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SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma
Intrahepatic cholangiocarcinoma (ICC) is the most common and deadly disease of the biliary tree due to its poor prognosis. Sal-like protein 4 (SALL4), a stem cell marker, has been identified as a potential target for aggressive hepatocellular carcinoma (HCC). In our study, 175 ICC cases with an aver...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694999/ https://www.ncbi.nlm.nih.gov/pubmed/26317546 |
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author | Deng, Gang Zhu, Lei Huang, Feizhou Nie, Wanpin Huang, Wei Xu, Hongbo Zheng, Shaopeng Yi, Zhongjie Wan, Tao |
author_facet | Deng, Gang Zhu, Lei Huang, Feizhou Nie, Wanpin Huang, Wei Xu, Hongbo Zheng, Shaopeng Yi, Zhongjie Wan, Tao |
author_sort | Deng, Gang |
collection | PubMed |
description | Intrahepatic cholangiocarcinoma (ICC) is the most common and deadly disease of the biliary tree due to its poor prognosis. Sal-like protein 4 (SALL4), a stem cell marker, has been identified as a potential target for aggressive hepatocellular carcinoma (HCC). In our study, 175 ICC cases with an average age of 55 years were included, and 53% (93/175) were male. And 28 adjacent non-tumor tissues were also collected. The SALL4-positive immunoreactivity was detected in a total of 102 ICC cases (58%), whereas all 28 adjacent tissues showed negative staining. Univariate analysis, showed that the SALL4-positive ICC cases had significantly more frequent lymph nodal metastasis (P = 0.0460), vascular invasion (P < 0.0001), and nerve invasion (P < 0.0001). Furthermore, the strong SALL4-positive cases (n = 7, 5 months) had shorter overall survival, when compared to moderate SALL4-positive (n = 46, 9 months) or SALL4-negative cases (n = 73, 7 months), respectively. Our data also suggest that SALL4 may be involved in the regulation of epithelial-mesenchymal transition (EMT) in ICC. Those results for the first time indicate an oncogenic role of SALL4 in ICC. Therefore, SALL4 may serve as a promising therapeutic target for ICC. |
format | Online Article Text |
id | pubmed-4694999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-46949992016-01-20 SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma Deng, Gang Zhu, Lei Huang, Feizhou Nie, Wanpin Huang, Wei Xu, Hongbo Zheng, Shaopeng Yi, Zhongjie Wan, Tao Oncotarget Research Paper Intrahepatic cholangiocarcinoma (ICC) is the most common and deadly disease of the biliary tree due to its poor prognosis. Sal-like protein 4 (SALL4), a stem cell marker, has been identified as a potential target for aggressive hepatocellular carcinoma (HCC). In our study, 175 ICC cases with an average age of 55 years were included, and 53% (93/175) were male. And 28 adjacent non-tumor tissues were also collected. The SALL4-positive immunoreactivity was detected in a total of 102 ICC cases (58%), whereas all 28 adjacent tissues showed negative staining. Univariate analysis, showed that the SALL4-positive ICC cases had significantly more frequent lymph nodal metastasis (P = 0.0460), vascular invasion (P < 0.0001), and nerve invasion (P < 0.0001). Furthermore, the strong SALL4-positive cases (n = 7, 5 months) had shorter overall survival, when compared to moderate SALL4-positive (n = 46, 9 months) or SALL4-negative cases (n = 73, 7 months), respectively. Our data also suggest that SALL4 may be involved in the regulation of epithelial-mesenchymal transition (EMT) in ICC. Those results for the first time indicate an oncogenic role of SALL4 in ICC. Therefore, SALL4 may serve as a promising therapeutic target for ICC. Impact Journals LLC 2015-08-07 /pmc/articles/PMC4694999/ /pubmed/26317546 Text en Copyright: © 2015 Deng et al. http://creativecommons.org/licenses/by/2.5/ 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 credited. |
spellingShingle | Research Paper Deng, Gang Zhu, Lei Huang, Feizhou Nie, Wanpin Huang, Wei Xu, Hongbo Zheng, Shaopeng Yi, Zhongjie Wan, Tao SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
title | SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
title_full | SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
title_fullStr | SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
title_full_unstemmed | SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
title_short | SALL4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
title_sort | sall4 is a novel therapeutic target in intrahepatic cholangiocarcinoma |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694999/ https://www.ncbi.nlm.nih.gov/pubmed/26317546 |
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