<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>7(2)</volume><submitter>El-Murr N</submitter><pubmed_abstract>Mismatch repair-deficient colorectal cancers (CRC) display widespread instability at DNA microsatellite sequences (MSI). Although MSI has been reported to commonly occur at coding repeats, leading to alterations in the function of a number of genes encoding cancer-related proteins, nothing is known about the putative impact of this process on non-coding microRNAs. In miRbase V15, we identified very few human microRNA genes with mono- or di-nucleotide repeats (n = 27). A mutational analysis of these sequences in a large series of MSI CRC cell lines and primary tumors underscored instability in 15 of the 24 microRNA genes successfully studied at variable frequencies ranging from 2.5% to 100%. Following a maximum likelihood statistical method, microRNA genes were separated into two groups tha</pubmed_abstract><journal>PloS one</journal><pagination>e31862</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3279428</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>MiRNA genes constitute new targets for microsatellite instability in colorectal cancer.</pubmed_title><pmcid>PMC3279428</pmcid><pubmed_authors>Abidi Z</pubmed_authors><pubmed_authors>Gaub MP</pubmed_authors><pubmed_authors>Lesuffleur T</pubmed_authors><pubmed_authors>Flejou JF</pubmed_authors><pubmed_authors>Hamelin R</pubmed_authors><pubmed_authors>El-Murr N</pubmed_authors><pubmed_authors>Wanherdrick K</pubmed_authors><pubmed_authors>Duval A</pubmed_authors><pubmed_authors>Svrcek M</pubmed_authors></additional><is_claimable>false</is_claimable><name>MiRNA genes constitute new targets for microsatellite instability in colorectal cancer.</name><description>Mismatch repair-deficient colorectal cancers (CRC) display widespread instability at DNA microsatellite sequences (MSI). Although MSI has been reported to commonly occur at coding repeats, leading to alterations in the function of a number of genes encoding cancer-related proteins, nothing is known about the putative impact of this process on non-coding microRNAs. In miRbase V15, we identified very few human microRNA genes with mono- or di-nucleotide repeats (n = 27). A mutational analysis of these sequences in a large series of MSI CRC cell lines and primary tumors underscored instability in 15 of the 24 microRNA genes successfully studied at variable frequencies ranging from 2.5% to 100%. Following a maximum likelihood statistical method, microRNA genes were separated into two groups tha</description><dates><release>2012-01-01T00:00:00Z</release><publication>2012</publication><modification>2026-05-02T06:09:15.712Z</modification><creation>2026-04-07T17:41:49.678Z</creation></dates><accession>S-EPMC3279428</accession><cross_references><pubmed>22348132</pubmed><doi>10.1371/journal.pone.0031862</doi></cross_references></HashMap>