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Functional miRNAs in breast cancer drug resistance.

作者信息

Hu Weizi, Tan Chunli, He Yunjie, Zhang Guangqin, Xu Yong, Tang Jinhai

机构信息

Department of General Surgery, The First Affiliated Hospital of Nanjing Medical University.

School of Basic Medicine and Clinical Pharmacy, China Pharmaceutical University.

出版信息

Onco Targets Ther. 2018 Mar 19;11:1529-1541. doi: 10.2147/OTT.S152462. eCollection 2018.


DOI:10.2147/OTT.S152462
PMID:29593419
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5865556/
Abstract

Owing to improved early surveillance and advanced therapy strategies, the current death rate due to breast cancer has decreased; nevertheless, drug resistance and relapse remain obstacles on the path to successful systematic treatment. Multiple mechanisms responsible for drug resistance have been elucidated, and miRNAs seem to play a major part in almost every aspect of cancer progression, including tumorigenesis, metastasis, and drug resistance. In recent years, exosomes have emerged as novel modes of intercellular signaling vehicles, initiating cell-cell communication through their fusion with target cell membranes, delivering functional molecules including miRNAs and proteins. This review particularly focuses on enumerating functional miRNAs involved in breast cancer drug resistance as well as their targets and related mechanisms. Subsequently, we discuss the prospects and challenges of miRNA function in drug resistance and highlight valuable approaches for the investigation of the role of exosomal miRNAs in breast cancer progression and drug resistance.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/368e/5865556/04163b3890e4/ott-11-1529Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/368e/5865556/04163b3890e4/ott-11-1529Fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/368e/5865556/04163b3890e4/ott-11-1529Fig1.jpg

相似文献

[1]
Functional miRNAs in breast cancer drug resistance.

Onco Targets Ther. 2018-3-19

[2]
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[3]
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[4]
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[5]
The Emerging Roles of Exosomal miRNAs in Breast Cancer Progression and Potential Clinical Applications.

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[6]
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Biomark Med. 2017-11-20

[7]
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[8]
Emerging roles of exosomal miRNAs in breast cancer drug resistance.

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[9]
Exosomal miRNAs and miRNA dysregulation in cancer-associated fibroblasts.

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[10]
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[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
Trials and Tribulations of MicroRNA Therapeutics.

Int J Mol Sci. 2024-1-25

[10]
miRNAs as biomarkers of therapeutic response to HER2-targeted treatment in breast cancer: A systematic review.

Biochem Biophys Rep. 2023-11-28

本文引用的文献

[1]
Exosomes derived from gemcitabine-resistant cells transfer malignant phenotypic traits via delivery of miRNA-222-3p.

Mol Cancer. 2017-7-25

[2]
MiR-146a-5p level in serum exosomes predicts therapeutic effect of cisplatin in non-small cell lung cancer.

Eur Rev Med Pharmacol Sci. 2017-6

[3]
Cisplatin-resistant lung cancer cell-derived exosomes increase cisplatin resistance of recipient cells in exosomal miR-100-5p-dependent manner.

Int J Nanomedicine. 2017-5-15

[4]
Exosomal transfer of tumor-associated macrophage-derived miR-21 confers cisplatin resistance in gastric cancer cells.

J Exp Clin Cancer Res. 2017-4-13

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MicroRNA-155 Controls Exosome Synthesis and Promotes Gemcitabine Resistance in Pancreatic Ductal Adenocarcinoma.

Sci Rep. 2017-2-15

[6]
MiR-24 induces chemotherapy resistance and hypoxic advantage in breast cancer.

Oncotarget. 2017-3-21

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Lapatinib resistance in HER2+ cancers: latest findings and new concepts on molecular mechanisms.

Tumour Biol. 2016-12

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miR-145 sensitizes breast cancer to doxorubicin by targeting multidrug resistance-associated protein-1.

Oncotarget. 2016-9-13

[9]
The miR-644a/CTBP1/p53 axis suppresses drug resistance by simultaneous inhibition of cell survival and epithelial-mesenchymal transition in breast cancer.

Oncotarget. 2016-8-2

[10]
miRNA-205 targets VEGFA and FGF2 and regulates resistance to chemotherapeutics in breast cancer.

Cell Death Dis. 2016-6-30

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