Drug-Induced Destabilization of Bcl-2 mRNA
药物诱导的 Bcl-2 mRNA 不稳定
基本信息
- 批准号:7911535
- 负责人:
- 金额:$ 13.92万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-08-01 至 2010-07-31
- 项目状态:已结题
- 来源:
- 关键词:3&apos Untranslated RegionsAcidsAffectAntineoplastic AgentsApoptosisApplications GrantsB-Cell LymphomasB-LymphocytesBe++ elementBerylliumBindingBinding SitesBiological AssayCell ExtractsCell LineCellsChronic Lymphocytic LeukemiaDevelopmentDown-RegulationDrug resistanceElementsFluorescence PolarizationFluorescence Resonance Energy TransferGenetic TranscriptionGrowthHL-60 CellsHL60HumanHuman VolunteersIndiumMCF7 cellMalignant NeoplasmsMapsMessenger RNAOkadaic AcidPaclitaxelPatientsPharmaceutical PreparationsPhosphorylationProtein BindingProteinsProteolysisRNA Recognition MotifRNA SequencesRecombinantsReportingResistanceRibonucleasesRibosomal RNARoboticsRoleScreening procedureStructureTestingTimeTransfectionTretinoinWorkbasecancer celldeletion analysisdesignhigh throughput screeninginhibitor/antagonistleukemiamRNA StabilitymRNA Transcript Degradationnovel strategiesnucleasenucleolinoverexpressionresearch studysmall moleculesmall molecule librariesvolunteer
项目摘要
DESCRIPTION (provided by applicant): Over expression of bcl-2 is an important component in the development of B-cell lymphomas and some B-cell leukemia as well as in the emergence of cellular resistance to certain anticancer drugs. The 3'-untranslated region (3'-UTR) of bcl-2 mRNA contains several AU-rich elements (AREs) that promote mRNA destabilization. We have observed that the protein, nucleolin, binds to ARE-1 in bcl-2 mRNA, potentially protecting this mRNA from nuclease degradation. Accordingly, the central hypothesis of this proposal is that nucleolin stabilizes bcl-2 mRNA through interaction with AREs in the 3'-UTR, and that ATRA, taxol and okadiac acid destabilize bcl-2 mRNA by inducing down regulation or inactivation of nucleolin. The studies proposed in the first specific aim will evaluate the effects of bcl-2 ARE's 1-4 on bcl-2 mRNA stability in extracts of HL-60, MCF-7 and purified B cells from normal volunteers and patients with B-cell chronic lymphocytic leukemia (CLL). This will be followed by testing the effects of taxol and ATRA on bcl-2 ARE mRNA stability in cell extracts. Aim 2 is to determine whether functional nucleolin-bcl-2 mRNA interactions occur in intact cells. The ability of recombinant nucleolin to stabilize the bcl-2 mRNAs containing destabilizing AREs (Specific Aim 1) will be tested using transfection assays. We will also determine if exogenous over expression of nucleolin in parental HL-60 cells or MCF-7 cells can confer resistance to ATRA (HL-60) or taxol (HL-60 and MCF-7) concomitant with increased bcl-2 mRNA and protein. Additional experiments will reveal if knockdown of nucleolin expression with siRNAs leads to destabilization of bcl-2 mRNA. The third specific aim is to identify the RNA binding domains of nucleolin that are involved in binding to bcl-2 ARE mRNA. Finally, the information generated in Aims 1-3 will guide the development of high-throughput, robotic screening of diverse chemical libraries to identify small molecules that specifically inhibit nucleolin binding to AREs in bcl-2 mRNA.
描述(由申请人提供):bcl-2的过度表达是B细胞淋巴瘤和一些B细胞白血病的发展以及细胞对某些抗癌药物产生耐药性的重要组成部分。 bcl-2 mRNA 的 3'-非翻译区 (3'-UTR) 包含多个富含 AU 的元件 (ARE),可促进 mRNA 不稳定。我们观察到核仁蛋白与 bcl-2 mRNA 中的 ARE-1 结合,可能保护该 mRNA 免受核酸酶降解。因此,该提议的中心假设是核仁素通过与 3'-UTR 中的 ARE 相互作用来稳定 bcl-2 mRNA,而 ATRA、紫杉醇和冈田酸通过诱导核仁素的下调或失活来不稳定 bcl-2 mRNA。第一个具体目标中提出的研究将评估 bcl-2 ARE 1-4 对正常志愿者和 B 细胞慢性病患者的 HL-60、MCF-7 和纯化 B 细胞提取物中 bcl-2 mRNA 稳定性的影响。淋巴细胞白血病(CLL)。随后将测试紫杉醇和 ATRA 对细胞提取物中 bcl-2 ARE mRNA 稳定性的影响。目标 2 是确定完整细胞中是否发生功能性核仁素-bcl-2 mRNA 相互作用。将使用转染测定来测试重组核仁素稳定含有不稳定 ARE 的 bcl-2 mRNA 的能力(具体目标 1)。我们还将确定亲本 HL-60 细胞或 MCF-7 细胞中核仁素的外源过度表达是否可以赋予对 ATRA (HL-60) 或紫杉醇 (HL-60 和 MCF-7) 的抗性,同时增加 bcl-2 mRNA 和蛋白质。其他实验将揭示用 siRNA 敲低核仁素表达是否会导致 bcl-2 mRNA 不稳定。第三个具体目标是鉴定参与与 bcl-2 ARE mRNA 结合的核仁素的 RNA 结合域。最后,目标 1-3 中生成的信息将指导各种化学文库的高通量机器人筛选的开发,以识别特异性抑制核仁素与 bcl-2 mRNA 中 ARE 结合的小分子。
项目成果
期刊论文数量(2)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Plasma membrane nucleolin is a receptor for the anticancer aptamer AS1411 in MV4-11 leukemia cells.
质膜核仁素是 MV4-11 白血病细胞中抗癌适体 AS1411 的受体。
- DOI:
- 发表时间:2009-11
- 期刊:
- 影响因子:3.6
- 作者:Soundararajan, Sridharan;Wang, Li;Sridharan, Vijayalakshmi;Chen, Weiwei;Courtenay;Jones, David;Spicer, Eleanor K;Fernandes, Daniel J
- 通讯作者:Fernandes, Daniel J
The nucleolin targeting aptamer AS1411 destabilizes Bcl-2 messenger RNA in human breast cancer cells.
核仁素靶向适体 AS1411 会破坏人乳腺癌细胞中 Bcl-2 信使 RNA 的稳定性。
- DOI:10.1158/0008-5472.can-07-5723
- 发表时间:2008-04-01
- 期刊:
- 影响因子:11.2
- 作者:S. Soundararajan;Weiwei Chen;E. Spicer;N. Courtenay;D. Fern;es;es
- 通讯作者:es
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Daniel J Fernandes其他文献
Influence of acid treatment on surface properties and in vivo performance of Ti6Al4V alloy for biomedical applications
酸处理对生物医学应用Ti6Al4V合金表面性能和体内性能的影响
- DOI:
10.1007/s10856-017-5977-5 - 发表时间:
2017-09-15 - 期刊:
- 影响因子:0
- 作者:
Daniel J Fernandes;R. Marques;C. Elias - 通讯作者:
C. Elias
Mechanical Performance of Nickel-titanium Archwires
镍钛弓丝的机械性能
- DOI:
10.1590/1516-1439.003615 - 发表时间:
2015-11-03 - 期刊:
- 影响因子:0
- 作者:
Daniel J Fernandes;C. Elias;Rafael Vidal;A. Mendes - 通讯作者:
A. Mendes
Force Relaxation Characteristics of Medium Force Orthodontic Latex Elastics: A Pilot Study
中力正畸乳胶弹性体的力松弛特性:初步研究
- DOI:
- 发表时间:
2011 - 期刊:
- 影响因子:0
- 作者:
Daniel J Fernandes;G. M. Abrahão;C. Elias;A. Mendes - 通讯作者:
A. Mendes
Corrosion Resistance of Absorbable Mg-Ca Based Alloys in Physiological Environment
可吸收镁钙基合金在生理环境中的耐腐蚀性能
- DOI:
- 发表时间:
2018 - 期刊:
- 影响因子:0
- 作者:
Daniel J Fernandes - 通讯作者:
Daniel J Fernandes
Mechanical Strength and Surface Roughness of Magnesium-Based Metallic Glasses
镁基金属玻璃的机械强度和表面粗糙度
- DOI:
10.1007/s11837-016-1964-4 - 发表时间:
2017-07-01 - 期刊:
- 影响因子:2.6
- 作者:
Daniel J Fernandes;C. Elias;Celso Renato Souza Resende;C. Bolfarini - 通讯作者:
C. Bolfarini
Daniel J Fernandes的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Daniel J Fernandes', 18)}}的其他基金
Drug-Induced Destabilization of Bcl-2 mRNA
药物诱导的 Bcl-2 mRNA 不稳定
- 批准号:
7361413 - 财政年份:2005
- 资助金额:
$ 13.92万 - 项目类别:
相似海外基金
Translational Regulation of SARS-CoV-2 in response to viral S protein-induced signaling
SARS-CoV-2 响应病毒 S 蛋白诱导信号传导的翻译调控
- 批准号:
10721101 - 财政年份:2023
- 资助金额:
$ 13.92万 - 项目类别:
Interplay between LINE-1 retrotransposons, condensins, and IFN
LINE-1 逆转录转座子、凝缩蛋白和 IFN 之间的相互作用
- 批准号:
10655795 - 财政年份:2023
- 资助金额:
$ 13.92万 - 项目类别:
Identification and characterization of small open reading frames translated during inflammation
炎症期间翻译的小开放阅读框的识别和表征
- 批准号:
10752246 - 财政年份:2023
- 资助金额:
$ 13.92万 - 项目类别:
Post-transcriptional regulation of germline mRNAs in C. elegans
线虫种系 mRNA 的转录后调控
- 批准号:
10610874 - 财政年份:2022
- 资助金额:
$ 13.92万 - 项目类别:
Atrial Natriuretic Peptide and Regulation of Cardiometabolic Health: A Genotype-Guided Human Physiological Study
心钠素和心脏代谢健康的调节:基因型引导的人类生理学研究
- 批准号:
10419574 - 财政年份:2022
- 资助金额:
$ 13.92万 - 项目类别: