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SGO1 is involved in the DNA damage response in MYCN-amplified neuroblastoma cells

Shugoshin 1 (SGO1) is required for accurate chromosome segregation during mitosis and meiosis; however, its other functions, especially at interphase, are not clearly understood. Here, we found that downregulation of SGO1 caused a synergistic phenotype in cells overexpressing MYCN. Downregulation of...

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Detalles Bibliográficos
Autores principales: Murakami-Tonami, Yuko, Ikeda, Haruna, Yamagishi, Ryota, Inayoshi, Mao, Inagaki, Shiho, Kishida, Satoshi, Komata, Yosuke, Jan Koster, J K, Takeuchi, Ichiro, Kondo, Yutaka, Maeda, Tohru, Sekido, Yoshitaka, Murakami, Hiroshi, Kadomatsu, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4990925/
https://www.ncbi.nlm.nih.gov/pubmed/27539729
http://dx.doi.org/10.1038/srep31615
Descripción
Sumario:Shugoshin 1 (SGO1) is required for accurate chromosome segregation during mitosis and meiosis; however, its other functions, especially at interphase, are not clearly understood. Here, we found that downregulation of SGO1 caused a synergistic phenotype in cells overexpressing MYCN. Downregulation of SGO1 impaired proliferation and induced DNA damage followed by a senescence-like phenotype only in MYCN-overexpressing neuroblastoma cells. In these cells, SGO1 knockdown induced DNA damage, even during interphase, and this effect was independent of cohesin. Furthermore, MYCN-promoted SGO1 transcription and SGO1 expression tended to be higher in MYCN- or MYC-overexpressing cancers. Together, these findings indicate that SGO1 plays a role in the DNA damage response in interphase. Therefore, we propose that SGO1 represents a potential molecular target for treatment of MYCN-amplified neuroblastoma.