Nrf2, A Target for Precision Oncology in Cancer Prognosis and Treatment.

IF 2.5 Q3 ONCOLOGY Journal of Cancer Prevention Pub Date : 2023-12-30 DOI:10.15430/JCP.2023.28.4.131
Hoang Kieu Chi Ngo, Hoang Le, Young-Joon Surh
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Abstract

Activating nuclear factor-erythroid 2-related factor (Nrf2), a master regulator of redox homeostasis, has been shown to suppress initiation of carcinogenesis in normal cells. However, this transcription factor has recently been reported to promote proliferation of some transformed or cancerous cells. In tumor cells, Nrf2 is prone to mutations that result in stabilization and concurrent accumulation of its protein product. A hyperactivated mutant form of Nrf2 could support the cancer cells for enhanced proliferation, invasiveness, and resistance to chemotherapeutic agents and radiotherapy, which are associated with a poor clinical outcome. Hence understanding mutations in Nrf2 would have a significant impact on the prognosis and treatment of cancer in the era of precision medicine. This perspective would provide an insight into the genetic alterations in Nrf2 and suggest the application of small molecules, RNAi, and genome editing technologies, particularly CRISR-Cas9, in therapeutic intervention of cancer in the context of the involvement of Nrf2 mutations.

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Nrf2,癌症预后和治疗中的精准肿瘤学靶点。
激活核因子-红细胞 2 相关因子(Nrf2)是氧化还原平衡的主要调节因子,已被证明可抑制正常细胞癌变的发生。然而,最近有报道称这种转录因子会促进一些转化细胞或癌细胞的增殖。在肿瘤细胞中,Nrf2 容易发生突变,导致其蛋白产物稳定并同时积累。Nrf2 的超活化突变形式可支持癌细胞增殖、侵袭性和对化疗药物和放疗的抵抗力增强,而这与不良的临床预后有关。因此,在精准医学时代,了解 Nrf2 的突变将对癌症的预后和治疗产生重大影响。这一观点将有助于深入了解 Nrf2 的基因改变,并建议在 Nrf2 基因突变的背景下,应用小分子、RNAi 和基因组编辑技术,特别是 CRISR-Cas9 对癌症进行治疗干预。
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