LY96基因是M2巨噬细胞相关的生物标志物,与肾细胞癌的免疫抑制有关

Weiquan Li, Xiangui Meng, Tiexi Yu, Xin Shi, Wei Dong, Hailong Ruan, Tao Wang, Wen Xiao
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引用次数: 1

摘要

淋巴细胞抗原96(LY96)被鉴定为多种肿瘤的致癌基因。然而,它在癌症中的作用尚未被探索。在这项研究中,使用几个公共肾脏癌症测序数据确定了LY96的异常表达。LY96的表达水平使用配对的临床样本进行验证。生存分析和ROC曲线用于检查其预后和诊断价值。基因集富集分析表明LY96可能影响免疫过程。免疫浸润分析结果表明LY96与肾细胞癌M2巨噬细胞浸润呈正相关。单细胞数据用于验证其与巨噬细胞的相关性。此外,LY96与各种免疫评分呈正相关,可能影响免疫治疗的疗效。药物筛选结果表明,LY96可能是vemurafenib和依托泊苷的靶点。进一步的实验证实了LY96和M2的空间共定位,敲低LY96可以抑制M2的极化。细胞活力实验表明,敲低LY96将导致M2巨噬细胞对依托泊苷的耐药性降低。研究表明,LY96可能是肾细胞癌的不利生物标志物,并可能通过促进M2巨噬细胞的浸润而促进癌症的进展。LY96可能是治疗RCC的新靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gene LY96 is an M2 macrophage-related biomarker and is associated with immunosuppression in renal cell carcinoma

Gene LY96 is an M2 macrophage-related biomarker and is associated with immunosuppression in renal cell carcinoma

Lymphocyte Antigen 96 (LY96) was identified as an oncogene in several tumors. However, its role in renal cancer has not been explored. In the study, LY96 is identified abnormally expressed using several public kidney cancer sequencing data. The expression level of LY96 is validated using paired clinical samples. Survival analyses and ROC curves are used to examine its prognostic and diagnostic value. Gene sets enrichment analyses (GSEA) show LY96 might influence immune processes. Then immune infiltration analyses results suggest that LY96 is positively correlated with M2 macrophages infiltration in RCC. Single-cell data are used to verify its association with macrophages. Moreover, LY96 is positively with various immune scores and might affect the efficacy of immunotherapy. Drug screening results show LY96 might be the target of vemurafenib and etoposide. Further experiments confirm the spatial co-localization of LY96 and M2, and knocking down LY96 can inhibit M2 polarization. Cell viability experiments indicate that knocking down LY96 would result in a decrease in the resistance of M2 macrophages to etoposide. The study shows LY96 could act as an unfavorable biomarker for RCC and possibly contribute to cancer progression by promoting the infiltration of M2 macrophage. LY96 could be a novel therapeutic target for RCC.

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