间皮素作为癌症免疫治疗的生物标志物和治疗靶点
Mesothelin as Biomarker and Therapeutic Target for Immunotherapy in Cancer.
癌症仍是一个关键的全球健康问题,原因在于发现晚、耐药和高死亡率。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:GHRL as a prognostic biomarker correlated with immune infiltrates and progression of precancerous lesions in gastric cancer.
GHRL as a prognostic biomarker correlated with immune infiltrates and progression of precancerous lesions in gastric cancer.
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GHRL 是 GC 患者的预后生物标志物,并且与 GC 癌前病变的进展相关。
Ghrelin是一种调节人体食欲和能量平衡的蛋白,由GHRL(ghrelin前体肽基因)编码。GHRL与癌变和免疫调节相关,但其与胃癌(GC)预后及TIL(肿瘤浸润淋巴细胞)的关系尚不明确。
本研究基于TIMER、GEPIA、GEO、STRING、UALCAN、TISIDB和Kaplan-Meier Plotter等数据库数据,评估GC患者中GHRL的转录表达、预后及不同临床病理特征,并分析其与肿瘤浸润免疫细胞的相关性。此外,研究使用R软件分析胃癌Correa级联过程。最后,采用定量实时PCR和免疫组化检测胃癌组织中的GHRL表达。
胃癌样本中的GHRL表达低于正常样本,并通过定量PCR和免疫组化验证。然而,样本类型、癌症分期和较差生存均与GHRL高表达相关。研究还发现,异型增生组织中的GHRL表达显著低于慢性非萎缩性胃炎(CNAG)及胃癌组织。GHRL高表达与胃癌患者的免疫调节因子、趋化因子以及B细胞、CD8⁺ T细胞、CD4⁺ T细胞、巨噬细胞、中性粒细胞和树突状细胞浸润水平相关。
GHRL是胃癌患者的预后生物标志物,并与胃癌癌前病变进展相关。GHRL可能通过调节肿瘤免疫微环境导致不良预后。未来开展研究以探索靶向GHRL治疗具有重要意义。
Ghrelin is a protein that regulate appetite and energy balance in the human body, which is encoded by the ghrelin prepropeptide gene (GHRL). GHRL is linked with carcinogenesis and immune regulation. However, the correlation of GHRL to prognosis and tumor-infiltrating lymphocytes in gastric cancer (GC) remains unclear.
In this study, we assessed the transcriptional expression, prognosis, and different clinicopathological features about GHRL and the correlation between GHRL and tumor infiltration immune cells in GC patients based on the data published in the following databases: TIMER, GEPIA, GEO, STRING, UALCAN, TISIDB, and Kaplan-Meier Plotter. Furthermore, R software analysis for GC Correa' cascade was also provided. Finally, GHRL expression in GC tissues was assayed using quantitative real-time polymerase chain reaction and immunohistochemistry.
We found that GHRL expression in GC samples was lower than in normal samples and verified by quantitative PCR (qPCR) and immunohistochemistry. However, sample type, cancer stage, and worse survival were correlated to high GHRL expression. We also found that the expression of GHRL in dysplasia was significantly lower than that in CNAG and in GC. High GHRL expression was connected with immunomodulators, chemokines, and infiltrating levels of B cells, CD8+ T cells, CD4+ T cells, macrophages, neutrophils, and dendritic cells in GC.
GHRL is a prognostic biomarker for GC patients, and it is correlated with progression of precancerous lesions in GC. It might lead to poor prognosis by regulating tumor immune microenvironment. Studies are important to explore therapeutic targeting GHRL in the future.
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