Literature DB >> 12427485

Anti-proliferative and differentiation-inducing activities of the green tea catechin epigallocatechin-3-gallate (EGCG) on the human eosinophilic leukemia EoL-1 cell line.

H L Lung1, W K Ip, C K Wong, N K Mak, Z Y Chen, K N Leung.   

Abstract

A novel approach for the treatment of leukemia is the differentiation therapy in which immature leukemia cells are induced to attain a mature phenotype when exposed to differentiation inducers, either alone or in combinations with other chemotherapeutic or chemopreventive drugs. Over the past decade, numerous studies indicated that green tea catechins (GTC) could suppress the growth and induce apoptosis on a number of human cancer cell lines. However, the differentiation-inducing activity of GTC on human tumors remains poorly understood. In the present study, the effect of the major GTC epigallocatechin-3-gallate (EGCG) on the proliferation and differentiation of a human eosinophilc leukemic cell line, EoL-1, was examined. Our results showed that EGCG suppressed the proliferation of the EoL-1 cells in a dose-dependent manner, with an estimated IC(50) value of 31.5 microM. On the other hand, EGCG at a concentration of 40 microM could trigger the EoL-1 cells to undergo morphological differentiation into mature eosinophil-like cells. Using RT-PCR and flow cytometry, it was found that EGCG upregulated the gene and protein expression of two eosinophil-specific granule proteins, the major basic protein (MBP) and eosinophil peroxidase (EPO), in EoL-1 cells. Taken together, our findings suggest that EGCG can exhibit anti-leukemic activity on a human eosinophilic cell line EoL-1 by suppressing the proliferation and by inducing the differentiation of the leukemia cells.

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Year:  2002        PMID: 12427485     DOI: 10.1016/s0024-3205(02)02236-1

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  8 in total

1.  A derivative of epigallocatechin-3-gallate induces apoptosis via SHP-1-mediated suppression of BCR-ABL and STAT3 signalling in chronic myelogenous leukaemia.

Authors:  Ji Hoon Jung; Miyong Yun; Eun-Jeong Choo; Sun-Hee Kim; Myoung-Seok Jeong; Deok-Beom Jung; Hyemin Lee; Eun-Ok Kim; Nobuo Kato; Bonglee Kim; Sanjay K Srivastava; Kunihiro Kaihatsu; Sung-Hoon Kim
Journal:  Br J Pharmacol       Date:  2015-06-04       Impact factor: 8.739

2.  Modulation of MPP+ uptake by tea and some of its components in Caco-2 cells.

Authors:  R Monteiro; C Calhau; F Martel; A Faria; N Mateus; I Azevedo
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  2005-10-22       Impact factor: 3.000

3.  Differential alterations in metabolic pattern of the spliceosomal UsnRNAs during pre-malignant lung lesions induced by benzo(a)pyrene: modulation by tea polyphenols.

Authors:  Sugata Manna; Sarmistha Banerjee; Prosenjit Saha; Anup Roy; Sukta Das; Chinmay Kr Panda
Journal:  Mol Cell Biochem       Date:  2006-05-23       Impact factor: 3.396

4.  Protective effect of theaflavins on neuron against 6-hydroxydopamine-induced apoptosis in SH-SY5Y cells.

Authors:  Zihua Luo; Yan Zhao; Yuefei Wang; Xianqiang Yang; Baolu Zhao
Journal:  J Clin Biochem Nutr       Date:  2011-09-13       Impact factor: 3.114

5.  Molecular Cytotoxic Mechanisms of 1-(3,4,5-Trihydroxyphenyl)-dodecylbenzoate in Human Leukemia Cell Lines.

Authors:  M F Maioral; L D S Bubniak; M A L Marzarotto; A C R De Moraes; P Leal; R Nunes; R A Yunes; M C Santos-Silva
Journal:  Indian J Pharm Sci       Date:  2016 Jan-Feb       Impact factor: 0.975

6.  Established Human Cell Lines as Models to Study Anti-leukemic Effects of Flavonoids.

Authors:  Katrin Sak; Hele Everaus
Journal:  Curr Genomics       Date:  2017-02       Impact factor: 2.236

Review 7.  A Comprehensive Insight on the Health Benefits and Phytoconstituents of Camellia sinensis and Recent Approaches for Its Quality Control.

Authors:  Maram M Aboulwafa; Fadia S Youssef; Haidy A Gad; Ahmed E Altyar; Mohamed M Al-Azizi; Mohamed L Ashour
Journal:  Antioxidants (Basel)       Date:  2019-10-06

8.  Reducing FASN expression sensitizes acute myeloid leukemia cells to differentiation therapy.

Authors:  Magali Humbert; Kristina Seiler; Severin Mosimann; Vreni Rentsch; Katyayani Sharma; Amit V Pandey; Sharon L McKenna; Mario P Tschan
Journal:  Cell Death Differ       Date:  2021-03-19       Impact factor: 15.828

  8 in total

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