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抗蠕虫药物作为癌症治疗中的新兴免疫调节剂

Anthelmintic Drugs as Emerging Immune Modulators in Cancer.

机构信息

Department of Systems Medicine, University of Rome "Tor Vergata", 00133 Rome, Italy.

Inflammatory Bowel Disease Research Laboratory, Department of Biological Sciences, Institute of Biotechnology, Federal University of Catalão (UFCAT), Catalão 75705-220, GO, Brazil.

出版信息

Int J Mol Sci. 2023 Mar 29;24(7):6446. doi: 10.3390/ijms24076446.

Abstract

Despite recent advances in treatment approaches, cancer is still one of the leading causes of death worldwide. Restoration of tumor immune surveillance represents a valid strategy to overcome the acquired resistance and cytotoxicity of conventional therapies in oncology and immunotherapeutic drugs, such as immune checkpoint inhibitors and immunogenic cell death inducers, and has substantially progressed the treatment of several malignancies and improved the clinical management of advanced disease. Unfortunately, because of tumor-intrinsic and/or -extrinsic mechanisms for escaping immune surveillance, only a fraction of patients clinically respond to and benefit from cancer immunotherapy. Accumulating evidence derived from studies of drug repositioning, that is, the strategy to identify new uses for approved or investigational drugs that are outside the scope of the original medical indication, has suggested that some anthelmintic drugs, in addition to their antineoplastic effects, exert important immunomodulatory actions on specific subsets of immune cell and related pathways. In this review, we report and discuss current knowledge on the impact of anthelmintic drugs on host immunity and their potential implication in cancer immunotherapy.

摘要

尽管近年来在治疗方法上取得了进展,但癌症仍然是全球主要的死亡原因之一。恢复肿瘤免疫监测代表了一种有效的策略,可以克服肿瘤学中常规疗法和免疫治疗药物(如免疫检查点抑制剂和免疫原性细胞死亡诱导剂)的获得性耐药性和细胞毒性,并大大推进了几种恶性肿瘤的治疗,并改善了晚期疾病的临床管理。不幸的是,由于肿瘤内在和/或外在的逃避免疫监测的机制,只有一小部分患者对癌症免疫疗法有临床反应并从中受益。药物重新定位(即确定已批准或正在研究的药物在原始医疗适应证范围之外的新用途的策略)的研究积累的证据表明,除了抗肿瘤作用外,一些驱虫药还对特定免疫细胞亚群和相关途径产生重要的免疫调节作用。在这篇综述中,我们报告和讨论了驱虫药对宿主免疫的影响及其在癌症免疫治疗中的潜在意义的最新知识。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df97/10094506/6dcab835e92c/ijms-24-06446-g001.jpg

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