Nanosensor-Based Phenotypic Screening for Precision Therapy of Cancer Stem Cells
Nanosensor-Based Phenotypic Screening for Precision Therapy of Cancer Stem Cells
批准号:
9371612
负责人:
Arthur M Mercurio
金额:
$30.0万
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-09-12 至 2019-09-10
关键词:
AnimalsBehaviorBiological MarkersBreast Cancer CellBreast Cancer PatientBreast CarcinomaCancer BiologyCell modelCell surfaceCellsCharacteristicsDataDevelopmentDrug usageFingerprintFluorescenceGoalsGoldIn VitroIndividualMammary NeoplasmsMeasurementMeasuresMethodsNeoplasm MetastasisOutputPatientsPhenotypePolymersPopulationPrecision therapeuticsPreclinical Drug EvaluationProcessPropertyProteinsRecurrenceResearchResearch PersonnelResistanceScreening for cancerSolid NeoplasmStem cellsSystemTechniquesTestingTherapeuticTherapeutic AgentsTherapeutic UsesToxic effectTrainingXenograft procedureanalogbasecancer stem cellchemotherapycytotoxicitydrug discoverydrug mechanismeffective therapyhigh throughput screeningin vivoindividual patientmalignant breast neoplasmmolecular phenotypenanomaterialsnanoparticlenanosensorsneoplastic cellnew therapeutic targetnovel therapeuticsparticlepersonalized medicinepersonalized therapeuticprogramsscreeningself-renewalsensorsmall moleculestemnesstherapeutic targettooltumortumor xenograft
中文摘要
项目摘要/摘要
基于纳米传感器的肿瘤干细胞精确治疗表型筛选
肿瘤干细胞(CSCs)具有干细胞特性,包括自我更新和
植入新的肿瘤。这些细胞对化疗有抵抗力,并与肿瘤有关。
复发和转移,使它们成为重要但具有挑战性的治疗靶点。在这
U01建议,我们将使用基于纳米颗粒的传感器来快速表型CSCs,使用
筛选能够区分小分子和纳米颗粒疗法的信息
CSCs向侵袭性较弱且对化疗药物更敏感的细胞分化。
目标1:罗特洛将开发一种强大的纳米粒子-聚合物高通量-高含量
用于区分CSC和非CSC肿瘤细胞模型的筛选(HT-HCS)方法
由Mercurio开发。
目标2:Rotello将使用HT-HCS平台来识别小分子和纳米粒子
对CSC细胞具有选择性体外毒性的治疗剂,Mercurio将验证其
影响乳腺癌细胞体外和体内行为的能力。
目标3:Mercurio将从患者分离的异种移植物(PDX)中分离CSCs,Rotello将使用
HT-HCS平台在体外确定精确的治疗策略,将通过
Mercurio有能力阻止个别肿瘤的发生和复发。
这项雄心勃勃的研究整合了摩科瑞(UMassWorcester)的癌症生物学专业知识
拥有罗特罗公司(UMassAmherst)的纳米材料和传感能力。这项研究将
由为该项目聚集的互补研究人员团队提供极大的便利,如
以及伍斯特大学广泛的动物能力和最先进的纳米材料
阿默斯特的设施。
英文摘要
Project Summary/Abstract
Nanosensor-Based Phenotypic Screening for Precision Therapy of Cancer Stem Cells
Cancer stem cells (CSCs) have stem cells characteristics, including the ability to self-renew and
populate new tumors. These cells are resistant to chemotherapy and are responsible for tumor
recurrence and metastasis, making them important yet challenging therapeutic targets. In this
U01 proposal, we will use a nanoparticle-based sensor to rapidly phenotype CSCs, using this
information to screen for small molecule and nanoparticle therapeutics capable of differentiating
CSCs to cells that are less aggressive and more susceptible to chemotherapeutics.
Aim 1: Rotello will develop a robust nanoparticle-polymer high throughput-high content
screening (HT-HCS) process for discriminating between CSC and non-CSC tumor cell models
developed by Mercurio.
Aim 2: Rotello will use the HT-HCS platform to identify small molecule and nanoparticle
therapeutic agents with selective in vitro toxicity to CSC cells, and Mercurio will validate their
ability to impact the in vitro and in vivo behavior of breast cancer cells.
Aim 3: Mercurio will isolate CSCs from patient-dervied xenografts (PDX), and Rotello will use the
HT-HCS platform to indentify precision therapeutic strategies in vitro that will be tested by
Mercurio for their ability to hinder the initiation and recurrence of individual tumors.
This ambitious research integrates the cancer biology expertise of Mercurio (UMass Worcester)
with the nanomaterials and sensing capabilities of Rotello (UMass Amherst). The research will
be greatly facilitated by the complementary team of researchers assembled for the project, as
well as the extensive animal capabilities at Worcester and state of the art nanomaterials
facilities at Amherst.
期刊论文(0)
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