HMGN1 plays a significant role in CRLF2 driven Down Syndrome leukemia and provides a potential therapeutic target in this high-risk cohort

Oncogene ◽  
2021 ◽  
Author(s):  
Elyse C. Page ◽  
Susan L. Heatley ◽  
Laura N. Eadie ◽  
Barbara J. McClure ◽  
Charles E. de Bock ◽  
...  
Oncotarget ◽  
2013 ◽  
Vol 4 (9) ◽  
pp. 1438-1448 ◽  
Author(s):  
Audrey Astori ◽  
Hanne Fredly ◽  
Thomas Aquinas Aloysius ◽  
Lars Bullinger ◽  
Véronique Mansat-De Mas ◽  
...  

2006 ◽  
Vol 70 (6) ◽  
pp. 2108-2115 ◽  
Author(s):  
Jun Fang ◽  
Quintin J. Quinones ◽  
Trevor L. Holman ◽  
Michael J. Morowitz ◽  
Qun Wang ◽  
...  

2020 ◽  
Vol 6 (6) ◽  
pp. 416-421
Author(s):  
David Van Ly ◽  
Duo Wang ◽  
Robert Max Conway ◽  
Michael Giblin ◽  
Sharron Liang ◽  
...  

Uveal melanoma (UM) is the commonest primary intraocular malignancy in adults. There is limited published data on lipid production in UM. Here, we describe the clinical, histological, immunohistochemical, and molecular findings in a ciliochoroidal melanoma with lipid production and expression of the enzyme HMG-CoA reductase. This case highlights an unusual UM tumour phenotype with a high-risk molecular metastatic profile and discusses tumour lipogenesis and activation of the mevalonate pathway as a potential therapeutic target in managing lipidised ciliochoroidal UM.


2021 ◽  
Author(s):  
Jiawei Sun ◽  
Dandan Song ◽  
yin song ◽  
Guoxiang Li ◽  
Pingping Meng ◽  
...  

Abstract BackgroundAlzheimer's disease (AD) is a progressive neurodegenerative disease characterized by complex pathobiological characteristics and still lacks accurate biomarkers in early diagnosis. Neuritin (NRN1) is a neurotrophic factor, which has active roles in neuronal plasticity and regeneration. Recent research suggests that Neuritin has been associated with loss of cognitive function, maybe a potential therapeutic target in AD. MethodsWe have clustered the upregulated miRNAs in AD and predicted the target miRNAs of Neuritin by bioinformatics analysis, found miR-188-5p may involve in the development of AD. ResultsIn the present study, we confirm the association between Neuritin and miR-188-5p expression in mice with AD. Besides, we provide evidence for the changes of cognition capacity, miR-188-5p and Neuritin levels in APP/PS1 mice. ConclusionOur results reveal a previously undefined mechanism that miR-188-5p plays a significant role in the development of AD by inhibiting the expression of target protein Neuritin.


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