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Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma
PURPOSE: The cell division cycle 7 (CDC7) is a serine/threonine kinase that is essential for DNA replication in human cells which has been identified to play a critical role in multiple cancer types. However, the expression and clinical significance of CDC7 in ESCC has never been reported. PATIENTS...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304257/ https://www.ncbi.nlm.nih.gov/pubmed/30588031 http://dx.doi.org/10.2147/OTT.S183629 |
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author | Cao, Ji-Xiang Lu, Yao |
author_facet | Cao, Ji-Xiang Lu, Yao |
author_sort | Cao, Ji-Xiang |
collection | PubMed |
description | PURPOSE: The cell division cycle 7 (CDC7) is a serine/threonine kinase that is essential for DNA replication in human cells which has been identified to play a critical role in multiple cancer types. However, the expression and clinical significance of CDC7 in ESCC has never been reported. PATIENTS AND METHODS: CDC7 expression was detected in 30 ESCC and matched adjacent normal tissues, and a series of loss-of-function and gain-of-function assays were performed to evaluate the effects of CDC7 on the proliferation, migration and invasion, and chemoresistance of ESCC cells. RESULTS: The results showed that CDC7 was highly expressed in ESCC tissues compared with matched adjacent normal tissues. Functional studies demonstrated that knockdown of CDC7 inhibited proliferation by arresting ESCC cells in the G0/G1 phase and inducing apoptosis. Knockdown of CDC7 also inhibited cell migration and invasion in ESCC cells. Furthermore, knockdown of CDC7 sensitized ESCC cells to Cis and 5-FU. CONCLUSION: Our results suggest that CDC7 is highly expressed in ESCC tissues, and silencing CDC7 enhances chemosensitivity of ESCC cells, providing a new avenue for ESCC therapy. |
format | Online Article Text |
id | pubmed-6304257 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63042572018-12-26 Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma Cao, Ji-Xiang Lu, Yao Onco Targets Ther Original Research PURPOSE: The cell division cycle 7 (CDC7) is a serine/threonine kinase that is essential for DNA replication in human cells which has been identified to play a critical role in multiple cancer types. However, the expression and clinical significance of CDC7 in ESCC has never been reported. PATIENTS AND METHODS: CDC7 expression was detected in 30 ESCC and matched adjacent normal tissues, and a series of loss-of-function and gain-of-function assays were performed to evaluate the effects of CDC7 on the proliferation, migration and invasion, and chemoresistance of ESCC cells. RESULTS: The results showed that CDC7 was highly expressed in ESCC tissues compared with matched adjacent normal tissues. Functional studies demonstrated that knockdown of CDC7 inhibited proliferation by arresting ESCC cells in the G0/G1 phase and inducing apoptosis. Knockdown of CDC7 also inhibited cell migration and invasion in ESCC cells. Furthermore, knockdown of CDC7 sensitized ESCC cells to Cis and 5-FU. CONCLUSION: Our results suggest that CDC7 is highly expressed in ESCC tissues, and silencing CDC7 enhances chemosensitivity of ESCC cells, providing a new avenue for ESCC therapy. Dove Medical Press 2018-12-20 /pmc/articles/PMC6304257/ /pubmed/30588031 http://dx.doi.org/10.2147/OTT.S183629 Text en © 2019 Cao and Lu. 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. |
spellingShingle | Original Research Cao, Ji-Xiang Lu, Yao Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
title | Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
title_full | Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
title_fullStr | Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
title_full_unstemmed | Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
title_short | Targeting CDC7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
title_sort | targeting cdc7 improves sensitivity to chemotherapy of esophageal squamous cell carcinoma |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6304257/ https://www.ncbi.nlm.nih.gov/pubmed/30588031 http://dx.doi.org/10.2147/OTT.S183629 |
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