KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis

KDM5c is a histone demethylase that specifically demethylates trimethylated and dimethylated H3 Lys-4 to play a central role in transcriptional repression. C-Jun is a proto-oncogene and promotes cell proliferation when ectopically accumulated, but can be ubiquitinated by SCF (FBXW7), leading to its...

Full description

Bibliographic Details
Main Authors: Haishan Lin, Nina Ma, Lei Zhao, Guowei Yang, Bangwei Cao
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-09-01
Series:Frontiers in Oncology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fonc.2020.535449/full
_version_ 1818354628986667008
author Haishan Lin
Nina Ma
Lei Zhao
Guowei Yang
Bangwei Cao
author_facet Haishan Lin
Nina Ma
Lei Zhao
Guowei Yang
Bangwei Cao
author_sort Haishan Lin
collection DOAJ
description KDM5c is a histone demethylase that specifically demethylates trimethylated and dimethylated H3 Lys-4 to play a central role in transcriptional repression. C-Jun is a proto-oncogene and promotes cell proliferation when ectopically accumulated, but can be ubiquitinated by SCF (FBXW7), leading to its degradation. FBXW7 is an E3 ubiquitin ligase of c-Jun, and exhibits carcinostasis in colon cancer. Here, we report that overexpression of KDM5c in human colon cancer cells results in attenuated FBXW7 transcription and accumulated c-Jun protein, leading to increased proliferation of colon cancer cells. We show that overexpression of KDM5c can result in increased c-Jun protein levels and decreased ubiquitin levels, with no significant change in mRNA levels of c-Jun. KDM5c overexpression blocks the ubiquitin-proteasome proteolytic pathway of c-Jun by down-regulating the expression of FBXW7. KDM5c down-regulation of FBXW7 occurs by demethylation of H3K4me3 at TSS and downstream of the FBXW7 gene. And interaction of KDM5c with H3K4me3 downstream of FBXW7 gene may be followed by recruitment of DNMT3b to methylate the spatially close CpG island located near the FBXW7 TSS. This methylation represses FBXW7 gene expression, which can reduce c-Jun degradation via the ubiquitin-proteasome pathway. TCGA database analysis revealed high expression of KDM5c in colon cancer tissues. KDM5c expression in colon cancer was correlated with poor overall survival of patients in the first 7 years. Data from TCGA showed that high expression of KDM5c was correlated with high DNA methylation of the FBXW7 gene, but was not positively correlated with methylation of the Jun gene. These results suggest that KDM5c regulation of colon cell proliferation is mainly mediated by the KDM5c-FBXW7-c-Jun axis.
first_indexed 2024-12-13T19:28:27Z
format Article
id doaj.art-56318d0be6e242e086695b698867faaa
institution Directory Open Access Journal
issn 2234-943X
language English
last_indexed 2024-12-13T19:28:27Z
publishDate 2020-09-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Oncology
spelling doaj.art-56318d0be6e242e086695b698867faaa2022-12-21T23:33:59ZengFrontiers Media S.A.Frontiers in Oncology2234-943X2020-09-011010.3389/fonc.2020.535449535449KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory AxisHaishan Lin0Nina Ma1Lei Zhao2Guowei Yang3Bangwei Cao4Cancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaCancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaCancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaDepartment of Tropical Medicine, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaCancer Center, Beijing Friendship Hospital, Capital Medical University, Beijing, ChinaKDM5c is a histone demethylase that specifically demethylates trimethylated and dimethylated H3 Lys-4 to play a central role in transcriptional repression. C-Jun is a proto-oncogene and promotes cell proliferation when ectopically accumulated, but can be ubiquitinated by SCF (FBXW7), leading to its degradation. FBXW7 is an E3 ubiquitin ligase of c-Jun, and exhibits carcinostasis in colon cancer. Here, we report that overexpression of KDM5c in human colon cancer cells results in attenuated FBXW7 transcription and accumulated c-Jun protein, leading to increased proliferation of colon cancer cells. We show that overexpression of KDM5c can result in increased c-Jun protein levels and decreased ubiquitin levels, with no significant change in mRNA levels of c-Jun. KDM5c overexpression blocks the ubiquitin-proteasome proteolytic pathway of c-Jun by down-regulating the expression of FBXW7. KDM5c down-regulation of FBXW7 occurs by demethylation of H3K4me3 at TSS and downstream of the FBXW7 gene. And interaction of KDM5c with H3K4me3 downstream of FBXW7 gene may be followed by recruitment of DNMT3b to methylate the spatially close CpG island located near the FBXW7 TSS. This methylation represses FBXW7 gene expression, which can reduce c-Jun degradation via the ubiquitin-proteasome pathway. TCGA database analysis revealed high expression of KDM5c in colon cancer tissues. KDM5c expression in colon cancer was correlated with poor overall survival of patients in the first 7 years. Data from TCGA showed that high expression of KDM5c was correlated with high DNA methylation of the FBXW7 gene, but was not positively correlated with methylation of the Jun gene. These results suggest that KDM5c regulation of colon cell proliferation is mainly mediated by the KDM5c-FBXW7-c-Jun axis.https://www.frontiersin.org/article/10.3389/fonc.2020.535449/fullKDM5cc-Jun oncogenecolon cancer cellFBXW7epigenetic modifier
spellingShingle Haishan Lin
Nina Ma
Lei Zhao
Guowei Yang
Bangwei Cao
KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis
Frontiers in Oncology
KDM5c
c-Jun oncogene
colon cancer cell
FBXW7
epigenetic modifier
title KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis
title_full KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis
title_fullStr KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis
title_full_unstemmed KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis
title_short KDM5c Promotes Colon Cancer Cell Proliferation Through the FBXW7-c-Jun Regulatory Axis
title_sort kdm5c promotes colon cancer cell proliferation through the fbxw7 c jun regulatory axis
topic KDM5c
c-Jun oncogene
colon cancer cell
FBXW7
epigenetic modifier
url https://www.frontiersin.org/article/10.3389/fonc.2020.535449/full
work_keys_str_mv AT haishanlin kdm5cpromotescoloncancercellproliferationthroughthefbxw7cjunregulatoryaxis
AT ninama kdm5cpromotescoloncancercellproliferationthroughthefbxw7cjunregulatoryaxis
AT leizhao kdm5cpromotescoloncancercellproliferationthroughthefbxw7cjunregulatoryaxis
AT guoweiyang kdm5cpromotescoloncancercellproliferationthroughthefbxw7cjunregulatoryaxis
AT bangweicao kdm5cpromotescoloncancercellproliferationthroughthefbxw7cjunregulatoryaxis