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靶向铁死亡:克服乳腺癌耐药性的一种有前景的策略。

Targeting ferroptosis: a promising strategy to overcome drug resistance in breast cancer.

作者信息

Peng Cuixin, Chen Yanning, Jiang Mingzhang

机构信息

Department of Pharmacy, West China Xiamen Hospital of Sichuan University, Xiamen, China.

出版信息

Front Oncol. 2024 Dec 20;14:1499125. doi: 10.3389/fonc.2024.1499125. eCollection 2024.


DOI:10.3389/fonc.2024.1499125
PMID:39759144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11695291/
Abstract

Breast cancer is one of the most prevalent malignancies affecting women worldwide, with its incidence increasingly observed in younger populations. In recent years, drug resistance has emerged as a significant challenge in the treatment of breast cancer, making it a central focus of contemporary research aimed at identifying strategies to overcome this issue. Growing evidence indicates that inducing ferroptosis through various mechanisms, particularly by inhibiting System Xc, depleting glutathione (GSH), and inactivating glutathione peroxidase 4 (GPX4), holds great potential in overcoming drug resistance in breast cancer. It is anticipated that therapies targeting ferroptosis will emerge as a promising strategy to reverse tumor resistance, offering new hope for breast cancer patients. This review will explore the latest advancements in understanding ferroptosis in the context of breast cancer drug resistance, with a particular emphasis on the roles of ferroptosis inducers and inhibitors, and the impact of ferroptotic pathways on overcoming drug resistance in breast cancer.

摘要

乳腺癌是全球影响女性的最常见恶性肿瘤之一,其发病率在年轻人群中日益增加。近年来,耐药性已成为乳腺癌治疗中的一项重大挑战,使其成为当代旨在确定克服这一问题策略的研究核心焦点。越来越多的证据表明,通过各种机制诱导铁死亡,特别是通过抑制Xc系统、消耗谷胱甘肽(GSH)和使谷胱甘肽过氧化物酶4(GPX4)失活,在克服乳腺癌耐药性方面具有巨大潜力。预计靶向铁死亡的疗法将成为逆转肿瘤耐药性的一种有前景的策略,为乳腺癌患者带来新的希望。本综述将探讨在乳腺癌耐药背景下理解铁死亡的最新进展,特别强调铁死亡诱导剂和抑制剂的作用,以及铁死亡途径对克服乳腺癌耐药性的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f978/11695291/fcc67f09810b/fonc-14-1499125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f978/11695291/fcc67f09810b/fonc-14-1499125-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f978/11695291/fcc67f09810b/fonc-14-1499125-g001.jpg

相似文献

[1]
Targeting ferroptosis: a promising strategy to overcome drug resistance in breast cancer.

Front Oncol. 2024-12-20

[2]
Ferroptosis as a promising targeted therapy for triple negative breast cancer.

Breast Cancer Res Treat. 2024-10

[3]
Directly targeting glutathione peroxidase 4 may be more effective than disrupting glutathione on ferroptosis-based cancer therapy.

Biochim Biophys Acta Gen Subj. 2020-1-18

[4]
Application of ferroptosis strategy to overcome tumor therapy resistance in breast and different cancer cells.

Iran J Basic Med Sci. 2024

[5]
Ferroptosis: a novel strategy to overcome chemoresistance in gynecological malignancies.

Front Cell Dev Biol. 2024-7-9

[6]
System X /GSH/GPX4 : An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy.

Front Pharmacol. 2022-8-29

[7]
An iron oxyhydroxide-based nanosystem sensitizes ferroptosis by a "Three-Pronged" strategy in breast cancer stem cells.

Acta Biomater. 2023-4-1

[8]
Potent nanoreactor-mediated ferroptosis-based strategy for the reversal of cancer chemoresistance to Sorafenib.

Acta Biomater. 2023-3-15

[9]
Multifunctional Sr/Se co-doped ZIF-8 nanozyme for chemo/chemodynamic synergistic tumor therapy apoptosis and ferroptosis.

Theranostics. 2024

[10]
Activatable nanomedicine for overcoming hypoxia-induced resistance to chemotherapy and inhibiting tumor growth by inducing collaborative apoptosis and ferroptosis in solid tumors.

Biomaterials. 2021-1

本文引用的文献

[1]
Formononetin triggers ferroptosis in triple-negative breast cancer cells by regulating the mTORC1/SREBP1/SCD1 pathway.

Front Pharmacol. 2024-9-27

[2]
Ferroptosis as a promising targeted therapy for triple negative breast cancer.

Breast Cancer Res Treat. 2024-10

[3]
Danggui Buxue Tang improves therapeutic efficacy of doxorubicin in triple negative breast cancer via ferroptosis.

J Ethnopharmacol. 2024-4-6

[4]
Glutathione depletion and dihydroorotate dehydrogenase inhibition actuated ferroptosis-augment to surmount triple-negative breast cancer.

Biomaterials. 2024-3

[5]
Yttrium Oxide nanoparticles induce cytotoxicity, genotoxicity, apoptosis, and ferroptosis in the human triple-negative breast cancer MDA-MB-231 cells.

BMC Cancer. 2023-11-27

[6]
SOCS1 acts as a ferroptosis driver to inhibit the progression and chemotherapy resistance of triple-negative breast cancer.

Carcinogenesis. 2023-12-2

[7]
Disulfiram/Copper Induce Ferroptosis in Triple-Negative Breast Cancer Cell Line MDA-MB-231.

Front Biosci (Landmark Ed). 2023-8-28

[8]
Irreversible HER2 inhibitors overcome resistance to the RSL3 ferroptosis inducer in non-HER2 amplified luminal breast cancer.

Cell Death Dis. 2023-8-18

[9]
Natural compound So-2 suppresses triple-negative breast cancer through inducing ferroptosis via downregulating transcription factor E2F7.

Arch Biochem Biophys. 2023-8

[10]
HSPB1 facilitates chemoresistance through inhibiting ferroptotic cancer cell death and regulating NF-κB signaling pathway in breast cancer.

Cell Death Dis. 2023-7-15

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