Engineering tumor-colonizing E. coli Nissle 1917 for detection and treatment of colorectal neoplasia

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作者
Candice R. Gurbatri
Georgette A. Radford
Laura Vrbanac
Jongwon Im
Elaine M. Thomas
Courtney Coker
Samuel R. Taylor
YoungUk Jang
Ayelet Sivan
Kyu Rhee
Anas A. Saleh
Tiffany Chien
Fereshteh Zandkarimi
Ioana Lia
Tamsin R. M. Lannagan
Tongtong Wang
Josephine A. Wright
Hiroki Kobayashi
Jia Q. Ng
Matt Lawrence
Tarik Sammour
Michelle Thomas
Mark Lewis
Lito Papanicolas
Joanne Perry
Tracy Fitzsimmons
Patricia Kaazan
Amanda Lim
Alexandra M. Stavropoulos
Dion A. Gouskos
Julie Marker
Cheri Ostroff
Geraint Rogers
Nicholas Arpaia
Daniel L. Worthley
Susan L. Woods
Tal Danino
机构
[1] Columbia University,Department of Biomedical Engineering
[2] University of Adelaide,Adelaide Medical School
[3] Weill Cornell-Rockefeller-Sloan Kettering Tri-Institutional MD-PhD program,Division of Infectious Diseases, Weill Department of Medicine
[4] Weill Cornell Medicine,Department of Chemistry
[5] Columbia University,Colorectal Unit, Department of Surgery
[6] South Australian Health and Medical Research Institute (SAHMRI),College of Medicine and Public Health
[7] Royal Adelaide Hospital,Department of Microbiology & Immunology
[8] Flinders University,Herbert Irving Comprehensive Cancer Center
[9] Cancer Voices SA,Data Science Institute
[10] University of South Australia,undefined
[11] Vagelos College of Physicians and Surgeons of Columbia University,undefined
[12] Columbia University,undefined
[13] Colonoscopy Clinic,undefined
[14] Columbia University,undefined
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摘要
Bioengineered probiotics enable new opportunities to improve colorectal cancer (CRC) screening, prevention and treatment. Here, first, we demonstrate selective colonization of colorectal adenomas after oral delivery of probiotic E. coli Nissle 1917 (EcN) to a genetically-engineered murine model of CRC predisposition and orthotopic models of CRC. We next undertake an interventional, double-blind, dual-centre, prospective clinical trial, in which CRC patients take either placebo or EcN for two weeks prior to resection of neoplastic and adjacent normal colorectal tissue (ACTRN12619000210178). We detect enrichment of EcN in tumor samples over normal tissue from probiotic-treated patients (primary outcome of the trial). Next, we develop early CRC intervention strategies. To detect lesions, we engineer EcN to produce a small molecule, salicylate. Oral delivery of this strain results in increased levels of salicylate in the urine of adenoma-bearing mice, in comparison to healthy controls. To assess therapeutic potential, we engineer EcN to locally release a cytokine, GM-CSF, and blocking nanobodies against PD-L1 and CTLA-4 at the neoplastic site, and demonstrate that oral delivery of this strain reduces adenoma burden by ~50%. Together, these results support the use of EcN as an orally-deliverable platform to detect disease and treat CRC through the production of screening and therapeutic molecules.
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