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Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene
An important task in understanding oncogenesis is the identification of those genes whose copy number and expression increase during tumorigenesis. Previously, in an effort to identify genes which could be used as molecular markers for glial tumors, we compared gene expression in glioblastoma to the...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Master Publishing Group
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614833/ https://www.ncbi.nlm.nih.gov/pubmed/23675241 |
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author | Kavsan, Vadym M. Baklaushev, Vladimir P. Balynska, Olena V. Iershov, Anton V. Areshkov, Pavlo O. Yusubalieva, Gaukhar M. Grinenko, Nadezhda Ph. Victorov, Ilya V. Rymar, Vadym I. Sanson, Marc Chekhonin, Vladimir P. |
author_facet | Kavsan, Vadym M. Baklaushev, Vladimir P. Balynska, Olena V. Iershov, Anton V. Areshkov, Pavlo O. Yusubalieva, Gaukhar M. Grinenko, Nadezhda Ph. Victorov, Ilya V. Rymar, Vadym I. Sanson, Marc Chekhonin, Vladimir P. |
author_sort | Kavsan, Vadym M. |
collection | PubMed |
description | An important task in understanding oncogenesis is the identification of those genes whose copy number and expression increase during tumorigenesis. Previously, in an effort to identify genes which could be used as molecular markers for glial tumors, we compared gene expression in glioblastoma to the normal brain cells. Among the genes with the most pronounced increased expression in tumors there was CHI3L1, encoding the secreted chitinase 3-like 1 protein (also known as HC gp-39 or YKL-40). Expression of CHI3L1 was found increased significantly in various tumors in comparison with corresponding normal tissues. Here we show that CHI3L1 can decrease the doubling time of 293 cells. We have also demonstrated that CHI3L1 allows the anchorage-independent growth in soft agar and, in addition, stable CHI3L1 expression made 293 cells tumorigenic: these cells stimulate the initiation of tumors after their xenograft transplantation into the Wistar rat brains. Thus, the overexpression of CHI3L1 is likely to be critical in the development of some tumors and when we gain more information about mechanisms of CHI3L1 oncogenicity, it could be used as one of the potential targets for anticancer therapy. |
format | Online Article Text |
id | pubmed-3614833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Master Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-36148332013-05-01 Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene Kavsan, Vadym M. Baklaushev, Vladimir P. Balynska, Olena V. Iershov, Anton V. Areshkov, Pavlo O. Yusubalieva, Gaukhar M. Grinenko, Nadezhda Ph. Victorov, Ilya V. Rymar, Vadym I. Sanson, Marc Chekhonin, Vladimir P. Int J Biomed Sci Article An important task in understanding oncogenesis is the identification of those genes whose copy number and expression increase during tumorigenesis. Previously, in an effort to identify genes which could be used as molecular markers for glial tumors, we compared gene expression in glioblastoma to the normal brain cells. Among the genes with the most pronounced increased expression in tumors there was CHI3L1, encoding the secreted chitinase 3-like 1 protein (also known as HC gp-39 or YKL-40). Expression of CHI3L1 was found increased significantly in various tumors in comparison with corresponding normal tissues. Here we show that CHI3L1 can decrease the doubling time of 293 cells. We have also demonstrated that CHI3L1 allows the anchorage-independent growth in soft agar and, in addition, stable CHI3L1 expression made 293 cells tumorigenic: these cells stimulate the initiation of tumors after their xenograft transplantation into the Wistar rat brains. Thus, the overexpression of CHI3L1 is likely to be critical in the development of some tumors and when we gain more information about mechanisms of CHI3L1 oncogenicity, it could be used as one of the potential targets for anticancer therapy. Master Publishing Group 2011-09 /pmc/articles/PMC3614833/ /pubmed/23675241 Text en © Vadym M. Kavsan et al. Licensee Master Publishing Group http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.5/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Kavsan, Vadym M. Baklaushev, Vladimir P. Balynska, Olena V. Iershov, Anton V. Areshkov, Pavlo O. Yusubalieva, Gaukhar M. Grinenko, Nadezhda Ph. Victorov, Ilya V. Rymar, Vadym I. Sanson, Marc Chekhonin, Vladimir P. Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene |
title | Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene |
title_full | Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene |
title_fullStr | Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene |
title_full_unstemmed | Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene |
title_short | Gene Encoding Chitinase 3-Like 1 Protein (CHI3L1) is a Putative Oncogene |
title_sort | gene encoding chitinase 3-like 1 protein (chi3l1) is a putative oncogene |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3614833/ https://www.ncbi.nlm.nih.gov/pubmed/23675241 |
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