Tumor hypoxia plays a crucial role in driving cancer progression and fostering resistance to therapies by contributing significantly to chemoresistance, radioresistance, angiogenesis, invasiveness, metastasis, altered cell metabolism, and genomic instability. Despite the challenges encountered in therapeutically addressing tumor hypoxia with conventional drugs, a noteworthy alternative has emerged through the utilization of anaerobic oncolytic bacteria. These bacteria exhibit a preference for accumulating and proliferating within the hypoxic regions of tumors, where they can initiate robust antitumor effects and immune responses. Through simple genetic manipulation or sophisticated synthetic bioengineering, these bacteria can be further optimized to improve safety and antitumor activities, or they can be combined synergistically with chemotherapies, radiation, or other immunotherapies. In this review, we explore the potential benefits and challenges associated with this innovative anticancer approach, addressing issues related to clinical translation, particularly as several strains have progressed to clinical evaluation.
Keyphrases
- cancer therapy
- endothelial cells
- clinical evaluation
- immune response
- drug delivery
- escherichia coli
- microbial community
- papillary thyroid
- copy number
- squamous cell carcinoma
- single cell
- stem cells
- cell therapy
- squamous cell
- toll like receptor
- dendritic cells
- oxidative stress
- wound healing
- radiation therapy
- inflammatory response
- climate change
- radiation induced