CLLU1 作为慢性淋巴性白血病的新兴生物标记物。

IF 3.4 3区 生物学 Q3 CELL BIOLOGY
Human Cell Pub Date : 2024-05-01 Epub Date: 2024-03-20 DOI:10.1007/s13577-024-01051-4
Chunmeng Rong, Chenhao Liang, Jinze Shen, Yuhua Zhang, Qurui Wang, Fang Yang, Yalu Chen, Yuqing Luo, Meier Gu, Panpan Gao, Yongming Xia, Shiwei Duan
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引用次数: 0

摘要

CLLU1是一种与慢性淋巴性白血病(CLL)相关的疾病特异性基因,位于染色体12q22上。以前的研究认为 CLLU1 是一种非编码 RNA;但最近的研究发现,其编码序列区域有可能编码一种类似于白细胞介素-4 的短肽。值得注意的是,在所有血液癌症中,只有慢性淋巴性白血病中检测到 CLLU1 的异常高表达。CLLU1 的高表达通常预示着更多的恶性病理特征和对患者不利的预后。重要的是,CLLU1 的表达水平不受时间推移或治疗干预的影响,因此成为一种新的预后标志物。本文从CLL预后和临床应用的角度全面总结了CLLU1的相关研究成果,旨在为该领域的后续理论和临床研究提供指导。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

CLLU1 as an emerging biomarker in chronic lymphoid leukemia.

CLLU1 as an emerging biomarker in chronic lymphoid leukemia.

CLLU1, a disease-specific gene associated with chronic lymphoid leukemia (CLL), is located on chromosome 12q22. Previous studies considered CLLU1 to be a non-coding RNA; however, recent research has discovered that its coding sequence region possesses the potential to encode a short peptide similar to interleukin-4. Remarkably, abnormally elevated expression of CLLU1 has only been detected in chronic lymphoid leukemia among all hematological cancers. High CLLU1 expression often indicates more malignant pathological features and an unfavorable prognosis for patients. Importantly, the expression level of CLLU1 remains unaffected by the passage of time or therapeutic interventions, thus rendering it a novel prognostic marker. This article provides a comprehensive summary of relevant research findings on CLLU1 in the context of CLL prognosis and clinical applications, aiming to guide subsequent theoretical and clinical investigations in this field.

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来源期刊
Human Cell
Human Cell CELL BIOLOGY-
CiteScore
5.90
自引率
2.30%
发文量
176
审稿时长
4.5 months
期刊介绍: Human Cell is the official English-language journal of the Japan Human Cell Society. The journal serves as a forum for international research on all aspects of the human cell, encompassing not only cell biology but also pathology, cytology, and oncology, including clinical oncology. Embryonic stem cells derived from animals, regenerative medicine using animal cells, and experimental animal models with implications for human diseases are covered as well. Submissions in any of the following categories will be considered: Research Articles, Cell Lines, Rapid Communications, Reviews, and Letters to the Editor. A brief clinical case report focusing on cellular responses to pathological insults in human studies may also be submitted as a Letter to the Editor in a concise and short format. Not only basic scientists but also gynecologists, oncologists, and other clinical scientists are welcome to submit work expressing new ideas or research using human cells.
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