Analysis of Fusobacterium persistence and antibiotic response in colorectal cancer.
Susan BullmanChandra S PedamalluEwa SicinskaThomas E ClancyXiaoyang ZhangDiana CaiDonna S NeubergKatherine HuangFatima GuevaraTimothy NelsonOtari ChipashviliTimothy HaganMark A WalkerAruna RamachandranBegoña DiosdadoGarazi SernaNuria MuletStefania LandolfiSantiago Ramon Y CajalRoberta FasaniAndrew J AguirreKimmie NgElena ÉlezShuji OginoJosep TaberneroCharles S FuchsWilliam C HahnPaolo G NuciforoMatthew L MeyersonPublished in: Science (New York, N.Y.) (2017)
Colorectal cancers comprise a complex mixture of malignant cells, nontransformed cells, and microorganisms. Fusobacterium nucleatum is among the most prevalent bacterial species in colorectal cancer tissues. Here we show that colonization of human colorectal cancers with Fusobacterium and its associated microbiome-including Bacteroides, Selenomonas, and Prevotella species-is maintained in distal metastases, demonstrating microbiome stability between paired primary and metastatic tumors. In situ hybridization analysis revealed that Fusobacterium is predominantly associated with cancer cells in the metastatic lesions. Mouse xenografts of human primary colorectal adenocarcinomas were found to retain viable Fusobacterium and its associated microbiome through successive passages. Treatment of mice bearing a colon cancer xenograft with the antibiotic metronidazole reduced Fusobacterium load, cancer cell proliferation, and overall tumor growth. These observations argue for further investigation of antimicrobial interventions as a potential treatment for patients with Fusobacterium-associated colorectal cancer.
Keyphrases
- induced apoptosis
- endothelial cells
- cell proliferation
- small cell lung cancer
- cell cycle arrest
- staphylococcus aureus
- oxidative stress
- minimally invasive
- type diabetes
- endoplasmic reticulum stress
- cell death
- single cell
- climate change
- combination therapy
- metabolic syndrome
- pi k akt
- replacement therapy
- human health
- skeletal muscle