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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
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.
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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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