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Updated: Aug 2, 2025

Bioluminescent Bacterial Imaging In Vivo
Published on: November 4, 2012
Using bugs as drugs: Administration of bacteria-related microbes to fight cancer
Jiawei Wang1, Debadyuti Ghosh2, Mohammed Maniruzzaman1
1Pharmaceutical Engineering and 3D Printing (PharmE3D) Lab, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA; Division of Molecular Pharmaceutics and Drug Delivery, College of Pharmacy, The University of Texas at Austin, Austin, TX 78712, USA.
Abstract:
Bioengineering of bacteria-related microbes has demonstrated a great potential in targeted cancer therapy. Presently, the major administration routes of bacteria-related microbes for cancer treatment include intravenous injection, intratumoral injection, intraperitoneal injection, and oral delivery. Routes of bacteria administration are critical since different delivery approaches might exert anticancer effects through diverse mechanisms. Herein, we provide an overview of the primary routes of bacteria administration as well as their advantages and limitations. Furthermore, we discuss that microencapsulation can overcome some of the associated challenges with the administration of free bacteria. We also review the latest advancements in combining functional particles with engineered bacteria to fight cancer, which can be coupled with conventional therapies to improve therapeutic effects. Moreover, we highlight the application prospect of emerging 3D bioprinting in cancer bacteriotherapy, which represents a new paradigm for personalized cancer treatment. Eventually, we provide insights into regulatory expectations and concerns regarding this field for the future translation from bench to clinic.
Insights
Engineered bacteria show promise for cancer therapy via various delivery routes. Strategies like microencapsulation and 3D bioprinting enhance efficacy and personalization in bacteriotherapy.
Area of Science:
- Biomedical Engineering
- Oncology
- Microbiology
Background:
- Engineered bacteria offer potential for targeted cancer therapy.
- Current administration routes include intravenous, intratumoral, intraperitoneal, and oral delivery.
- The route of administration influences the mechanisms of anticancer effects.
Purpose of the Study:
- To provide an overview of bacteria administration routes for cancer treatment.
- To discuss challenges and solutions, including microencapsulation.
- To review advancements in combining engineered bacteria with functional particles and 3D bioprinting for personalized cancer therapy.
Main Methods:
- Literature review of bacteria administration routes in cancer therapy.
- Discussion of microencapsulation techniques for bacteria delivery.
- Exploration of synergistic approaches combining engineered bacteria with functional particles and 3D bioprinting.
- Analysis of regulatory considerations for clinical translation.
Main Results:
- Different administration routes have distinct advantages, limitations, and mechanisms of action.
- Microencapsulation can mitigate challenges associated with free bacteria administration.
- Combining engineered bacteria with functional particles and 3D bioprinting shows potential for enhanced and personalized cancer treatment.
- Regulatory aspects are crucial for the clinical translation of bacteriotherapy.
Conclusions:
- Optimizing bacteria administration routes is key for effective cancer bacteriotherapy.
- Advanced strategies like microencapsulation, functional particle conjugation, and 3D bioprinting are advancing the field.
- Personalized cancer treatment through engineered bacteria holds significant future promise, pending regulatory considerations.
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