A combined array-based comparative genomic hybridization and functional library screening approach identifies mir-30d as an oncomir in cancer.

Détails

Ressource 1Télécharger: BIB_CFABD2FA201F.P001.pdf (4042.09 [Ko])
Etat: Public
Version: de l'auteur⸱e
ID Serval
serval:BIB_CFABD2FA201F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
A combined array-based comparative genomic hybridization and functional library screening approach identifies mir-30d as an oncomir in cancer.
Périodique
Cancer Research
Auteur⸱e⸱s
Li N., Kaur S., Greshock J., Lassus H., Zhong X., Wang Y., Leminen A., Shao Z., Hu X., Liang S., Katsaros D., Huang Q., Bützow R., Weber B.L., Coukos G., Zhang L.
ISSN
1538-7445 (Electronic)
ISSN-L
0008-5472
Statut éditorial
Publié
Date de publication
2012
Volume
72
Numéro
1
Pages
154-164
Langue
anglais
Notes
Publication types: Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't Publication Status: ppublish
Résumé
Oncomirs are microRNAs (miRNA) that acts as oncogenes or tumor suppressor genes. Efficient identification of oncomirs remains a challenge. Here we report a novel, clinically guided genetic screening approach for the identification of oncomirs, identifying mir-30d through this strategy. mir-30d regulates tumor cell proliferation, apoptosis, senescence, and migration. The chromosomal locus harboring mir-30d was amplified in more than 30% of multiple types of human solid tumors (n = 1,283). Importantly, higher levels of mir-30d expression were associated significantly with poor clinical outcomes in ovarian cancer patients (n = 330, P = 0.0016). Mechanistic investigations suggested that mir-30d regulates a large number of cancer-associated genes, including the apoptotic caspase CASP3. The guided genetic screening approach validated by this study offers a powerful tool to identify oncomirs that may have utility as biomarkers or targets for drug development.
Mots-clé
Animals, Apoptosis/genetics, Cell Proliferation, Chromosome Mapping, Comparative Genomic Hybridization, Female, Humans, In Situ Hybridization, Mice, MicroRNAs/genetics, Ovarian Neoplasms/genetics, Ovarian Neoplasms/pathology, Polymorphism, Single Nucleotide, Real-Time Polymerase Chain Reaction
Pubmed
Web of science
Open Access
Oui
Création de la notice
14/10/2014 11:42
Dernière modification de la notice
20/08/2019 15:50
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