Bugs as Drugs: Organoids and Engineered Microbes Unite to Rewrite Cancerâs Corrupted Code |
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What if preventing cancer in high-risk children didnât come in a pillâbut in a programmed microbe?
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Our newest initiative, B.A.D. (Bugs As Drugs), harnesses engineered gut microbes to intercept colorectal cancer at the sourceâbefore it can even begin, and math to objectively track cancer risk.
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đ§Ş About the origin of the âB.A.D Bugs as Drugsâ program: Led by a transdisciplinary team of experts at UC San DiegoâDrs. Dennis Kuo, Amir Zarrinpar, Pradipta Ghosh and collaboratorsâand funded by CureBound Inc, this program seeks to put to the test a radical concept, originally innovated by the Zarrinpar Lab: that engineered native bacteria (ENB; built with support from an NIH U01 mechanism (NCI)Â can be designed to detect and correct cellular dysfunctions that drive colorectal cancer (CRC) in patients with inherited predispositions, like Familial Adenomatous Polyposis (FAP) and Lynch Syndrome.
At the heart of this work is HUMANOIDâ˘, a unique biobank of patient-derived organoids (PDOs) that harbor real-world genetic predispositions. These PDOs offer human-relevant models that surpass what mice can replicateâcapturing both complex genetic factors and the microbial dynamics that shape cancer risk. The biobank was originally built with support from an NIH UG3/UH3 mechanism (NCATS) and bolstered by the dedication of physician-scientist Dr. Sherry Huang (former UC San Diego Associate Dean and now Vice Provost at UT Southwestern) and continues through efforts of Dr. Dennis Kuo and Dr. Nidhi Goyal. This biobank will now be leveraged to study how engineered bacteria might reshape the gut ecosystem in real time, simulating the high-stakes biological duel that unfolds as ENBs colonize and correct. These bugs donât just coexistâthey surveil, intervene, and restore balance with a single, sustainable dose. Together with personalized diagnostics, this approach could redefine what cancer prevention looks likeâespecially for children at highest risk.
Together with AI/ML-driven analyses, this platform doesnât just model CRC riskâit measures how precisely ENBs can reduce it.
The result: a potentially transformative approach to cancer prevention, especially for children carrying the highest inherited risk.
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đĄ What Makes 'Bugs As Drugs' Unique? |
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âď¸ One-and-Done Dosing: A single administration delivers lasting therapeutic effects
đ§ Synthetic Smarts: Engineered to detect and respond to oncogenic changes in real time
đ§Ź Native Bacterial Hosts: Minimally invasive, with high biological compatibility
đ§Ť Tested on Organoids: Personalized in real time using patient-derived cells
đŻ Designed for Precision: Integrates human gene signatures with microbial modulators
This bold initiative goes beyond discoveryâit's about building the future of preventive medicine and redefining cancer care, especially as colorectal cancer rates are skyrocketing in young adults.Â
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đŹ The Big Questions B.A.D Will Answer: |
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1.Can we prevent colon adenomas in children with a 100% lifetime risk of CRC (e.g., FAP)?
2.How can synthetic biology turn gut bacteria into long-term therapeutic allies?
3.Will this microbial therapy reduce the need for invasive preventive surgeries like colectomies?
4.Can we generalize this platform for other genetically predisposed cancers?
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đŠâđŹ Meet the B.A.D Program team |
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Program team (from Left to Right): Dennis Kuo [PED], Pradipta Ghosh [MED, CMM], Amir Zarrinpar [MED], Courtney Tindle [CMM], Saptarshi Sinha [CMM] and Nidhi Goyal [PED].
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If successful, this approach could revolutionize preventive medicine, offering the first-ever sustainable therapy for inherited CRC syndromes. It opens the door to a future where âbugs as drugsâ become the new norm for preventing cancers and chronic diseasesâespecially in children. Efforts are also expected to help launch new interdisciplinary initiatives at the crossroads of leverage synthetic biology and PDOs.
This project touches multiple CureBound investment pillars:
𩺠Prevention & Diagnostic Tools
đ§Ź Novel Therapeutics & Platforms
đ§ Pediatric Cancers
Stay tuned for updates as we move from lab bench to preclinical modelsâtoward the first microbe-based cancer prevention therapy. Got an idea on how you can use organoids? Contact: Courtney Tindle at ctindle@health.ucsd.edu
đ HUMANOIDâ˘: Meet Us at Phase Zero.
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How Can HUMANOIDâ˘Â Help Your Research? |
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Test Hypotheses:Â Use human organoids to validate your research ideas and push boundaries.
- Drive Discoveries: Tap into our cutting-edge models to uncover new treatments, novel biomarkers and even therapeutic interventions (small molecules, antibodies, CRISPR/RNA interference).
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Test Drug Toxicity & Efficacy:Â Get precise results that could accelerate your journey from the lab to real-world applications.
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