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Updated: Apr 5, 2026

Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
Published on: July 28, 2010
JMJD5 is a potential oncogene for colon carcinogenesis
Ru Zhang1, Qingjun Huang1, Yinpeng Li1
1Department of Gastroenterology, Shenzhen People's Hospital, The Second Affiliated Hospital of Jinan University Shenzhen, P. R. China.
Objective:
To observe the effects of Jumonji C domain-containing (JMJD) 5 depletion on colon cancer (CC).
Methods:
A short-hairpin RNA targeting JMJD5 was transfected into a lentivirus to make Lv-shJMJD5 for infection into the Caco-2 human cell. Besides, a negative control shRNA was constructed. The mRNA and protein levels of JMJD5 were determined by quantitative real-time polymerase chain reaction (qRT-PCR) and western blotting, respectively. Cell proliferation, migration, and invasion were assessed by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT), soft agar colony assay and transwell assay, respectively. In addition, immunohistochemical (IHC) staining was performed to investigate the expression of JMJD5 in adjacent normal tissues and tumor tissues from patients with CC.
Results:
Compared with control group, mRNA and protein levels of JMJD5 was significantly reduced after infection with Lv-shJMJD5 (P<0.05), and Caco-2 cell proliferation, migration, and invasion were all obviously inhibited (P<0.05). The results of IHC showed that JMJD5 was significantly up-regulated compared with normal tissues (P<0.01). Additionally, follow-up data demonstrated that the survival rate of patients with high expression of JMJD5 was obviously lower than that with low expression (P<0.01).
Conclusions:
JMJD5 depletion could significantly inhibit human CC cell proliferation, migration, and invasion, implying that JMJD5 might be a potential oncogene.
Insights
Depleting Jumonji C domain-containing (JMJD) 5 significantly inhibits colon cancer cell proliferation, migration, and invasion. JMJD5 is upregulated in colon cancer tissues and linked to lower patient survival rates, suggesting it may be an oncogene.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Colon cancer (CC) remains a significant global health challenge.
- Understanding the molecular mechanisms driving CC progression is crucial for developing effective therapies.
Purpose of the Study:
- To investigate the role of Jumonji C domain-containing (JMJD) 5 in the development and progression of colon cancer.
- To evaluate the impact of JMJD5 depletion on colon cancer cell behavior in vitro and its expression in patient tissues.
Main Methods:
- JMJD5 was depleted in Caco-2 human colon cancer cells using lentiviral short-hairpin RNA (shRNA).
- Quantitative real-time polymerase chain reaction (qRT-PCR) and western blotting assessed JMJD5 mRNA and protein levels.
- Cell proliferation, migration, and invasion were evaluated using MTT assays, soft agar colony formation assays, and Transwell assays, respectively.
- Immunohistochemical (IHC) staining analyzed JMJD5 expression in CC patient tissues and adjacent normal tissues.
Main Results:
- JMJD5 depletion significantly reduced JMJD5 mRNA and protein levels in Caco-2 cells.
- Inhibition of JMJD5 significantly suppressed colon cancer cell proliferation, migration, and invasion.
- JMJD5 was found to be significantly upregulated in colon cancer tissues compared to normal adjacent tissues.
- High JMJD5 expression in patients correlated with a significantly lower survival rate.
Conclusions:
- JMJD5 depletion effectively inhibits colon cancer cell proliferation, migration, and invasion.
- JMJD5 is upregulated in colon cancer and associated with poor patient prognosis.
- These findings suggest that JMJD5 acts as a potential oncogene in colon cancer and may represent a therapeutic target.
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