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Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma

LIM and SH3 domain protein (LASP-1) is responsible for the development of several types of human cancers via the interaction with other proteins; however, the precise biological functions of proteins interacting with LASP-1 are not fully clarified. Although the role of LASP-1 in hepatocarcinogenesis...

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Autores principales: Kong, Fan-Yun, Zhu, Ting, Li, Nan, Cai, Yun-Fei, Zhou, Kai, Wei, Xiao, Kou, Yan-Bo, You, Hong-Juan, Zheng, Kui-Yang, Tang, Ren-Xian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339786/
https://www.ncbi.nlm.nih.gov/pubmed/28266596
http://dx.doi.org/10.1038/srep44017
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author Kong, Fan-Yun
Zhu, Ting
Li, Nan
Cai, Yun-Fei
Zhou, Kai
Wei, Xiao
Kou, Yan-Bo
You, Hong-Juan
Zheng, Kui-Yang
Tang, Ren-Xian
author_facet Kong, Fan-Yun
Zhu, Ting
Li, Nan
Cai, Yun-Fei
Zhou, Kai
Wei, Xiao
Kou, Yan-Bo
You, Hong-Juan
Zheng, Kui-Yang
Tang, Ren-Xian
author_sort Kong, Fan-Yun
collection PubMed
description LIM and SH3 domain protein (LASP-1) is responsible for the development of several types of human cancers via the interaction with other proteins; however, the precise biological functions of proteins interacting with LASP-1 are not fully clarified. Although the role of LASP-1 in hepatocarcinogenesis has been reported, the implication of LASP-1 interactors in HBV-related hepatocellular carcinoma (HCC) is not clearly evaluated. We obtained information regarding LASP-1 interactors from public databases and published studies. Via bioinformatics analysis, we found that LASP-1 interactors were related to distinct molecular functions and associated with various biological processes. Through an integrated network analysis of the interaction and pathways of LASP-1 interactors, cross-talk between different proteins and associated pathways was found. In addition, LASP-1 and several its interactors are significantly altered in HBV-related HCC through microarray analysis and could form a complex co-expression network. In the disease, LASP-1 and its interactors were further predicted to be regulated by a complex interaction network composed of different transcription factors. Besides, numerous LASP-1 interactors were associated with various clinical factors and related to the survival and recurrence of HBV-related HCC. Taken together, these results could help enrich our understanding of LASP-1 interactors and their relationships with HBV-related HCC.
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spelling pubmed-53397862017-03-10 Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma Kong, Fan-Yun Zhu, Ting Li, Nan Cai, Yun-Fei Zhou, Kai Wei, Xiao Kou, Yan-Bo You, Hong-Juan Zheng, Kui-Yang Tang, Ren-Xian Sci Rep Article LIM and SH3 domain protein (LASP-1) is responsible for the development of several types of human cancers via the interaction with other proteins; however, the precise biological functions of proteins interacting with LASP-1 are not fully clarified. Although the role of LASP-1 in hepatocarcinogenesis has been reported, the implication of LASP-1 interactors in HBV-related hepatocellular carcinoma (HCC) is not clearly evaluated. We obtained information regarding LASP-1 interactors from public databases and published studies. Via bioinformatics analysis, we found that LASP-1 interactors were related to distinct molecular functions and associated with various biological processes. Through an integrated network analysis of the interaction and pathways of LASP-1 interactors, cross-talk between different proteins and associated pathways was found. In addition, LASP-1 and several its interactors are significantly altered in HBV-related HCC through microarray analysis and could form a complex co-expression network. In the disease, LASP-1 and its interactors were further predicted to be regulated by a complex interaction network composed of different transcription factors. Besides, numerous LASP-1 interactors were associated with various clinical factors and related to the survival and recurrence of HBV-related HCC. Taken together, these results could help enrich our understanding of LASP-1 interactors and their relationships with HBV-related HCC. Nature Publishing Group 2017-03-07 /pmc/articles/PMC5339786/ /pubmed/28266596 http://dx.doi.org/10.1038/srep44017 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Kong, Fan-Yun
Zhu, Ting
Li, Nan
Cai, Yun-Fei
Zhou, Kai
Wei, Xiao
Kou, Yan-Bo
You, Hong-Juan
Zheng, Kui-Yang
Tang, Ren-Xian
Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma
title Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma
title_full Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma
title_fullStr Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma
title_full_unstemmed Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma
title_short Bioinformatics analysis of the proteins interacting with LASP-1 and their association with HBV-related hepatocellular carcinoma
title_sort bioinformatics analysis of the proteins interacting with lasp-1 and their association with hbv-related hepatocellular carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339786/
https://www.ncbi.nlm.nih.gov/pubmed/28266596
http://dx.doi.org/10.1038/srep44017
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