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小儿急性淋巴细胞白血病患者脑脊液的蛋白质组学分析:一项初步研究。

Proteomic analysis of cerebrospinal fluid in pediatric acute lymphoblastic leukemia patients: a pilot study.

作者信息

Guo Linghong, Ren Honghong, Zeng Hao, Gong Yanqiu, Ma Xuelei

机构信息

Department of Biotherapy, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University and Collaborative Innovation Center of Biotherapy, Chengdu 610041, People's Republic of China,

West China School of Medicine, Sichuan University, Chengdu, People's Republic of China.

出版信息

Onco Targets Ther. 2019 May 17;12:3859-3868. doi: 10.2147/OTT.S193616. eCollection 2019.

Abstract

PURPOSE

Involvement of central nervous system in acute lymphoblastic leukemia (CNSL) remains one of the major causes of pediatric acute lymphoblastic leukemia (ALL) treatment failure. However, the current understanding of the pathological process of CNSL is still limited. This study aimed to better understand the protein expression in cerebrospinal fluid (CSF) of ALL and discover valuable prognostic biomarkers.

MATERIALS AND METHODS

CSF samples were obtained from ALL patients and healthy controls. Comparative proteomic profiling using label-free liquid chromatography-tandem mass spectrometry was performed to detect differentially expressed proteins.

RESULTS

In the present study, 51 differentially expressed proteins were found. Among them, two core clusters including ten proteins (TIMP1, LGALS3BP, A2M, FN1, AHSG, HRG, ITIH4, CF I, C2, and C4a) might be crucial for tumorigenesis and progression of ALL and can be potentially valuable indicators of CNSL.

CONCLUSION

These differentially expressed proteins of ALL children with central nervous system involvement and normal children may work as diagnostic and prognostic factors of ALL patients.

摘要

目的

中枢神经系统受累于急性淋巴细胞白血病(CNSL)仍是小儿急性淋巴细胞白血病(ALL)治疗失败的主要原因之一。然而,目前对CNSL病理过程的了解仍然有限。本研究旨在更好地了解ALL患者脑脊液(CSF)中的蛋白质表达情况,并发现有价值的预后生物标志物。

材料与方法

从ALL患者和健康对照中获取CSF样本。采用无标记液相色谱-串联质谱法进行比较蛋白质组分析,以检测差异表达的蛋白质。

结果

在本研究中,共发现51种差异表达的蛋白质。其中,两个核心簇包含十种蛋白质(TIMP1、LGALS3BP、A2M、FN1、AHSG、HRG、ITIH4、CF I、C2和C4a),可能对ALL的肿瘤发生和进展至关重要,并且可能是CNSL的潜在有价值指标。

结论

这些ALL患儿中枢神经系统受累组与正常儿童之间差异表达的蛋白质可能作为ALL患者的诊断和预后因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9ded/6527054/84825d74f3f3/ott-12-3859Fig1.jpg

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