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Updated: Mar 24, 2026

Studying TGF-β Signaling and TGF-β-induced Epithelial-to-mesenchymal Transition in Breast Cancer and Normal Cells
Published on: October 27, 2020
STARD13-correlated ceRNA network inhibits EMT and metastasis of breast cancer
Xiaoman Li1,2, Lufeng Zheng1,2, Feng Zhang1,2
1School of Life Science and Technology, China Pharmaceutical University, Nanjing, People's Republic of China.
Abstract:
Competing endogenous RNAs (ceRNAs) network has been correlated with the initiation and development of cancer. Here, we identify CDH5, HOXD1, and HOXD10 as putative STARD13 ceRNAs and they display concordant patterns with STARD13 in different metastatic potential breast cancer cell lines and tissues. Notably, 3'UTRs of these genes suppress breast cancer metastasis via inhibiting epithelial-mesenchymal transition (EMT) in vitro and in vivo, which are activated through the crosstalk between STARD13 and its ceRNAs in 3'UTR- and miRNA-dependent manners. In addition, Kaplan-Meier survival analysis reveals that mRNA level of STARD13 and its ceRNAs is remarkably associated with survival of breast cancer patients. These results suggest that 3'UTRs of CDH5, HOXD1, and HOXD10 inhibit breast cancer metastasis via serving as STARD13 ceRNAs.
Insights
The study identifies CDH5, HOXD1, and HOXD10 as competing endogenous RNAs (ceRNAs) that suppress breast cancer metastasis by interacting with STARD13. Higher levels of these ceRNAs correlate with improved patient survival.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Competing endogenous RNAs (ceRNAs) play a role in cancer initiation and progression.
- Understanding ceRNA networks is crucial for developing novel cancer therapies.
Purpose of the Study:
- To identify novel ceRNAs involved in breast cancer metastasis.
- To elucidate the mechanism by which these ceRNAs regulate metastasis.
- To assess the prognostic value of these ceRNAs in breast cancer patients.
Main Methods:
- Identification of STARD13 ceRNAs using expression profiling in breast cancer cell lines and tissues.
- In vitro and in vivo experiments to assess the role of identified ceRNAs in epithelial-mesenchymal transition (EMT) and metastasis.
- Kaplan-Meier survival analysis to correlate ceRNA expression with patient survival.
Main Results:
- CDH5, HOXD1, and HOXD10 were identified as putative STARD13 ceRNAs, showing concordant expression patterns with STARD13 in breast cancer.
- The 3'UTRs of CDH5, HOXD1, and HOXD10 were found to suppress breast cancer metastasis by inhibiting EMT, mediated by crosstalk with STARD13.
- High mRNA levels of STARD13 and its identified ceRNAs were significantly associated with better survival outcomes in breast cancer patients.
Conclusions:
- CDH5, HOXD1, and HOXD10 function as STARD13 ceRNAs, inhibiting breast cancer metastasis through EMT suppression.
- The STARD13-ceRNA network involving CDH5, HOXD1, and HOXD10 holds potential as a prognostic biomarker for breast cancer.
- Targeting this ceRNA network could offer a therapeutic strategy for reducing breast cancer metastasis.
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