Department of Neurosurgery, Shaoxing People's Hospital, Shaoxing, 312000, Zhejiang, China.
Department of Neurosurgery, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310020, Zhejiang, China.
Mol Cancer. 2022 Oct 28;21(1):204. doi: 10.1186/s12943-022-01668-9.
Brain cancer is regarded among the deadliest forms of cancer worldwide. The distinct tumor microenvironment and inherent characteristics of brain tumor cells virtually render them resistant to the majority of conventional and advanced therapies. Oxidative stress (OS) is a key disruptor of normal brain homeostasis and is involved in carcinogenesis of different forms of brain cancers. Thus, antioxidants may inhibit tumorigenesis by preventing OS induced by various oncogenic factors. Antioxidants are hypothesized to inhibit cancer initiation by endorsing DNA repair and suppressing cancer progression by creating an energy crisis for preneoplastic cells, resulting in antiproliferative effects. These effects are referred to as chemopreventive effects mediated by an antioxidant mechanism. In addition, antioxidants minimize chemotherapy-induced nonspecific organ toxicity and prolong survival. Antioxidants also support the prooxidant chemistry that demonstrate chemotherapeutic potential, particularly at high or pharmacological doses and trigger OS by promoting free radical production, which is essential for activating cell death pathways. A growing body of evidence also revealed the roles of exogenous antioxidants as adjuvants and their ability to reverse chemoresistance. In this review, we explain the influences of different exogenous and endogenous antioxidants on brain cancers with reference to their chemopreventive and chemotherapeutic roles. The role of antioxidants on metabolic reprogramming and their influence on downstream signaling events induced by tumor suppressor gene mutations are critically discussed. Finally, the review hypothesized that both pro- and antioxidant roles are involved in the anticancer mechanisms of the antioxidant molecules by killing neoplastic cells and inhibiting tumor recurrence followed by conventional cancer treatments. The requirements of pro- and antioxidant effects of exogenous antioxidants in brain tumor treatment under different conditions are critically discussed along with the reasons behind the conflicting outcomes in different reports. Finally, we also mention the influencing factors that regulate the pharmacology of the exogenous antioxidants in brain cancer treatment. In conclusion, to achieve consistent clinical outcomes with antioxidant treatments in brain cancers, rigorous mechanistic studies are required with respect to the types, forms, and stages of brain tumors. The concomitant treatment regimens also need adequate consideration.
脑癌被认为是全球最致命的癌症之一。独特的肿瘤微环境和脑肿瘤细胞的固有特性使它们几乎对大多数常规和先进的治疗方法都具有耐药性。氧化应激(OS)是正常脑内稳态的关键破坏因素,并且涉及不同形式脑癌的癌变。因此,抗氧化剂可以通过防止各种致癌因子引起的 OS 来抑制肿瘤发生。抗氧化剂通过促进 DNA 修复和通过为肿瘤前细胞制造能量危机来抑制癌症进展来抑制癌症发生,从而产生抗增殖作用。这些作用被称为通过抗氧化机制介导的化学预防作用。此外,抗氧化剂可以最大程度地减少化疗引起的非特异性器官毒性并延长生存期。抗氧化剂还支持表现出化学治疗潜力的促氧化剂化学物质,特别是在高剂量或药理学剂量下通过促进自由基产生来触发 OS,这对于激活细胞死亡途径至关重要。越来越多的证据还揭示了外源性抗氧化剂作为佐剂的作用及其逆转化学抗性的能力。在本综述中,我们参考它们的化学预防和化学治疗作用,解释了不同外源性和内源性抗氧化剂对脑癌的影响。批判性地讨论了抗氧化剂对代谢重编程的作用及其对肿瘤抑制基因突变诱导的下游信号事件的影响。最后,该综述假设,通过杀死肿瘤细胞和抑制肿瘤复发,抗氧化分子的抗癌机制涉及抗氧化和促氧化剂作用,随后是常规癌症治疗。批判性地讨论了不同条件下脑肿瘤治疗中外源性抗氧化剂的促氧化剂和抗氧化剂作用的要求,以及不同报告中结果冲突的原因。最后,我们还提到了调节脑癌治疗中外源性抗氧化剂药理学的影响因素。总之,为了在脑癌的抗氧化治疗中获得一致的临床结果,需要针对脑肿瘤的类型、形式和阶段进行严格的机制研究。同时也需要充分考虑伴随的治疗方案。