Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B

Abstract Mitogen‐activated protein kinase 14 (MAPK14), which plays an important role in DNA damage and repair, is activated by various environmental stress and proinflammatory cytokines. It is highly active in a variety of tumors, acting as a tumor promoter or suppressor, but its role in clear cell...

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Main Authors: Junlong Liu, Xiuyue Yu, Hongyuan Yu, Bitian Liu, Zhe Zhang, Chuize Kong, Zhenhua Li
Format: Article
Language:English
Published: Wiley 2020-02-01
Series:Cancer Medicine
Subjects:
Online Access:https://doi.org/10.1002/cam4.2795
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author Junlong Liu
Xiuyue Yu
Hongyuan Yu
Bitian Liu
Zhe Zhang
Chuize Kong
Zhenhua Li
author_facet Junlong Liu
Xiuyue Yu
Hongyuan Yu
Bitian Liu
Zhe Zhang
Chuize Kong
Zhenhua Li
author_sort Junlong Liu
collection DOAJ
description Abstract Mitogen‐activated protein kinase 14 (MAPK14), which plays an important role in DNA damage and repair, is activated by various environmental stress and proinflammatory cytokines. It is highly active in a variety of tumors, acting as a tumor promoter or suppressor, but its role in clear cell renal cell carcinoma (ccRCC) has not been elucidated. Cell division cycle 25B (CDC25B) is involved in cell cycle regulation and is highly expressed in many malignant tumors. The transcription levels of MAPK14 and CDC25B in 72 pairs of ccRCC and adjacent healthy tissues from the cancer genome atlas database and the protein expression levels in 66 pairs of clinical samples were analyzed in this study. After MAPK14 was knocked down by small interfering RNA (siRNA), P‐MAPK14 and CDC25B protein levels decreased. Subsequently, Western blot and co‐immunoprecipitation demonstrated that P‐MAPK14 could bind to CDC25B, potentially maintaining its stability. The proliferation and migration of ccRCC cell lines were suppressed by siRNA knockdown of MAPK14, however, that could be partially reversed by the overexpression of CDC25B. These results suggest that downregulation of MAPK14 and P‐MAPK14 could inhibit the proliferation and migration of ccRCC by downregulating CDC25B.
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spelling doaj.art-7997b168142a49d1861b8946f12730c02022-12-22T04:11:27ZengWileyCancer Medicine2045-76342020-02-01931183119510.1002/cam4.2795Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25BJunlong Liu0Xiuyue Yu1Hongyuan Yu2Bitian Liu3Zhe Zhang4Chuize Kong5Zhenhua Li6Department of Urology The First Hospital of China Medical University Shenyang P. R. ChinaDepartment of Urology The First Hospital of China Medical University Shenyang P. R. ChinaDepartment of Urology The First Hospital of China Medical University Shenyang P. R. ChinaDepartment of Urology Shengjing Hospital of China Medical University Shenyang P. R. ChinaDepartment of Urology The First Hospital of China Medical University Shenyang P. R. ChinaDepartment of Urology The First Hospital of China Medical University Shenyang P. R. ChinaDepartment of Urology The First Hospital of China Medical University Shenyang P. R. ChinaAbstract Mitogen‐activated protein kinase 14 (MAPK14), which plays an important role in DNA damage and repair, is activated by various environmental stress and proinflammatory cytokines. It is highly active in a variety of tumors, acting as a tumor promoter or suppressor, but its role in clear cell renal cell carcinoma (ccRCC) has not been elucidated. Cell division cycle 25B (CDC25B) is involved in cell cycle regulation and is highly expressed in many malignant tumors. The transcription levels of MAPK14 and CDC25B in 72 pairs of ccRCC and adjacent healthy tissues from the cancer genome atlas database and the protein expression levels in 66 pairs of clinical samples were analyzed in this study. After MAPK14 was knocked down by small interfering RNA (siRNA), P‐MAPK14 and CDC25B protein levels decreased. Subsequently, Western blot and co‐immunoprecipitation demonstrated that P‐MAPK14 could bind to CDC25B, potentially maintaining its stability. The proliferation and migration of ccRCC cell lines were suppressed by siRNA knockdown of MAPK14, however, that could be partially reversed by the overexpression of CDC25B. These results suggest that downregulation of MAPK14 and P‐MAPK14 could inhibit the proliferation and migration of ccRCC by downregulating CDC25B.https://doi.org/10.1002/cam4.2795CDC25Bclear cell renal cell carcinomaDNA damage and repairMAPK14P‐MAPK14
spellingShingle Junlong Liu
Xiuyue Yu
Hongyuan Yu
Bitian Liu
Zhe Zhang
Chuize Kong
Zhenhua Li
Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B
Cancer Medicine
CDC25B
clear cell renal cell carcinoma
DNA damage and repair
MAPK14
P‐MAPK14
title Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B
title_full Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B
title_fullStr Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B
title_full_unstemmed Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B
title_short Knockdown of MAPK14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of CDC25B
title_sort knockdown of mapk14 inhibits the proliferation and migration of clear cell renal cell carcinoma by downregulating the expression of cdc25b
topic CDC25B
clear cell renal cell carcinoma
DNA damage and repair
MAPK14
P‐MAPK14
url https://doi.org/10.1002/cam4.2795
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