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吲哚衍生物作为乳腺癌抗癌剂的最新研究进展。

Recent Development in Indole Derivatives as Anticancer Agents for Breast Cancer.

机构信息

Laboratory of Natural Products, Department of Pharmaceutical Sciences and Natural Products, Central University of Punjab, Bathinda (Pb) -151001, India.

出版信息

Anticancer Agents Med Chem. 2019;19(8):962-983. doi: 10.2174/1871520619666190312125602.

Abstract

BACKGROUND

Breast Cancer (BC) is the second most common cause of cancer related deaths in women. Due to severe side effects and multidrug resistance, current therapies like hormonal therapy, surgery, radiotherapy and chemotherapy become ineffective. Also, the existing drugs for BC treatment are associated with several drawbacks such as poor oral bioavailability, non-selectivity and poor pharmacodynamics properties. Therefore, there is an urgent need for the development of more effective and safer anti BC agents.

OBJECTIVE

This article explored in detail the possibilities of indole-based heterocyclic compounds as anticancer agents with breast cancer as their major target.

METHODS

Recent literature related to indole derivatives endowed with encouraging anti BC potential is reviewed. With special focus on BC, this review offers a detailed account of multiple mechanisms of action of various indole derivatives: aromatase inhibitor, tubulin inhibitor, microtubule inhibitor, targeting estrogen receptor, DNA-binding mechanism, induction of apoptosis, inhibition of PI3K/AkT/NFkB/mTOR, and HDAC inhibitors, by which these derivatives have shown promising anticancer potential.

RESULTS

Exhaustive literature survey indicated that indole derivatives are associated with properties of inducing apoptosis and disturbing tubulin assembly. Indoles are also associated with the inhibition of NFkB/mTOR/PI3K/AkT and regulation of estrogen-mediated activity. Furthermore, indole derivatives have been found to modulate critical targets such as topoisomerase and HDAC. These derivatives have shown significant activity against breast cancer cells.

CONCLUSION

In BC, indole derivatives seem to be quite competent and act through various mechanisms that are well established in case of BC. This review has shown that indole derivatives can further be explored for the betterment of BC chemotherapy. A lot of potential is still hidden which demands to be discovered for upgrading BC chemotherapy.

摘要

背景

乳腺癌(BC)是女性癌症相关死亡的第二大主要原因。由于严重的副作用和多药耐药性,目前的治疗方法,如激素治疗、手术、放疗和化疗,变得无效。此外,用于 BC 治疗的现有药物存在许多缺点,如口服生物利用度差、非选择性和差的药效学特性。因此,迫切需要开发更有效和更安全的抗 BC 药物。

目的

本文详细探讨了吲哚杂环化合物作为抗癌药物的可能性,其主要靶标是乳腺癌。

方法

综述了与具有令人鼓舞的抗 BC 潜力的吲哚衍生物相关的最新文献。特别关注 BC,本综述详细描述了各种吲哚衍生物的多种作用机制:芳香酶抑制剂、微管抑制剂、微管抑制剂、靶向雌激素受体、DNA 结合机制、诱导细胞凋亡、抑制 PI3K/AkT/NFkB/mTOR 和 HDAC 抑制剂,这些衍生物表现出有希望的抗癌潜力。

结果

详尽的文献调查表明,吲哚衍生物与诱导细胞凋亡和干扰微管组装有关。吲哚还与抑制 NFkB/mTOR/PI3K/AkT 和调节雌激素介导的活性有关。此外,已发现吲哚衍生物可以调节拓扑异构酶和 HDAC 等关键靶标。这些衍生物对乳腺癌细胞表现出显著的活性。

结论

在 BC 中,吲哚衍生物似乎相当有能力,并通过在 BC 中已确立的各种机制发挥作用。本综述表明,吲哚衍生物可以进一步探索用于改善 BC 化疗。仍然隐藏着大量的潜力,需要被发现,以提高 BC 化疗。

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