TY - JOUR
T1 - Lactobacillus brevis T2102 suppresses the growth of colorectal cancer cells by activating SIRT1
AU - Harada, Gakuro
AU - Pattarawat, Pawat
AU - Ito, Kenji
AU - Matsumoto, Takashi
AU - Hasegawa, Takanori
AU - Katakura, Yoshinori
N1 - Funding Information:
The authors would like to thank N. Oshima (GE Healthcare) for her expert assistance with the IN Cell Analyzer 1000. This work was supported in part by JSPS KAKENHI Grant Numbers 15J07800 and 24580190 .
Publisher Copyright:
© 2016 Elsevier Ltd.
PY - 2016/5/1
Y1 - 2016/5/1
N2 - SIRT1 is known to have critical functions in the maintenance of homeostasis and cell survival, and it confers anti-ageing effects on cells and tissues. To identify novel foods and food ingredients with potential anti-ageing functions, a novel system for screening substances that activate the SIRT1 promoter in human colorectal cancer cells was established. We screened several lactic acid bacteria (LAB) and identified Lactobacillus brevis T2102 as a SIRT1-activating strain of LAB. T2102 inactivated β-catenin through SIRT1-mediated deacetylation and consequently suppressed the growth of the human colorectal cancer cell line DLD-1. Furthermore, T2102-induced degradation of β-catenin repressed transcription of the human telomerase reverse transcriptase (hTERT) gene, one of the target genes of β-catenin, which led to the induction of cellular senescence and concomitant growth suppression of DLD-1. These results indicate that SIRT1-activating T2102 might be a promising candidate for developing novel functional foods with anti-cancer properties.
AB - SIRT1 is known to have critical functions in the maintenance of homeostasis and cell survival, and it confers anti-ageing effects on cells and tissues. To identify novel foods and food ingredients with potential anti-ageing functions, a novel system for screening substances that activate the SIRT1 promoter in human colorectal cancer cells was established. We screened several lactic acid bacteria (LAB) and identified Lactobacillus brevis T2102 as a SIRT1-activating strain of LAB. T2102 inactivated β-catenin through SIRT1-mediated deacetylation and consequently suppressed the growth of the human colorectal cancer cell line DLD-1. Furthermore, T2102-induced degradation of β-catenin repressed transcription of the human telomerase reverse transcriptase (hTERT) gene, one of the target genes of β-catenin, which led to the induction of cellular senescence and concomitant growth suppression of DLD-1. These results indicate that SIRT1-activating T2102 might be a promising candidate for developing novel functional foods with anti-cancer properties.
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U2 - 10.1016/j.jff.2016.01.016
DO - 10.1016/j.jff.2016.01.016
M3 - Article
AN - SCOPUS:84961154479
SN - 1756-4646
VL - 23
SP - 444
EP - 452
JO - Journal of Functional Foods
JF - Journal of Functional Foods
ER -