IP6 reduces colorectal cancer metastasis by mediating the interaction of gut microbiota with host genes.
IP6 reduces colorectal cancer metastasis by mediating the interaction of gut microbiota with host genes.
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IP6通过介导肠道微生物群与宿主基因的相互作用减少结直肠癌转移。
DOI:
10.3389/fnut.2022.979135
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发表时间:
2022
影响因子:
5
通讯作者:
Li, Hui
中科院分区:
文献类型:
--
作者:
Lan, Tong-Tong;Song, Yang;Liu, Xiao-Han;Liu, Cui-Ping;Zhao, Hui-Chao;Han, Yi-Sa;Wang, Chu-Hui;Yang, Ning;Xu, Zhen;Tao, Meng;Li, Hui
Inositol hexaphosphate (IP6) is a phytochemical widely found in grains and legumes that plays an anti-cancer role. However, the mechanism underlying the inhibition of colorectal cancer metastasis by IP6 through host genes, gut microbiota, and their interactions remain elusive. In this study, 16S rRNA sequencing was used to study the effect of IP6 on gut microbiota in an orthotopic transplantation model of colorectal cancer mice. The transcriptome was used to study the changes of host genes in metastasis and the relationship with gut microbiota. The results showed that the gut microbiota composition of model mice was significantly different from that of normal mice. The beta diversity partly tended to return to the normal level after IP6 intervention. Especially, Lactobacillus helveticus and Lactococcus lactis were recovered after IP6-treated. Enrichment analysis showed that the enrichment score of the Cytokine-Cytokine receptor interaction signal pathway decreased after IP6 treatment compared to the model group. Further analysis of differentially expressed genes (DEGs) in this pathway showed that IP6 reduced the expression of the Tnfrsf1b gene related to the area of liver metastasis, and the Tnfrsf1b gene was negatively correlated with the relative abundance of Lactobacillus helveticus. Our results presented that host gene, microbiome and their interaction may serve as promising targets for the mechanism of IP6 intervention in colorectal cancer metastasis.
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DOI:
10.1158/1541-7786.mcr-10-0210
发表时间:
2011-12
期刊:
Molecular cancer research : MCR
影响因子:
--
作者:
Hamilton KE;Simmons JG;Ding S;Van Landeghem L;Lund PK
通讯作者:
Lund PK
DOI:
10.1136/bmj.c5504
发表时间:
2010-10-26
期刊:
BMJ (Clinical research ed.)
影响因子:
--
作者:
Kirkegaard H;Johnsen NF;Christensen J;Frederiksen K;Overvad K;Tjønneland A
通讯作者:
Tjønneland A
影响因子:
2.8
作者:
Eun, Chang Soo;Kim, Yong Seok;Park, Yoon Kyung
通讯作者:
Park, Yoon Kyung
影响因子:
3.8
作者:
Hackl C;Neumann P;Gerken M;Loss M;Klinkhammer-Schalke M;Schlitt HJ
通讯作者:
Schlitt HJ
影响因子:
4
作者:
Liu, Xiaohan;Liu, Cuiping;Song, Yang
通讯作者:
Song, Yang