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Identification and characterization of a novel human hepatocellular carcinoma-associated gene
To investigate liver cancer-associated genes and to explore the molecular basis of liver cancer genesis, we have cloned a novel hepatocellular carcinoma (HCC)-related gene with a transcript of 2520 base pairs in length named HCCA2 by mRNA differential display polymerase chain reaction (DDPCR) and sc...
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2001
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375167/ https://www.ncbi.nlm.nih.gov/pubmed/11710830 http://dx.doi.org/10.1054/bjoc.2001.2059 |
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author | Wang, Z-X Wang, H-Y Wu, M-C |
author_facet | Wang, Z-X Wang, H-Y Wu, M-C |
author_sort | Wang, Z-X |
collection | PubMed |
description | To investigate liver cancer-associated genes and to explore the molecular basis of liver cancer genesis, we have cloned a novel hepatocellular carcinoma (HCC)-related gene with a transcript of 2520 base pairs in length named HCCA2 by mRNA differential display polymerase chain reaction (DDPCR) and screening a placenta cDNA library. No significant homologous protein with known genes was found. Western blot analysis showed that HCCA2 could be expressed in transfected 293 cells. Northern hybridization analysis showed that HCCA2 mRNA was expressed in 79% (34/43) patients with HCC, most of whom had significantly high expression in HCC tissues, while not expressed in corresponding noncancerous liver tissues. The clinical pathological data showed that the HCCA2 was significantly associated with the invasion of tumour capsule (P= 0.0007) and the expression of ki-67 protein (P= 0.0022). Immunohistochemical staining confirmed that the HCCA2 protein was localized in cytoplasm of liver cancer tissues. According to amino acid analysis of the protein and its localization, it may play a role in a cascade of intracellular signal transduction because the protein was characterized with two Src homology 3 (SH3) binding-domains and several functional motifs of phophorylation. © 2001 Cancer Research Campaign http://www.bjcancer.com |
format | Text |
id | pubmed-2375167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2001 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23751672009-09-10 Identification and characterization of a novel human hepatocellular carcinoma-associated gene Wang, Z-X Wang, H-Y Wu, M-C Br J Cancer Regular Article To investigate liver cancer-associated genes and to explore the molecular basis of liver cancer genesis, we have cloned a novel hepatocellular carcinoma (HCC)-related gene with a transcript of 2520 base pairs in length named HCCA2 by mRNA differential display polymerase chain reaction (DDPCR) and screening a placenta cDNA library. No significant homologous protein with known genes was found. Western blot analysis showed that HCCA2 could be expressed in transfected 293 cells. Northern hybridization analysis showed that HCCA2 mRNA was expressed in 79% (34/43) patients with HCC, most of whom had significantly high expression in HCC tissues, while not expressed in corresponding noncancerous liver tissues. The clinical pathological data showed that the HCCA2 was significantly associated with the invasion of tumour capsule (P= 0.0007) and the expression of ki-67 protein (P= 0.0022). Immunohistochemical staining confirmed that the HCCA2 protein was localized in cytoplasm of liver cancer tissues. According to amino acid analysis of the protein and its localization, it may play a role in a cascade of intracellular signal transduction because the protein was characterized with two Src homology 3 (SH3) binding-domains and several functional motifs of phophorylation. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-10 /pmc/articles/PMC2375167/ /pubmed/11710830 http://dx.doi.org/10.1054/bjoc.2001.2059 Text en Copyright © 2001 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article Wang, Z-X Wang, H-Y Wu, M-C Identification and characterization of a novel human hepatocellular carcinoma-associated gene |
title | Identification and characterization of a novel human hepatocellular carcinoma-associated gene |
title_full | Identification and characterization of a novel human hepatocellular carcinoma-associated gene |
title_fullStr | Identification and characterization of a novel human hepatocellular carcinoma-associated gene |
title_full_unstemmed | Identification and characterization of a novel human hepatocellular carcinoma-associated gene |
title_short | Identification and characterization of a novel human hepatocellular carcinoma-associated gene |
title_sort | identification and characterization of a novel human hepatocellular carcinoma-associated gene |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375167/ https://www.ncbi.nlm.nih.gov/pubmed/11710830 http://dx.doi.org/10.1054/bjoc.2001.2059 |
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