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长链非编码RNA参与癌症多柔比星耐药性的研究进展

Insights into the involvement of long non-coding RNAs in doxorubicin resistance of cancer.

作者信息

Zhang Hai-Bo, Hu Yang, Deng Jun-Li, Fang Guo-Ying, Zeng Ying

机构信息

Department of Pharmacy, Hangzhou Women's Hospital (Hangzhou Maternity and Child Health Care Hospital), Hangzhou, China.

Guangzhou Institute of Respiratory Disease and China State Key Laboratory of Respiratory Disease, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

出版信息

Front Pharmacol. 2023 Sep 15;14:1243934. doi: 10.3389/fphar.2023.1243934. eCollection 2023.


DOI:10.3389/fphar.2023.1243934
PMID:37781691
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10540237/
Abstract

Doxorubicin is one of the most classical chemotherapeutic drugs for the treatment of cancer. However, resistance to the cytotoxic effects of doxorubicin in tumor cells remains a major obstacle. Aberrant expression of long non-coding RNAs (lncRNAs) has been associated with tumorigenesis and development via regulation of chromatin remodeling, transcription, and post-transcriptional processing. Emerging studies have also revealed that dysregulation of lncRNAs mediates the development of drug resistance through multiple molecules and pathways. In this review, we focus on the role and mechanism of lncRNAs in the progress of doxorubicin resistance in various cancers, which mainly include cellular drug transport, cell cycle disorder, anti-apoptosis, epithelial-mesenchymal transition, cancer stem cells, autophagy, tumor microenvironment, metabolic reprogramming and signaling pathways. This review is aimed to provide potential therapeutic targets for future cancer therapy, especially for the reversal of chemoresistance.

摘要

阿霉素是治疗癌症最经典的化疗药物之一。然而,肿瘤细胞对阿霉素细胞毒性作用的耐药性仍然是一个主要障碍。长链非编码RNA(lncRNAs)的异常表达通过调控染色质重塑、转录和转录后加工与肿瘤发生发展相关。新兴研究还表明,lncRNAs的失调通过多种分子和途径介导耐药性的发展。在这篇综述中,我们聚焦于lncRNAs在各种癌症阿霉素耐药进展中的作用和机制,主要包括细胞药物转运、细胞周期紊乱、抗凋亡、上皮-间质转化、癌症干细胞、自噬、肿瘤微环境、代谢重编程和信号通路。这篇综述旨在为未来癌症治疗,尤其是化疗耐药的逆转提供潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/fa2722bc224b/fphar-14-1243934-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/32b519bd287e/fphar-14-1243934-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/4645ff2c0169/fphar-14-1243934-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/38c132e452bf/fphar-14-1243934-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/ac9ce1b95bf3/fphar-14-1243934-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/c4cda6f0ab47/fphar-14-1243934-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/abf17d4d4062/fphar-14-1243934-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/fa2722bc224b/fphar-14-1243934-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/32b519bd287e/fphar-14-1243934-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/4645ff2c0169/fphar-14-1243934-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/38c132e452bf/fphar-14-1243934-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/ac9ce1b95bf3/fphar-14-1243934-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/c4cda6f0ab47/fphar-14-1243934-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/abf17d4d4062/fphar-14-1243934-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/812a/10540237/fa2722bc224b/fphar-14-1243934-g007.jpg

相似文献

[1]
Insights into the involvement of long non-coding RNAs in doxorubicin resistance of cancer.

Front Pharmacol. 2023-9-15

[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]
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[10]
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引用本文的文献

[1]
Epigenetic Drivers of Chemoresistance in Nucleobase and Nucleoside Analog Therapies.

Biology (Basel). 2025-7-9

[2]
SEQSIM: A novel bioinformatics tool for comparisons of promoter regions-a case study of calcium binding protein spermatid associated 1 (CABS1).

BMC Bioinformatics. 2025-6-9

[3]
Regulation of immune-mediated chemoresistance in cancer by lncRNAs: an in-depth review of signaling pathways.

Naunyn Schmiedebergs Arch Pharmacol. 2025-4-9

[4]
NONHSAT141192.2 Facilitates the Stemness and Radioresistance of Glioma Stem Cells via the Regulation of PIK3R3 and SOX2.

CNS Neurosci Ther. 2025-2

[5]
Nanoparticles (NPs)-mediated lncMALAT1 silencing to reverse cisplatin resistance for effective hepatocellular carcinoma therapy.

Front Pharmacol. 2024-7-30

[6]
MALSU1-mediated regulation of mitochondrial function governs proliferation and doxorubicin resistance in triple-negative breast cancer cells.

Mol Cell Biochem. 2025-2

本文引用的文献

[1]
CL4-modified exosomes deliver lncRNA DARS-AS1 siRNA to suppress triple-negative breast cancer progression and attenuate doxorubicin resistance by inhibiting autophagy.

Int J Biol Macromol. 2023-10-1

[2]
Clinical insights into small cell lung cancer: Tumor heterogeneity, diagnosis, therapy, and future directions.

CA Cancer J Clin. 2023

[3]
LncRNA FGD5-AS1 potentiates autophagy-associated doxorubicin resistance by regulating the miR-154-5p/WNT5A axis in osteosarcoma.

Cell Biol Int. 2022-11

[4]
Sonic hedgehog pathway for the treatment of inflammatory diseases: implications and opportunities for future research.

J Immunother Cancer. 2022-6

[5]
The lncARSR/PTEN/Akt/nuclear factor-kappa B feedback regulatory loop contributes to doxorubicin resistance in hepatocellular carcinoma.

J Biochem Mol Toxicol. 2022-9

[6]
A novel LncRNA PTH-AS upregulates interferon-related DNA damage resistance signature genes and promotes metastasis in human breast cancer xenografts.

J Biol Chem. 2022-7

[7]
LncRNA SNHG10 suppresses the development of doxorubicin resistance by downregulating miR-302b in triple-negative breast cancer.

Bioengineered. 2022-5

[8]
LncRNA MALAT1 promotes breast cancer progression and doxorubicin resistance via regulating miR-570-3p.

Biomed J. 2021-12

[9]
Targeting the lncRNA DUXAP8/miR-29a/ Network Restores Doxorubicin Chemosensitivity PI3K-AKT-mTOR Signaling and Synergizes With Inotuzumab Ozogamicin in Chemotherapy-Resistant B-Cell Acute Lymphoblastic Leukemia.

Front Oncol. 2022-3-2

[10]
LncRNA PVT1 contributes to invasion and doxorubicin resistance of bladder cancer cells through promoting MDM2 expression and AURKB-mediated p53 ubiquitination.

Environ Toxicol. 2022-6

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