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Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia

Background. Nucleophosmin 1 (NPM1) plays an important role in ribosomal synthesis and malignancies, but NPM1 mutations occur rarely in the blast-crisis and chronic-phase chronic myelogenous leukemia (CML) patients. The NPM1-associated gene set (GCM_NPM1), in total 116 genes including NPM1, was chose...

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Autores principales: Wang, Fengfeng, Chan, Lawrence W. C., Tsui, Nancy B. Y., Wong, S. C. Cesar, Siu, Parco M., Yip, S. P., Yung, Benjamin Y. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413041/
https://www.ncbi.nlm.nih.gov/pubmed/25961029
http://dx.doi.org/10.1155/2015/610595
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author Wang, Fengfeng
Chan, Lawrence W. C.
Tsui, Nancy B. Y.
Wong, S. C. Cesar
Siu, Parco M.
Yip, S. P.
Yung, Benjamin Y. M.
author_facet Wang, Fengfeng
Chan, Lawrence W. C.
Tsui, Nancy B. Y.
Wong, S. C. Cesar
Siu, Parco M.
Yip, S. P.
Yung, Benjamin Y. M.
author_sort Wang, Fengfeng
collection PubMed
description Background. Nucleophosmin 1 (NPM1) plays an important role in ribosomal synthesis and malignancies, but NPM1 mutations occur rarely in the blast-crisis and chronic-phase chronic myelogenous leukemia (CML) patients. The NPM1-associated gene set (GCM_NPM1), in total 116 genes including NPM1, was chosen as the candidate gene set for the coexpression analysis. We wonder if NPM1-associated genes can affect the ribosomal synthesis and translation process in CML. Results. We presented a distribution-based approach for gene pair classification by identifying a disease-specific cutoff point that classified the coexpressed gene pairs into strong and weak coexpression structures. The differences in the coexpression patterns between the normal and the CML groups were reflected from the overall structure by performing two-sample Kolmogorov-Smirnov test. Our developed method effectively identified the coexpression pattern differences from the overall structure: P  value = 1.71 × 10(−22) < 0.05 for the maximum deviation D = 0.109. Moreover, we found that genes involved in the ribosomal synthesis and translation process tended to be coexpressed in the CML group. Conclusion. Our developed method can identify the coexpression difference between two different groups. Dysregulation of ribosomal synthesis and translation process may be related to the CML disease. Our significant findings may provide useful information for the novel CML mechanism exploration and cancer treatment.
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spelling pubmed-44130412015-05-10 Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia Wang, Fengfeng Chan, Lawrence W. C. Tsui, Nancy B. Y. Wong, S. C. Cesar Siu, Parco M. Yip, S. P. Yung, Benjamin Y. M. Biomed Res Int Research Article Background. Nucleophosmin 1 (NPM1) plays an important role in ribosomal synthesis and malignancies, but NPM1 mutations occur rarely in the blast-crisis and chronic-phase chronic myelogenous leukemia (CML) patients. The NPM1-associated gene set (GCM_NPM1), in total 116 genes including NPM1, was chosen as the candidate gene set for the coexpression analysis. We wonder if NPM1-associated genes can affect the ribosomal synthesis and translation process in CML. Results. We presented a distribution-based approach for gene pair classification by identifying a disease-specific cutoff point that classified the coexpressed gene pairs into strong and weak coexpression structures. The differences in the coexpression patterns between the normal and the CML groups were reflected from the overall structure by performing two-sample Kolmogorov-Smirnov test. Our developed method effectively identified the coexpression pattern differences from the overall structure: P  value = 1.71 × 10(−22) < 0.05 for the maximum deviation D = 0.109. Moreover, we found that genes involved in the ribosomal synthesis and translation process tended to be coexpressed in the CML group. Conclusion. Our developed method can identify the coexpression difference between two different groups. Dysregulation of ribosomal synthesis and translation process may be related to the CML disease. Our significant findings may provide useful information for the novel CML mechanism exploration and cancer treatment. Hindawi Publishing Corporation 2015 2015-04-15 /pmc/articles/PMC4413041/ /pubmed/25961029 http://dx.doi.org/10.1155/2015/610595 Text en Copyright © 2015 Fengfeng Wang et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Fengfeng
Chan, Lawrence W. C.
Tsui, Nancy B. Y.
Wong, S. C. Cesar
Siu, Parco M.
Yip, S. P.
Yung, Benjamin Y. M.
Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia
title Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia
title_full Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia
title_fullStr Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia
title_full_unstemmed Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia
title_short Coexpression Pattern Analysis of NPM1-Associated Genes in Chronic Myelogenous Leukemia
title_sort coexpression pattern analysis of npm1-associated genes in chronic myelogenous leukemia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4413041/
https://www.ncbi.nlm.nih.gov/pubmed/25961029
http://dx.doi.org/10.1155/2015/610595
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