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Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma
BACKGROUND: The identification of fusion genes such as SYT-SSX1/SSX2, PAX3-FOXO1, TPM3/TPM4-ALK and EWS-FLI1 in human sarcomas has provided important insight into the diagnosis and targeted therapy of sarcomas. No recurrent fusion has been reported in human osteosarcoma. METHODS: Transcriptome seque...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197299/ https://www.ncbi.nlm.nih.gov/pubmed/25300797 http://dx.doi.org/10.1186/s13045-014-0076-2 |
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author | Yang, Jilong Annala, Matti Ji, Ping Wang, Guowen Zheng, Hong Codgell, David Du, Xiaoling Fang, Zhiwei Sun, Baocun Nykter, Matti Chen, Kexin Zhang, Wei |
author_facet | Yang, Jilong Annala, Matti Ji, Ping Wang, Guowen Zheng, Hong Codgell, David Du, Xiaoling Fang, Zhiwei Sun, Baocun Nykter, Matti Chen, Kexin Zhang, Wei |
author_sort | Yang, Jilong |
collection | PubMed |
description | BACKGROUND: The identification of fusion genes such as SYT-SSX1/SSX2, PAX3-FOXO1, TPM3/TPM4-ALK and EWS-FLI1 in human sarcomas has provided important insight into the diagnosis and targeted therapy of sarcomas. No recurrent fusion has been reported in human osteosarcoma. METHODS: Transcriptome sequencing was used to characterize the gene fusions and mutations in 11 human osteosarcomas. RESULTS: Nine of 11 samples were found to harbor genetic inactivating alterations in the TP53 pathway. Two recurrent fusion genes associated with the 12q locus, LRP1-SNRNP25 and KCNMB4-CCND3, were identified and validated by RT-PCR, Sanger sequencing and fluorescence in situ hybridization, and were found to be osteosarcoma specific in a validation cohort of 240 other sarcomas. Expression of LRP1-SNRNP25 fusion gene promoted SAOS-2 osteosarcoma cell migration and invasion. Expression of KCNMB4-CCND3 fusion gene promoted SAOS-2 cell migration. CONCLUSIONS: Our study represents the first whole transcriptome analysis of untreated human osteosarcoma. Our discovery of two osteosarcoma specific fusion genes associated with osteosarcoma cellular motility highlights the heterogeneity of osteosarcoma and provides opportunities for new treatment modalities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13045-014-0076-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4197299 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-41972992014-10-16 Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma Yang, Jilong Annala, Matti Ji, Ping Wang, Guowen Zheng, Hong Codgell, David Du, Xiaoling Fang, Zhiwei Sun, Baocun Nykter, Matti Chen, Kexin Zhang, Wei J Hematol Oncol Research BACKGROUND: The identification of fusion genes such as SYT-SSX1/SSX2, PAX3-FOXO1, TPM3/TPM4-ALK and EWS-FLI1 in human sarcomas has provided important insight into the diagnosis and targeted therapy of sarcomas. No recurrent fusion has been reported in human osteosarcoma. METHODS: Transcriptome sequencing was used to characterize the gene fusions and mutations in 11 human osteosarcomas. RESULTS: Nine of 11 samples were found to harbor genetic inactivating alterations in the TP53 pathway. Two recurrent fusion genes associated with the 12q locus, LRP1-SNRNP25 and KCNMB4-CCND3, were identified and validated by RT-PCR, Sanger sequencing and fluorescence in situ hybridization, and were found to be osteosarcoma specific in a validation cohort of 240 other sarcomas. Expression of LRP1-SNRNP25 fusion gene promoted SAOS-2 osteosarcoma cell migration and invasion. Expression of KCNMB4-CCND3 fusion gene promoted SAOS-2 cell migration. CONCLUSIONS: Our study represents the first whole transcriptome analysis of untreated human osteosarcoma. Our discovery of two osteosarcoma specific fusion genes associated with osteosarcoma cellular motility highlights the heterogeneity of osteosarcoma and provides opportunities for new treatment modalities. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13045-014-0076-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-10-10 /pmc/articles/PMC4197299/ /pubmed/25300797 http://dx.doi.org/10.1186/s13045-014-0076-2 Text en © Yang et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Yang, Jilong Annala, Matti Ji, Ping Wang, Guowen Zheng, Hong Codgell, David Du, Xiaoling Fang, Zhiwei Sun, Baocun Nykter, Matti Chen, Kexin Zhang, Wei Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma |
title | Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma |
title_full | Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma |
title_fullStr | Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma |
title_full_unstemmed | Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma |
title_short | Recurrent LRP1-SNRNP25 and KCNMB4-CCND3 fusion genes promote tumor cell motility in human osteosarcoma |
title_sort | recurrent lrp1-snrnp25 and kcnmb4-ccnd3 fusion genes promote tumor cell motility in human osteosarcoma |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4197299/ https://www.ncbi.nlm.nih.gov/pubmed/25300797 http://dx.doi.org/10.1186/s13045-014-0076-2 |
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