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Updated: Jan 2, 2026

Impedance-based Real-time Measurement of Cancer Cell Migration and Invasion
Published on: April 2, 2020
Inhibition of human cervical cancer cell invasion by IL-37 involving runt related transcription factor 2 suppression
Ping Ouyang1, Kun Wu1,2, Liudan Su1,2
1Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Dongguan Scientific Research Center, Guangdong Medical University, Dongguan 523808, China.
Background:
IL-37 is a newly anti-inflammatory cytokine whose function is largely unknown in cancer. Our preliminary experiment found IL-37 could inhibit the invasion of human cervical cancer (CC) cells and influence the expression of RUNX family whose function was also unclear in CC. The present study aims to further investigate the effects of IL-37 on cell invasion and runt related transcription factor 2 (RUNX2) expression in CC cell lines.
Methods:
Firstly, plasmid overexpressing IL-37 or RUNX2 was transfected into Siha and C33A cells by Hilymax. Then, the effects of IL-37 on the mRNA expression of RUNX1, RUNX2 and RUNX3 gene were detected by quantitative real-time polymerase chain reaction. Protein expression was measured by Western blot and the grayscale scanning analysis. Finally, the effects of IL-37 or RUNX2 on cell invasion were tested by transwell assay.
Results:
IL-37 inhibited the mRNA expression of RUNX1 and RUNX2, and increased that of RUNX3 in CC cells. Among the three RUNX genes, RUNX2 showed the most significant change in mRNA expression (decreased by78.5% in Siha cells and by 61.5% in C33A cells) and thus was chosen for the following study. Overexpressed IL-37 inhibited cell invasion by 36.23% in Siha cells (P<0.05) and 26.21% in C33A cells (P<0.01). Overexpression of RUNX2 promoted cell invasion. Up-regulation of IL-37 suppressed markedly the mRNA and protein expression of RUNX2. Furthermore, overexpressed RUNX2 partially restored the inhibited cell invasion by IL-37 to 86.62% in Siha cells (P<0.01) and 87.08% in C33A cells (P<0.01).
Conclusions:
IL-37 can significantly inhibit the cell invasion of Siha and C33A cells, which involves the suppression of RUNX2.
Insights
Interleukin-37 (IL-37) inhibits human cervical cancer cell invasion by suppressing RUNX2 expression. This finding highlights IL-37 as a potential therapeutic target for cervical cancer treatment.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- Interleukin-37 (IL-37) is an anti-inflammatory cytokine with largely unknown roles in cancer.
- Preliminary studies suggest IL-37 inhibits cervical cancer (CC) cell invasion and affects RUNX family gene expression.
- The function of RUNX family genes in CC is also not well understood.
Purpose of the Study:
- To investigate the effects of IL-37 on cell invasion in CC cell lines.
- To determine the impact of IL-37 on the expression of runt related transcription factor 2 (RUNX2) in CC cells.
Main Methods:
- Transfection of Siha and C33A cells with plasmids overexpressing IL-37 or RUNX2.
- Quantitative real-time PCR to detect RUNX1, RUNX2, and RUNX3 mRNA expression.
- Western blot analysis for protein expression and grayscale scanning.
- Transwell assays to evaluate cell invasion.
Main Results:
- IL-37 suppressed RUNX1 and RUNX2 mRNA expression while increasing RUNX3 mRNA levels.
- Overexpression of IL-37 significantly inhibited cell invasion in both Siha and C33A cell lines.
- IL-37 suppressed both mRNA and protein expression of RUNX2.
- Overexpression of RUNX2 partially reversed the inhibitory effect of IL-37 on cell invasion.
Conclusions:
- IL-37 significantly inhibits the invasion of cervical cancer cells (Siha and C33A).
- This inhibitory effect of IL-37 on cell invasion is mediated through the suppression of RUNX2 expression.
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