Oral poliovirus vaccine-induced programmed cell death involves both intrinsic and extrinsic pathways in human colorectal cancer cells
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Updated: Feb 2, 2026

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Published on: May 16, 2025
Sareh Zhand1, Seyed Masoud Hosseini1, Alijan Tabarraei2
1Department of Microbiology, Faculty of Biological Sciences and Technology, Shahid Beheshti University, Tehran, Iran.
Purpose:
Colorectal cancer (CRC) is one of the most common causes of cancer death throughout the world. Replication-competent viruses, which are naturally able to infect and lyse tumor cells, seem to be promising in this field. The aim of this study was to evaluate the potential of oral poliovirus vaccine (OPV) on human CRC cells and elucidate the mechanism of apoptosis induction.
Materials And Methods:
Protein and gene expression of poliovirus (PV) receptor (CD155) on four human CRC cell lines including HCT116, SW480, HT-29, and Caco-2 and normal fetal human colon (FHC) cell line as a control were examined by flow cytometry and SYBR Green Real-Time PCR, respectively. Cytotoxicity of OPV on indicated cell lines was tested using MTT assay. The ability of OPV on apoptosis induction for both intrinsic and extrinsic pathways was examined using caspase-8 and caspase-9 colorimetric assay kits. The PV propagation in mentioned cell lines was investigated, and the quantity of viral yields (cells associated and extracellular) was determined using TaqMan PCR.
Results:
CD155 mRNA and protein were expressed significantly higher in studied CRC cell lines rather than the normal cell line (P=0). OPV induced cell death in a time- and dose-dependent manner in human CRC cells. Apoptosis through both extrinsic and intrinsic pathways was detected in CRC cells with the minimum level found in FHC. PV viral load was significantly correlated with apoptosis via extrinsic (R=0.945, P=0.0001) and intrinsic (R=0.756, P=0.001) pathways.
Conclusion:
This study suggests that OPV has potential for clinical treatment of CRC. However further studies in animal models (tumor xenografts) are needed to be certain that it is qualified enough for treatment of CRC.
Insights
Oral poliovirus vaccine (OPV) shows promise for treating colorectal cancer (CRC) by inducing apoptosis in cancer cells. Further research in animal models is recommended to confirm its therapeutic potential for CRC.
Area of Science:
- Oncolytic virotherapy
- Molecular oncology
- Cancer cell biology
Background:
- Colorectal cancer (CRC) is a leading cause of cancer mortality worldwide.
- Replication-competent viruses are being explored for their ability to infect and lyse tumor cells.
- Oral poliovirus vaccine (OPV) is investigated for its potential anti-cancer properties.
Purpose of the Study:
- To evaluate the efficacy of OPV against human CRC cells.
- To investigate the mechanism of apoptosis induction by OPV in CRC.
- To assess the expression of the poliovirus receptor (CD155) in CRC cells.
Main Methods:
- Assessed CD155 expression using flow cytometry and RT-PCR.
- Determined OPV cytotoxicity via MTT assay.
- Quantified apoptosis induction through caspase-8 and caspase-9 assays.
- Measured poliovirus (PV) propagation using TaqMan PCR.
Main Results:
- CRC cell lines exhibited significantly higher CD155 expression compared to normal colon cells.
- OPV demonstrated time- and dose-dependent cytotoxicity against CRC cells.
- OPV induced apoptosis via both extrinsic and intrinsic pathways, correlating with viral load.
Conclusions:
- OPV exhibits potential as a clinical treatment for colorectal cancer.
- Further investigation in animal models (tumor xenografts) is warranted to validate OPV's therapeutic application in CRC.
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