌症中的具体作用和机制仍不清楚。泛癌症的转录组和临床数据来自 TCGA 数据库。采用 K-M 生存曲线和单变量 Cox 进行预后分析。采用CIBERSORT和TIMER算法计算免疫细胞浸润。基因组富集分析(GSEA)用于研究NXPH4的功能。Western 印迹验证了 NXPH4 在结肠癌中的差异表达。功能试验(CCK-8、平板克隆性试验、伤口愈合试验和 Transwell 试验)证实了 NXPH4 对结肠癌细胞增殖、侵袭和迁移的影响。NXPH4 在泛癌症中的失调表明,它有可能成为某些癌症(包括结肠癌和肝癌)的诊断和预后标志物。泛癌中 NXPH4 的高表达可能与拷贝数增加和低甲基化有关。泛癌中 NXPH4 的表达与免疫微环境中的免疫细胞浸润密切相关。NXPH4 的表达与免疫疗法和化疗的易感性有关。Western 印迹进一步证实了 NXPH4 在结肠癌中的高表达。经功能测试验证,敲除 NXPH4 能显著抑制结肠癌细胞株 HT-29 和 HCT116 的增殖、侵袭和迁移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
NXPH4 can be used as a biomarker for pan-cancer and promotes colon cancer progression
NXPH4 promotes cancer proliferation and invasion. However, its specific role and mechanism in cancer remain unclear. Transcriptome and clinical data for pan-cancer were derived from the TCGA database. K-M survival curve and univariate Cox were used for prognostic analysis. CIBERSORT and TIMER algorithms were employed to calculate immune cell infiltration. Gene set enrichment analysis (GSEA) was employed for investigating the function of NXPH4. Western blot verified differential expression of NXPH4 in colon cancer. Functional assays (CCK-8, plate clonogenicity assay, wound healing assay, and Transwell assay) confirmed the impact of NXPH4 on proliferation, invasion, and migration of colon cancer cells. Dysregulation of NXPH4 in pan-cancer suggests its potential as a diagnostic and prognostic marker for certain cancers, including colon and liver cancer. High expression of NXPH4 in pan-cancer might be associated with the increase in copy number and hypomethylation. NXPH4 expression in pan-cancer is substantially linked to immune cell infiltration in the immune microenvironment. NXPH4 expression is associated with the susceptibility to immunotherapy and chemotherapy. Western blot further confirmed the higher expression of NXPH4 in colon cancer. Knockdown of NXPH4 significantly suppresses proliferation, invasion, and migration of colon cancer cell lines HT-29 and HCT116, as validated by functional assays.
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