miR-1285-3p Controls Colorectal Cancer Proliferation and Escape from Apoptosis through DAPK2.
Antineoplastic Agents
/ pharmacology
Apoptosis
/ drug effects
Cell Cycle Checkpoints
Cell Line, Tumor
Cell Proliferation
/ drug effects
Colonic Neoplasms
/ genetics
Colorectal Neoplasms
/ genetics
Death-Associated Protein Kinases
/ genetics
Gene Expression Regulation, Neoplastic
/ drug effects
Humans
MicroRNAs
/ genetics
Neoplastic Stem Cells
Oligonucleotides
DAPK2
LNAs
apoptosis
cancer stem cells
cell cycle
colorectal cancer
microRNAs
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
31 Mar 2020
31 Mar 2020
Historique:
received:
29
01
2020
revised:
23
03
2020
accepted:
29
03
2020
entrez:
5
4
2020
pubmed:
5
4
2020
medline:
8
1
2021
Statut:
epublish
Résumé
MicroRNAs are tiny but powerful regulators of gene expression at the post-transcriptional level. Aberrant expression of oncogenic and tumor-suppressor microRNAs has been recognized as a common feature of human cancers. Colorectal cancer represents a major clinical challenge in the developed world and the design of innovative therapeutic approaches relies on the identification of novel biological targets. Here, we perform a functional screening in colorectal cancer cells using a library of locked nucleic acid (LNA)-modified anti-miRs in order to unveil putative oncogenic microRNAs whose inhibition yields a cytotoxic effect. We identify miR-1285-3p and further explore the effect of its targeting in both commercial cell lines and primary colorectal cancer stem cells, finding induction of cell cycle arrest and apoptosis. We show that DAPK2, a known tumor-suppressor, is a novel miR-1285 target and mediates both the anti-proliferative and the pro-apoptotic effects of miR-1285 depletion. Altogether, our findings uncover a novel oncogenic microRNA in colorectal cancer and lay the foundation for further studies aiming at the development of possible therapeutic strategies based on miR-1285 targeting.
Identifiants
pubmed: 32244500
pii: ijms21072423
doi: 10.3390/ijms21072423
pmc: PMC7177834
pii:
doi:
Substances chimiques
Antineoplastic Agents
0
MIRN1285 microRNA, human
0
MicroRNAs
0
Oligonucleotides
0
locked nucleic acid
0
DAPK2 protein, human
EC 2.7.11.1
Death-Associated Protein Kinases
EC 2.7.11.1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Associazione Italiana per la Ricerca sul Cancro
ID : Investigator Grant 13431
Déclaration de conflit d'intérêts
Supplementary Materials: The following are available online at www.mdpi.com/1422-0067/21/7/2423/s1.
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