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Targeting Triple Negative Breast Cancer With Oncolytic Adenoviruses
Gabriela Green-Tripp1, Callum Nattress1,2, Gunnel Halldén1
1Centre for Biomarkers and Biotherapeutics, Barts Cancer Institute, Queen Mary University of London, London, United Kingdom.
Frontiers in Molecular Biosciences
|July 11, 2022
Summary
Oncolytic adenoviruses (OAds) show promise in treating triple-negative breast cancer (TNBC) by selectively destroying cancer cells and activating immune responses. Combinations with existing therapies enhance efficacy, offering new hope for improved patient outcomes.
Area of Science:
- Oncolytic virotherapy
- Cancer immunology
- Breast cancer therapeutics
Background:
- Breast cancer (BC) is a leading cause of cancer death globally.
- Triple-negative breast cancer (TNBC) lacks effective targeted therapies and has a poor prognosis.
- Current TNBC treatments face challenges with resistance and limited efficacy.
Purpose of the Study:
- To review the potential of oncolytic adenoviruses (OAds) as a novel therapeutic strategy for TNBC.
- To evaluate OAds efficacy in preclinical and clinical settings, alone and in combination therapies.
- To discuss OAds' mechanisms, limitations, and future directions for improving patient outcomes.
Main Methods:
- Review of preclinical studies on OAds in TNBC cell lines and xenografts.
- Analysis of clinical trial data for OAds in various cancers, including breast cancer.
- Examination of OAds combined with standard treatments, targeted agents (EGFR, AR, PARP inhibitors), and immunotherapies.
Main Results:
- OAds demonstrate selective tumor lysis and immune response recruitment in TNBC models.
- Combinations of OAds with PARP inhibitors (e.g., Olaparib) show enhanced anti-tumor effects.
- OAds combined with immune checkpoint inhibitors or cytokine expression show promising results.
Conclusions:
- OAds represent a promising new therapeutic avenue for TNBC and other breast cancers.
- Combination strategies significantly enhance OAds' anti-tumor activity and therapeutic potential.
- Further research is needed to optimize OAds for metastatic disease, immune activation, and intratumoral spread.
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