Department of Oncology, University of Torino, Candiolo, Italy.
Candiolo Cancer Institute-IRCCS-FPO, Candiolo, Italy.
Mol Oncol. 2021 Feb;15(2):327-346. doi: 10.1002/1878-0261.12867. Epub 2020 Dec 23.
Transcription factor EB (TFEB) represents an emerging player in cancer biology. Together with microphthalmia-associated transcription factor, transcription factor E3 and transcription factor EC, TFEB belongs to the microphthalmia family of bHLH-leucine zipper transcription factors that may be implicated in human melanomas, renal and pancreatic cancers. TFEB was originally described as being translocated in a juvenile subset of pediatric renal cell carcinoma; however, whole-genome sequencing reported that somatic mutations were sporadically found in many different cancers. Besides its oncogenic activity, TFEB controls the autophagy-lysosomal pathway by recognizing a recurrent motif present in the promoter regions of a set of genes that participate in lysosome biogenesis; furthermore, its dysregulation was found to have a crucial pathogenic role in different tumors by modulating the autophagy process. Other than regulating cancer cell-autonomous responses, recent findings indicate that TFEB participates in the regulation of cellular functions of the tumor microenvironment. Here, we review the emerging role of TFEB in regulating cancer cell behavior and choreographing tumor-microenvironment interaction. Recognizing TFEB as a hub of network of signals exchanged within the tumor between cancer and stroma cells provides a fresh perspective on the molecular principles of tumor self-organization, promising to reveal numerous new and potentially druggable vulnerabilities.
转录因子 EB(TFEB)是癌症生物学中的一个新兴角色。与小眼畸形相关转录因子、转录因子 E3 和转录因子 EC 一起,TFEB 属于小眼畸形家族的碱性螺旋-环-螺旋亮氨酸拉链转录因子,可能与人类黑色素瘤、肾细胞癌和胰腺癌有关。TFEB 最初被描述为在小儿肾细胞癌的少年亚群中易位;然而,全基因组测序报告称,体细胞突变在许多不同的癌症中偶尔被发现。除了其致癌活性外,TFEB 通过识别一组参与溶酶体生物发生的基因启动子区域中存在的重复基序来控制自噬-溶酶体途径;此外,通过调节自噬过程,其失调被发现对不同肿瘤具有关键的致病作用。除了调节癌细胞自主反应外,最近的发现表明 TFEB 参与调节肿瘤微环境中的细胞功能。在这里,我们回顾了 TFEB 在调节癌细胞行为和协调肿瘤微环境相互作用方面的新作用。将 TFEB 识别为肿瘤内癌细胞和基质细胞之间交换信号的网络的枢纽,为肿瘤自我组织的分子原理提供了新的视角,有望揭示许多新的、潜在可药物治疗的弱点。