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CLEC10A 是肺腺癌的预后生物标志物,与临床病理特征和免疫浸润相关。

CLEC10A is a prognostic biomarker and correlated with clinical pathologic features and immune infiltrates in lung adenocarcinoma.

机构信息

Department of Oncology, Xiangya Hospital, Central South University, Changsha, China.

Key Laboratory for Molecular Radiation Oncology of Hunan Province, Xiangya Hospital, Central South University, Changsha, China.

出版信息

J Cell Mol Med. 2021 Apr;25(7):3391-3399. doi: 10.1111/jcmm.16416. Epub 2021 Mar 2.

Abstract

CLEC10A, (C-type lectin domain family 10, member A), as the member of C-type lectin receptors (CLRs), plays a vital role in modulating innate immunity and adaptive immunity and has shown great potential as an immunotherapy target for cancers. However, there is no functional research of CLEC10A in prognostic risk, immunotherapy or any other treatment of lung adenocarcinoma (LUAD). We performed bioinformatics analysis on LUAD data downloaded from TCGA (The Cancer Genome Atlas) and GEO (Gene Expression Omnibus), and jointly analysed with online databases such as HPA, LinkedOmics, TIMER, ESTIMATE and TISIDB. We found that lower expression of CLEC10A was accompanied with worse outcomes of LUAD patients. Moreover, CLEC10A expression was significantly correlated with a variety of the tumour-infiltrating immune cells (TIICs). As a promising prognosis predictor and potential immunotherapy target, the potential influence and mechanisms of CLEC10A in LUAD deserve further exploring.

摘要

CLEC10A(C 型凝集素结构域家族 10,成员 A)作为 C 型凝集素受体(CLRs)的成员,在调节先天免疫和适应性免疫方面发挥着重要作用,并且作为癌症免疫治疗的靶点具有巨大的潜力。然而,在肺腺癌(LUAD)的预后风险、免疫治疗或任何其他治疗中,CLEC10A 的功能研究还没有开展。我们对从 TCGA(癌症基因组图谱)和 GEO(基因表达综合数据库)下载的 LUAD 数据进行了生物信息学分析,并与 HPA、LinkedOmics、TIMER、ESTIMATE 和 TISIDB 等在线数据库进行了联合分析。我们发现 CLEC10A 表达水平较低与 LUAD 患者的预后较差有关。此外,CLEC10A 表达与多种肿瘤浸润免疫细胞(TIICs)显著相关。作为一个有前途的预后预测因子和潜在的免疫治疗靶点,CLEC10A 在 LUAD 中的潜在影响和机制值得进一步探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bb31/8034442/0c05950309e1/JCMM-25-3391-g004.jpg

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