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Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts
We have shown earlier that overexpression of the human mitochondrial ribosomal protein MRPS18-2 (S18-2) led to immortalization of primary rat embryonic fibroblasts. The derived cells expressed the embryonic stem cell markers, and cellular pathways that control cell proliferation, oxidative phosphory...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673247/ https://www.ncbi.nlm.nih.gov/pubmed/26023799 |
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author | Darekar, Suhas D. Mushtaq, Muhammad Gurrapu, Sreeharsha Kovalevska, Larysa Drummond, Catherine Petruchek, Maria Tirinato, Luca Di Fabrizio, Enzo Carbone, Ennio Kashuba, Elena |
author_facet | Darekar, Suhas D. Mushtaq, Muhammad Gurrapu, Sreeharsha Kovalevska, Larysa Drummond, Catherine Petruchek, Maria Tirinato, Luca Di Fabrizio, Enzo Carbone, Ennio Kashuba, Elena |
author_sort | Darekar, Suhas D. |
collection | PubMed |
description | We have shown earlier that overexpression of the human mitochondrial ribosomal protein MRPS18-2 (S18-2) led to immortalization of primary rat embryonic fibroblasts. The derived cells expressed the embryonic stem cell markers, and cellular pathways that control cell proliferation, oxidative phosphorylation, cellular respiration, and other redox reactions were activated in the immortalized cells. Here we report that, upon overexpression of S18-2 protein, primary rat skin fibroblasts underwent cell transformation. Cells passed more than 300 population doublings, and two out of three tested clones gave rise to tumors in experimental animals. Transformed cells showed anchorage-independent growth and loss of contact inhibition; they expressed epithelial markers, such as E-cadherin and β-catenin. Transformed cells showed increased telomerase activity, disturbance of the cell cycle, and chromosomal instability. Taken together, our data suggest that S18-2 is a newly identified oncoprotein that may be involved in cancerogenesis. |
format | Online Article Text |
id | pubmed-4673247 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-46732472015-12-22 Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts Darekar, Suhas D. Mushtaq, Muhammad Gurrapu, Sreeharsha Kovalevska, Larysa Drummond, Catherine Petruchek, Maria Tirinato, Luca Di Fabrizio, Enzo Carbone, Ennio Kashuba, Elena Oncotarget Research Paper We have shown earlier that overexpression of the human mitochondrial ribosomal protein MRPS18-2 (S18-2) led to immortalization of primary rat embryonic fibroblasts. The derived cells expressed the embryonic stem cell markers, and cellular pathways that control cell proliferation, oxidative phosphorylation, cellular respiration, and other redox reactions were activated in the immortalized cells. Here we report that, upon overexpression of S18-2 protein, primary rat skin fibroblasts underwent cell transformation. Cells passed more than 300 population doublings, and two out of three tested clones gave rise to tumors in experimental animals. Transformed cells showed anchorage-independent growth and loss of contact inhibition; they expressed epithelial markers, such as E-cadherin and β-catenin. Transformed cells showed increased telomerase activity, disturbance of the cell cycle, and chromosomal instability. Taken together, our data suggest that S18-2 is a newly identified oncoprotein that may be involved in cancerogenesis. Impact Journals LLC 2015-05-12 /pmc/articles/PMC4673247/ /pubmed/26023799 Text en Copyright: © 2015 Darekar et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Darekar, Suhas D. Mushtaq, Muhammad Gurrapu, Sreeharsha Kovalevska, Larysa Drummond, Catherine Petruchek, Maria Tirinato, Luca Di Fabrizio, Enzo Carbone, Ennio Kashuba, Elena Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
title | Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
title_full | Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
title_fullStr | Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
title_full_unstemmed | Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
title_short | Mitochondrial ribosomal protein S18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
title_sort | mitochondrial ribosomal protein s18-2 evokes chromosomal instability and transforms primary rat skin fibroblasts |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4673247/ https://www.ncbi.nlm.nih.gov/pubmed/26023799 |
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