Emory University Lung Cancer SPORE
埃默里大学肺癌孢子
基本信息
- 批准号:10685410
- 负责人:
- 金额:$ 183.99万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-07-10 至 2024-05-31
- 项目状态:已结题
- 来源:
- 关键词:ABCG2 geneAddressAnimal Cancer ModelAnimal ModelAreaAwardBiological MarkersBiometryCD8-Positive T-LymphocytesCancer EtiologyCancer PatientCell Fate ControlCessation of lifeCollaborationsComprehensive Cancer CenterCoupledDataDedicationsDependenceDeuteriumDevelopmentDiagnosisDiseaseDrug resistanceEpidermal Growth Factor ReceptorFundingGoalsHealth SciencesHealthcare SystemsHematologyHumanImmune checkpoint inhibitorImmunologic FactorsImmunologistImmunotherapyIn VitroInstitutionInvestigationIonizing radiationJournalsKRAS2 geneLabelLocationMERTK geneMalignant NeoplasmsMalignant neoplasm of lungMediatorMedical OncologyModernizationMolecularMolecular TargetMutateMutationNeoadjuvant TherapyNon-Small-Cell Lung CarcinomaOncologistOutcomePD-1 blockadePathologyPatient-Focused OutcomesPatientsPhenotypePhosphorylationPhosphorylation SitePlayPrognostic MarkerPropertyPublishingRadiation therapyRecommendationReproduction sporesResearchResearch PersonnelResistanceResource SharingRoleSDZ RADSafetyScientistSignal TransductionSiteT-LymphocyteTP53 geneTechnologyTestingTherapeutic AgentsTherapy trialTreatment EfficacyTumor ImmunityUniversitiesWorkanti-PD1 therapyanti-canceranticancer researchantitumor effectbiomedical informaticscancer therapycareerclinical applicationclinical efficacyclinical investigationdrug discoveryexperienceimprovedimproved outcomein vivoinhibitorinnovationlung cancer cellmTOR inhibitionmedical schoolsmembermolecular targeted therapiesmortalitymultidisciplinarymutantnovelnovel strategiesnovel therapeutic interventionpatient populationphase 1 studypreclinical developmentprogrammed cell death protein 1programsradiation resistanceresistance mechanismsmall moleculestemstem-like celltargeted agenttargeted treatmenttherapeutic targettherapy resistanttranslational goaltranslational scientisttumortumorigenesis
项目摘要
OVERVIEW SUMMARY/ABSTRACT
Lung cancer is the leading cause of cancer-related deaths, with more than 1.6 million deaths/year globally. It is
often diagnosed at an advanced stage and is associated with poor outcomes for the majority of patients. This
application for a lung cancer SPORE award from Emory University brings together an outstanding and multi-
disciplinary team of oncologists, immunologists, drug discovery experts, and translational researchers dedicated
to lung cancer research to address critical questions that will improve the outcome for patients with this lethal
disease. Our proposed program will have significant impact in two crucial areas of lung cancer management:
enhancing the efficacy of immunotherapy and overcoming treatment resistance through the development of
novel molecularly targeted agents. Through strong teamwork carried out by this highly collaborative team of
dedicated investigators, and building on exciting data published in leading journals by our group since our
previous SPORE application, this revised submission aims to achieve substantial improvements in the
management of patients with non-small cell lung cancer (NSCLC), through three overall Specific Aims: Aim 1:
To evaluate stem-like T cells and improve efficacy of checkpoint inhibitors in NSCLC (Project 1); Aim 2:
To target MERTK to improve outcomes for EGFR-mutated NSCLC (Project 2); and Aim 3: To target Bax
signaling to overcome treatment resistance in NSCLC (Project 3). The Emory Lung Cancer SPORE program
will be supported by close interaction with the Administrative Core (Core 1), Pathology Core (Core 2) and the
Biostatistics and Biomedical Informatics Core (Core 3), and will conduct Career Enhancement and
Developmental Research Programs (CEP and DRP). The SPORE program will benefit from regular advice and
recommendations from External and Internal Advisory Board members regarding its progress and direction. Our
program will receive strong institutional support including modern research space, excellent shared resources,
and a significant level of matching funds (totaling $2.25M) from the Winship Cancer Institute of Emory University
(an NCI-designated Comprehensive Cancer Center), Emory University Woodruff Health Sciences Center, Emory
Healthcare System, Emory School of Medicine, and the Department of Hematology and Medical Oncology.
Through team-driven innovative research efforts in immunotherapies and molecularly targeted therapeutics, we
are confident that this SPORE program, in collaboration with other lung cancer SPORE sites, will have a major
positive impact on the management of lung cancer.
概述摘要/摘要
肺癌是与癌症相关死亡的主要原因,全球每年超过160万人死亡。这是
通常在晚期诊断出,大多数患者的结局差。这
埃默里大学(Emory University)申请肺癌孢子奖召集
肿瘤学家,免疫学家,药物发现专家和翻译研究人员的纪律团队敬业
肺癌研究以解决关键问题,以改善这种致命患者的结果
疾病。我们提出的计划将在肺癌管理的两个关键领域产生重大影响:
通过发展,增强免疫疗法和克服治疗抗性的功效
新型分子靶向剂。通过这个高度协作的团队实施的强大团队合作
专门的调查人员,并基于我们小组在领先期刊上发表的令人兴奋的数据以来
以前的孢子应用程序,此修订后的提交旨在实现
通过三个总体特定目的管理非小细胞肺癌(NSCLC)患者的管理:目标1:
评估样干细胞并提高NSCLC检查点抑制剂的功效(项目1);目标2:
靶向MERTK,以改善EGFR突变的NSCLC的结果(项目2);和目标3:针对Bax
信号传导以克服NSCLC的治疗耐药性(项目3)。埃默里肺癌孢子计划
与行政核心(核心1),病理核心(核心2)和
生物统计学和生物医学信息学核心(核心3),并将进行职业增强和
发展研究计划(CEP和DRP)。孢子计划将从常规建议中受益,
外部和内部咨询委员会成员就其进度和方向的建议。我们的
计划将获得强大的机构支持,包括现代研究空间,出色的共享资源,
以及来自埃默里大学Winship癌症研究所的大量匹配资金(总计225万美元)
(NCI指定的综合癌症中心),Emory University Woodruff Health Sciences Center,Emory
医疗保健系统,埃默里医学院以及血液学和医学肿瘤学系。
通过团队驱动的免疫疗法和分子靶向疗法的创新研究工作,我们
相信该孢子计划与其他肺癌孢子站点合作,将有一个主要
对肺癌治疗的积极影响。
项目成果
期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Hope and Challenges: Immunotherapy in EGFR-Mutant NSCLC Patients.
- DOI:10.3390/biomedicines11112916
- 发表时间:2023-10-28
- 期刊:
- 影响因子:4.7
- 作者:
- 通讯作者:
Targeting MERTK and AXL in EGFR Mutant Non-Small Cell Lung Cancer.
- DOI:10.3390/cancers13225639
- 发表时间:2021-11-11
- 期刊:
- 影响因子:5.2
- 作者:Yan D;Earp HS;DeRyckere D;Graham DK
- 通讯作者:Graham DK
TMPRSS2 and SARS-CoV-2 SPIKE interaction assay for uHTS.
- DOI:10.1093/jmcb/mjad017
- 发表时间:2023-08-03
- 期刊:
- 影响因子:5.5
- 作者:
- 通讯作者:
Spatially variant immune infiltration scoring in human cancer tissues.
- DOI:10.1038/s41698-022-00305-4
- 发表时间:2022-09-01
- 期刊:
- 影响因子:7.9
- 作者:Allam, Mayar;Hu, Thomas;Lee, Jeongjin;Aldrich, Jeffrey;Badve, Sunil S.;Gokmen-Polar, Yesim;Bhave, Manali;Ramalingam, Suresh S.;Schneider, Frank;Coskun, Ahmet F.
- 通讯作者:Coskun, Ahmet F.
Multiplexed protein profiling reveals spatial subcellular signaling networks.
- DOI:10.1016/j.isci.2022.104980
- 发表时间:2022-09-16
- 期刊:
- 影响因子:5.8
- 作者:Cai, Shuangyi;Hu, Thomas;Venkatesan, Mythreye;Allam, Mayar;Schneider, Frank;Ramalingam, Suresh S.;Sun, Shi-Yong;Coskun, Ahmet F.
- 通讯作者:Coskun, Ahmet F.
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{{ truncateString('HAIAN FU', 18)}}的其他基金
Deciphering LKB1-associated immunotherapy resistance in lung adenocarcinoma (LUAD)
解读肺腺癌 (LUAD) 中 LKB1 相关免疫治疗耐药性
- 批准号:
10411665 - 财政年份:2022
- 资助金额:
$ 183.99万 - 项目类别:
Deciphering LKB1-associated immunotherapy resistance in lung adenocarcinoma (LUAD)
解读肺腺癌 (LUAD) 中 LKB1 相关免疫治疗耐药性
- 批准号:
10631134 - 财政年份:2022
- 资助金额:
$ 183.99万 - 项目类别:
Project 2: Reversing STING-mediated immunosuppression in LKB1-mutant lung adenocarcinoma
项目 2:逆转 LKB1 突变型肺腺癌中 STING 介导的免疫抑制
- 批准号:
10631142 - 财政年份:2022
- 资助金额:
$ 183.99万 - 项目类别:
Project 2: Reversing STING-mediated immunosuppression in LKB1-mutant lung adenocarcinoma
项目 2:逆转 LKB1 突变型肺腺癌中 STING 介导的免疫抑制
- 批准号:
10411667 - 财政年份:2022
- 资助金额:
$ 183.99万 - 项目类别:
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相似海外基金
Project 2: Targeting MERTK to improve outcomes for EGFR-mutated NSCLC
项目 2:靶向 MERTK 改善 EGFR 突变 NSCLC 的预后
- 批准号:
10685418 - 财政年份:2019
- 资助金额:
$ 183.99万 - 项目类别:
Project 2: Targeting MERTK to improve outcomes for EGFR-mutated NSCLC
项目 2:靶向 MERTK 改善 EGFR 突变 NSCLC 的预后
- 批准号:
10210199 - 财政年份:2019
- 资助金额:
$ 183.99万 - 项目类别: