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含葡萄球菌核酸酶和Tudor结构域蛋白1:癌症中一个新出现的治疗靶点(综述)

Staphylococcal nuclease and tudor domain-containing protein 1: An emerging therapeutic target in cancer (Review).

作者信息

Rai Santosh Kumar, Khan Mohd Imran, Kumar Rakesh, Patil Rakesh Ishwar, Dhawan Sanjeev, Panwar Amit, Kumar Anil

机构信息

New Drug Discovery Research, Mankind Research Centre Unit-1, Mankind Pharma Limited, Gurugram, Haryana 122051, India.

出版信息

Mol Clin Oncol. 2025 Jul 17;23(4):86. doi: 10.3892/mco.2025.2881. eCollection 2025 Oct.

Abstract

Staphylococcal nuclease and tudor domain-containing protein 1 (SND1) is an oncoprotein that is overexpressed in various types of cancer, including breast, prostate, lung, colorectal and hepatocellular carcinomas, as well as malignant gliomas, especially in cases of advanced and metastatic cancer. SND1 has a significant role in tumour development via its interactions with RNA and partner proteins. SND1 functions as a nuclease within the RNA-induced silencing complex, where small RNAs (such as siRNAs or miRNAs) bind to ribonucleoproteins to mediate RNA interference and silencing of tumour suppressor genes. Metadherin (MTDH) has been identified as an important protein partner of SND1, and the SND1-MTDH interaction has been reported to drive tumour initiation, metastasis and immune evasion in various types of cancer. Therefore, SND1 is considered as a crucial target for cancer therapy, and multiple approaches have been explored to inhibit its nuclease activity or disrupt its interaction with MTDH. In the present review, both the oncogenic functions of SND1 and therapeutic strategies that target either its binding to RNA or its interaction with MTDH are investigated.

摘要

含葡萄球菌核酸酶和 Tudor 结构域蛋白 1(SND1)是一种癌蛋白,在包括乳腺癌、前列腺癌、肺癌、结直肠癌和肝细胞癌以及恶性胶质瘤在内的多种癌症类型中均有过表达,尤其是在晚期和转移性癌症病例中。SND1 通过与 RNA 和伴侣蛋白相互作用,在肿瘤发生发展中发挥重要作用。SND1 在 RNA 诱导沉默复合体中作为核酸酶发挥作用,小 RNA(如 siRNA 或 miRNA)在此与核糖核蛋白结合,介导 RNA 干扰和肿瘤抑制基因沉默。黏附素(MTDH)已被确定为 SND1 的重要蛋白伴侣,据报道,SND1-MTDH 相互作用在多种癌症类型中驱动肿瘤起始、转移和免疫逃逸。因此,SND1 被认为是癌症治疗的关键靶点,人们已探索多种方法来抑制其核酸酶活性或破坏其与 MTDH 的相互作用。在本综述中,我们研究了 SND1 的致癌功能以及针对其与 RNA 结合或与 MTDH 相互作用的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a478/12311766/66830f7d10ac/mco-23-04-02881-g00.jpg

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