MicroRNA-139-5p regulates proliferation of hematopoietic progenitors and is repressed during BCR-ABL-mediated leukemogenesis.
@article{Choi2016MicroRNA1395pRP,
title={MicroRNA-139-5p regulates proliferation of hematopoietic progenitors and is repressed during BCR-ABL-mediated leukemogenesis.},
author={Jinwook Choi and Young‐Kook Kim and Kyungsoo Park and J J Nah and Sung-Soo Yoon and Dong-Wook Kim and V. Narry Kim and Rho Hyun Seong},
journal={Blood},
year={2016},
volume={128 17},
pages={
2117-2129
}
}MicroRNAs (miRNAs) have emerged as important regulators of the immune system. However, despite this prominence, our understanding of the function of miRNAs in the early hematopoietic stages is incomplete. In this study, we found that miR-139-5p negatively regulated the proliferation of hematopoietic stem cells and progenitor cells and that downregulation of miR-139-5p expression was associated with hematopoietic malignancy, such as chronic myeloid leukemia (CML). Knockdown of miR-139-5p…
20 Citations
miR-139-5p Regulates the Proliferation of Acute Promyelocytic Leukemia Cells by Targeting MNT
- Biology, MedicineJournal of oncology
- 2021
Evaluated the effects of miRNAs on leukocytosis during induction therapy of APL patients and identified that MNT was a target of miR-139-5p and significantly inhibited the proliferation, invasion, and migration function of NB4 cells through targeting MNT.
MiR-139-5p negatively regulates PMP22 to repress cell proliferation by targeting the NF-κB signaling pathway in gastric cancer
- Biology, ChemistryInternational journal of biological sciences
- 2020
The results showed overexpression of miR-139-5p significantly suppressed growth and prolifration in GC cells and inhibited tumor growth in nude mice xenografted with GC cells, suggesting that miR+5p and PMP22 might be important diagnostic or therapeutic targets for gastric cancer and other human diseases.
Tumor suppressor miR‐139‐5p targets Tspan3 and regulates the progression of acute myeloid leukemia through the PI3K/Akt pathway
- BiologyJournal of cellular biochemistry
- 2019
It is concluded that miR‐139‐5p suppressed the leukemogenesis in AML cells by targeting Tspan3 through inactivation of the PI3K/Akt pathway, providing a better understanding of AML progression.
MicroRNA 34a promotes ionizing radiation–induced DNA damage repair in murine hematopoietic stem cells
- BiologyFASEB journal : official publication of the Federation of American Societies for Experimental Biology
- 2019
It is demonstrated that miR‐34a contributes to promoting HSCs' survival after irradiation, which provides a promising approach for protecting HSC’s from IR.
MicroRNA in leukemia: Tumor suppressors and oncogenes with prognostic potential
- BiologyJournal of cellular physiology
- 2019
Various miRNAs as tumor suppressor and oncogene which could be introduced as therapeutic targets in treatment of leukemia are summarized.
Diagnostic, prognostic, and therapeutic significance of miR-139-5p in cancers.
- BiologyLife sciences
- 2020
MiRNA-142-3p increases radiosensitivity in human umbilical cord blood mononuclear cells by inhibiting the expression of CD133
- BiologyScientific Reports
- 2018
A novel regulation pathway in hematopoietic stem cells is elucidated and a potential therapeutic approach for blood system diseases therapy is suggested.
Alteration of microRNA profiles by a novel inhibitor of human La protein in HBV‐transformed human hepatoma cells
- BiologyJournal of medical virology
- 2018
Insight is provided into the molecular mechanism of the action of HBSC11 against HBV infection and will support the development of antiviral drugs targeting La protein.
Long noncoding RNA lnc-NAP sponges mmu-miR-139-5p to modulate Nanog functions in mouse ESCs and embryos
- BiologyRNA biology
- 2020
This work identifies mmu-miR-139-5p as a new regulator for Nanog by targeting Nanog 3′ untranslated region (UTR) to repress Nanog expression in mouse ESCs and embryos, and reveals a feed-forward regulatory loop of Nanog through the participation of lnc-NAP.
miR-139-5p protects septic mice with acute lung injury by inhibiting Toll-like receptor 4/Myeloid differentiation factor 88/Nuclear factor-&mac_kgr;B signaling pathway
- Biology, MedicineClinics
- 2021
OBJECTIVES: To investigate the role of miR-139-5p and the TLR4/MyD88/NF-κB signaling pathway in acute lung injury in septic mice. METHOD: A total of 140 healthy male SPF C57BL/6 mice were divided…
References
SHOWING 1-10 OF 51 REFERENCES
miR-139-5p controls translation in myeloid leukemia through EIF4G2
- BiologyOncogene
- 2016
Elevated miR-139-5p expression is associated with a favorable outcome in a cohort of 165 pediatric patients with AML, and mir-139 acts as a global tumor suppressor-miR in AML by controlling protein translation.
ICL-induced miR139-3p and miR199a-3p have opposite roles in hematopoietic cell expansion and leukemic transformation.
- BiologyBlood
- 2015
Interstrand crosslinks (ICLs) are toxic DNA lesions that cause severe genomic damage during replication, especially in Fanconi anemia pathway-deficient cells. This results in progressive bone marrow…
microRNA-29a induces aberrant self-renewal capacity in hematopoietic progenitors, biased myeloid development, and acute myeloid leukemia
- BiologyThe Journal of experimental medicine
- 2010
It is suggested that miR-29a initiates AML by converting myeloid progenitors into self-renewing LSC and regulates early hematopoiesis.
MicroRNA miR-125a controls hematopoietic stem cell number
- BiologyProceedings of the National Academy of Sciences
- 2010
It is reported that the microRNA processing enzyme Dicer is essential for stem cell persistence in vivo and a specific microRNA, miR-125a, controls the size of the stem cell population by regulating hematopoietic stem/progenitor cell (HSPC) apoptosis.
MicroRNA-125b expands hematopoietic stem cells and enriches for the lymphoid-balanced and lymphoid-biased subsets
- BiologyProceedings of the National Academy of Sciences
- 2010
Overexpression of miR-125b in mouse HSC enhances their function, demonstrated through serial transplantation of highly purified HSC, and enriches for the previously described Slamf1loCD34− lymphoid-balanced and the Slamf 1negCD34+ lymphoids-biased cell subsets within the multipotent HSC (CD34-KLS) fraction.
Regulation of RAP1B by miR-139 suppresses human colorectal carcinoma cell proliferation.
- BiologyThe international journal of biochemistry & cell biology
- 2012
Attenuation of miR-126 Activity Expands HSC In Vivo without Exhaustion
- BiologyCell stem cell
- 2012
MicroRNAs enriched in hematopoietic stem cells differentially regulate long-term hematopoietic output
- BiologyProceedings of the National Academy of Sciences
- 2010
An in vivo gain-of-function screen found that three of these miRNAs conferred a competitive advantage to engrafting hematopoietic cells, whereas other HSCMiRNAs attenuated production of blood cells.
The microRNA miR-139 suppresses metastasis and progression of hepatocellular carcinoma by down-regulating Rho-kinase 2.
- Biology, MedicineGastroenterology
- 2011
Overexpression of miR-139 in HCC cells significantly reduced cell migration and invasion in vitro and the incidence and severity of lung metastasis from orthotopic liver tumors in mice.
Attenuation of the beta-catenin/TCF4 complex in colorectal cancer cells induces several growth-suppressive microRNAs that target cancer promoting genes
- BiologyOncogene
- 2012
This study demonstrates that multiple miRNAs are upregulated as a consequence of forced attenuation of Wnt signaling in CRC cells, and some of these mi RNAs inhibit cell growth with concomitant suppression of several growth-stimulatory cancer-related genes.