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Updated: Jan 29, 2026

Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
OLFM4 Inhibits Epithelial-Mesenchymal Transition and Metastatic Potential of Cervical Cancer Cells
Juan Li1, Chunyan Liu2, Dawei Li3
1Department of Pathology, Qianfoshan Hospital Affiliated with Shandong University, Jinan, Shandong, P.R. China.
Abstract:
OLFM4 has been shown to play an important role in tumor initiation and progression. This study aims to investigate the role of OLFM4 in metastatic cervical cancer and its underlying mechanism. Here we discover that OLFM4 expression is significantly reduced in metastatic cervical cancer. Accordingly, overexpression of OLFM4 inhibits epithelial-mesenchymal transition (EMT), migration, and invasion in human cervical cancer cells. To further explore its molecular mechanisms, we reveal that OLFM4 augmentation interferes with mTOR signaling pathway, and the suppressive effects of OLFM4 on cell migration and invasion are largely weakened by phosphatidic acid (PA)-induced mTOR signal activation, which implicates the potential role of the mTOR pathway in OLFM4-related cervical metastasis. In conclusion, our results confirm OLFM4 as a tumor suppressor that inhibits cervical cancer metastasis by regulating mTOR signal pathway.
Insights
OlfM4 (Olfactomedin 4) acts as a tumor suppressor in cervical cancer. Its reduced expression promotes metastasis, while its restoration inhibits cancer cell migration and invasion via the mTOR pathway.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Metastasis Research
Background:
- Olfactomedin 4 (OLFM4) is implicated in tumor initiation and progression.
- The role of OLFM4 in cervical cancer metastasis remains to be fully elucidated.
Purpose of the Study:
- To investigate the function of OLFM4 in metastatic cervical cancer.
- To identify the molecular mechanisms underlying OLFM4's role in cervical cancer progression.
Main Methods:
- Analysis of OLFM4 expression in metastatic cervical cancer tissues.
- Overexpression of OLFM4 in human cervical cancer cell lines.
- Assessment of cell migration and invasion.
- Investigation of the mTOR signaling pathway and its interaction with OLFM4.
Main Results:
- OLFM4 expression is significantly decreased in metastatic cervical cancer.
- Overexpression of OLFM4 suppresses epithelial-mesenchymal transition (EMT), migration, and invasion.
- OLFM4 augmentation interferes with the mTOR signaling pathway.
- Activation of mTOR signaling by phosphatidic acid (PA) partially reverses the inhibitory effects of OLFM4.
Conclusions:
- OLFM4 functions as a tumor suppressor in cervical cancer.
- OLFM4 inhibits cervical cancer cell metastasis by regulating the mTOR signaling pathway.
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