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WWP1在慢性淋巴细胞白血病中的异常表达及临床意义

OBJECTIVE: This study aims to investigate the expression of E3 ubiquitin-ligase(WWP1)in chronic lymphocytic leukemia(CLL)patients and analyze its correlation with clinical prognostic indicators(TP53, CD38, IGHV mutation)and its prognostic value. METHODS: A total of 48 CLL patients and 9 age-matched...

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Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial office of Chinese Journal of Hematology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595860/
https://www.ncbi.nlm.nih.gov/pubmed/33113605
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.09.006
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collection PubMed
description OBJECTIVE: This study aims to investigate the expression of E3 ubiquitin-ligase(WWP1)in chronic lymphocytic leukemia(CLL)patients and analyze its correlation with clinical prognostic indicators(TP53, CD38, IGHV mutation)and its prognostic value. METHODS: A total of 48 CLL patients and 9 age-matched normal subjects were enrolled in the study. The WWP1 expression was detected by SYBR Green-based real-time PCR, and the clinical relationship was analyzed by GraphPad Prism software. RESULTS: The WWP1 median expression was 0.007(95% CI 0.005–0.010)in the normal control group and 0.031(95% CI 0.019–0.044)in the CLL group(P<0.001). A sub-groups analysis implicated a statistically significant result(P=0.022), showing that the median time from a relatively high and low transcription level of WWP1 to the first treatment was 24 months and 35 months, respectively. Positive CD38 and ZAP-70 expressions were associated with a higher WWP1 expression(P=0.012 and 0.029, respectively). CONCLUSION: An abnormal WWP1 mRNA expression was found in CLL patients with significant correlation with ZAP-70 and CD38 expressions, and WWP1 may become a new supplement of CLL prognostic markers.
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spelling pubmed-75958602020-10-30 WWP1在慢性淋巴细胞白血病中的异常表达及临床意义 Zhonghua Xue Ye Xue Za Zhi 论著 OBJECTIVE: This study aims to investigate the expression of E3 ubiquitin-ligase(WWP1)in chronic lymphocytic leukemia(CLL)patients and analyze its correlation with clinical prognostic indicators(TP53, CD38, IGHV mutation)and its prognostic value. METHODS: A total of 48 CLL patients and 9 age-matched normal subjects were enrolled in the study. The WWP1 expression was detected by SYBR Green-based real-time PCR, and the clinical relationship was analyzed by GraphPad Prism software. RESULTS: The WWP1 median expression was 0.007(95% CI 0.005–0.010)in the normal control group and 0.031(95% CI 0.019–0.044)in the CLL group(P<0.001). A sub-groups analysis implicated a statistically significant result(P=0.022), showing that the median time from a relatively high and low transcription level of WWP1 to the first treatment was 24 months and 35 months, respectively. Positive CD38 and ZAP-70 expressions were associated with a higher WWP1 expression(P=0.012 and 0.029, respectively). CONCLUSION: An abnormal WWP1 mRNA expression was found in CLL patients with significant correlation with ZAP-70 and CD38 expressions, and WWP1 may become a new supplement of CLL prognostic markers. Editorial office of Chinese Journal of Hematology 2020-09 /pmc/articles/PMC7595860/ /pubmed/33113605 http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.09.006 Text en 2020年版权归中华医学会所有 http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution 3.0 License (CC-BY-NC). The Copyright own by Publisher. Without authorization, shall not reprint, except this publication article, shall not use this publication format design. Unless otherwise stated, all articles published in this journal do not represent the views of the Chinese Medical Association or the editorial board of this journal.
spellingShingle 论著
WWP1在慢性淋巴细胞白血病中的异常表达及临床意义
title WWP1在慢性淋巴细胞白血病中的异常表达及临床意义
title_full WWP1在慢性淋巴细胞白血病中的异常表达及临床意义
title_fullStr WWP1在慢性淋巴细胞白血病中的异常表达及临床意义
title_full_unstemmed WWP1在慢性淋巴细胞白血病中的异常表达及临床意义
title_short WWP1在慢性淋巴细胞白血病中的异常表达及临床意义
title_sort wwp1在慢性淋巴细胞白血病中的异常表达及临床意义
topic 论著
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7595860/
https://www.ncbi.nlm.nih.gov/pubmed/33113605
http://dx.doi.org/10.3760/cma.j.issn.0253-2727.2020.09.006
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