Targeting miRNAs involved in cancer stem cell and EMT regulation: An emerging concept in overcoming drug resistance - PubMed (original) (raw)
Review
Targeting miRNAs involved in cancer stem cell and EMT regulation: An emerging concept in overcoming drug resistance
Zhiwei Wang et al. Drug Resist Updat. 2010 Aug-Oct.
Abstract
Although chemotherapy is an important therapeutic strategy for cancer treatment, it fails to eliminate all tumor cells due to intrinsic or acquired drug resistance, which is the most common cause of tumor recurrence. Emerging evidence suggests an intricate role of cancer stem cells (CSCs) and epithelial-mesenchymal transition (EMT)-type cells in anticancer drug resistance. Recent studies also demonstrated that microRNAs (miRNAs) play critical roles in the regulation of drug resistance. Here we will discuss current knowledge regarding CSCs, EMT and the role of regulation by miRNAs in the context of drug resistance, tumor recurrence and metastasis. A better understanding of the molecular intricacies of drug-resistant cells will help to design novel therapeutic strategies by selective targeting of CSCs and EMT-phenotypic cells through alterations in the expression of specific miRNAs towards eradicating tumor recurrence and metastasis. A particular promising lead is the potential synergistic combination of natural compounds that affect critical miRNAs, such as curcumin or epigallocatechin-3-gallate (EGCG) with chemotherapeutic agents.
Copyright © 2010 Elsevier Ltd. All rights reserved.
Figures
Figure 1
The connection between EMT, cancer stem cells, and miRNA. EMT cells have cancer stem cell-like features, and CSCs exhibit mesenchymal phenotype. Aberrant miRNA expression has been correlated with the formation of CSCs and the acquisition of EMT phenotype. miRNAs affect and connect CSCs through regulation of EMT.
Similar articles
- Regulating miRNA by natural agents as a new strategy for cancer treatment.
Sethi S, Li Y, Sarkar FH. Sethi S, et al. Curr Drug Targets. 2013 Sep;14(10):1167-74. doi: 10.2174/13894501113149990189. Curr Drug Targets. 2013. PMID: 23834152 Free PMC article. Review. - The Role of Cancer Stem Cells in Recurrent and Drug-Resistant Lung Cancer.
Suresh R, Ali S, Ahmad A, Philip PA, Sarkar FH. Suresh R, et al. Adv Exp Med Biol. 2016;890:57-74. doi: 10.1007/978-3-319-24932-2_4. Adv Exp Med Biol. 2016. PMID: 26703799 Review. - Targeting microRNAs in epithelial-to-mesenchymal transition-induced cancer stem cells: therapeutic approaches in cancer.
Garg M. Garg M. Expert Opin Ther Targets. 2015 Feb;19(2):285-97. doi: 10.1517/14728222.2014.975794. Epub 2015 Jan 7. Expert Opin Ther Targets. 2015. PMID: 25563894 Review. - Pancreatic cancer stem cells: emerging target for designing novel therapy.
Li Y, Kong D, Ahmad A, Bao B, Sarkar FH. Li Y, et al. Cancer Lett. 2013 Sep 10;338(1):94-100. doi: 10.1016/j.canlet.2012.03.018. Epub 2012 Mar 20. Cancer Lett. 2013. PMID: 22445908 Free PMC article. Review. - MicroRNAs and cancer stem cells: the sword and the shield.
Sun X, Jiao X, Pestell TG, Fan C, Qin S, Mirabelli E, Ren H, Pestell RG. Sun X, et al. Oncogene. 2014 Oct 16;33(42):4967-77. doi: 10.1038/onc.2013.492. Epub 2013 Nov 18. Oncogene. 2014. PMID: 24240682 Review.
Cited by
- LncRNA SNHG6 sponges miR-101 and induces tamoxifen resistance in breast cancer cells through induction of EMT.
Khan MI, Ahmad A. Khan MI, et al. Front Oncol. 2022 Sep 23;12:1015428. doi: 10.3389/fonc.2022.1015428. eCollection 2022. Front Oncol. 2022. PMID: 36212408 Free PMC article. - Implications of microRNAs in colorectal cancer development, diagnosis, prognosis, and therapeutics.
Zhai H, Ju J. Zhai H, et al. Front Genet. 2011 Nov 3;2(78):78. doi: 10.3389/fgene.2011.00078. Front Genet. 2011. PMID: 22114584 Free PMC article. - G protein pathway suppressor 2 (GPS2) acts as a tumor suppressor in liposarcoma.
Huang XD, Xiao FJ, Wang SX, Yin RH, Lu CR, Li QF, Liu N, Zhang Y, Wang LS, Li PY. Huang XD, et al. Tumour Biol. 2016 Oct;37(10):13333-13343. doi: 10.1007/s13277-016-5220-x. Epub 2016 Jul 26. Tumour Biol. 2016. PMID: 27460081 Free PMC article. - Promising Druggable Target in Head and Neck Squamous Cell Carcinoma: Wnt Signaling.
Aminuddin A, Ng PY. Aminuddin A, et al. Front Pharmacol. 2016 Aug 12;7:244. doi: 10.3389/fphar.2016.00244. eCollection 2016. Front Pharmacol. 2016. PMID: 27570510 Free PMC article. Review. - Morphine promotes cancer stem cell properties, contributing to chemoresistance in breast cancer.
Niu DG, Peng F, Zhang W, Guan Z, Zhao HD, Li JL, Wang KL, Li TT, Zhang Y, Zheng FM, Xu F, Han QN, Gao P, Wen QP, Liu Q. Niu DG, et al. Oncotarget. 2015 Feb 28;6(6):3963-76. doi: 10.18632/oncotarget.2894. Oncotarget. 2015. PMID: 25686831 Free PMC article.
References
- Aboody KS, Najbauer J, Danks MK. Stem and progenitor cell-mediated tumor selective gene therapy. Gene Ther. 2008;15:739–752. - PubMed
- Adam L, Zhong M, Choi W, Qi W, Nicoloso M, Arora A, Calin G, Wang H, Siefker-Radtke A, McConkey D, Bar-Eli M, Dinney C. miR-200 expression regulates epithelial-to-mesenchymal transition in bladder cancer cells and reverses resistance to epidermal growth factor receptor therapy. Clin Cancer Res. 2009;15:5060–5072. - PMC - PubMed
Publication types
MeSH terms
Substances
Grants and funding
- R01 CA083695-09/CA/NCI NIH HHS/United States
- 1R01CA101870/CA/NCI NIH HHS/United States
- R01 CA131151/CA/NCI NIH HHS/United States
- 5R01CA131151/CA/NCI NIH HHS/United States
- R01 CA101870-05/CA/NCI NIH HHS/United States
- 5P20-CA101936/CA/NCI NIH HHS/United States
- 1R01CA132794/CA/NCI NIH HHS/United States
- P20 CA101936/CA/NCI NIH HHS/United States
- 5R01CA083695/CA/NCI NIH HHS/United States
- R01 CA101870/CA/NCI NIH HHS/United States
- R01 CA131151-04/CA/NCI NIH HHS/United States
- R01 CA132794-03/CA/NCI NIH HHS/United States
- R01 CA132794/CA/NCI NIH HHS/United States
- R01 CA083695/CA/NCI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources