Ferroptosis-targeting drugs in breast cancer.

IF 4.3 4区 医学 Q1 PHARMACOLOGY & PHARMACY Journal of Drug Targeting Pub Date : 2025-01-01 Epub Date: 2024-09-05 DOI:10.1080/1061186X.2024.2399181
Shuxian Zhang, Lijuan Guo, Ran Tao, Shuangping Liu
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Abstract

In 2020, breast cancer surpassed lung cancer as the most common cancer in the world for the first time. Due to the resistance of some breast cancer cell lines to apoptosis, the therapeutic effect of anti-breast cancer drugs is limited. According to recent report, the susceptibility of breast cancer cells to ferroptosis affects the progress, prognosis and drug resistance of breast cancer. For instance, roblitinib induces ferroptosis of trastuzumab-resistant human epidermal growth factor receptor 2 (HER2)-positive breast cancer cells by diminishing fibroblast growth factor receptor 4 (FGFR4) expression, thereby augmenting the susceptibility of these cells to HER2-targeted therapies. In tamoxifen-resistant breast cancer cells, Fascin exacerbates their resistance by repressing solute carrier family 7 member 11 (SLC7A11) expression, which in turn heightens their responsiveness to tamoxifen. In recent years, Chinese herbs extracts and therapeutic drugs have been demonstrated to elicit ferroptosis in breast cancer cells by modulating a spectrum of regulatory factors pertinent to ferroptosis, including SLC7A11, glutathione peroxidase 4 (GPX4), acyl-CoA synthetase long chain family member 4 (ACSL4), and haem oxygenase 1 (HO-1). Here, we review the roles and mechanisms of Chinese herbal extracts and therapeutic drugs in regulating ferroptosis in breast cancer, providing potential therapeutic options for anti-breast cancer.

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乳腺癌中的铁蛋白沉积靶向药物
2020 年,乳腺癌首次超过肺癌,成为全球最常见的癌症。由于一些乳腺癌细胞株对细胞凋亡具有抗性,抗乳腺癌药物的治疗效果有限。最新报告显示,乳腺癌细胞对铁凋亡的敏感性会影响乳腺癌的进展、预后和耐药性。例如,罗格列替尼通过降低成纤维细胞生长因子受体4(FGFR4)的表达,诱导曲妥珠单抗耐药的人表皮生长因子受体2(HER2)阳性乳腺癌细胞发生铁变态反应,从而提高这些细胞对HER2靶向疗法的敏感性。在他莫昔芬耐药的乳腺癌细胞中,法斯金通过抑制溶质运载家族 7 成员 11(SLC7A11)的表达,加剧了这些细胞的耐药性,进而提高了它们对他莫昔芬的反应性。近年来,中草药提取物和治疗药物通过调节一系列与铁氧化相关的调节因子,包括 SLC7A11、谷胱甘肽过氧化物酶 4 (GPX4)、酰基-CoA 合成酶长链家族成员 4 (ACSL4) 和血红素加氧酶 1 (HO-1),已被证实能诱导乳腺癌细胞的铁氧化。在此,我们综述了中药提取物和治疗药物在调节乳腺癌铁氧化过程中的作用和机制,为抗乳腺癌提供了潜在的治疗方案。
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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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