DF/HCC Prostate SPORE
DF/HCC 前列腺孢子
基本信息
- 批准号:10628270
- 负责人:
- 金额:$ 258.56万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2023
- 资助国家:美国
- 起止时间:2023-09-01 至 2028-08-31
- 项目状态:未结题
- 来源:
- 关键词:AccelerationAcuteAddressAndrogen ReceptorAutopsyBackBasic ScienceBiologicalBiological AssayBiological MarkersBiometryBloodBlood specimenCancer BiologyCancer CenterCancer EtiologyCaringCessation of lifeClinicalClinical InvestigatorClinical ResearchClinical SciencesClinical TrialsCollaborationsCommunicationCommunitiesComputational BiologyDana-Farber Cancer InstituteDataDedicationsDevelopmentDiagnosisDiseaseDisease ResistanceEZH2 geneEarly DiagnosisEarly treatmentEnsureEnvironmentEpigenetic ProcessFosteringFundingGeneral HospitalsGenomicsGoalsGrowthHospitalsIndividualInfrastructureInstitutionIsraelLaboratoriesLaboratory ResearchLeadMachine LearningMalignant NeoplasmsMalignant neoplasm of prostateMassachusettsMedical centerMentorsMolecularMorbidity - disease rateNeoadjuvant TherapyNewly DiagnosedPathologyPathway interactionsPatient advocacyPatientsPhenotypePopulation SciencesPre-Clinical ModelPrincipal InvestigatorPrognostic MarkerProstateProstate Cancer therapyRecruitment ActivityResearchResearch PersonnelResistanceResistance developmentResourcesServicesSpecimenTherapeuticTissuesTranslatingTranslational ResearchTranslationsUnited StatesWorkWritinganticancer researchbench to bedsidebiomarker developmentbiomarker discoverybiomarker drivencancer genomicscancer initiationcareercastration resistant prostate cancerclinical translationcohortcombatdata sharingdeep learningdrug standardepigenomefollow-uphigh riskimprovedindividualized medicineinnovationinsightmeetingsmenmodel developmentmortalitynext generationnext generation sequencingnovelnovel strategiespatient populationpre-clinicalprecision medicineprecision oncologypreclinical studyprogramsprostate cancer riskrepositoryresistance mechanismsuccesstherapy resistanttranslational approachtranslational cancer researchtranslational scientisttumortumor progression
项目摘要
PROJECT SUMMARY – OVERALL
The Dana-Farber/Harvard Cancer Center (DF/HCC) Prostate SPORE seeks to improve the understanding
and treatment of prostate cancer using a highly translational approach. The application consists of three
Projects, three Cores, a Developmental Research Program and a Career Enhancement Program. The
SPORE infrastructure will facilitate interactions and collaboration within our thriving community of basic,
clinical, and population science researchers dedicated to prostate cancer research. Each project addresses
a fundamental challenge that contributes to prostate cancer morbidity and mortality. Project 1 leverages
tumor specimens from patients with high-risk prostate cancer treated with neoadjuvant therapies to
understand how tumors respond and resist acute potent androgen receptor blockade and to develop novel
strategies to improve cure rates and combat resistance. Project 2 will develop innovative strategies to target
the epigenome in later stages of advanced castration resistant prostate cancer and will develop a first-in-field
clinical trial focused on co-targeting EZH2 and PARP. Project 3 delves deep into biomarkers in localized
prostate cancer, leveraging innovations in computation and biologically-guided deep learning, to deliver on
precision cancer medicine in this disease state. The ability to understand why some localized prostate
cancers are phenotypically aggressive and predict which localized prostate cancers will behave in this
manner addresses a large clinical unmet need. Each of these projects combines elegant preclinical work with
innovative clinical studies led by DF/HCC investigators. Core A, the Administrative Core, will be the center for
scientific, fiscal and administrative oversight. It will lead efforts in planning and communication, and also
house the Patient Advocacy Committee. Core A will ensure that the DF/HCC infrastructure supports the
SPORE clinical and translational research efforts. Core B, the Biostatistics and Computational Biology core,
will provide specialized expertise in biostatistics and the management of genomic and other next generation
sequencing data and data sharing. Core C, the Biospecimen and Pathology Core, will maintain tissue/blood
repositories for the SPORE projects as well as other investigators within the prostate cancer program. It will
provide critical expertise and pathology services including next generation molecular assays and will help
facilitate the use of fresh tumor specimens including rapid autopsies for patient derived model development
to accelerate translational investigation. The Developmental Research and Career Enhancement Programs
will identify and fund innovative projects that address basic, translational, and clinical research questions and
unmet needs in prostate cancer and will support early career and new prostate cancer investigators. These
programs will actively recruit and retain researchers from diverse backgrounds to foster cutting-edge and
impactful prostate cancer translational science. We anticipate that the DF/HCC Prostate SPORE will make
substantial scientific discoveries in the field and translate directly into benefits for men with prostate cancer.
项目概要-总体
丹娜-法伯/哈佛癌症中心(DF/HCC)前列腺孢子寻求提高理解
以及使用高度翻译的方法治疗前列腺癌。该应用程序包括三个
项目,三个核心,发展研究计划和职业提升计划。的
SPORE基础设施将促进我们蓬勃发展的基本社区内的互动和协作,
致力于前列腺癌研究的临床和人口科学研究人员。每个项目都涉及
这是导致前列腺癌发病率和死亡率的根本挑战。项目1利用
来自用新辅助疗法治疗的高危前列腺癌患者的肿瘤标本,
了解肿瘤如何响应和抵抗急性强效雄激素受体阻断,并开发新的
提高治愈率和抵抗力的战略。项目2将制定创新战略,
在晚期去势抵抗性前列腺癌的后期阶段的表观基因组,并将开发一个第一个在该领域
临床试验集中在共同靶向EZH 2和PARP。项目3深入研究生物标志物,
前列腺癌,利用计算和生物引导的深度学习方面的创新来实现
精准的癌症治疗能够理解为什么一些局限性前列腺
癌症是表型侵略性的,并预测哪些局限性前列腺癌将在这种情况下表现。
方式解决了大量临床未满足的需求。这些项目中的每一个都结合了优雅的临床前工作,
由DF/HCC研究者领导的创新临床研究。核心A,即行政核心,将成为
科学、财政和行政监督。它将领导规划和沟通方面的努力,并且还
病人权益保护委员会核心A将确保DF/HCC基础设施支持
开展临床和转化研究工作。核心B,生物统计学和计算生物学核心,
将提供生物统计学和管理基因组和其他下一代的专业知识,
测序数据和数据共享。核心C,生物标本和病理学核心,将保持组织/血液
存储库的孢子项目以及其他研究人员在前列腺癌计划。它将
提供关键的专业知识和病理学服务,包括下一代分子检测,并将帮助
促进新鲜肿瘤标本的使用,包括用于患者衍生模型开发的快速尸检
加快翻译研究发展研究和职业提升计划
将确定并资助创新项目,解决基础,转化和临床研究问题,
前列腺癌未满足的需求,并将支持早期职业和新的前列腺癌研究人员。这些
计划将积极招募和留住来自不同背景的研究人员,以培养尖端和
影响力前列腺癌转化科学我们预计DF/HCC前列腺孢子将使
该领域的重大科学发现,并直接转化为前列腺癌患者的益处。
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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Steven P. Balk其他文献
Recognition of cluster of differentiation 1 antigens by human CD4−CD8>− cytolytic T lymphocyte
人 CD4−CD8>−细胞毒性 T 淋巴细胞对分化簇 1 抗原簇的识别
- DOI:
10.1038/341447a0 - 发表时间:
1989-10-05 - 期刊:
- 影响因子:48.500
- 作者:
Steven Porcelli;Michael B. Brenner;Julia L. Greenstein;Cox Terhorst;Steven P. Balk;Paul A. Bleicher - 通讯作者:
Paul A. Bleicher
Specific reversal of cytolytic T cell-target cell functional binding is induced by free target cells.
游离靶细胞诱导溶细胞性 T 细胞与靶细胞功能结合的特异性逆转。
- DOI:
10.4049/jimmunol.127.1.51 - 发表时间:
1981 - 期刊:
- 影响因子:4.4
- 作者:
Steven P. Balk;M. Mescher - 通讯作者:
M. Mescher
BH3 mimetics targeting BCL-XL have efficacy in solid tumors with RB1 loss and replication stress
靶向 BCL-XL 的 BH3 模拟物在具有 RB1 缺失和复制应激的实体瘤中具有疗效
- DOI:
10.1038/s41467-025-60238-x - 发表时间:
2025-05-28 - 期刊:
- 影响因子:15.700
- 作者:
Andreas Varkaris;Keshan Wang;Mannan Nouri;Nina Kozlova;Daniel R. Schmidt;Anastasia Stavridi;Seiji Arai;Nicholas Ambrosio;Larysa Poluben;Juan M. Jimenez-Vacas;Daniel Westaby;Juliet Carmichael;Fang Xie;Ines Figueiredo;Lorenzo Buroni;Antje Neeb;Bora Gurel;Nicholas Chevalier;Lisha Brown;Olga Voznesensky;Shao-Yong Chen;Joshua W. Russo;Xin Yuan;Dejan Juric;Himisha Beltran;Johann S. De Bono;Matthew G. Vander Heiden;David J. Einstein;Taru Muranen;Eva Corey;Adam Sharp;Steven P. Balk - 通讯作者:
Steven P. Balk
Inhibiteurs de kinase moelle osseuse sur chromosome x (bmx) et leurs utilisations
X 染色体上的骨摩尔激酶抑制剂 (bmx) 及其用途
- DOI:
- 发表时间:
2013 - 期刊:
- 影响因子:0
- 作者:
Nathanael S. Gray;Steven P. Balk;Qingsong Liu;Sen Chen - 通讯作者:
Sen Chen
665 EFFECT OF NEOADJUVANT ABIRATERONE ACETATE PLUS LEUPROLIDE ACETATE ON PSA, PATHOLOGIC RESPONSE, AND INTRAPROSTATIC/SERUM ANDROGEN LEVELS IN LOCALIZED HIGH-RISK PROSTATE CANCER: RESULTS OF A RANDOMIZED PHASE 2 STUDY
- DOI:
10.1016/j.juro.2013.02.220 - 发表时间:
2013-04-01 - 期刊:
- 影响因子:
- 作者:
Jerome P. Richie;Robert B. Montgomery;Christopher J. Logothetis;Glenn J. Bubley;Bruce L. Dalkin;Martin G. Sanda;Massimo F. Loda;Rosina T. Lis;Lawrence D. True;Patricia Troncoso;Elizabeth M. Genega;Steven P. Balk;Elahe A. Mostaghel;Trevor M. Penning;Peter S. Nelson;Wanling Xie;Christopher M. Haqq;NamPhuong Tran;Weimin Peng;Daniel Tamae - 通讯作者:
Daniel Tamae
Steven P. Balk的其他文献
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{{ truncateString('Steven P. Balk', 18)}}的其他基金
WNT5a/ROR2-Mediated Hippo Pathway Activation in Prostate Cancer
前列腺癌中 WNT5a/ROR2 介导的 Hippo 通路激活
- 批准号:
10734173 - 财政年份:2023
- 资助金额:
$ 258.56万 - 项目类别:
Enhancing the Efficacy of Docetaxel in Prostate Cancer
增强多西紫杉醇治疗前列腺癌的疗效
- 批准号:
10665071 - 财政年份:2022
- 资助金额:
$ 258.56万 - 项目类别:
Prostate Cancer Vulnerabilities to BH3 Mimetic Drugs
前列腺癌对 BH3 模拟药物的脆弱性
- 批准号:
10407648 - 财政年份:2021
- 资助金额:
$ 258.56万 - 项目类别:
Prostate Cancer Vulnerabilities to BH3 Mimetic Drugs
前列腺癌对 BH3 模拟药物的脆弱性
- 批准号:
10279279 - 财政年份:2021
- 资助金额:
$ 258.56万 - 项目类别:
SOX9 Mediation of AR and ERG Driven Prostate Cancer
SOX9 介导 AR 和 ERG 驱动的前列腺癌
- 批准号:
9477598 - 财政年份:2014
- 资助金额:
$ 258.56万 - 项目类别:
SOX9 Mediation of AR and ERG Driven Prostate Cancer
SOX9 介导 AR 和 ERG 驱动的前列腺癌
- 批准号:
8653225 - 财政年份:2014
- 资助金额:
$ 258.56万 - 项目类别:
SOX9 Mediation of AR and ERG Driven Prostate Cancer
SOX9 介导 AR 和 ERG 驱动的前列腺癌
- 批准号:
9269164 - 财政年份:2014
- 资助金额:
$ 258.56万 - 项目类别:
Androgen Receptor Action in Castration Resistant Prostate Cancer
雄激素受体在去势抵抗性前列腺癌中的作用
- 批准号:
8475909 - 财政年份:2013
- 资助金额:
$ 258.56万 - 项目类别:
Project 2: Mechanisms Driving AR Full Length and Splice Variant Activities and Antagonist Resistance
项目 2:驱动 AR 全长和剪接变体活动和拮抗剂耐药性的机制
- 批准号:
10363640 - 财政年份:2013
- 资助金额:
$ 258.56万 - 项目类别:
Androgen Receptor Action in Castration Resistant Prostate Cancer
雄激素受体在去势抵抗性前列腺癌中的作用
- 批准号:
10363638 - 财政年份:2013
- 资助金额:
$ 258.56万 - 项目类别:
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