Oncolytic adenoviruses in bladder and kidney cancers: emerging strategies and next frontiers

Jia Yao1, Dmitry M Shayakhmetov1,2,3

  • 1Departments of Pediatrics and Medicine, Lowance Center for Human Immunology, Emory University School of Medicine, Atlanta, GA, United States.

Frontiers in Microbiology
|December 25, 2025
PubMed

Insights

Engineered oncolytic adenoviruses (OAds) show promise for treating renal and bladder cancers. Advances in OAd design and combination therapies enhance their potential as effective cancer treatments.

Area of Science:

  • Oncolytic virotherapy
  • Cancer gene therapy
  • Urologic oncology

Background:

  • Oncolytic adenoviruses (OAds) are engineered viruses that selectively infect and kill cancer cells.
  • Significant progress has been made in tailoring OAds for enhanced antitumor specificity and efficacy.
  • Understanding adenovirus biology, cancer pathology, and tumor immunology is crucial for OAd development.

Purpose of the Study:

  • To review recent advances in engineered oncolytic adenoviruses for renal and bladder cancers.
  • To summarize preclinical and clinical findings on OAd safety and efficacy.
  • To highlight the therapeutic potential of OAds for patients with limited treatment options.

Main Methods:

  • Review of current literature on oncolytic adenovirus engineering.
  • Analysis of preclinical studies in animal models of renal and bladder cancer.
  • Summary of clinical trial data on OAd safety and efficacy in cancer patients.

Main Results:

  • Engineered OAds demonstrate enhanced antitumor specificity and efficacy.
  • Combination therapies involving OAds show synergistic effects.
  • Preclinical studies show tumor suppression, and clinical trials indicate favorable safety and efficacy.

Conclusions:

  • Engineered oncolytic adenoviruses represent a promising novel therapeutic strategy.
  • OAds offer significant potential for treating renal and bladder cancers.
  • Further development and clinical application of OAds are warranted for patients with limited options.

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