Personalized Cancer Therapy Guided by Photoacoustic Chemical Imaging (PACI) of Tumor Microenvironment (TME)
肿瘤微环境(TME)光声化学成像(PACI)引导的个性化癌症治疗
基本信息
- 批准号:10186721
- 负责人:
- 金额:$ 62.38万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2020
- 资助国家:美国
- 起止时间:2020-06-08 至 2025-05-31
- 项目状态:未结题
- 来源:
- 关键词:AcidosisAffectAftercareAnimal ModelCancer PatientChemicalsClinical ManagementComplexCorrelation StudiesEarly treatmentEcosystemEnsureFundingHealth PersonnelHypoxiaImageImaging technologyImmuno-ChemotherapyImmunotherapyIndividualLasersLightMalignant NeoplasmsMapsMedicineMetabolicModelingModificationMolecular BiologyMusNeoplasm MetastasisOutcomes ResearchOxygenPatient imagingPatient-Focused OutcomesPatient-derived xenograft models of breast cancerPatientsPenetrationPharmaceutical PreparationsPhysiologicalPlayPotassiumPublicationsRadiation therapyRadioResearchResistanceResolutionShapesSignal TransductionSolid NeoplasmSpatial DistributionSpeedSystemT cell therapyTechnologyTestingTissuesTranslational ResearchTreatment outcomeTriad Acrylic ResinUltrasonographyWarburg Effectbasecancer imagingcancer therapychemical propertyclinical translationexperiencehyperkalemiaimage guidedin vivomalignant breast neoplasmmembermouse modelnanomedicinenanoprobenanosensorsnoveloptimal treatmentspatient derived xenograft modelpersonalized cancer therapyphotoacoustic imagingresponsespatiotemporaltooltreatment planningtreatment responsetumortumor heterogeneitytumor microenvironmenttumor xenograft
项目摘要
Title: Personalized Cancer Therapy Guided by Photoacoustic Chemical Imaging (PACI)
of Tumor Microenvironment (TME)
Abstract:
Tumors are often found in an altered metabolic state, which leads to anomalous chemical composition, such as
hypoxia (low oxygen level), acidosis (low pH level), and hyperkalemia (high potassium concentration). These
three form a “therapy resistance triad (O2, pH, and K+)”, suppressing cancer’s responses to radio-, chemo-,
and immuno-therapy. As each triad member’s concentration is strongly relevant to cancer progress and
response to therapy, a non-invasive, sensitive, and reliable approach for evaluating their temporal and spatial
distributions in the tumor microenvironment (TME) in vivo, non-invasively, is highly desirable. To fill this serious
and long-standing gap in technology, we introduce a novel set of O2, pH, and K+ sensing nanoprobes that, in
combination with the emerging photoacoustic imaging technology, enables quantitative mapping of the O2, pH,
and K+ levels in solid tumors in vivo. The central hypothesis of this proposed research is that, enabled by our
photoacoustic chemical imaging (PACI) powered with sensitive chemical indicator nanoprobes, we can image
and quantitatively evaluate the spatio-temporal distributions of the TME’s therapy resistance triad (O2, pH, and
K+), at depths of up to a few centimeters, in vivo and in a non-invasive fashion, and then correlate with cancer
responses to treatments via radio-, chemo-, and immuno-therapy. This hypothesis will be examined rigorously
using orthotopic patient derived xenograft (PDX) breast cancer mouse models. To enable a comprehensive
understanding of the technology’s capabilities, as well as limitations, the imaging results from PACI of the TME
will be compared for a wide variety of PDX tumor models and treatment situations. To examine the central
hypothesis, our research will focus on three specific aims: Aim 1. Understand tumor response to radio-therapy
by PACI of the TME; Aim 2. Understand tumor response to chemo-therapy by PACI of the TME; and Aim 3.
Understand tumor response to immuno-therapy by PACI of the TME.
Potential impact: As the orthotopic PDX tumors faithfully resemble the original tumors in cancer patients,
including their TME, chemical imaging of these PDX tumors, combined with studying the correlations of the
imaging findings with the cancer responses to therapies, could have a large impact on translational research
and clinical management of breast cancer, e.g. helping to discriminate the most suitable treatment plan or
alternative plan for individual cancer patients. By the end of this funding period, we will objectively test and
thoroughly verify whether the novel PACI technology powered by sensitive nanoprobes can image the TME’s
chemical properties of PDX mouse tumors in vivo, non-invasively, for predicting the cancer responses to radio-
, chemo-, and immuno-therapy. Once successfully validated, the proposed strategy could shed new light on
imaging-guided personalized cancer medicine, so as to hopefully ensure an optimal treatment outcome.
题目:光声化学成像(PACI)指导下的个性化癌症治疗
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Raoul Kopelman其他文献
Raoul Kopelman的其他文献
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{{ truncateString('Raoul Kopelman', 18)}}的其他基金
Personalized Cancer Therapy Guided by Photoacoustic Chemical Imaging (PACI) of Tumor Microenvironment (TME)
肿瘤微环境(TME)光声化学成像(PACI)引导的个性化癌症治疗
- 批准号:
10452531 - 财政年份:2020
- 资助金额:
$ 62.38万 - 项目类别:
Photonic Nanosonophores for Functional and Structural Imaging
用于功能和结构成像的光子纳米声载体
- 批准号:
8830441 - 财政年份:2014
- 资助金额:
$ 62.38万 - 项目类别:
Photonic Nanosonophores for Functional and Structural Imaging
用于功能和结构成像的光子纳米声载体
- 批准号:
9017968 - 财政年份:2014
- 资助金额:
$ 62.38万 - 项目类别:
Photonic Nanosonophores for Functional and Structural Imaging
用于功能和结构成像的光子纳米声载体
- 批准号:
8576590 - 财政年份:2014
- 资助金额:
$ 62.38万 - 项目类别:
Magnetorotation: a Rapid Assay for Single Cell Drug Sensitivity of Cancer Cells
磁旋转:癌细胞单细胞药物敏感性的快速测定
- 批准号:
8154084 - 财政年份:2011
- 资助金额:
$ 62.38万 - 项目类别:
Magnetorotation: a Rapid Assay for Single Cell Drug Sensitivity of Cancer Cells
磁旋转:癌细胞单细胞药物敏感性的快速测定
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8332762 - 财政年份:2011
- 资助金额:
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Ultra Rapid Monitoring of Bacterial Nano-Growth and Antibiotic Susceptibility
细菌纳米生长和抗生素敏感性的超快速监测
- 批准号:
7659942 - 财政年份:2009
- 资助金额:
$ 62.38万 - 项目类别:
Ultra Rapid Monitoring of Bacterial Nano-Growth and Antibiotic Susceptibility
细菌纳米生长和抗生素敏感性的超快速监测
- 批准号:
7826724 - 财政年份:2009
- 资助金额:
$ 62.38万 - 项目类别:
Nanobiophotonics Enabled Tumor Surgery and Intraoperative PDT
纳米生物光子学支持肿瘤手术和术中 PDT
- 批准号:
7914680 - 财政年份:2009
- 资助金额:
$ 62.38万 - 项目类别:
Nanobiophotonics Enabled Tumor Surgery and Intraoperative PDT
纳米生物光子学支持肿瘤手术和术中 PDT
- 批准号:
7665205 - 财政年份:2007
- 资助金额:
$ 62.38万 - 项目类别:
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