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Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer
The aim of the present study was to investigate the expression of keratin 20 (KRT20) and placenta specific 8 (PLAC8) in gastrointestinal (GI) cancer with various differentiation phenotypes. The present study retrospectively investigated archived formalin-fixed paraffin-embedded tissue samples from 1...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947936/ https://www.ncbi.nlm.nih.gov/pubmed/31974611 http://dx.doi.org/10.3892/mmr.2019.10871 |
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author | Hung, Chih-Sheng Wang, Yen-Chieh Guo, Jiun-Wen Yang, Ruey-Neng Lee, Chia-Long Shen, Ming-Hung Huang, Chi-Cheng Huang, Chi-Jung Yang, Jhih-Yun Liu, Chih-Yi |
author_facet | Hung, Chih-Sheng Wang, Yen-Chieh Guo, Jiun-Wen Yang, Ruey-Neng Lee, Chia-Long Shen, Ming-Hung Huang, Chi-Cheng Huang, Chi-Jung Yang, Jhih-Yun Liu, Chih-Yi |
author_sort | Hung, Chih-Sheng |
collection | PubMed |
description | The aim of the present study was to investigate the expression of keratin 20 (KRT20) and placenta specific 8 (PLAC8) in gastrointestinal (GI) cancer with various differentiation phenotypes. The present study retrospectively investigated archived formalin-fixed paraffin-embedded tissue samples from 12 patients at different stages of GI cancer [four with gastric cancer, four with pancreatic cancer and four with colorectal cancer (CRC)]. The stages were pre-determined, according to differentiation phenotypes, by a pathologist of the Department of Pathology at Sijhih Cathay General Hospital. KRT20 and PLAC8 expression levels were assessed using immunohistochemistry. The CRC cell lines SW620 and Caco-2 were used to assess interactions between KRT20 and PLAC8 via reverse transcription-quantitative PCR. PLAC8 and KRT20 expression was observed consistently only in the well-differentiated CRC tissue samples. Low KRT20 expression levels were observed in the PLAC8 knockdown SW620 cells. In addition, there was a positive association between PLAC8 and KRT20 expression in the differentiated Caco-2 cells. According to the results of the present study, the differentiation status of GI cancer influenced KRT20 expression, particularly in CRC, which may explain why patients with well-differentiated CRC display better clinical outcomes. Therefore, the prognostic significance of KRT20 and PLAC8 may be particularly crucial for patients with CRC displaying a well-differentiated phenotype. |
format | Online Article Text |
id | pubmed-6947936 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-69479362020-01-13 Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer Hung, Chih-Sheng Wang, Yen-Chieh Guo, Jiun-Wen Yang, Ruey-Neng Lee, Chia-Long Shen, Ming-Hung Huang, Chi-Cheng Huang, Chi-Jung Yang, Jhih-Yun Liu, Chih-Yi Mol Med Rep Articles The aim of the present study was to investigate the expression of keratin 20 (KRT20) and placenta specific 8 (PLAC8) in gastrointestinal (GI) cancer with various differentiation phenotypes. The present study retrospectively investigated archived formalin-fixed paraffin-embedded tissue samples from 12 patients at different stages of GI cancer [four with gastric cancer, four with pancreatic cancer and four with colorectal cancer (CRC)]. The stages were pre-determined, according to differentiation phenotypes, by a pathologist of the Department of Pathology at Sijhih Cathay General Hospital. KRT20 and PLAC8 expression levels were assessed using immunohistochemistry. The CRC cell lines SW620 and Caco-2 were used to assess interactions between KRT20 and PLAC8 via reverse transcription-quantitative PCR. PLAC8 and KRT20 expression was observed consistently only in the well-differentiated CRC tissue samples. Low KRT20 expression levels were observed in the PLAC8 knockdown SW620 cells. In addition, there was a positive association between PLAC8 and KRT20 expression in the differentiated Caco-2 cells. According to the results of the present study, the differentiation status of GI cancer influenced KRT20 expression, particularly in CRC, which may explain why patients with well-differentiated CRC display better clinical outcomes. Therefore, the prognostic significance of KRT20 and PLAC8 may be particularly crucial for patients with CRC displaying a well-differentiated phenotype. D.A. Spandidos 2020-02 2019-12-06 /pmc/articles/PMC6947936/ /pubmed/31974611 http://dx.doi.org/10.3892/mmr.2019.10871 Text en Copyright: © Hung et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Articles Hung, Chih-Sheng Wang, Yen-Chieh Guo, Jiun-Wen Yang, Ruey-Neng Lee, Chia-Long Shen, Ming-Hung Huang, Chi-Cheng Huang, Chi-Jung Yang, Jhih-Yun Liu, Chih-Yi Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
title | Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
title_full | Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
title_fullStr | Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
title_full_unstemmed | Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
title_short | Expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
title_sort | expression pattern of placenta specific 8 and keratin 20 in different types of gastrointestinal cancer |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6947936/ https://www.ncbi.nlm.nih.gov/pubmed/31974611 http://dx.doi.org/10.3892/mmr.2019.10871 |
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