Hirose Wataru, Oshikiri Hiroyuki, Taguchi Keiko, Yamamoto Masayuki
Department of Medical Biochemistry, Tohoku University Graduate School of Medicine, 2-1 Seiryo-Machi, Aoba, Sendai 980-8575, Japan.
Department of Surgery, Tohoku University Graduate School of Medicine, Sendai 980-8575, Japan.
Cancers (Basel). 2022 Sep 27;14(19):4702. doi: 10.3390/cancers14194702.
NRF2 (nuclear factor erythroid 2-related factor 2) is a transcription factor that regulates the expression of many cytoprotective genes. NRF2 activation is mainly regulated by KEAP1 (kelch-like ECH-associated protein 1) through ubiquitination and proteasome degradation. Esophageal cancer is classified histologically into two major types: esophageal squamous cell carcinoma (ESCC) and esophageal adenocarcinoma (EAC). ESCC harbors more genetic alterations in the KEAP-NRF2 system than EAC does, which results in NRF2 activation in these cancers. NRF2-addicted ESCC exhibits increased malignancy and acquisition of resistance to chemoradiotherapy. Therefore, it has been recognized that the development of drugs targeting the KEAP1-NRF2 system based on the molecular dissection of NRF2 function is important and urgent for the treatment of ESCC, along with efficient clinical screening for NRF2-addicted ESCC patients. Recently, the fate of NRF2-activated cells in esophageal tissues, which was under the influence of strong cell competition, and its relationship to the pathogenesis of ESCC, was clarified. In this review, we will summarize the current knowledge of the KEAP1-NRF2 system and the treatment of ESCC. We propose three main strategies for the treatment of NRF2-addicted cancer: (1) NRF2 inhibitors, (2) synthetic lethal drugs for NRF2-addicted cancers, and (3) NRF2 inducers of the host defense system.
核因子E2相关因子2(NRF2)是一种转录因子,可调节许多细胞保护基因的表达。NRF2的激活主要由kelch样ECH相关蛋白1(KEAP1)通过泛素化和蛋白酶体降解来调节。食管癌在组织学上主要分为两种类型:食管鳞状细胞癌(ESCC)和食管腺癌(EAC)。与EAC相比,ESCC在KEAP-NRF2系统中存在更多的基因改变,这导致这些癌症中NRF2的激活。对NRF2成瘾的ESCC表现出更高的恶性程度并获得了对放化疗的抗性。因此,基于对NRF2功能的分子剖析,开发针对KEAP1-NRF2系统的药物对于ESCC的治疗以及对NRF2成瘾的ESCC患者进行有效的临床筛查都非常重要且紧迫。最近,在强大的细胞竞争影响下食管组织中NRF2激活细胞的命运及其与ESCC发病机制的关系得到了阐明。在这篇综述中,我们将总结关于KEAP1-NRF2系统和ESCC治疗的当前知识。我们提出了三种治疗对NRF2成瘾癌症的主要策略:(1)NRF2抑制剂,(2)针对对NRF2成瘾癌症的合成致死药物,以及(3)宿主防御系统的NRF2诱导剂。