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June 5, 2013New England Journal of Medicine350 citationsOpen Access

Characterization of Uterine Leiomyomas by Whole-Genome Sequencing

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MMMiika MehineEKEevi KaasinenNMNetta Mäkinen

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Abstract

Chromosome shattering and reassembly resembling chromothripsis (a single genomic event that results in focal losses and rearrangements in multiple genomic regions) is a major cause of chromosomal abnormalities in uterine leiomyomas; we propose that tumorigenesis occurs when tissue-specific tumor-promoting changes are formed through these events. Chromothripsis has previously been associated with aggressive cancer; its common occurrence in leiomyomas suggests that it also has a role in the genesis and progression of benign tumors. We observed that multiple separate tumors could be seeded from a single lineage of uterine leiomyoma cells. (Funded by the Academy of Finland Center of Excellence program and others.).

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Cite This Study

Mehine et al. (2013) studied this question.

synapsesocial.com/papers/69daa1a33bc1ef7225684353https://doi.org/10.1056/nejmoa1302736
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