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解析卵巢癌耐药机制及克服耐药策略的研究进展:综述

Deciphering resistance mechanisms and novel strategies to overcome drug resistance in ovarian cancer: a comprehensive review.

机构信息

Infectious Diseases Research Center, Birjand University of Medical Sciences, Birjand, Iran.

Department of Midwifery, Ministry of Health and Medical Education, Tehran, Iran.

出版信息

Oncol Res. 2024 Apr 23;32(5):831-847. doi: 10.32604/or.2024.031006. eCollection 2024.


DOI:10.32604/or.2024.031006
PMID:38686048
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11055988/
Abstract

Ovarian cancer is among the most lethal gynecological cancers, primarily due to the lack of specific symptoms leading to an advanced-stage diagnosis and resistance to chemotherapy. Drug resistance (DR) poses the most significant challenge in treating patients with existing drugs. The Food and Drug Administration (FDA) has recently approved three new therapeutic drugs, including two poly (ADP-ribose) polymerase (PARP) inhibitors (olaparib and niraparib) and one vascular endothelial growth factor (VEGF) inhibitor (bevacizumab) for maintenance therapy. However, resistance to these new drugs has emerged. Therefore, understanding the mechanisms of DR and exploring new approaches to overcome them is crucial for effective management. In this review, we summarize the major molecular mechanisms of DR and discuss novel strategies to combat DR.

摘要

卵巢癌是最致命的妇科癌症之一,主要是由于缺乏特定的症状导致晚期诊断和对化疗的耐药性。耐药性 (DR) 是治疗现有药物患者的最大挑战。美国食品和药物管理局 (FDA) 最近批准了三种新的治疗药物,包括两种聚 (ADP-核糖) 聚合酶 (PARP) 抑制剂 (奥拉帕利和尼拉帕利) 和一种血管内皮生长因子 (VEGF) 抑制剂 (贝伐珠单抗) 用于维持治疗。然而,这些新药已经出现耐药性。因此,了解 DR 的机制并探索克服 DR 的新方法对于有效管理至关重要。在这篇综述中,我们总结了 DR 的主要分子机制,并讨论了克服 DR 的新策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/bb4e20617b98/OncolRes-32-31006-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/16eaa7e76a40/OncolRes-32-31006-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/d56f589b0b42/OncolRes-32-31006-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/bb4e20617b98/OncolRes-32-31006-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/16eaa7e76a40/OncolRes-32-31006-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/d56f589b0b42/OncolRes-32-31006-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b2fe/11055988/bb4e20617b98/OncolRes-32-31006-f003.jpg

相似文献

[1]
Deciphering resistance mechanisms and novel strategies to overcome drug resistance in ovarian cancer: a comprehensive review.

Oncol Res. 2024

[2]
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[3]
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[4]
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[7]
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[8]
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[9]
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[2]
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[4]
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[5]
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本文引用的文献

[1]
Oxidative Stress Inducers in Cancer Therapy: Preclinical and Clinical Evidence.

Antioxidants (Basel). 2023-5-26

[2]
Liposomes for Tumor Targeted Therapy: A Review.

Int J Mol Sci. 2023-1-31

[3]
2-Phenethylamines in Medicinal Chemistry: A Review.

Molecules. 2023-1-14

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Signals transduced by Eph receptors and ephrin ligands converge on MAP kinase and AKT pathways in human cancers.

Cell Signal. 2023-4

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Mechanisms of Drug Resistance in Ovarian Cancer and Associated Gene Targets.

Cancers (Basel). 2022-12-18

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Aetiology, Epidemiology, Histopathology, Classification, Detailed Evaluation, and Treatment of Ovarian Cancer.

Cureus. 2022-10-21

[7]
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Int J Mol Sci. 2022-10-10

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Multidrug Resistance in Cancer: Understanding Molecular Mechanisms, Immunoprevention and Therapeutic Approaches.

Front Oncol. 2022-6-23

[9]
Mechanisms of chemotherapy resistance in ovarian cancer.

Cancer Drug Resist. 2022-4-3

[10]
Guidelines for measuring reactive oxygen species and oxidative damage in cells and in vivo.

Nat Metab. 2022-6

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