A Signature of Differentially Expressed Micrornas in Lymphoblastoid Cells from Shwachman-Diamond Syndrome Patients Indicates Possible Molecular Targets for Mirna Therapeutics

小RNA 生物 癌症研究 表型 髓样 基因 分子生物学 遗传学
作者
Jessica Gasparello,Chiara Papi,Giulia Breveglieri,Elisabetta D’Aversa,Valentino Bezzerri,Giovanna D’Amico,Marco Cipolli,Roberto Gambari,Monica Borgatti,Alessia Finotti
出处
期刊:Blood [Elsevier BV]
卷期号:134 (Supplement_1): 2504-2504 被引量:1
标识
DOI:10.1182/blood-2019-128607
摘要

In the Shwachman-Diamond syndrome (SDS), mutations of the gene encoding for the SBDS protein causes several hematological disorders, including neutropenia and myelodysplastic syndrome (MDS), with high risk of acute myeloid leukemia (AML).MicroRNAs (miRNAs) are small noncoding RNAs regulating gene expression by sequence-selective targeting of mRNAs, leading to translational repression or mRNA degradation. Low miRNA expression is associated with the accumulation of target mRNAs; high miRNA content causes low expression of target mRNAs. In almost all hematological disorders microRNAs were found dysregulated, and often these alterations of miRNAlevels are associated with the phenotype of the disease and tumor onset and progression. In order to verify possible involvement of microRNA in the SDS phenotype, we determined whether the microRNA pattern differentiate Lymphoblastoid Cell Cultures (LCC) derived from SDS patients from healthy subjects-derived LCC. To this aim Next Generation Sequencing (NGS) was performed using Illumina NextSeq500 platform and a signature of 11 up-regulated (hsa-miR-1260b, hsa-miR-1270, hsa-miR-1278, hsa-miR-1294, hsa-miR-296-5p, hsa-miR-34a-3p, hsa-miR-423-3p, hsa-miR-4513, hsa-miR-4521, hsa-miR-6732-3p, hsa-miR-744-3p) and 7 down-regulated (hsa-miR-148a-3p, hsa-miR-148a-5p, hsa-miR-181a-3p, hsa-miR-29b-3p, hsa-miR-29c-3p, hsa-miR-30d-5p, hsa-miR-660-5p) miRNAs was found in SDS cell cultures compared with controls. The differential expression of the microRNAs identified as dysregulated was confirmed by droplet-digital RT-PCR (ddRT-PCR). In consideration of the possible involvement of microRNAs in the STAT3 hyperactivation and interleukin-6 (IL-6) dysregulation, the 7 miRNAs down-regulated in SDS-LCC were analyzed. Among this miRNA set, miR-148a-5p might be of interest, because it targets the 3'UTR of IL-6 mRNA (position 71-78 of IL-6 3'UTR). MicroRNA miR-148a-5p down-regulation can participate to the IL-6 upregulation in SDS-LCC, demonstrated in LCC supernatants by Bio-Plex analysis of the secretome. Moreover, in consideration of the fact that LCC from SDS patients are characterized by up-regulated mTOR phosphorylation (Bezzerri et al, Sci Rep 2016) possibly associated with down-regulation of PTEN (a validated inhibitor of mTOR phosphorylation), PTEN transcript and protein levels were analyzed in SDS-LCC by RT-PCR and Western Blotting analysis. The data obtained suggest a down regulation of PTEN in SDS-LCC. In order to investigate the possible correlation between PTEN down-regulation and microRNA content in lymphoblastoid cells of SDS patients, we verified whether some of the up-regulated microRNAs found in the NGS analysis were potential regulators of PTEN. When the 11 up-regulated miRNAs were compared with 81 validated PTEN regulating miRNAs (www. mirtarbase.mbc.nctu.edu.tw), two microRNAs were identified: miR-34a-3p and miR-744-3p. Of relevance, the relative expression of miR-34a-3p and miR-744-3p was found variable among the cells from the different SDS patients. When the PTEN expression was related with the miR-34a-3p and miR-744-3p levels, an inverse correlation was found between the miR-34a-3p and miR-744-3p levels and PTEN gene expression. This study allows proposing molecules mimicking miR-148a-5p function in order to reduction of IL-6 expression. On the other hand, miR-34a-3p and miR-744-3p might be considered as possible targets of antagomiRNA molecules, for increasing PTEN expression in SDS patients. Altogether, these data support the concept themicroRNAs might participate to the phenotype of lymphoblastoid cells of SDS patients, therefore being potential molecular targets for miRNA therapeutics of Shwachman-Diamond syndrome. Acknowledgements: This study was supported by a FIR and a FAR fund of Ferrara University to AF, and by a fund from the Italian Ministry of Health (MOH) to VB, MB and GB. Disclosures Bezzerri: Marco Cipolli, Valentino Bezzerri, Baroukh Maurice Assael: Patents & Royalties: WO2018/050706 A1 "Method of treatment of Shwachman-Diamond syndrome". Cipolli:Marco Cipolli, Valentino Bezzerri, Baroukh Maurice Assael: Patents & Royalties: WO2018/050706 A1 "Method of treatment of Shwachman-Diamond syndrome".

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
自由如风完成签到 ,获得积分10
1秒前
1秒前
vans如意完成签到 ,获得积分10
2秒前
梁哲铭完成签到,获得积分10
3秒前
Jenna完成签到 ,获得积分10
5秒前
5秒前
留柿完成签到,获得积分10
5秒前
王明月完成签到 ,获得积分10
5秒前
干净的雅青完成签到,获得积分10
6秒前
6秒前
如意代秋完成签到,获得积分20
7秒前
YUANYUAN1111完成签到 ,获得积分10
7秒前
sandra发布了新的文献求助10
9秒前
科研通AI6.4应助阿拉伯芮采纳,获得10
10秒前
5AGAME完成签到,获得积分10
13秒前
Liu完成签到 ,获得积分0
13秒前
13秒前
spring_IMU完成签到,获得积分10
13秒前
14秒前
共享精神应助全鑫采纳,获得10
18秒前
王cc发布了新的文献求助10
18秒前
无限的信封完成签到,获得积分20
19秒前
小明完成签到,获得积分0
19秒前
shuoliu完成签到 ,获得积分10
20秒前
科研通AI6.1应助褚明雪采纳,获得10
20秒前
科研三井泽完成签到,获得积分10
21秒前
22秒前
之后再说咯完成签到,获得积分10
22秒前
tumankol完成签到 ,获得积分10
24秒前
星辰大海应助aa采纳,获得10
25秒前
yang完成签到,获得积分10
25秒前
123发布了新的文献求助10
26秒前
宇文鹏煊完成签到 ,获得积分10
28秒前
cdercder应助yy采纳,获得10
29秒前
chen完成签到,获得积分10
29秒前
科研通AI2S应助YYY采纳,获得10
30秒前
30秒前
全鑫发布了新的文献求助10
34秒前
37秒前
高分求助中
液晶指向矢仿真分析数据集 8888
Invited Discussant 63O and 64O 1000
Ideology and Meaning-Making under the Putin Regime 750
Thermal effects on behaviour of clay–structure interface under partial drainage 500
Petrology and Plate Tectonics 500
Writing Systems 500
A Handbook of User Experience Research & Design in Libraries 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6895836
求助须知:如何正确求助?哪些是违规求助? 8591589
关于积分的说明 18243206
捐赠科研通 6291699
什么是DOI,文献DOI怎么找? 3060424
关于科研通互助平台的介绍 2078937
邀请新用户注册赠送积分活动 2038242