The JMJD2A demethylase regulates apoptosis and proliferation in colon cancer cells
Tae-Dong Kim1, Sook Shin, William L Berry
1Department of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma 73104, USA.
Abstract:
JMJD2A is a transcriptional cofactor and enzyme that catalyzes demethylation of histone H3 lysines 9 and 36 and is overexpressed in human tumors, but its role in oncogenesis remains unclear. Here, we show that JMJD2A interacts with the tumor suppressor p53 both in vitro and in HCT116 colon cancer cells. Chromatin immunoprecipitation assays demonstrated that JMJD2A was recruited together with p53 to the promoter of the p21 cell cycle inhibitor upon stimulation with the DNA damaging agent, adriamycin. Downregulation of JMJD2A resulted in increased expression of p21 and of the pro-apoptotic Puma protein, whereas levels of the anti-apoptotic Bcl-2 protein were decreased. Furthermore, JMJD2A knock-down led to reduced HCT116, DLD-1 and HT-29 colon cancer cell proliferation, while overexpression of JMJD2A enhanced HCT116 proliferation in low serum media. Finally, JMJD2A depletion induced apoptosis in HCT116 cells and this effect was less pronounced in the absence of p53. Collectively, these data indicate that JMJD2A is a novel promoter of colon cancer cell proliferation and survival, which mediates its effects in p53-dependent and -independent ways. JMJD2A may therefore be a valid target to sensitize tumor cells to chemotherapy-induced cell death and growth suppression.
Insights
JMJD2A promotes colon cancer cell growth and survival by interacting with p53. Reducing JMJD2A levels can suppress tumor cell proliferation and enhance apoptosis, suggesting it as a therapeutic target.
Area of Science:
- Oncology
- Molecular Biology
- Epigenetics
Background:
- JMJD2A is an enzyme overexpressed in tumors.
- Its role in cancer development is not fully understood.
Purpose of the Study:
- To investigate the role of JMJD2A in colon cancer.
- To explore the interaction between JMJD2A and the tumor suppressor p53.
Main Methods:
- In vitro and cellular assays (HCT116 cells).
- Chromatin immunoprecipitation (ChIP) assays.
- Gene knockdown and overexpression studies.
- Cell proliferation and apoptosis assays.
Main Results:
- JMJD2A interacts with p53 and is recruited to the p21 promoter.
- JMJD2A downregulation increases p21 and Puma, decreases Bcl-2.
- JMJD2A knockdown reduces colon cancer cell proliferation.
- JMJD2A depletion induces p53-dependent and -independent apoptosis.
Conclusions:
- JMJD2A promotes colon cancer cell proliferation and survival.
- JMJD2A is a potential therapeutic target for sensitizing tumors to chemotherapy.
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