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Updated: Jun 25, 2026

Measuring Growth and Gene Expression Dynamics of Tumor-Targeted S. Typhimurium Bacteria
Published on: July 6, 2013
Cancer metastasis directly eradicated by targeted therapy with a modified Salmonella typhimurium
Katsuhiro Hayashi1, Ming Zhao, Kensuke Yamauchi
1AntiCancer, Inc., 7917 Ostrow Street, San Diego, CA 92111, USA.
Abstract:
Cancer metastasis is the life-threatening aspect of cancer and is usually resistant to standard treatment. We report here a targeted therapy strategy for cancer metastasis using a genetically-modified strain of Salmonella typhimurium. The genetically-modified strain of S. typhimurium is auxotrophic for the amino acids arginine and leucine. These mutations preclude growth in normal tissue but do not reduce bacterial virulence in cancer cells. The tumor-targeting strain of S. typhimurium, termed A1-R, and expressing green fluorescent protein (GFP), was administered to both axillary lymph and popliteal lymph node metastasis of human pancreatic cancer and fibrosarcoma, respectively, as well as lung metastasis of the fibrosarcoma in nude mice. The bacteria were delivered via a lymphatic channel to target the lymph node metastases and systemically via the tail vein to target the lung metastasis. The cancer cells expressed red fluorescent protein (RFP) in the cytoplasm and GFP in the nucleus linked to histone H2B, enabling color-coded real-time imaging of the bacteria targeting the metastatic tumors. After 7-21 days of treatment, the metastases were eradicated without the need of chemotherapy or any other treatment. No adverse effects were observed. This new strategy demonstrates the clinical potential of targeting and curing cancer metastasis with engineered bacteria without the need of toxic chemotherapy.
Insights
Engineered Salmonella typhimurium bacteria eradicated cancer metastasis in mice. This novel therapy targets tumors, offering a potential chemotherapy-free treatment for advanced cancers.
Area of Science:
- Oncology
- Microbiology
- Biotechnology
Background:
- Cancer metastasis is a primary cause of cancer-related mortality.
- Metastatic cancers are often resistant to conventional therapies.
- Targeted therapies are crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the efficacy of genetically modified Salmonella typhimurium (A1-R) as a targeted therapy for cancer metastasis.
- To evaluate the safety and effectiveness of A1-R in eradicating metastatic tumors in preclinical models.
- To demonstrate a novel, non-chemotherapeutic approach for treating metastatic disease.
Main Methods:
- Developed a genetically modified Salmonella typhimurium strain (A1-R) auxotrophic for arginine and leucine.
- Administered A1-R via lymphatic channels and tail vein injection to target lymph node and lung metastases in nude mice.
- Utilized fluorescent proteins (GFP and RFP) for real-time imaging of bacterial targeting and tumor response.
Main Results:
- Complete eradication of axillary lymph node metastasis (pancreatic cancer) and popliteal lymph node metastasis (fibrosarcoma) within 7-21 days.
- Successful eradication of lung metastasis (fibrosarcoma) in nude mice.
- No adverse effects observed in treated animals, indicating a favorable safety profile.
Conclusions:
- Genetically engineered Salmonella typhimurium (A1-R) demonstrates significant potential for treating cancer metastasis.
- This bacterial therapy offers a promising alternative to toxic chemotherapy for metastatic cancers.
- The study highlights the clinical feasibility of using engineered bacteria for targeted cancer treatment.
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