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骨髓基质细胞抗原 2:肿瘤生物学、信号通路与治疗靶点(综述)。

Bone marrow stromal cell antigen 2: Tumor biology, signaling pathway and therapeutic targeting (Review).

机构信息

Department of Endocrinology, Affiliated Hospital of Jining Medical University, Jining Medical University, Jining, Shandong 272029, P.R. China.

Collaborative Innovation Center, Jining Medical University, Jining, Shandong 272067, P.R. China.

出版信息

Oncol Rep. 2024 Mar;51(3). doi: 10.3892/or.2024.8704. Epub 2024 Jan 19.

Abstract

Bone marrow stromal cell antigen 2 (BST2) is a type II transmembrane protein that serves critical roles in antiretroviral defense in the innate immune response. In addition, it has been suggested that BST2 is highly expressed in various types of human cancer and high BST2 expression is related to different clinicopathological parameters in cancer. The molecular mechanism underlying BST2 as a potential tumor biomarker in human solid tumors has been reported on; however, to the best of our knowledge, there has been no review published on the molecular mechanism of BST2 in human solid tumors. The present review focuses on human BST2 expression, structure and functions; the molecular mechanisms of BST2 in breast cancer, hepatocellular carcinoma, gastrointestinal tumor and other solid tumors; the therapeutic potential of BST2; and the possibility of BST2 as a potential marker. BST2 is involved in cell membrane integrity and lipid raft formation, which can activate epidermal growth factor receptor signaling pathways, providing a potential mechanistic link between BST2 and tumorigenesis. Notably, BST2 may be considered a universal tumor biomarker and a potential therapeutical target.

摘要

骨髓基质细胞抗原 2(BST2)是一种 II 型跨膜蛋白,在先天免疫反应中的抗逆转录病毒防御中发挥关键作用。此外,有研究表明,BST2 在多种人类癌症中高度表达,高表达 BST2 与癌症的不同临床病理参数有关。BST2 作为人类实体瘤中潜在的肿瘤标志物的分子机制已经有报道;然而,据我们所知,目前尚无关于 BST2 在人类实体瘤中分子机制的综述。本综述重点介绍了人类 BST2 的表达、结构和功能;BST2 在乳腺癌、肝癌、胃肠道肿瘤等实体瘤中的分子机制;BST2 的治疗潜力;以及 BST2 作为潜在标志物的可能性。BST2 参与细胞膜完整性和脂筏形成,可激活表皮生长因子受体信号通路,为 BST2 与肿瘤发生之间提供了潜在的机制联系。值得注意的是,BST2 可能被认为是一种通用的肿瘤标志物和潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/03e2/10828922/cacdc1e7a050/or-51-03-08704-g00.jpg

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