抗坏血酸在癌症治疗中的应用--是时候重新审视了

Izuegbuna Ogochukwu
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摘要

引言和目的。在过去的几十年里,关于抗坏血酸(AA)可作为抗肿瘤疗法发挥作用的假设产生了许多相互矛盾的报道。尽管存在争议,但越来越多的证据表明,抗坏血酸具有作为抗肿瘤药物发挥作用的潜力。最近的研究揭示了 AA 的药代动力学和对癌细胞的各种作用机制。这催生了不同的临床前研究,有报告称 AA 对各种癌症具有良好的活性。材料和方法。使用 PubMed 数据库对有关抗坏血酸治疗癌症的文献进行了综述。研究仅限于摘要和可用的全文文章。文献分析。临床试验也证明了不同剂量抗坏血酸的安全性和耐受性。人们注意到 AA 是一种多靶点制剂,可作为促氧化细胞毒制剂、抗癌表观遗传调节剂和免疫调节剂。在不同的癌症中,AA 还能与标准化疗方案产生协同作用。尽管 AA 潜力巨大,但目前仍严重缺乏 III 期临床试验。最近的 VITALITY III 期研究表明,AA 可作为一种辅助靶向疗法用于治疗 ras 基因突变的癌症。因此,有必要进行更多标准化临床试验,以帮助确定癌症亚型和能产生最大疗效的 AA 组合方案。在这篇综述中,探讨了 AA 的多效应作用机制以及癌症治疗中的各种临床前和临床研究。此外,还就 AA 和标准癌症治疗方案的有效策略以及未来发展方向提出了建议。研究表明,抗坏血酸可通过不同的作用机制诱导各种癌症类型的细胞死亡。一些临床试验和病例报告显示了其在联合化疗中的疗效,其药理作用途径可以是静脉注射或口服。不过,联合用药时可能会影响某些药物的作用。此外,应确定剂量以发挥最大药理作用。结论抗坏血酸具有提供安全、经济的抗肿瘤治疗选择的潜力,尤其是在联合治疗中。其潜力需要通过临床试验进一步研究。
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Ascorbic acid in cancer management – time for a second look
Introduction and aim. Over the past decades, the hypotheses that ascorbic acid (AA) can play a role as an anti-neoplastic therapy have generated many conflicting reports. Despite the controversies, mounting evidence has shown that AA has the potential to play a role as an anti-neoplastic agent. Recent studies have unraveled its pharmacokinetics and various mechanism of action on cancer cells. This has spawned different preclinical studies with reports of good activities against various cancers. Material and methods. A review of the literature regarding ascorbic acid in the management of cancer was performed using the PubMed database. The research was limited to abstracts and available full-text articles. Analysis of the literature. Clinical trials have also demonstrated its safety and tolerability across different dosages. AA has been noted as a multitargeting agent that acts as a pro-oxidative cytotoxic agent, anti-cancer epigenetic regulator and immune modulator. AA has also been shown act synergistically with standard chemotherapy regimens in different cancers. Despite its potentials, phase III clinical trials are seriously lacking. The recent phase III VITALITY study shows that AA may play a role as an adjunct targeted therapy for ras-mutated cancers. Therefore, there is need to for more standardized clinical trials to help identify cancer subtypes and AA combination regimens that can show the most benefits. In this review, the pleiotropic mechanism of action of AA was explored as well as various preclinical and clinical studies in cancer therapy. In addition, recommendations were also made for effective strategies towards an AA and standard cancer regimens in treatment as well as future directions. Ascorbic acid has been shown to induce cell death in various cancer types through different mechanisms of action. Several clinical trials and case reports have shown its efficacy in combination chemotherapy, and the pharmacological route of action can be either intravenous or oral. However, it can impair the actions of some drugs when given in combination. Also, dosage should be determined for maximal pharmacologic action. Conclusion. Ascorbic acid has the potential to provide safe and cost-effective antineoplastic treatment option especially in combination therapy. Its potential needs to be further investigated through clinical trials.
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