Hiring Non-toxic Virus Nanoparticles to Count Cancer Biomarker Molecules
Hiring Non-toxic Virus Nanoparticles to Count Cancer Biomarker Molecules
批准号:
9070724
负责人:
Chuanbin Mao
金额:
$19.52万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2015
资助国家:
美国
项目状态:
已结题
起止时间:
2015-09-01 至 2018-08-31
关键词:
AffectBacteriaBacteriophage T7BacteriophagesBindingBiological MarkersBody FluidsBuffersCancer PatientCapsidCatalogingCatalogsClinicalColorComplementComplementary DNAComplexDNADetectionDiagnosisEngineeringEyeFamilyFiberFluorescenceGene ExpressionGenetic EngineeringGenetic TranscriptionGoalsGoldHealthHumanInfectionLightMagnetic nanoparticlesMagnetismMalignant NeoplasmsMalignant neoplasm of prostateMethodsMicroRNAsNanotechnologyOligonucleotidesPatientsPeptidesPhage DisplayPolymerase Chain ReactionPropertyProteinsRNARecombinantsReportingReproducibilityReverse TranscriptionRiskSamplingSeriesSerumSodium ChlorideStructureSurfaceTailTechniquesTestingTimeTissuesTumor TissueUntranslated RNAVirusWaterbasecancer biomarkerscancer diagnosiscancer typecirculating microRNAcostdesignimprovedmicroRNA biomarkersnanoparticlenovelspecific biomarkers
中文摘要
前列腺癌的一种生物标记物,称为microRNAs(MiRNAs),在癌症患者的血清中有独特的水平。因此,检测它们将使我们能够更早地诊断前列腺癌。目前,这类生物标志物只能通过实时定量聚合酶链式反应进行检测。然而,当该技术用于低水平的miRNAs检测时,不能产生可重复性和可靠的结果。为了能够可靠地在低水平上定量前列腺癌特异的miRNAs,我们提出了一种超敏感的策略,即雇佣无毒的病毒纳米颗粒来探测miRNAs。这一策略是基于这样一个事实,即病毒纳米颗粒可以被设计成能够发出三种不同的光,并与纳米颗粒形成复合物,以捕获目标miRNAs。因此,在一个平台上检测多个靶miRNAs是可能的,因为当三个不同的荧光分子出现在病毒纳米粒的表面时,病毒纳米粒可以发射三个不同的荧光来检测三个不同的靶miRNAs。我们在这个项目中的目标是开发新的策略,以定量血清样本中的多个前列腺癌miRNA生物标记物,包括三个针对前列腺癌的靶miRNAs。我们的目标是实现检测血清中前列腺癌生物标记物的高灵敏度、准确性和重复性。本项目将开发一种新的简便方法,可以准确地检测前列腺癌的生物标志物,从而可以用于前列腺癌的早期诊断。
英文摘要
A type of biomarkers for prostate cancer, called microRNAs (miRNAs), has a unique level in serum from cancer patients. Hence, detecting them will allow us to diagnose prostate cancer earlier. Currently, this type of biomarkers can only be detected by quantitative real-time polymerase chain reaction. However, this technique does not generate reproducible and reliable results when it is used to detect miRNAs at a low level. To be able to reliably quantify prostate cancer-specific miRNAs at a low level, we propose an ultrasensitive strategy that hires non-toxic virus nanoparticles for probing the miRNAs. This strategy is based on the fact that the virus nanoparticles can be engineered to become capable of emitting three different lights and form complex with nanoparticles for capturing the target miRNAs. It is thus possible to detect multiple target miRNAs in one platform because the virus nanoparticles can emit three different fluorescence lights for detecting three different target miRNAs when three different fluorescent molecules are presented on the surface of the virus nanoparticles. Our objective in this project is to develop the new strategy in order to quantify multiple prostate cancer miRNA biomarkers in serum samples, including three target miRNAs specific for the prostate cancer. We aim to achieve high sensitivity, accuracy, and reproducibility for detecting the prostate cancer biomarkers in serum. This project will develop a new facile method that can precisely detect the prostate cancer biomarkers and thus can be used for early prostate cancer diagnosis.
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DOI:
10.1038/srep19047
发表时间:
2016-01-08
期刊:
Scientific reports
影响因子:
4.6
作者:
[Ning C, Wang S, Zhu Y, Zhong M, Lin X, Zhang Y, Tan G, Li M, Yin Z, Yu P, Wang X, Li Y, He T, Chen W, Wang Y, Mao C]
通讯作者:
Mao C
DOI:
10.1021/acs.accounts.5b00557
发表时间:
2016-06-21
期刊:
Accounts of chemical research
影响因子:
18.3
作者:
[Cao B, Yang M, Mao C]
通讯作者:
Mao C
Cross Talk Between Autophagy and Apoptosis Contributes to ZnO Nanoparticle-Induced Human Osteosarcoma Cell Death.
自噬和细胞凋亡之间的相互作用导致氧化锌纳米粒子诱导的人骨肉瘤细胞死亡
DOI:
10.1002/adhm.201800332
发表时间:
2018-09
期刊:
Advanced healthcare materials
影响因子:
10
作者:
[He G, Ma Y, Zhu Y, Yong L, Liu X, Wang P, Liang C, Yang C, Zhao Z, Hai B, Pan X, Liu Z, Liu X, Mao C]
通讯作者:
Mao C
DOI:
10.7150/thno.19748
发表时间:
2017
期刊:
Theranostics
影响因子:
12.4
作者:
[Yu P, Ning C, Zhang Y, Tan G, Lin Z, Liu S, Wang X, Yang H, Li K, Yi X, Zhu Y, Mao C]
通讯作者:
Mao C
Corrigendum to "Untangling the response of bone tumor cells and bone forming cells to matrix stiffness and adhesion ligand density by means of hydrogels" [Biomaterials 188 (2019) 130-143].
“通过水凝胶解开骨肿瘤细胞和骨形成细胞对基质硬度和粘附配体密度的反应”的勘误表[Biomaterials 188 (2019) 130-143]。
DOI:
10.1016/j.biomaterials.2019.119663
发表时间:
2020
期刊:
Biomaterials
影响因子:
14
作者:
[Jiang,Tongmeng, Zhao,Jinmin, Yu,Shan, Mao,Zhengwei, Gao,Changyou, Zhu,Ye, Mao,Chuanbin, Zheng,Li]
通讯作者:
Zheng,Li
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