TY - JOUR
T1 - Modulation of telomerase activity in cancer cells by dietary compounds
T2 - A review
AU - Eitsuka, Takahiro
AU - Nakagawa, Kiyotaka
AU - Kato, Shunji
AU - Ito, Junya
AU - Otoki, Yurika
AU - Takasu, Soo
AU - Shimizu, Naoki
AU - Takahashi, Takumi
AU - Miyazawa, Teruo
N1 - Funding Information:
Some of the work presented in this review was partly supported by a grant from The Tojuro Iijima Foundation for Food Science and Technology, and JSPS KAKENHI Grant Numbers 19780105, 25450185, 17K07803.
Publisher Copyright:
© 2018 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2018/2/6
Y1 - 2018/2/6
N2 - Telomerase is expressed in ~90% of human cancer cell lines and tumor specimens, whereas its enzymatic activity is not detectable in most human somatic cells, suggesting that telomerase represents a highly attractive target for selective cancer treatment. Accordingly, various classes of telomerase inhibitors have been screened and developed in recent years. We and other researchers have successfully found that some dietary compounds can modulate telomerase activity in cancer cells. Telomerase inhibitors derived from food are subdivided into two groups: one group directly blocks the enzymatic activity of telomerase (e.g., catechin and sulfoquinovosyldiacylglycerol), and the other downregulates the expression of human telomerase reverse transcriptase (hTERT), the catalytic subunit of human telomerase, via signal transduction pathways (e.g., retinoic acid and tocotrienol). In contrast, a few dietary components, including genistein and glycated lipid, induce cellular telomerase activity in several types of cancer cells, suggesting that they may be involved in tumor progression. This review summarizes the current knowledge about the effects of dietary factors on telomerase regulation in cancer cells and discusses their molecular mechanisms of action.
AB - Telomerase is expressed in ~90% of human cancer cell lines and tumor specimens, whereas its enzymatic activity is not detectable in most human somatic cells, suggesting that telomerase represents a highly attractive target for selective cancer treatment. Accordingly, various classes of telomerase inhibitors have been screened and developed in recent years. We and other researchers have successfully found that some dietary compounds can modulate telomerase activity in cancer cells. Telomerase inhibitors derived from food are subdivided into two groups: one group directly blocks the enzymatic activity of telomerase (e.g., catechin and sulfoquinovosyldiacylglycerol), and the other downregulates the expression of human telomerase reverse transcriptase (hTERT), the catalytic subunit of human telomerase, via signal transduction pathways (e.g., retinoic acid and tocotrienol). In contrast, a few dietary components, including genistein and glycated lipid, induce cellular telomerase activity in several types of cancer cells, suggesting that they may be involved in tumor progression. This review summarizes the current knowledge about the effects of dietary factors on telomerase regulation in cancer cells and discusses their molecular mechanisms of action.
KW - Cancer
KW - Dietary compound
KW - HTERT
KW - Telomerase
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U2 - 10.3390/ijms19020478
DO - 10.3390/ijms19020478
M3 - Review article
C2 - 29415465
AN - SCOPUS:85041548332
SN - 1422-0067
VL - 19
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
IS - 2
M1 - 478
ER -