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从 miRNA 角度看 T 细胞急性淋巴细胞白血病:基本概念、实验方法和潜在的生物标志物。

T-cell acute lymphoblastic leukemia from miRNA perspective: Basic concepts, experimental approaches, and potential biomarkers.

机构信息

Institute of Human Genetics, Polish Academy of Sciences, Poznań, Poland.

出版信息

Blood Rev. 2018 Nov;32(6):457-472. doi: 10.1016/j.blre.2018.04.003. Epub 2018 Apr 12.


DOI:10.1016/j.blre.2018.04.003
PMID:29703513
Abstract

T-cell acute lymphoblastic leukemia (T-ALL) is a rare, aggressive and heterogeneous malignancy originating from T-cell precursors. The mechanisms of T-ALL pathogenesis related to non-protein coding part of the genome are currently intensively studied. miRNAs are short, non-coding molecules acting as negative regulators of gene expression which shape phenotype of cells in a complex and context-specific manner. miRNAs may act as oncogenes or tumor suppressors; several miRNAs have been related to drug resistance and treatment response in various malignancies. Here we present the review of the state-of-the-art knowledge on the role of miRNAs in T-ALL pathogenesis, with detailed overview of the studies reporting on miRNAs with oncogenic and tumor suppressor potential. We discuss whether miRNAs might be considered candidate biomarkers of prognosis in T-ALL and leukemia subtype-specific markers. We also describe experimental approaches and a typical workflow applied in research on the involvement of miRNAs in oncogenesis.

摘要

T 细胞急性淋巴细胞白血病(T-ALL)是一种罕见的、侵袭性的和异质性的恶性肿瘤,起源于 T 细胞前体。目前正在深入研究与基因组非蛋白编码部分相关的 T-ALL 发病机制。miRNA 是短的非编码分子,作为基因表达的负调节剂,以复杂和特定于上下文的方式塑造细胞的表型。miRNA 可以作为癌基因或肿瘤抑制因子;在各种恶性肿瘤中,已经有几种 miRNA 与耐药性和治疗反应有关。在这里,我们介绍了 miRNA 在 T-ALL 发病机制中的作用的最新知识,详细介绍了报告具有致癌和肿瘤抑制潜力的 miRNA 的研究。我们讨论了 miRNA 是否可以被认为是 T-ALL 预后的候选生物标志物和白血病亚型特异性标志物。我们还描述了应用于 miRNA 参与致癌作用研究的实验方法和典型工作流程。

相似文献

[1]
T-cell acute lymphoblastic leukemia from miRNA perspective: Basic concepts, experimental approaches, and potential biomarkers.

Blood Rev. 2018-4-12

[2]
MicroRNAs and their involvement in T-ALL: A brief overview.

Adv Biol Regul. 2019-12

[3]
microRNAs regulate TAL1 expression in T-cell acute lymphoblastic leukemia.

Oncotarget. 2016-2-16

[4]
Comprehensive Investigation of miRNome Identifies Novel Candidate miRNA-mRNA Interactions Implicated in T-Cell Acute Lymphoblastic Leukemia.

Neoplasia. 2019-2-11

[5]
A cooperative microRNA-tumor suppressor gene network in acute T-cell lymphoblastic leukemia (T-ALL).

Nat Genet. 2011-6-5

[6]
Characterization of a set of tumor suppressor microRNAs in T cell acute lymphoblastic leukemia.

Sci Signal. 2014-11-18

[7]
Identification of Endogenous Control miRNAs for RT-qPCR in T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2018-9-20

[8]
New insight into the role of miRNAs in leukemia.

Sci China C Life Sci. 2009-3

[9]
OncomiR or antioncomiR: Role of miRNAs in Acute Myeloid Leukemia.

Leuk Lymphoma. 2018-9-6

[10]
Cooperative control of tumor suppressor genes by a network of oncogenic microRNAs.

Cell Cycle. 2011-9-1

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[2]
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Cancer Cell Int. 2025-3-19

[3]
CD99 tumor associated antigen is a potential target for antibody therapy of T-cell acute lymphoblastic leukemia.

Explor Target Antitumor Ther. 2024

[4]
The Effects of Resveratrol, Gallic Acid, and Piperine on the Expression of miR-17, miR-92b, miR-181a, miR-222, BAX, BCL-2, MCL-1, WT1, c-Kit, and CEBPA in Human Acute Myeloid Leukemia Cells and Their Roles in Apoptosis.

Biochem Genet. 2024-8

[5]
Diagnostic significance of dysregulated miRNAs in T-cell malignancies and their metabolic roles.

Front Oncol. 2023-8-10

[6]
MicroRNAs as Modulators of the Immune Response in T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2022-1-13

[7]
MicroRNA as a Prognostic and Diagnostic Marker in T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2021-5-18

[8]
Comprehensive Overview of Gene Rearrangements in Childhood T-Cell Acute Lymphoblastic Leukaemia.

Int J Mol Sci. 2021-1-15

[9]
Influence of variants of the , , and genes on susceptibility to acute lymphoblastic leukemia in an admixed population from the brazilian amazon.

Am J Transl Res. 2020-12-15

[10]
miR-22-3p Negatively Affects Tumor Progression in T-Cell Acute Lymphoblastic Leukemia.

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