Yu Jiale, Guo Zhijuan, Zhang Junyi
Inner Mongolia Medical University, Hohhot, China.
School of Basic Medicine, Chifeng University, Chifeng, China.
Front Oncol. 2024 Nov 4;14:1468484. doi: 10.3389/fonc.2024.1468484. eCollection 2024.
The Schlafen (SLFN) gene family has emerged as a critical subject of study in recent years, given its involvement in an array of cellular functions such as proliferation, differentiation, immune responses, viral infection inhibition, and DNA replication. Additionally, SLFN genes are linked to chemosensitivity, playing a pivotal role in treating malignant tumors. Human SLFNs comprise three domains: the N-terminal, middle (M), and C-terminal. The N- and C-terminal domains demonstrate nuclease and helicase/ATPase activities, respectively. Meanwhile, the M-domain likely functions as a linker that connects the enzymatic domains of the N- and C-terminals and may engage in interactions with other proteins. This paper aims to present a comprehensive overview of the SLFN family's structure and sequence, examine its significance in various tumors, and explore its connection with immune infiltrating cells and immune checkpoints. The objective is to assess the potential of SLFNs as vital targets in cancer therapy and propose novel strategies for combined treatment approaches.
近年来,Schlafen(SLFN)基因家族已成为一个关键的研究对象,因为它参与了一系列细胞功能,如增殖、分化、免疫反应、病毒感染抑制和DNA复制。此外,SLFN基因与化疗敏感性有关,在恶性肿瘤治疗中发挥着关键作用。人类SLFNs包含三个结构域:N端、中间(M)端和C端。N端和C端结构域分别表现出核酸酶和螺旋酶/ATP酶活性。同时,M结构域可能作为连接N端和C端酶结构域的连接体,并可能与其他蛋白质相互作用。本文旨在全面概述SLFN家族的结构和序列,研究其在各种肿瘤中的意义,并探讨其与免疫浸润细胞和免疫检查点的关系。目的是评估SLFNs作为癌症治疗重要靶点的潜力,并提出联合治疗方法的新策略。