| Literature DB >> 24714101 |
Hannes Spittel1, Florian Kubek, Katharina Kreskowski, Monika Ziegler, Elisabeth Klein, Ahmed B Hamid, Nadezda Kosyakova, Gopakumar Radhakrishnan, Annelore Junge, Peter Kozlowski, Berndt Schulze, Thomas Martin, Dagmar Huhle, Karl Mehnert, Laura Rodríguez, Mehmet A Ergun, Catherine Sarri, Mariela Militaru, Fedora Stipoljev, Hanne Tittelbach, Faezeh Vasheghani, Marcelo de Bello Cioffi, Shaymaa S Hussein, Xiaobo Fan, Marianne Volleth, Thomas Liehr.
Abstract
Small supernumerary marker chromosomes (sSMC) are known for being present in mosaic form as 47,+mar/46 in >50% of the cases with this kind of extra chromosomes. However, no detailed studies have been done for the mitotic stability of sSMC so far, mainly due to the lack of a corresponding in vitro model system. Recently, we established an sSMC-cell bank (Else Kröner-Fresenius-sSMC-cellbank) with >150 cell lines. Therefore, 93 selected sSMC cases were studied here for the presence of the corresponding marker chromosomes before and after Epstein-Barr virus-induced immortalization. The obtained results showed that dicentric inverted duplicated-shaped sSMC are by far more stable in vitro than monocentric centric minute- or ring-shaped sSMC. Simultaneously, a review of the literature revealed that a comparable shape-dependent mitotic stability can be found in vivo in sSMC carriers. Additionally, a possible impact of the age of the sSMC carrier on mitotic stability was found: sSMC cell lines established from patients between 10-20 years of age were predominantly mitotically unstable. The latter finding was independent of the sSMC shape. The present study shows that in vitro models can lead to new and exciting insights into the biology of this genetically and clinically heterogeneous patient group.Entities:
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Year: 2014 PMID: 24714101 DOI: 10.1159/000360776
Source DB: PubMed Journal: Cytogenet Genome Res ISSN: 1424-8581 Impact factor: 1.636