Fusobacterium species are distinctly associated with patients with Lynch syndrome colorectal cancer

被引:4
|
作者
Salim, Felix [1 ]
Mizutani, Sayaka [1 ,2 ]
Shiba, Satoshi [3 ]
Takamaru, Hiroyuki [4 ]
Yamada, Masayoshi [4 ]
Nakajima, Takeshi [4 ]
Yachida, Tatsuo [6 ]
Soga, Tomoyoshi [7 ]
Saito, Yutaka [4 ]
Fukuda, Shinji [7 ,8 ,9 ,10 ,11 ,12 ]
Yachida, Shinichi [5 ,13 ]
Yamada, Takuji [1 ,11 ,12 ,14 ]
机构
[1] Tokyo Inst Technol, Sch Life Sci & Technol, Meguro Ku, Tokyo 1528550, Japan
[2] Japan Soc Promot Sci, Tokyo, Japan
[3] Natl Canc Ctr, Res Inst, Div Canc Genom, Chuo Ku, Tokyo 1040045, Japan
[4] Natl Canc Ctr, Endoscopy Div, Chuo Ku, Tokyo 1040045, Japan
[5] Osaka Univ, Grad Sch Med, Dept Canc Genome Informat, Suita, Osaka 5650871, Japan
[6] Kagawa Univ, Fac Med, Dept Gastroenterol & Neurol, Miki Cho, Kagawa 7610793, Japan
[7] Keio Univ, Inst Adv Biosci, Tsuruoka, Yamagata 9970052, Japan
[8] Kanagawa Inst Ind Sci & Technol, Gut Environm Design Grp, Kawasaki, Kanagawa 2100821, Japan
[9] Univ Tsukuba, Transborder Med Res Ctr, Tsukuba, Ibaraki 3058575, Japan
[10] Juntendo Univ, Grad Sch Med, Lab Regenerat Microbiol, Bunkyo Ku, Tokyo 1138421, Japan
[11] Metagen Inc, Tsuruoka, Yamagata 9970052, Japan
[12] Metagen Theurapeut Inc, Tsuruoka, Yamagata 9970052, Japan
[13] Osaka Univ, Inst Open & Transdisciplinary Res Initiat OTRI, Integrated Frontier Res Med Sci Div, Suita, Osaka 5650871, Japan
[14] Digzyme Inc, Minato Ku, Tokyo 1050004, Japan
关键词
GUT MICROBIOTA; NUCLEATUM; FAP2; CELL; ALIGNMENT; GLUTAMATE; BINDING; PROTEIN;
D O I
10.1016/j.isci.2024.110181
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Accumulating evidence demonstrates clear correlation between the gut microbiota and sporadic colorectal cancer (CRC). Despite this, there is limited understanding of the association between the gut micro- biota and CRC in Lynch Syndrome (LS), a hereditary type of CRC. Here, we analyzed fecal shotgun metagenomic and targeted metabolomic of 71 Japanese LS subjects. A previously published Japanese sporadic CRC cohort, which includes non-LS controls, was utilized as a non-LS cohort (n = 437). LS subjects exhibited reduced microbial diversity and low- Faecalibacterium enterotypes compared to non-LS. Patients with LS- CRC had higher levels of Fusobacterium nucleatum and fap2. Differential fecal metabolites and functional genes suggest heightened degradation of lysine and arginine in LS-CRC. A comparison between LS and non-LS subjects prior to adenoma formation revealed distinct fecal metabolites of LS subjects. These findings suggest that the gut microbiota plays a more responsive role in CRC tumorigenesis in patients with LS than those without LS.
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页数:24
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