Department of Gastroenterology, Xinqiao Hospital, Third Military Medical University (Army Medical University), Chongqing, 400037, China.
Department of Medicine, University of California San Diego, San Diego, CA, 92093, USA.
Cell Commun Signal. 2018 Jun 15;16(1):31. doi: 10.1186/s12964-018-0242-1.
The MiT/TFE transcription factors play a pivotal role in the regulation of autophagy and lysosomal biogenesis. The subcellular localization and activity of MiT/TFE proteins are primarily regulated through phosphorylation. And the phosphorylated protein is retained in the cytoplasm and subsequently translocates to the nucleus upon dephosphorylation, where it stimulates the expression of hundreds of genes, leading to lysosomal biogenesis and autophagy induction. The transcription factor-mediated lysosome-to-nucleus signaling can be directly controlled by several signaling molecules involved in the mTORC1, PKC, and AKT pathways. MiT/TFE family members have attracted much attention owing to their intracellular clearance of pathogenic factors in numerous diseases. Recently, multiple studies have also revealed the MiT/TFE proteins as master regulators of cellular metabolic reprogramming, converging on autophagic and lysosomal function and playing a critical role in cancer, suggesting that novel therapeutic strategies could be based on the modulation of MiT/TFE family member activity. Here, we present an overview of the latest research on MiT/TFE transcriptional factors and their potential mechanisms in cancer.
MiT/TFE 转录因子在自噬和溶酶体生物发生的调节中发挥关键作用。MiT/TFE 蛋白的亚细胞定位和活性主要通过磷酸化调节。磷酸化的蛋白质保留在细胞质中,并在去磷酸化后易位到细胞核,在那里它刺激数百个基因的表达,导致溶酶体生物发生和自噬诱导。转录因子介导的溶酶体到细胞核的信号可以直接被几个参与 mTORC1、PKC 和 AKT 途径的信号分子控制。由于 MiT/TFE 家族成员在多种疾病中清除了细胞内的致病因子,因此引起了广泛关注。最近的多项研究还揭示了 MiT/TFE 蛋白作为细胞代谢重编程的主要调节剂,它们与自噬和溶酶体功能收敛,并在癌症中发挥关键作用,这表明可以基于调节 MiT/TFE 家族成员的活性来制定新的治疗策略。在这里,我们概述了关于 MiT/TFE 转录因子及其在癌症中潜在机制的最新研究。