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The clinicopathological and prognostic significances of Dkk3 expression in cancers: A bioinformatics analysis
Background:
Dkk3 protein attenuates the expression of Wnt3a, Wnt5a and LRP6, and their interaction, and interacts with βTrCP to suppress wnt/β-catenin pathway.
Methods:
We performed a bioinformatics analysis of Dkk3 mRNA expression through Oncomine, TCGA and Kaplan-Meier plotter databases up to July 10, 2017.
Results:
Up-regulated Dkk3 expression was higher in gastric, breast, and ovarian cancers than normal tissues (p< 0.05). Bitter's database showed a higher Dkk3 expression in ovarian cytoadenocarcinoma than clear cell adenocarcinoma (p< 0.05). Dkk3 was more expressed in ductal breast cancer in situ than invasive ductal breast cancer (p< 0.05), in mixed lobular and ductal cancer, and lobular cancer than ductal breast cancer (p< 0.05). In TCGA data, Dkk3 expression was lower in gastric cancers with than without Barret's esophagus (p< 0.05), in intestinal-type than diffuse-type cancers (p< 0.05), and in the cancers of elder than younger patients (p< 0.05). Dkk3 expression was higher in squamous cell carcinoma than adenocarcinoma (p< 0.05). Dkk3 expression was higher in ductal than lobular breast cancer, or in younger than elder patients with breast cancer (p< 0.05). According to Kaplan-Meier plotter, Dkk3 expression was negatively correlated with overall, progression-free, relapse-free or distant-metastasis-free survival rate of gastric, breast or ovarian cancer patients, but versa for lung cancer patients (p< 0.05).
Conclusion:
Dkk3 expression might be employed as a potential marker to indicate carcinogenesis and histogenesis, even prognosis.
Insights
Dickkopf-3 (Dkk3) expression is elevated in several cancers, including gastric, breast, and ovarian. Dkk3 levels correlate with cancer progression and patient survival, suggesting its potential as a diagnostic marker.
Area of Science:
- Molecular oncology
- Cancer biology
- Biomarker discovery
Background:
- Dickkopf-3 (Dkk3) protein negatively regulates Wnt signaling pathways by inhibiting Wnt ligands (Wnt3a, Wnt5a) and LRP6, and interacting with βTrCP to suppress the Wnt/β-catenin pathway.
- Aberrant Wnt signaling is implicated in various cancers.
Purpose of the Study:
- To investigate the expression patterns of Dkk3 mRNA in different cancer types.
- To analyze the correlation between Dkk3 expression and clinicopathological features and patient survival.
Main Methods:
- Bioinformatics analysis of Dkk3 mRNA expression using Oncomine, TCGA, and Kaplan-Meier plotter databases.
- Data analysis included comparisons across various cancer types, subtypes, and patient demographics.
Main Results:
- Dkk3 expression was significantly higher in gastric, breast, and ovarian cancers compared to normal tissues.
- Specific cancer subtypes, such as ovarian cytoadenocarcinoma and ductal breast cancer, showed higher Dkk3 levels.
- Dkk3 expression was negatively correlated with overall survival in gastric, breast, and ovarian cancers, but positively correlated in lung cancer.
Conclusions:
- Dkk3 expression may serve as a potential biomarker for cancer diagnosis, indicating carcinogenesis and histogenesis.
- Dkk3 levels could be a prognostic indicator for patient outcomes in several cancer types.
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