Abdominal Oncology Ward, Cancer Center, West China Hospital, Sichuan University, Chengdu 610041, China.
Int J Mol Sci. 2023 Mar 2;24(5):4820. doi: 10.3390/ijms24054820.
Pancreatic cancer is one of the most lethal malignant diseases due to its high invasiveness, early metastatic properties, rapid disease progression, and typically late diagnosis. Notably, the capacity for pancreatic cancer cells to undergo epithelial-mesenchymal transition (EMT) is key to their tumorigenic and metastatic potential, and is a feature that can explain the therapeutic resistance of such cancers to treatment. Epigenetic modifications are a central molecular feature of EMT, for which histone modifications are most prevalent. The modification of histones is a dynamic process typically carried out by pairs of reverse catalytic enzymes, and the functions of these enzymes are increasingly relevant to our improved understanding of cancer. In this review, we discuss the mechanisms through which histone-modifying enzymes regulate EMT in pancreatic cancer.
胰腺癌是最致命的恶性疾病之一,因为它具有高侵袭性、早期转移性、疾病进展迅速和通常晚期诊断的特点。值得注意的是,胰腺癌细胞发生上皮-间充质转化(EMT)的能力是其致瘤和转移潜能的关键,也是此类癌症对治疗产生耐药性的一个特征。表观遗传修饰是 EMT 的一个主要分子特征,其中组蛋白修饰最为普遍。组蛋白的修饰是一个典型由两对反向催化酶进行的动态过程,这些酶的功能与我们对癌症的认识的提高越来越相关。在这篇综述中,我们讨论了组蛋白修饰酶调节胰腺癌 EMT 的机制。