The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation

碩士 === 長庚大學 === 基礎醫學研究所 === 93 === Human myelogenous leukemia K562 cells were induced to undergo erythroid differentiation by treatment with hydroxyurea (HU). However, the cellular mechanism by which HU exert its effects on tumor cells, leading to inhibition of cell growth and induction of different...

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Main Authors: Heui Chung Chu, 朱惠君
Other Authors: Yat Ming Yung
Format: Others
Language:en_US
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/50157673613118504268
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spelling ndltd-TW-093CGU003250832016-06-08T04:13:35Z http://ndltd.ncl.edu.tw/handle/50157673613118504268 The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation 在羥基尿素誘發慢性骨髓性血癌K562細胞分化中核仁磷酸蛋白nucleophosmin/B23的生物角色 Heui Chung Chu 朱惠君 碩士 長庚大學 基礎醫學研究所 93 Human myelogenous leukemia K562 cells were induced to undergo erythroid differentiation by treatment with hydroxyurea (HU). However, the cellular mechanism by which HU exert its effects on tumor cells, leading to inhibition of cell growth and induction of differentiation markers, are largely unknown. This study examined (1) the role of different mitogen-activated protein kinase signal transduction pathways in HU-induced erythroid differentiation of K562 cells. (2) The mechanism of down regulation of nucleophosmin (NPM)/ B23 promoter during HU- induced erythroid differentiation. (3) To study the biological role of B23 in K562 cell differentiation induced by HU. Here, we show that the relationship between NPM / B23 and interferon regulatory factor- 1 (IRF-1), mediates down-stream target gene activation that during HU-induced erythroid differentiation of K562 cells. Thus, this study indicate effects of HU on down regulation of NPM/ B23 may be caused by inhibition of histone deacetylase 1(HDAC 1). Yat Ming Yung 翁一鳴 2005 學位論文 ; thesis 66 en_US
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description 碩士 === 長庚大學 === 基礎醫學研究所 === 93 === Human myelogenous leukemia K562 cells were induced to undergo erythroid differentiation by treatment with hydroxyurea (HU). However, the cellular mechanism by which HU exert its effects on tumor cells, leading to inhibition of cell growth and induction of differentiation markers, are largely unknown. This study examined (1) the role of different mitogen-activated protein kinase signal transduction pathways in HU-induced erythroid differentiation of K562 cells. (2) The mechanism of down regulation of nucleophosmin (NPM)/ B23 promoter during HU- induced erythroid differentiation. (3) To study the biological role of B23 in K562 cell differentiation induced by HU. Here, we show that the relationship between NPM / B23 and interferon regulatory factor- 1 (IRF-1), mediates down-stream target gene activation that during HU-induced erythroid differentiation of K562 cells. Thus, this study indicate effects of HU on down regulation of NPM/ B23 may be caused by inhibition of histone deacetylase 1(HDAC 1).
author2 Yat Ming Yung
author_facet Yat Ming Yung
Heui Chung Chu
朱惠君
author Heui Chung Chu
朱惠君
spellingShingle Heui Chung Chu
朱惠君
The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation
author_sort Heui Chung Chu
title The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation
title_short The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation
title_full The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation
title_fullStr The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation
title_full_unstemmed The biological role of Nucleophosmin/ B23 in hydroxyurea- induced K562 cell differentiation
title_sort biological role of nucleophosmin/ b23 in hydroxyurea- induced k562 cell differentiation
publishDate 2005
url http://ndltd.ncl.edu.tw/handle/50157673613118504268
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