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基于靶点的抗癌吲哚衍生物用于开发抗神经胶质瘤药物。

Target-Based Anticancer Indole Derivatives for the Development of Anti-Glioblastoma Agents.

机构信息

Department of Pharmacy, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy.

出版信息

Molecules. 2023 Mar 13;28(6):2587. doi: 10.3390/molecules28062587.

Abstract

Glioblastoma (GBM) is the most aggressive and frequent primary brain tumor, with a poor prognosis and the highest mortality rate. Currently, GBM therapy consists of surgical resection of the tumor, radiotherapy, and adjuvant chemotherapy with temozolomide. Consistently, there are poor treatment options and only modest anticancer efficacy is achieved; therefore, there is still a need for the development of new effective therapies for GBM. Indole is considered one of the most privileged scaffolds in heterocyclic chemistry, so it may serve as an effective probe for the development of new drug candidates against challenging diseases, including GBM. This review analyzes the therapeutic benefit and clinical development of novel indole-based derivatives investigated as promising anti-GBM agents. The existing indole-based compounds which are in the pre-clinical and clinical stages of development against GBM are reported, with particular reference to the most recent advances between 2013 and 2022. The main mechanisms of action underlying their anti-GBM efficacy, such as protein kinase, tubulin and p53 pathway inhibition, are also discussed. The final goal is to pave the way for medicinal chemists in the future design and development of novel effective indole-based anti-GBM agents.

摘要

胶质母细胞瘤(GBM)是最具侵袭性和最常见的原发性脑肿瘤,预后不良,死亡率最高。目前,GBM 的治疗包括肿瘤的手术切除、放疗和替莫唑胺辅助化疗。一致的是,治疗选择很差,仅取得了适度的抗癌疗效;因此,仍然需要开发新的有效治疗胶质母细胞瘤的方法。吲哚被认为是杂环化学中最具特权的支架之一,因此它可能成为开发针对包括胶质母细胞瘤在内的挑战性疾病的新候选药物的有效探针。本综述分析了新型吲哚衍生物作为有前途的抗 GBM 药物的治疗益处和临床开发。报告了现有处于临床前和临床阶段开发的针对 GBM 的基于吲哚的化合物,特别提到了 2013 年至 2022 年之间的最新进展。还讨论了它们抗 GBM 疗效的主要作用机制,如蛋白激酶、微管蛋白和 p53 途径抑制。最终目标是为未来的药物化学家设计和开发新型有效的基于吲哚的抗 GBM 药物铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ada6/10056347/9d391b6654fc/molecules-28-02587-ch001.jpg

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