Shantou University of Medical College, Shantou, 515000, China.
Department of General Surgery, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, No. 106 Zhongshan Er Road, Guangzhou, 510080, China.
Clin Transl Oncol. 2020 Dec;22(12):2244-2252. doi: 10.1007/s12094-020-02365-z. Epub 2020 May 18.
Family with sequence similarity 83 members H (FAM83H) is one member of Family with sequence similarity 83 (FAM83) family, which possess oncogenic properties in several types of cancer. However, the potential function of FAM83H in pancreatic cancer (PC) still remain unknown.
This study aims to explore the role of FAM83H during pancreatic carcinogenesis and the regulation of immune infiltration in PC.
In the current study, the clinical significance and potential biological of FAM83H were evaluated by bioinformatics analysis. Possible associations between FAM83H expression and tumor immunity were analyzed using ESTIMATE algorithm and single-sample gene set enrichment analysis (ssGSEA).
FAM83H expression was significantly upregulated in tumor tissues, and positively associated with higher histologic grade, tumor recurrence, and worse prognosis. FAM83H overexpression is notably associated with KRAS activation. And functional enrichment analysis demonstrated that FAM83H may be involved in positive regulation of cell proliferation and migration, Ras protein signal transduction, regulation of cell-matrix adhesion, epithelial to mesenchymal transition (EMT), TGF-β receptor signaling in EMT, and activated NOTCH transmits signal to the nucleus. ESTIMATE algorithm and ssGSEA demonstrated that FAM83H overexpression suppressed the infiltration and antitumor activity of tumor-infiltrating lymphocytes (TILs), especially for CD8 T cells. Besides, FAM83H overexpression significantly correlated with low expression of TIL-related gene markers (e.g. CD8A, CD8B, CD2, CD3D, and CD3E).
The study suggests that FAM83H overexpression predicts poor prognosis and correlates with less CD8 T cells infiltration and Ras-PI3K-Akt-mTOR signaling pathway in PC.
家族序列相似性 83 成员 H(FAM83H)是家族序列相似性 83(FAM83)家族的成员之一,在多种类型的癌症中具有致癌特性。然而,FAM83H 在胰腺癌(PC)中的潜在功能仍不清楚。
本研究旨在探讨 FAM83H 在胰腺癌发生过程中的作用及其对 PC 肿瘤免疫浸润的调节作用。
本研究通过生物信息学分析评估 FAM83H 的临床意义和潜在生物学功能。使用 ESTIMATE 算法和单样本基因集富集分析(ssGSEA)分析 FAM83H 表达与肿瘤免疫之间的可能关联。
FAM83H 在肿瘤组织中表达明显上调,与较高的组织学分级、肿瘤复发和预后不良呈正相关。FAM83H 的过表达与 KRAS 激活显著相关。功能富集分析表明,FAM83H 可能参与细胞增殖和迁移的正调控、Ras 蛋白信号转导、细胞-基质黏附的调节、上皮间质转化(EMT)、EMT 中的 TGF-β 受体信号转导以及激活的 NOTCH 向核内传递信号。ESTIMATE 算法和 ssGSEA 表明,FAM83H 过表达抑制肿瘤浸润淋巴细胞(TIL)的浸润和抗肿瘤活性,特别是 CD8 T 细胞。此外,FAM83H 过表达与 TIL 相关基因标志物(如 CD8A、CD8B、CD2、CD3D 和 CD3E)的低表达显著相关。
该研究表明,FAM83H 过表达预示着不良的预后,并与 PC 中 CD8 T 细胞浸润减少和 Ras-PI3K-Akt-mTOR 信号通路相关。