Combating chemoresistance in breast cancer: exploring tumour microenvironment, combination therapies and drug repurposing strategies.

IF 3.9 4区 医学 Q1 PHARMACOLOGY & PHARMACY
Shazia Sofi, Nusrat Jan, Gowhar Masoodi, Aijaz Ahmad Mir, Manzoor Ahmad Mir
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引用次数: 0

Abstract

Chemoresistance in breast cancer (BC) is a challenge that remains paramount in its treatment. Since the current therapies are insufficient to address chemoresistance, more potent strategies are urgently required to enhance current treatment plans. Chemoresistance in cancer can arise from a variety of molecular mechanisms, like drug efflux, decreased drug uptake, enhanced DNA repair mechanisms, the ability of cancer cells to avoid apoptosis, tumour heterogeneity and significant alterations in the tumour microenvironment, where interactions between cancer cells, cancer-associated fibroblasts, immune cells and the extracellular matrix contribute to a supportive environment that allows tumours to survive treatment and escape therapy. The available therapeutic strategies include combination therapies, immunotherapies, epigenetic modulators and drug delivery systems based on nanoparticles are a few promising strategies towards overcoming chemoresistance. Drug repurposing provides a practical and economical means to combat resistance through FDA-approved anticancer agents. Second, the incorporation of immune checkpoint inhibitors (ICIs), PARP inhibitors and metabolic modulators enhances the efficacy of treatments even further. Here in this article, we have reviewed the latest developments in the management of chemoresistance with a focus on innovative therapeutic approaches, innovative therapies targeting the tumour microenvironment, strategic drug repurposing and meticulously designed clinical trials in the treatment of BC.

对抗乳腺癌的化疗耐药:探索肿瘤微环境,联合治疗和药物再利用策略。
乳腺癌(BC)的化疗耐药仍然是其治疗中最重要的挑战。由于目前的治疗方法不足以解决化疗耐药问题,因此迫切需要更有效的策略来加强目前的治疗计划。癌症的化疗耐药可能源于多种分子机制,如药物外排、药物摄取减少、DNA修复机制增强、癌细胞避免凋亡的能力、肿瘤异质性和肿瘤微环境的显著改变,其中癌细胞、癌症相关成纤维细胞、免疫细胞和细胞外基质之间的相互作用有助于形成一个支持性环境,使肿瘤能够在治疗中存活并逃避治疗。现有的治疗策略包括联合疗法、免疫疗法、表观遗传调节剂和基于纳米颗粒的药物传递系统,这些都是克服化疗耐药的一些有希望的策略。通过fda批准的抗癌药物,药物再利用提供了一种实用而经济的方法来对抗耐药性。其次,免疫检查点抑制剂(ICIs)、PARP抑制剂和代谢调节剂的结合进一步提高了治疗的疗效。在这篇文章中,我们回顾了化疗耐药管理的最新进展,重点是创新治疗方法,针对肿瘤微环境的创新疗法,策略性药物再利用和精心设计的BC治疗临床试验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
9.10
自引率
0.00%
发文量
165
审稿时长
2 months
期刊介绍: Journal of Drug Targeting publishes papers and reviews on all aspects of drug delivery and targeting for molecular and macromolecular drugs including the design and characterization of carrier systems (whether colloidal, protein or polymeric) for both vitro and/or in vivo applications of these drugs. Papers are not restricted to drugs delivered by way of a carrier, but also include studies on molecular and macromolecular drugs that are designed to target specific cellular or extra-cellular molecules. As such the journal publishes results on the activity, delivery and targeting of therapeutic peptides/proteins and nucleic acids including genes/plasmid DNA, gene silencing nucleic acids (e.g. small interfering (si)RNA, antisense oligonucleotides, ribozymes, DNAzymes), as well as aptamers, mononucleotides and monoclonal antibodies and their conjugates. The diagnostic application of targeting technologies as well as targeted delivery of diagnostic and imaging agents also fall within the scope of the journal. In addition, papers are sought on self-regulating systems, systems responsive to their environment and to external stimuli and those that can produce programmed, pulsed and otherwise complex delivery patterns.
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