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Brush border myosin Ia inactivation in gastric but not endometrial tumors

Brush border Myosin Ia (MYO1A) has been shown to be frequently mutated in colorectal tumors with microsatellite instability (MSI) and to have tumor suppressor activity in intestinal tumors. Here, we investigated the frequency of frameshift mutations in the A8 microsatellite in exon 28 of MYO1A in MS...

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Main Authors: Mazzolini, Rocco (Author) , Rodrigues, Paulo (Author) , Bazzocco, Sarah (Author) , Dopeso, Higinio (Author) , Ferreira, Ana M. (Author) , Mateo-Lozano, Silvia (Author) , Andretta, Elena (Author) , Wörner, Stefan M. (Author) , Alazzouzi, Hafid (Author) , Landolfi, Stefania (Author) , Hernandez-Losa, Javier (Author) , Macaya, Irati (Author) , Suzuki, Hiromu (Author) , Cajal, Santiago Ramón y (Author) , Mooseker, Mark S. (Author) , Mariadason, John M. (Author) , Gebert, Johannes (Author) , Hofstra, Robert M. W. (Author) , Reventós, Jaume (Author) , Yamamoto, Hiroyuki (Author) , Schwartz, Simo (Author) , Arango, Diego (Author)
Format: Article (Journal)
Language:English
Published: 2013
In: International journal of cancer
Year: 2013, Volume: 132, Issue: 8, Pages: 1790-1799
ISSN:1097-0215
DOI:10.1002/ijc.27856
Online Access:Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1002/ijc.27856
Verlag, lizenzpflichtig, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.27856
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Author Notes:Rocco Mazzolini, Paulo Rodrigues, Sarah Bazzocco, Higinio Dopeso, Ana M. Ferreira, Silvia Mateo-Lozano, Elena Andretta, Stefan M. Woerner, Hafid Alazzouzi, Stefania Landolfi, Javier Hernandez-Losa, Irati Macaya, Hiromu Suzuki, Santiago Ramón y Cajal, Mark S. Mooseker, John M. Mariadason, Johannes Gebert, Robert M.W. Hofstra, Jaume Reventós, Hiroyuki Yamamoto, Simo Schwartz, Jr. and Diego Arango
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Summary:Brush border Myosin Ia (MYO1A) has been shown to be frequently mutated in colorectal tumors with microsatellite instability (MSI) and to have tumor suppressor activity in intestinal tumors. Here, we investigated the frequency of frameshift mutations in the A8 microsatellite in exon 28 of MYO1A in MSI gastric and endometrial tumors and found a high mutation rate in gastric (22/47; 46.8%) but not endometrial (3/48; 6.2%) tumors. Using a regression model, we show that MYO1A mutations are likely to confer a growth advantage to gastric, but not endometrial tumors. The mutant MYO1A7A protein was shown to lose its membrane localization in gastric cancer cells and a cycloheximide-chase assay demonstrated that the mutant MYO1A7A protein has reduced stability compared to the wild type MYO1A. Frequent MYO1A promoter hypermethylation was also found in gastric tumors. Promoter methylation negatively correlates with MYO1A mRNA expression in a series of 58 non-MSI gastric primary tumors (Pearson's r = −0.46; p = 0.0003) but not in a cohort of 54 non-MSI endometrial tumors and treatment of gastric cancer cells showing high MYO1A promoter methylation with the demethylating agent 5-aza-2′-deoxycytidine, resulted in a significant increase of MYO1A mRNA levels. We found that normal gastric epithelial cells, but not normal endometrial cells, express high levels of MYO1A. Therefore, when considered together, our findings suggest that MYO1A has tumor suppressor activity in the normal gastric epithelium but not in the normal endometrium and inactivation of MYO1A either genetically or epigenetically may confer gastric epithelial cells a growth advantage.
Item Description:First published: 24 September 2012
Gesehen am 08.07.2021
Physical Description:Online Resource
ISSN:1097-0215
DOI:10.1002/ijc.27856

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