Shazia Sofi, Nusrat Jan, Gowhar Masoodi, Aijaz Ahmad Mir, Manzoor Ahmad Mir
{"title":"Combating chemoresistance in breast cancer: exploring tumour microenvironment, combination therapies and drug repurposing strategies.","authors":"Shazia Sofi, Nusrat Jan, Gowhar Masoodi, Aijaz Ahmad Mir, Manzoor Ahmad Mir","doi":"10.1080/1061186X.2025.2550589","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":15573,"journal":{"name":"Journal of Drug Targeting","volume":" ","pages":"1-22"},"PeriodicalIF":3.9000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Drug Targeting","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/1061186X.2025.2550589","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
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.
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.