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Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms

Human chromosomal region 13q14 is a deletion hotspot in prostate cancer, multiple myeloma, and chronic lymphocytic leukemia. This region is believed to host multiple tumor suppressors. Chromosome Condensation 1-like (CHC1L) is located at 13q14, and found within the smallest common region of loss of...

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Autores principales: Spillane, David R., Wang, Ding Yan, Newbigging, Susan, Wang, Youdong, Shi, Chang-Xin, Cho, Hae-Ra, Shimizu, Hiroki, Gramolini, Anthony, Liu, Mingyao, Wen, Xiao-Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546397/
https://www.ncbi.nlm.nih.gov/pubmed/26291700
http://dx.doi.org/10.1371/journal.pone.0135755
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author Spillane, David R.
Wang, Ding Yan
Newbigging, Susan
Wang, Youdong
Shi, Chang-Xin
Cho, Hae-Ra
Shimizu, Hiroki
Gramolini, Anthony
Liu, Mingyao
Wen, Xiao-Yan
author_facet Spillane, David R.
Wang, Ding Yan
Newbigging, Susan
Wang, Youdong
Shi, Chang-Xin
Cho, Hae-Ra
Shimizu, Hiroki
Gramolini, Anthony
Liu, Mingyao
Wen, Xiao-Yan
author_sort Spillane, David R.
collection PubMed
description Human chromosomal region 13q14 is a deletion hotspot in prostate cancer, multiple myeloma, and chronic lymphocytic leukemia. This region is believed to host multiple tumor suppressors. Chromosome Condensation 1-like (CHC1L) is located at 13q14, and found within the smallest common region of loss of heterozygosity in prostate cancer. Decreased expression of CHC1L is linked to pathogenesis and progression of both prostate cancer and multiple myeloma. However, there is no direct evidence for CHC1L’s putative tumor suppressing role in current literature. Presently, we describe the generation and characterization of Chc1L knockout mice. Chc1L (-/-) mice do not develop cancer at a young age, but bone marrow and spleen cells from 8–12 week-old mice display an exaggerated proliferative response. By approximately two years of age, knockout and heterozygote mice have a markedly increased incidence of tumorigenesis compared to wild-type controls, with tumors occurring mainly in the spleen, mesenteric lymph nodes, liver and intestinal tract. Histopathological analysis found that most heterozygote and knockout mice succumb to either Histiocytic Sarcoma or Histiocyte-Associated Lymphoma. Our study suggests that Chc1L is involved in suppression of these two histiocyte-rich neoplasms in mice and supports clinical data suggesting that CHC1L loss of function is an important step in the pathogenesis of cancers containing 13q14 deletion.
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spelling pubmed-45463972015-08-26 Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms Spillane, David R. Wang, Ding Yan Newbigging, Susan Wang, Youdong Shi, Chang-Xin Cho, Hae-Ra Shimizu, Hiroki Gramolini, Anthony Liu, Mingyao Wen, Xiao-Yan PLoS One Research Article Human chromosomal region 13q14 is a deletion hotspot in prostate cancer, multiple myeloma, and chronic lymphocytic leukemia. This region is believed to host multiple tumor suppressors. Chromosome Condensation 1-like (CHC1L) is located at 13q14, and found within the smallest common region of loss of heterozygosity in prostate cancer. Decreased expression of CHC1L is linked to pathogenesis and progression of both prostate cancer and multiple myeloma. However, there is no direct evidence for CHC1L’s putative tumor suppressing role in current literature. Presently, we describe the generation and characterization of Chc1L knockout mice. Chc1L (-/-) mice do not develop cancer at a young age, but bone marrow and spleen cells from 8–12 week-old mice display an exaggerated proliferative response. By approximately two years of age, knockout and heterozygote mice have a markedly increased incidence of tumorigenesis compared to wild-type controls, with tumors occurring mainly in the spleen, mesenteric lymph nodes, liver and intestinal tract. Histopathological analysis found that most heterozygote and knockout mice succumb to either Histiocytic Sarcoma or Histiocyte-Associated Lymphoma. Our study suggests that Chc1L is involved in suppression of these two histiocyte-rich neoplasms in mice and supports clinical data suggesting that CHC1L loss of function is an important step in the pathogenesis of cancers containing 13q14 deletion. Public Library of Science 2015-08-20 /pmc/articles/PMC4546397/ /pubmed/26291700 http://dx.doi.org/10.1371/journal.pone.0135755 Text en © 2015 Spillane et al http://creativecommons.org/licenses/by/4.0/ 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 properly credited.
spellingShingle Research Article
Spillane, David R.
Wang, Ding Yan
Newbigging, Susan
Wang, Youdong
Shi, Chang-Xin
Cho, Hae-Ra
Shimizu, Hiroki
Gramolini, Anthony
Liu, Mingyao
Wen, Xiao-Yan
Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms
title Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms
title_full Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms
title_fullStr Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms
title_full_unstemmed Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms
title_short Chromosome Condensation 1-Like (Chc1L) Is a Novel Tumor Suppressor Involved in Development of Histiocyte-Rich Neoplasms
title_sort chromosome condensation 1-like (chc1l) is a novel tumor suppressor involved in development of histiocyte-rich neoplasms
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4546397/
https://www.ncbi.nlm.nih.gov/pubmed/26291700
http://dx.doi.org/10.1371/journal.pone.0135755
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