Colorectal cancer mutational profiles correlate with defined microbial communities in the tumor microenvironment

被引:73
作者
Burns, Michael B. [1 ,2 ,3 ]
Montassier, Emmanuel [4 ,5 ]
Abrahante, Juan [6 ]
Priya, Sambhawa [1 ,2 ]
Niccum, David E. [7 ]
Khoruts, Alexander [7 ,8 ]
Starr, Timothy K. [1 ,9 ,10 ]
Knights, Dan [4 ,11 ]
Blekhman, Ran [1 ,2 ]
机构
[1] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Ecol Evolut & Behav, St Paul, MN 55108 USA
[3] Loyola Univ Chicago, Dept Biol, Chicago, IL 60611 USA
[4] Univ Minnesota, Dept Comp Sci & Engn, Minneapolis, MN USA
[5] Univ Nantes, MiHAR lab, F-44000 Nantes, France
[6] Univ Minnesota, Univ Minnesota Informat Inst, Minneapolis, MN USA
[7] Univ Minnesota, Dept Med, Div Gastroenterol, Minneapolis, MN USA
[8] Univ Minnesota, Ctr Immunol, Minneapolis, MN USA
[9] Univ Minnesota, Mason Canc Ctr, Minneapolis, MN USA
[10] Univ Minnesota, Dept Obstet Gynecol & Womens Hlth, Minneapolis, MN USA
[11] Univ Minnesota, Coll Biol Sci, BioTechnol Inst, Minneapolis, MN USA
关键词
P75 NEUROTROPHIN RECEPTOR; HUMAN GUT MICROBIOME; GROWTH-FACTOR RECEPTOR; MOLECULAR CHARACTERIZATION; FUSOBACTERIUM-NUCLEATUM; COLON; CELLS; GENE; INFLAMMATION; ASSOCIATIONS;
D O I
10.1371/journal.pgen.1007376
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Variation in the gut microbiome has been linked to colorectal cancer (CRC), as well as to host genetic variation. However, we do not know whether, in addition to baseline host genetics, somatic mutational profiles in CRC tumors interact with the surrounding tumor microbiome, and if so, whether these changes can be used to understand microbe-host interactions with potential functional biological relevance. Here, we characterized the association between CRC microbial communities and tumor mutations using microbiome profiling and whole-exome sequencing in 44 pairs of tumors and matched normal tissues. We found statistically significant associations between loss-of-function mutations in tumor genes and shifts in the abundances of specific sets of bacterial taxa, suggestive of potential functional interaction. This correlation allows us to statistically predict interactions between loss-of-function tumor mutations in cancer-related genes and pathways, including MAPK and Wnt signaling, solely based on the composition of the microbiome. In conclusion, our study shows that CRC microbiomes are correlated with tumor mutational profiles, pointing towards possible mechanisms of molecular interaction.
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页数:24
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