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Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients

Green tea polyphenols (TEA) are known to exhibit antioxidative activity as well as tumor‐suppressing activity. In order to examine the tumor‐suppressing activity of TEA against adult T‐cell leukemia (ATL), we cultivated peripheral blood T lymphocytes of ATL patients (ATL PBLs), an HTLV‐I‐infected T‐...

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Autores principales: Li, Hong‐Chuan, Yashiki, Shinji, Sonoda, Junichiro, Lou, Hong, Ghosh, Subrata K., Byrnes, John J., Lema, Carolina, Fujiyoshi, Toshinobu, Karasuyama, Mitsuaki, Sonoda, Shunro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926221/
https://www.ncbi.nlm.nih.gov/pubmed/10744042
http://dx.doi.org/10.1111/j.1349-7006.2000.tb00857.x
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author Li, Hong‐Chuan
Yashiki, Shinji
Sonoda, Junichiro
Lou, Hong
Ghosh, Subrata K.
Byrnes, John J.
Lema, Carolina
Fujiyoshi, Toshinobu
Karasuyama, Mitsuaki
Sonoda, Shunro
author_facet Li, Hong‐Chuan
Yashiki, Shinji
Sonoda, Junichiro
Lou, Hong
Ghosh, Subrata K.
Byrnes, John J.
Lema, Carolina
Fujiyoshi, Toshinobu
Karasuyama, Mitsuaki
Sonoda, Shunro
author_sort Li, Hong‐Chuan
collection PubMed
description Green tea polyphenols (TEA) are known to exhibit antioxidative activity as well as tumor‐suppressing activity. In order to examine the tumor‐suppressing activity of TEA against adult T‐cell leukemia (ATL), we cultivated peripheral blood T lymphocytes of ATL patients (ATL PBLs), an HTLV‐I‐infected T‐cell line (KODV) and healthy controls (normal PBLs) for 3 days in the presence of TEA and its main constituent, epigallocatechin‐3‐gallate (EGCg), to measure cell proliferation and apoptosis, and to quantitate mRNAs of HTLV‐I pX and β‐actin genes of the cultured cells. Growth of ATL PBLs was significantly inhibited by 9–27 μg/ml of TEA and EGCg, in contrast to minimal growth inhibition of T cells of normal PBLs. Inhibition of KODV was intermediate between ATL PBLs and normal PBLs. The ATL PBLs and KODV treated with 27 μg/ml of either TEA or EGCg induced apoptotic DNA fragmentation, producing terminal deoxynucleotidyl transferase‐mediated dUTP‐biotin nick end labeling (TUNEL)‐positive cells, while the normal PBLs treated with the same concentration of TEA or EGCg produced a negligibly small number of TUNEL‐positive cells, in which apoptotic DNA fragmentation was not detectable. Expression of HTLV‐I pX mRNA was suppressed more than 90% in ATL PBLs by treatment with 3–27 μg/ml of either TEA or EGCg, while expression of β‐actin mRNA was much less suppressed by treatment with the same concentration of TEA or EGCg. These results indicate that TEA and EGCg inhibit growth of ATL PBLs, as well as HTLV‐I‐infected T‐cells, by suppressing HTLV‐I pX gene expression and inducing apoptotic cell death.
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spelling pubmed-59262212018-05-11 Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients Li, Hong‐Chuan Yashiki, Shinji Sonoda, Junichiro Lou, Hong Ghosh, Subrata K. Byrnes, John J. Lema, Carolina Fujiyoshi, Toshinobu Karasuyama, Mitsuaki Sonoda, Shunro Jpn J Cancer Res Article Green tea polyphenols (TEA) are known to exhibit antioxidative activity as well as tumor‐suppressing activity. In order to examine the tumor‐suppressing activity of TEA against adult T‐cell leukemia (ATL), we cultivated peripheral blood T lymphocytes of ATL patients (ATL PBLs), an HTLV‐I‐infected T‐cell line (KODV) and healthy controls (normal PBLs) for 3 days in the presence of TEA and its main constituent, epigallocatechin‐3‐gallate (EGCg), to measure cell proliferation and apoptosis, and to quantitate mRNAs of HTLV‐I pX and β‐actin genes of the cultured cells. Growth of ATL PBLs was significantly inhibited by 9–27 μg/ml of TEA and EGCg, in contrast to minimal growth inhibition of T cells of normal PBLs. Inhibition of KODV was intermediate between ATL PBLs and normal PBLs. The ATL PBLs and KODV treated with 27 μg/ml of either TEA or EGCg induced apoptotic DNA fragmentation, producing terminal deoxynucleotidyl transferase‐mediated dUTP‐biotin nick end labeling (TUNEL)‐positive cells, while the normal PBLs treated with the same concentration of TEA or EGCg produced a negligibly small number of TUNEL‐positive cells, in which apoptotic DNA fragmentation was not detectable. Expression of HTLV‐I pX mRNA was suppressed more than 90% in ATL PBLs by treatment with 3–27 μg/ml of either TEA or EGCg, while expression of β‐actin mRNA was much less suppressed by treatment with the same concentration of TEA or EGCg. These results indicate that TEA and EGCg inhibit growth of ATL PBLs, as well as HTLV‐I‐infected T‐cells, by suppressing HTLV‐I pX gene expression and inducing apoptotic cell death. Blackwell Publishing Ltd 2000-01 /pmc/articles/PMC5926221/ /pubmed/10744042 http://dx.doi.org/10.1111/j.1349-7006.2000.tb00857.x Text en
spellingShingle Article
Li, Hong‐Chuan
Yashiki, Shinji
Sonoda, Junichiro
Lou, Hong
Ghosh, Subrata K.
Byrnes, John J.
Lema, Carolina
Fujiyoshi, Toshinobu
Karasuyama, Mitsuaki
Sonoda, Shunro
Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients
title Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients
title_full Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients
title_fullStr Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients
title_full_unstemmed Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients
title_short Green Tea Polyphenols Induce Apoptosis in vitro in Peripheral Blood T Lymphocytes of Adult T‐Cell Leukemia Patients
title_sort green tea polyphenols induce apoptosis in vitro in peripheral blood t lymphocytes of adult t‐cell leukemia patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5926221/
https://www.ncbi.nlm.nih.gov/pubmed/10744042
http://dx.doi.org/10.1111/j.1349-7006.2000.tb00857.x
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