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Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers
PURPOSE: The zinc finger protein, ZBTB48, is a telomere-associated protein. It was renamed as telomeric zinc finger-associated protein (TZAP) binding to elongated telomeres. However, its expression level was not measured in cancers. PATIENTS AND METHODS: We analyzed TZAP mRNA levels in 60 colorectal...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751716/ https://www.ncbi.nlm.nih.gov/pubmed/33364783 http://dx.doi.org/10.2147/OTT.S274394 |
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author | Jung, Soo-Jung Seo, Yu-Ri Park, Won-Jin Heo, Yu-Ran Lee, Yun-Han Kim, Shin Lee, Jae-Ho |
author_facet | Jung, Soo-Jung Seo, Yu-Ri Park, Won-Jin Heo, Yu-Ran Lee, Yun-Han Kim, Shin Lee, Jae-Ho |
author_sort | Jung, Soo-Jung |
collection | PubMed |
description | PURPOSE: The zinc finger protein, ZBTB48, is a telomere-associated protein. It was renamed as telomeric zinc finger-associated protein (TZAP) binding to elongated telomeres. However, its expression level was not measured in cancers. PATIENTS AND METHODS: We analyzed TZAP mRNA levels in 60 colorectal cancers (CRC) and its correlation with telomere length and TERT was studied. RESULTS: TZAP mRNA in CRC was higher statistically than that in paired non-cancerous tissues (p = 0.033). Higher TZAP was found in carcinoembryonic antigen (CEA)-positive CRCs (>5 ng/mL) (p = 0.012). Shorter telomere was found in CRCs with high TZAP expression than that with low TZAP expression (p = 0.010). According to quantitative correlation analysis, TZAP has a correlation with age (r = −0.349, p = 0.007), TERT (r = 0.279, p = 0.041) and telomere length (r = −0.305, p = 0.021). TZAP expression did not harbor prognostic value in CRC. Inhibition of TZAP expression by siRNA suppresses cell growth in HT29 cells; however, it resulted in increased cell viability in HCT116 cells. TZAP inhibition induces a decrease in mRNA levels of TERT in both HT29 and HCT116 cells. TCGA data analysis showed higher expression of TZAP showed poorer overall survival in colon cancer (p = 0.001); however, it did not have a significance in rectal cancer (p = 0.951). CONCLUSION: We suggested that TZAP may be a possible biomarker for CRC. |
format | Online Article Text |
id | pubmed-7751716 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-77517162020-12-22 Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers Jung, Soo-Jung Seo, Yu-Ri Park, Won-Jin Heo, Yu-Ran Lee, Yun-Han Kim, Shin Lee, Jae-Ho Onco Targets Ther Original Research PURPOSE: The zinc finger protein, ZBTB48, is a telomere-associated protein. It was renamed as telomeric zinc finger-associated protein (TZAP) binding to elongated telomeres. However, its expression level was not measured in cancers. PATIENTS AND METHODS: We analyzed TZAP mRNA levels in 60 colorectal cancers (CRC) and its correlation with telomere length and TERT was studied. RESULTS: TZAP mRNA in CRC was higher statistically than that in paired non-cancerous tissues (p = 0.033). Higher TZAP was found in carcinoembryonic antigen (CEA)-positive CRCs (>5 ng/mL) (p = 0.012). Shorter telomere was found in CRCs with high TZAP expression than that with low TZAP expression (p = 0.010). According to quantitative correlation analysis, TZAP has a correlation with age (r = −0.349, p = 0.007), TERT (r = 0.279, p = 0.041) and telomere length (r = −0.305, p = 0.021). TZAP expression did not harbor prognostic value in CRC. Inhibition of TZAP expression by siRNA suppresses cell growth in HT29 cells; however, it resulted in increased cell viability in HCT116 cells. TZAP inhibition induces a decrease in mRNA levels of TERT in both HT29 and HCT116 cells. TCGA data analysis showed higher expression of TZAP showed poorer overall survival in colon cancer (p = 0.001); however, it did not have a significance in rectal cancer (p = 0.951). CONCLUSION: We suggested that TZAP may be a possible biomarker for CRC. Dove 2020-12-17 /pmc/articles/PMC7751716/ /pubmed/33364783 http://dx.doi.org/10.2147/OTT.S274394 Text en © 2020 Jung et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Jung, Soo-Jung Seo, Yu-Ri Park, Won-Jin Heo, Yu-Ran Lee, Yun-Han Kim, Shin Lee, Jae-Ho Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers |
title | Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers |
title_full | Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers |
title_fullStr | Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers |
title_full_unstemmed | Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers |
title_short | Clinicopathological Characteristics of TZAP Expression in Colorectal Cancers |
title_sort | clinicopathological characteristics of tzap expression in colorectal cancers |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7751716/ https://www.ncbi.nlm.nih.gov/pubmed/33364783 http://dx.doi.org/10.2147/OTT.S274394 |
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