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TRIM47通过促进波形蛋白的K63连接泛素化来促进下咽癌和喉癌的进展。

TRIM47 promotes hypopharyngeal and laryngeal cancers progression through promoting K63-linked ubiquitination of vimentin.

作者信息

Qin Shichao, Chang Fen, Sun Xiangkai, Li Zinan, Wang Yin, Lei Dapeng

机构信息

Department of Otorhinolaryngology, Qilu Hospital of Shandong University, Jinan, Shandong, China.

NHC Key Laboratory of Otorhinolaryngology (Shandong University), Jinan, Shandong, China.

出版信息

Cancer Sci. 2025 Feb;116(2):367-380. doi: 10.1111/cas.16397. Epub 2024 Nov 25.

Abstract

Hypopharyngeal and laryngeal cancers which belong to head and neck squamous cell carcinoma (HNSCC) are the two most malignant types of head and neck cancer, characterized by a low 5-year survival rate, high recurrence and metastasis rate. It is vital to explore strategies to suppress metastasis and improve prognosis for patients with these cancers. In this research, we analyzed the clinical data and found that E3 ubiquitin ligase TRIM47 was upregulated in cancer tissues of hypopharyngeal cancer and was closely associated with poor survival outcomes. In terms of mechanism, we performed tandem affinity chromatography and denatured Ni-NTA Agarose pulldown. As a result, TRIM47 was found to interact with vimentin and control vimentin stabilization through ubiquitination, specifically in the form of K63 chains. Importantly, through experiments of cancer cell viability and migration, we found that TRIM47 could enhance the proliferation and metastasis abilities of cancer cells in a vimentin-dependent manner, thus promoting the advancement of hypopharyngeal and laryngeal cancers. TRIM47 was verified to regulate cancer cells metastasis in vivo using metastasis models. All these results imply that TRIM47 emerges as a potential biomarker for early diagnosis and metastasis prediction of hypopharyngeal and laryngeal cancers and represents a promising therapeutic target.

摘要

下咽癌和喉癌属于头颈部鳞状细胞癌(HNSCC),是头颈部癌症中最具侵袭性的两种类型,其特点是5年生存率低、复发和转移率高。探索抑制转移和改善这些癌症患者预后的策略至关重要。在本研究中,我们分析了临床数据,发现E3泛素连接酶TRIM47在下咽癌组织中上调,且与不良生存结果密切相关。在机制方面,我们进行了串联亲和层析和变性镍-nta琼脂糖下拉实验。结果发现,TRIM47与波形蛋白相互作用,并通过泛素化控制波形蛋白的稳定性,具体是以K63链的形式。重要的是,通过癌细胞活力和迁移实验,我们发现TRIM47可以以波形蛋白依赖的方式增强癌细胞的增殖和转移能力,从而促进下咽癌和喉癌的进展。使用转移模型在体内验证了TRIM47对癌细胞转移的调节作用。所有这些结果表明,TRIM47有望成为下咽癌和喉癌早期诊断和转移预测的潜在生物标志物,并代表一个有前景的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f64/11786321/961d869f79b7/CAS-116-367-g001.jpg

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