CD44s Induces miR-629-3p Expression in Association with Cisplatin Resistance in Head and Neck Cancer Cells.
SAS cell
apoptosis
cancer stem cell
cisplatin resistance
miR-629-3p
migration
Journal
Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829
Informations de publication
Date de publication:
01 Apr 2020
01 Apr 2020
Historique:
received:
20
03
2020
accepted:
31
03
2020
entrez:
5
4
2020
pubmed:
5
4
2020
medline:
5
4
2020
Statut:
epublish
Résumé
Cisplatin (cis-diamminedichloroplatinum II [CDDP] ) is a well-known chemotherapeutic drug that has been used for the treatment of various types of human cancers, including head and neck cancer. Cisplatin exerts anticancer effects by causing DNA damage, replication defects, transcriptional inhibition, cell cycle arrest, and the induction of apoptosis. However, drug resistance is one of the most serious problems with cancer chemotherapy, and it causes expected therapeutic effects to not always be achieved. Here, we analyzed global microRNA (miRNA) expression in CD44 standard form (CD44s)-expressing SAS cells, and we identified miR-629-3p as being responsible for acquiring anticancer drug resistance in head and neck cancer. The introduction of miR-629-3p expression inhibited apoptotic cell death under cisplatin treatment conditions, and it promoted cell migration. Among the computationally predicted target genes of miR-629-3p, we found that a number of gene expressions were suppressed by the transfection with miR-629-3p. Using a xenografting model, we showed that miR-629-3p conferred cisplatin resistance to SAS cells. Clinically, increased miR-629-3p expression tended to be associated with decreased survival in head and neck cancer patients. In conclusion, our data suggest that the increased expression of miR-629-3p provides a mechanism of cisplatin resistance in head and neck cancer and may serve as a therapeutic target to reverse chemotherapy resistance.
Identifiants
pubmed: 32244823
pii: cancers12040856
doi: 10.3390/cancers12040856
pmc: PMC7226407
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : Japan Agency for Medical Research and Development
ID : 16ae0101011h0003
Organisme : Japan Society for the Promotion of Science
ID : 17K17110
Organisme : Japan Society for the Promotion of Science
ID : 17H04991
Références
Oral Oncol. 2018 Jan;76:1-7
pubmed: 29290280
Cell. 2013 Jul 18;154(2):311-324
pubmed: 23830207
Nat Commun. 2015 Jun 12;6:7318
pubmed: 26065921
PLoS One. 2013 Dec 10;8(12):e81735
pubmed: 24339958
Onco Targets Ther. 2017 Mar 20;10:1695-1705
pubmed: 28356756
Nat Rev Cancer. 2013 Oct;13(10):714-26
pubmed: 24060863
Nat Rev Mol Cell Biol. 2003 Jan;4(1):33-45
pubmed: 12511867
Oncotarget. 2018 Jan 13;9(11):10029-10041
pubmed: 29515788
Nature. 2008 Jan 10;451(7175):147-52
pubmed: 18185580
Cell Stem Cell. 2014 Mar 6;14(3):275-91
pubmed: 24607403
Onco Targets Ther. 2015 Mar 04;8:557-65
pubmed: 25784815
Nat Rev Cancer. 2006 Nov;6(11):857-66
pubmed: 17060945
JCI Insight. 2016 Nov 03;1(18):e83654
pubmed: 27812537
Artif Cells Nanomed Biotechnol. 2019 Dec;47(1):3286-3296
pubmed: 31379200
Onco Targets Ther. 2016 Mar 29;9:1813-22
pubmed: 27099514
Proc Natl Acad Sci U S A. 2007 Jan 16;104(3):973-8
pubmed: 17210912
Breast Cancer Res. 2017 Jun 19;19(1):72
pubmed: 28629464
CA Cancer J Clin. 2018 Nov;68(6):394-424
pubmed: 30207593
Lung Cancer. 2014 Feb;83(2):154-62
pubmed: 24360396
Jpn J Clin Oncol. 2015 Jan;45(1):2-6
pubmed: 25411434
Onco Targets Ther. 2018 Nov 05;11:7853-7864
pubmed: 30464532