| Literature DB >> 33557274 |
Donatella Conconi1, Serena Redaelli1, Andrea Alberto Lissoni1,2, Chiara Cilibrasi3, Patrizia Perego4, Eugenio Gautiero5, Elena Sala5, Mariachiara Paderno1,2, Leda Dalprà1, Fabio Landoni1,2, Marialuisa Lavitrano1, Gaia Roversi1,5, Angela Bentivegna1.
Abstract
Uterine smooth muscle tumors of uncertain malignant potential (STUMPs) represent a heterogeneous group of tumors that cannot be histologically diagnosed as unequivocally benign or malignant. For this reason, many authors are working to obtain a better definition of diagnostic and prognostic criteria. In this work, we analyzed the genomic and epigenomic profile of uterine smooth muscle tumors (USMTs) in order to find similarities and differences between STUMPs, leiomyosarcomas (LMSs) and leiomyomas (LMs), and possibly identify prognostic factors in this group of tumors. Array-CGH data on 23 USMTs demonstrated the presence of a more similar genomic profile between STUMPs and LMSs. Some genes, such as PRKDC and PUM2, with a potential prognostic value, were never previously associated with STUMP. The methylation data appears to be very promising, especially with regards to the divergent profile found in the sample that relapsed, characterized by an overall CGI hypomethylation. Finally, the Gene Ontology analysis highlighted some cancer genes that could play a pivotal role in the unexpected aggressive behavior that can be found in some of these tumors. These genes could prove to be prognostic markers in the future.Entities:
Keywords: Genome Wide DNA Methylation; array-CGH; copy number alterations; uterine STUMP
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Year: 2021 PMID: 33557274 PMCID: PMC7914585 DOI: 10.3390/ijms22041580
Source DB: PubMed Journal: Int J Mol Sci ISSN: 1422-0067 Impact factor: 5.923