Stanford and Northrop Grumman proposal for the Oncology Models Forum
Stanford and Northrop Grumman proposal for the Oncology Models Forum
批准号:
9762589
负责人:
ATUL J BUTTE
金额:
$91.28万
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 2021-08-31
关键词:
AddressAreaAwardBioinformaticsCancer ModelCatalogsCommunicable DiseasesCommunitiesCommunity Clinical Oncology ProgramCredentialingDataData AnalysesDatabasesDiagnosticDisease modelEducational workshopEnsureFeedbackFundingFunding MechanismsFutureGenetically Engineered MouseGoalsHourHumanHypersensitivityImmunologyInbred MouseInstitutesKnowledgeLearningMalignant NeoplasmsManuscriptsMarylandMissionModelingMusNIH Program AnnouncementsNanotechnologyNational Cancer InstituteNatureOnline SystemsOutputParticipantPublished CommentPublishingResearchResearch PersonnelResourcesRoleScienceServicesSiteSoftware EngineeringStructureSupport ContractsTechnologyTherapeuticTranslationsUniversitiesValidationXenograft procedurebiomedical informaticsbiomedical ontologycommunity buildingdata modelingdata sharingdesignexperiencehuman datainnovationknowledge basemeetingsmouse modeloncologyopen sourcepre-clinicalprogramspublic health relevanceskillssoftware developmentsuccesssupport networktechnology developmenttooltranslational cancer researchtransplant modeltumorweb sitewebinar
中文摘要
描述(由申请人提供):肿瘤学模型论坛(OMF)的使命是调整、利用和整合癌症小鼠模型的数据和知识,以推动在癌症诊断、治疗和疾病模型的发现方面取得更快的成功。2014年6月初,美国国家癌症研究所(NCI)发布了PAR-14-239,将OMF描述为“一个全面的信息资源,以指导生成、验证和认证新模型,告知它们的实际用途,推进建模技术,[并]提供可用的模型资源、程序和服务的目录。”为了最大限度地利用现有资源,这个在线网站被指定使用现有的开源科学网站框架HUBZO,避免了从零开始创建一个新的科学网站的昂贵费用。OMF被设计为一个社区建设工具,有在线论坛和年度会议。具体内容将由与OMF并行资助的协作R01提供。临床前的小鼠和人在小鼠的模型对未来的癌症转化至关重要。2013年发表了4300多篇描述或使用癌症小鼠模型的手稿,包括异种移植和移植模型、自发模型、近交系小鼠和基因工程小鼠模型(GEMM)。NCI癌症模型数据库(CaMOD)现在列出了数千种在一个或多个部位容易发生肿瘤的小鼠模型。但关于这些模型的数据分散在众多资源中。未来利用癌症小鼠模型研究的成功不再那么依赖于新模型的持续创建,而更多地依赖于对数千个现有模型的验证、对这些模型上的知识和数据的透明访问、模型数据与人类数据的比较以及研究社区的组织。我们计划开发肿瘤学模型论坛(OMF)来实现这些目标。我们提议的OMF将整合关于癌症小鼠模型的结构化和非结构化数据和知识,使新的发现和新的翻译工具的开发成为可能。
英文摘要
DESCRIPTION (provided by applicant): The mission for the Oncology Models Forum (OMF) is to align, harness and integrate data and knowledge of cancer mouse models to drive more rapid success in the discovery of diagnostics, therapeutics, and models of disease in cancer. In early June 2014, the National Cancer Institute (NCI) released PAR-14-239 describing the OMF as a "comprehensive resource for information to guide generating, validating, and credentialing new models, informing their practical uses, advancing modeling technologies, [and] providing catalogs of available models resources, programs, and services." To maximize the use of available resources, this online site was prescribed to use HUBzero, an existing open-source scientific website framework, avoiding the expensive creation of a new scientific website from scratch. The OMF was designed as a community-building tool, with online discussion forums and an annual meeting. Specific content will be provided from the collaborative R01s funded in parallel to the OMF. Pre-clinical mouse and human-in-mouse models are critical to future translation in cancer. More than 4,300 manuscripts were published in 2013 describing or using cancer mouse models, including xenografts and transplantation models, spontaneous models, inbred mice, and genetically engineered mouse models (GEMM). The NCI Cancer Models Database (caMOD) now lists thousands of mouse models that are prone to develop tumors in one or more sites. But data on these models is scattered across numerous resources. Future success in research using cancer mouse models is now less dependent on the continued creation of new models, and more dependent on the validation of the thousands of currently available models, transparent access to knowledge and data on these models, comparisons of model data with human data, and organization of the research community. We plan to develop the Oncology Models Forum (OMF) to accomplish these goals. Our proposed OMF will integrate structured and unstructured data and knowledge on cancer mouse models, enabling new discoveries and the development of new translational tools.
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Do Cancer Clinical Trial Populations Truly Represent Cancer Patients? A Comparison of Open Clinical Trials to the Cancer Genome Atlas
癌症临床试验人群是否真正代表癌症患者?
DOI:
10.1142/9789814749411_0029
发表时间:
2016
期刊:
Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing
影响因子:
--
作者:
[N. Geifman, A. Butte]
通讯作者:
A. Butte
Widespread parainflammation in human cancer.
人类癌症中广泛的副炎症。
DOI:
10.1186/s13059-016-0995-z
发表时间:
2016-07-08
期刊:
Genome biology
影响因子:
12.3
作者:
[Aran D, Lasry A, Zinger A, Biton M, Pikarsky E, Hellman A, Butte AJ, Ben-Neriah Y]
通讯作者:
Ben-Neriah Y
DOI:
10.1016/s1470-2045(17)30698-8
发表时间:
2017-11
期刊:
The Lancet. Oncology
影响因子:
--
作者:
[Jaffee EM, Dang CV, Agus DB, Alexander BM, Anderson KC, Ashworth A, Barker AD, Bastani R, Bhatia S, Bluestone JA, Brawley O, Butte AJ, Coit DG, Davidson NE, Davis M, DePinho RA, Diasio RB, Draetta G, Frazier AL, Futreal A, Gambhir SS, Ganz PA, Garraway L, Gerson S, Gupta S, Heath J, Hoffman RI, Hudis C, Hughes-Halbert C, Ibrahim R, Jadvar H, Kavanagh B, Kittles R, Le QT, Lippman SM, Mankoff D, Mardis ER, Mayer DK, McMasters K, Meropol NJ, Mitchell B, Naredi P, Ornish D, Pawlik TM, Peppercorn J, Pomper MG, Raghavan D, Ritchie C, Schwarz SW, Sullivan R, Wahl R, Wolchok JD, Wong SL, Yung A]
通讯作者:
Yung A
DOI:
10.1038/sdata.2016.27
发表时间:
2016-05-10
期刊:
Scientific data
影响因子:
9.8
作者:
[Geifman N, Butte AJ]
通讯作者:
Butte AJ
DOI:
10.1158/0008-5472.can-16-3383
发表时间:
2017-07-15
期刊:
Cancer research
影响因子:
11.2
作者:
[Lasry A, Aran D, Butte AJ, Ben-Neriah Y]
通讯作者:
Ben-Neriah Y
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