Hassan Sara M, Farid Alyaa, Panda Siva S, Bekheit Mohamed S, Dinkins Holden, Fayad Walid, Girgis Adel S
Biotechnology Department, Faculty of Science, Cairo University, Giza 12613, Egypt.
Department of Chemistry and Biochemistry, Augusta University, Augusta, GA 30912, USA.
Pharmaceuticals (Basel). 2024 Jul 10;17(7):922. doi: 10.3390/ph17070922.
Cancer remains a formidable global health challenge, with current treatment modalities such as chemotherapy, radiotherapy, surgery, and targeted therapy often hindered by low efficacy and adverse side effects. The indole scaffold, a prominent heterocyclic structure, has emerged as a promising candidate in the fight against cancer. This review consolidates recent advancements in developing natural and synthetic indolyl analogs, highlighting their antiproliferative activities against various cancer types over the past five years. These analogs are categorized based on their efficacy against common cancer types, supported by biochemical assays demonstrating their antiproliferative properties. In this review, emphasis is placed on elucidating the mechanisms of action of these compounds. Given the limitations of conventional cancer therapies, developing targeted therapeutics with enhanced selectivity and reduced side effects remains a critical focus in oncological research.
癌症仍然是一项严峻的全球健康挑战,当前的治疗方式,如化疗、放疗、手术和靶向治疗,常常受到疗效不佳和副作用的阻碍。吲哚骨架作为一种重要的杂环结构,已成为抗癌斗争中一个有前景的候选物。本综述总结了开发天然和合成吲哚类似物的最新进展,重点介绍了它们在过去五年中对各种癌症类型的抗增殖活性。这些类似物根据其对常见癌症类型的疗效进行分类,并通过生化分析证明其抗增殖特性。在本综述中,重点是阐明这些化合物的作用机制。鉴于传统癌症治疗方法的局限性,开发具有更高选择性和更低副作用的靶向治疗药物仍然是肿瘤学研究的关键重点。