CLLU1 as an emerging biomarker in chronic lymphoid leukemia.

Biomarker CLLU1 Chronic lymphoid leukemia Non-coding RNA Prognosis

Journal

Human cell
ISSN: 1749-0774
Titre abrégé: Hum Cell
Pays: Japan
ID NLM: 8912329

Informations de publication

Date de publication:
20 Mar 2024
Historique:
received: 18 11 2023
accepted: 26 02 2024
medline: 20 3 2024
pubmed: 20 3 2024
entrez: 20 3 2024
Statut: aheadofprint

Résumé

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.

Identifiants

pubmed: 38507118
doi: 10.1007/s13577-024-01051-4
pii: 10.1007/s13577-024-01051-4
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : the Natural Science Foundation project of Ningbo Science and Technology Bureau
ID : 2022J040

Informations de copyright

© 2024. The Author(s) under exclusive licence to Japan Human Cell Society.

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Auteurs

Chunmeng Rong (C)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China.

Chenhao Liang (C)

Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, China.

Jinze Shen (J)

Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, China.

Yuhua Zhang (Y)

Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, China.

Qurui Wang (Q)

Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, China.

Fang Yang (F)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China.

Yalu Chen (Y)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China.

Yuqing Luo (Y)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China.

Meier Gu (M)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China.

Panpan Gao (P)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China.

Yongming Xia (Y)

Department of Hematology, Yuyao People's Hospital of Zhejiang Province, Ningbo, Zhejiang, China. yy_xyzlnk@163.com.

Shiwei Duan (S)

Key Laboratory of Novel Targets and Drug Study for Neural Repair of Zhejiang Province, School of Medicine, Hangzhou City University, Hangzhou, Zhejiang, China. duansw@hzcu.edu.cn.

Classifications MeSH