Exploring enterovirus pathogenesis and cancer therapy potential through reverse genetics

Shijin Wang1,2, Qing Yu2,3, Junfeng Zhou4

  • 1Cancer Center, The First Hospital of Jilin University, Changchun 130021 China.

Biosafety and Health
|February 4, 2026
PubMed

Insights

Oncolytic enteroviruses (EVs) show promise for cancer treatment due to tumor-specific targeting. Reverse genetics advances understanding of EV infection and aids development of novel immunotherapies.

Area of Science:

  • Virology
  • Oncology
  • Molecular Biology

Background:

  • Oncolytic viruses are emerging as potent anticancer agents.
  • Enteroviruses (EVs) exhibit specific tropism for tumor cells, making them attractive candidates for oncolysis.
  • Reverse genetics has become a powerful tool for studying viral mechanisms and developing therapeutic applications.

Purpose of the Study:

  • To review the progress and potential clinical applications of reverse genetics in the development of oncolytic enteroviruses.
  • To explore the characteristics of EVs and the role of reverse genetics in understanding their infection mechanisms and oncolytic potential.
  • To highlight specific enteroviruses with oncolytic roles and their significance in cancer immunotherapy.

Main Methods:

  • Review of scientific literature on oncolytic enteroviruses and reverse genetics.
  • Analysis of studies investigating enterovirus tropism and pathogenesis.
  • Discussion of specific enterovirus serotypes with demonstrated oncolytic activity.

Main Results:

  • Reverse genetics has significantly advanced the understanding of enterovirus infection mechanisms and pathogenesis.
  • Specific enteroviruses, including EV-A71, CV-B3, Echo-7, CV-A21, and poliovirus, have shown oncolytic potential.
  • The application of reverse genetics facilitates the development of engineered oncolytic enteroviruses for cancer therapy.

Conclusions:

  • Oncolytic enteroviruses engineered using reverse genetics offer a promising avenue for cancer treatment.
  • The tumor-specific tropism of certain EVs enhances their potential as targeted oncolytic agents.
  • Further research and clinical translation of oncolytic EVs hold significant promise for cancer immunotherapy.

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