RRC ID 77098
著者 Chen Y, Yang S, Tavormina J, Tampe D, Zeisberg M, Wang H, Mahadevan KK, Wu CJ, Sugimoto H, Chang CC, Jenq RR, McAndrews KM, Kalluri R.
タイトル Oncogenic collagen I homotrimers from cancer cells bind to α3β1 integrin and impact tumor microbiome and immunity to promote pancreatic cancer.
ジャーナル Cancer Cell
Abstract In contrast to normal type I collagen (Col1) heterotrimer (α1/α2/α1) produced by fibroblasts, pancreatic cancer cells specifically produce unique Col1 homotrimer (α1/α1/α1). Col1 homotrimer results from epigenetic suppression of the Col1a2 gene and promotes oncogenic signaling, cancer cell proliferation, tumor organoid formation, and growth via α3β1 integrin on cancer cells, associated with tumor microbiome enriched in anaerobic Bacteroidales in hypoxic and immunosuppressive tumors. Deletion of Col1 homotrimers increases overall survival of mice with pancreatic ductal adenocarcinoma (PDAC), associated with reprograming of the tumor microbiome with increased microaerophilic Campylobacterales, which can be reversed with broad-spectrum antibiotics. Deletion of Col1 homotrimers enhances T cell infiltration and enables efficacy of anti-PD-1 immunotherapy. This study identifies the functional impact of Col1 homotrimers on tumor microbiome and tumor immunity, implicating Col1 homotrimer-α3β1 integrin signaling axis as a cancer-specific therapeutic target.
巻・号 40(8)
ページ 818-834.e9
公開日 2022-8-8
DOI 10.1016/j.ccell.2022.06.011
PII S1535-6108(22)00275-6
PMID 35868307
PMC PMC9831277
MeSH Animals Carcinogenesis Carcinoma, Pancreatic Ductal* / genetics Collagen Collagen Type I Integrin alpha3beta1 Mice Microbiota* Pancreatic Neoplasms* / genetics
IF 26.602
リソース情報
ヒト・動物細胞 T3M-4(RCB1021)