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微小 RNA 作为 T 细胞急性淋巴细胞白血病免疫反应的调节剂。

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

机构信息

Department of Molecular Medicine, Sapienza University of Rome, 00161 Roma, Italy.

Department of Experimental Medicine, Sapienza University of Rome, 00161 Roma, Italy.

出版信息

Int J Mol Sci. 2022 Jan 13;23(2):829. doi: 10.3390/ijms23020829.


DOI:10.3390/ijms23020829
PMID:35055013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8776227/
Abstract

Acute lymphoblastic leukaemia (ALL) is an aggressive haematological tumour driven by the malignant transformation and expansion of B-cell (B-ALL) or T-cell (T-ALL) progenitors. The evolution of T-ALL pathogenesis encompasses different master developmental pathways, including the main role played by Notch in cell fate choices during tissue differentiation. Recently, a growing body of evidence has highlighted epigenetic changes, particularly the altered expression of microRNAs (miRNAs), as a critical molecular mechanism to sustain T-ALL. The immune response is emerging as key factor in the complex multistep process of cancer but the role of miRNAs in anti-leukaemia response remains elusive. In this review we analyse the available literature on miRNAs as tuners of the immune response in T-ALL, focusing on their role in Natural Killer, T, T-regulatory and Myeloid-derived suppressor cells. A better understanding of this molecular crosstalk may provide the basis for the development of potential immunotherapeutic strategies in the leukemia field.

摘要

急性淋巴细胞白血病(ALL)是一种侵袭性血液系统肿瘤,由 B 细胞(B-ALL)或 T 细胞(T-ALL)前体细胞的恶性转化和扩增驱动。T-ALL 发病机制的演变包含不同的主要发育途径,包括 Notch 在组织分化过程中细胞命运选择中的主要作用。最近,越来越多的证据强调了表观遗传变化,特别是 microRNAs(miRNAs)的表达改变,作为维持 T-ALL 的关键分子机制。免疫反应是癌症复杂多步骤过程中的关键因素,但 miRNA 在抗白血病反应中的作用仍不清楚。在这篇综述中,我们分析了 miRNA 作为 T-ALL 中免疫反应调节剂的现有文献,重点关注它们在自然杀伤细胞、T 细胞、T 调节细胞和髓源抑制细胞中的作用。对这种分子串扰的更好理解可能为白血病领域潜在免疫治疗策略的发展提供基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ef/8776227/a71a0134b641/ijms-23-00829-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ef/8776227/a71a0134b641/ijms-23-00829-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/06ef/8776227/a71a0134b641/ijms-23-00829-g001.jpg

相似文献

[1]
MicroRNAs as Modulators of the Immune Response in T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2022-1-13

[2]
Myeloid-derived suppressor cells and regulatory T cells share common immunoregulatory pathways-related microRNAs that are dysregulated by acute lymphoblastic leukemia and chemotherapy.

Hum Immunol. 2021-1

[3]
The NF-κB1/p50 Subunit Influences the Notch/IL-6-Driven Expansion of Myeloid-Derived Suppressor Cells in Murine T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2024-9-13

[4]
The impact of microRNAs on myeloid-derived suppressor cells in cancer.

Hum Immunol. 2021-9

[5]
DNA methylation-mediated silencing of microRNA-204 enhances T cell acute lymphoblastic leukemia by up-regulating MMP-2 and MMP-9 via NF-κB.

J Cell Mol Med. 2021-3

[6]
Notch and NF-kB signaling pathways regulate miR-223/FBXW7 axis in T-cell acute lymphoblastic leukemia.

Leukemia. 2014-4-14

[7]
MiR-7 Functions as a Tumor Suppressor by Targeting the Oncogenes TAL1 in T-Cell Acute Lymphoblastic Leukemia.

Technol Cancer Res Treat. 2020

[8]
MicroRNA-128-3p is a novel oncomiR targeting PHF6 in T-cell acute lymphoblastic leukemia.

Haematologica. 2014-8

[9]
T-cell acute lymphoblastic leukemia from miRNA perspective: Basic concepts, experimental approaches, and potential biomarkers.

Blood Rev. 2018-4-12

[10]
NF-κB1 Regulates Immune Environment and Outcome of Notch-Dependent T-Cell Acute Lymphoblastic Leukemia.

Front Immunol. 2020-4-3

引用本文的文献

[1]
Notch Inhibitors and BH3 Mimetics in T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2024-11-29

[2]
The NF-κB1/p50 Subunit Influences the Notch/IL-6-Driven Expansion of Myeloid-Derived Suppressor Cells in Murine T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2024-9-13

[3]
Notch3-regulated microRNAs impair CXCR4-dependent maturation of thymocytes allowing maintenance and progression of T-ALL.

Oncogene. 2024-8

[4]
Role of microRNAs in Immune Regulation with Translational and Clinical Applications.

Int J Mol Sci. 2024-2-5

[5]
Role of microRNAs in B-Cell Compartment: Development, Proliferation and Hematological Diseases.

Biomedicines. 2022-8-18

[6]
Implication of microRNAs in Carcinogenesis with Emphasis on Hematological Malignancies and Clinical Translation.

Int J Mol Sci. 2022-5-23

本文引用的文献

[1]
Targeting Notch to Maximize Chemotherapeutic Benefits: Rationale, Advanced Strategies, and Future Perspectives.

Cancers (Basel). 2021-10-12

[2]
Cell-intrinsic and -extrinsic roles of miRNAs in regulating T cell immunity.

Immunol Rev. 2021-11

[3]
Activated natural killer cells predict poor clinical prognosis in high-risk B- and T-cell acute lymphoblastic leukemia.

Blood. 2021-10-21

[4]
MicroRNA as a Prognostic and Diagnostic Marker in T-Cell Acute Lymphoblastic Leukemia.

Int J Mol Sci. 2021-5-18

[5]
The impact of microRNAs on myeloid-derived suppressor cells in cancer.

Hum Immunol. 2021-9

[6]
B-cell acute lymphoblastic leukemia-related microRNAs: uncovering their diverse and special roles.

Am J Cancer Res. 2021-4-15

[7]
MicroRNA-325 inhibits the proliferation and induces the apoptosis of T cell acute lymphoblastic leukemia cells in a BAG2-dependent manner.

Exp Ther Med. 2021-6

[8]
Mechanisms of Immune Evasion in Acute Lymphoblastic Leukemia.

Cancers (Basel). 2021-3-26

[9]
Exosomal microRNA panels as biomarkers for hematological malignancies.

Curr Probl Cancer. 2021-10

[10]
The depletion of Circ-PRKDC enhances autophagy and apoptosis in T-cell acute lymphoblastic leukemia via microRNA-653-5p/Reelin mediation of the PI3K/AKT/mTOR signaling pathway.

Kaohsiung J Med Sci. 2021-5

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