(PQA-4) Organoid Omics To Detect And Defeat Ductal Pancreatic Cancer
(PQA-4) 类器官组学检测和战胜导管胰腺癌
基本信息
- 批准号:9336271
- 负责人:
- 金额:$ 55.27万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-09-22 至 2018-08-31
- 项目状态:已结题
- 来源:
- 关键词:AntibodiesBiological ModelsCancer PatientCell Culture SystemCell surfaceCellsCellularityClinicalClustered Regularly Interspaced Short Palindromic RepeatsDataDevelopmentDiagnosisDiagnosticDiseaseDisease ManagementDistantDuctalDuctal Epithelial CellEarly DiagnosisEnzymesEpitopesEvaluationExcisionFailureGene ExpressionGoalsHeterogeneityHumanImplantInvestigationLaboratoriesLesionMalignant - descriptorMalignant NeoplasmsMalignant neoplasm of pancreasMediatingMediator of activation proteinMetastatic AdenocarcinomaMolecularMolecular AnalysisMusNormal CellOperative Surgical ProceduresOrganoidsPancreasPancreatic Ductal AdenocarcinomaPancreatic ductPatient riskPatientsPolysaccharidesPopulationPrecancerous ConditionsPremalignantPremalignant CellPrimary NeoplasmProteomicsRecurrenceResectedSiteStromal CellsSurvival RateSystemTechniquesTherapeuticTimeTissuesTumorigenicityWorkbiomarker panelcancer cellcell growthcell typedesigndiagnostic biomarkergenome editingglycosylationhuman tissuein vivoinsightknock-downmouse modelneoplasticnovelnovel therapeutic interventionoverexpressionpotential biomarkerpreventpublic health relevancerelapse risksingle cell analysisstudy populationtargeted agenttargeted treatmenttherapeutic candidatetherapeutic developmenttherapeutic targettooltranscriptome sequencingtranscriptomicstumortumor progressiontumorigenic
项目摘要
DESCRIPTION (provided by applicant): The lethality of pancreatic ductal adenocarcinoma is universal, even in patients who present with small primary tumors and undergo surgery with curative intent. Therefore, determining whether there are specific molecular alterations contributing to the final transformation of pre- malignant cells, both for early detection and for patients with precursor lesions adjacent to their surgical resection site, may have clinical benefits. Since the investigation of pancreatic cancer in human and mouse tissues is challenging due to the low neoplastic cellularity and poorly defined tumor margins, we have developed a novel organoid cell culture system to expand primary mouse and human normal, pre-malignant and malignant pancreatic ductal cells. These organoids will be comprehensively analyzed for molecular alterations using transcriptomic, proteomic and other omics level approaches in order to identify candidates that correlate with the earliest stages of pancreatic cancer progression. Specific molecular alterations will be considered for potential therapeutic and/or diagnostic development in mouse and human tissues, using conventional and single cell analyses. Such findings will enable the identification of at risk patients, development of new therapeutic strategies, and provide new insights regarding how to prevent pancreatic cancer occurrence and recurrence. Significance The failure of disease management in pancreatic cancer patients following surgery is due to either local tumor regrowth or distant metastatic spread. In addition, if pre-malignant cells that are likely transform into a frank malignancy could
be identified and treated before forming a tumor, many lives could be saved. In order to detect and treat pre-malignant cells that are poised to become tumorigenic in mice and patients, we will develop new organoid model systems and use these systems to better characterize and understand the transition from a pre- malignant disease state to invasive, metastatic adenocarcinoma.
描述(由申请人提供):胰腺导管腺癌的致死率是普遍的,即使是原发肿瘤较小并接受手术治疗的患者。因此,确定是否存在特定的分子改变有助于恶性前病变细胞的最终转化,无论是对早期发现还是对手术切除部位附近的前驱病变患者,都可能具有临床益处。由于肿瘤细胞密度低且肿瘤边缘不明确,在人类和小鼠组织中研究胰腺癌具有挑战性,因此我们开发了一种新的类器官细胞培养系统来扩增小鼠和人类原代正常、癌前和恶性胰腺导管细胞。这些类器官将使用转录组学、蛋白质组学和其他组学水平的方法进行全面的分子改变分析,以确定与胰腺癌早期进展相关的候选器官。使用常规和单细胞分析,将考虑对小鼠和人体组织的潜在治疗和/或诊断发展进行特定的分子改变。这些发现将有助于识别高危患者,开发新的治疗策略,并为如何预防胰腺癌的发生和复发提供新的见解。意义胰腺癌患者手术后疾病管理失败的原因可能是肿瘤局部再生或远处转移扩散。此外,如果癌前细胞有可能转变为恶性肿瘤
项目成果
期刊论文数量(3)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Quid pro Quo: A Tumor is Not Alone.
- DOI:10.1016/j.molmed.2017.03.007
- 发表时间:2017-05
- 期刊:
- 影响因子:13.6
- 作者:C. Sacristán;D. Tuveson
- 通讯作者:C. Sacristán;D. Tuveson
CRISPR-Induced TMPRSS2-ERG Gene Fusions in Mouse Prostate Organoids.
- DOI:
- 发表时间:2017
- 期刊:
- 影响因子:0
- 作者:E. Driehuis;H. Clevers
- 通讯作者:E. Driehuis;H. Clevers
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David A Tuveson其他文献
Modeling human lung cancer in mice: similarities and shortcomings
在小鼠中模拟人类肺癌:相似性与不足之处
- DOI:
10.1038/sj.onc.1203107 - 发表时间:
1999-09-20 - 期刊:
- 影响因子:7.300
- 作者:
David A Tuveson;Tyler Jacks - 通讯作者:
Tyler Jacks
David A Tuveson的其他文献
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{{ truncateString('David A Tuveson', 18)}}的其他基金
Nrf2 Regulation of Ductal Pancreatic Cancer Etiology and Treatment Response
Nrf2 对导管胰腺癌病因和治疗反应的调节
- 批准号:
10056198 - 财政年份:2016
- 资助金额:
$ 55.27万 - 项目类别:
(PQA-4) Organoid Omics To Detect And Defeat Ductal Pancreatic Cancer
(PQA-4) 类器官组学检测和战胜导管胰腺癌
- 批准号:
9122093 - 财政年份:2014
- 资助金额:
$ 55.27万 - 项目类别:
(PQA-4) Organoid Omics To Detect And Defeat Ductal Pancreatic Cancer
(PQA-4) 类器官组学检测和战胜导管胰腺癌
- 批准号:
8792084 - 财政年份:2014
- 资助金额:
$ 55.27万 - 项目类别:
(PQA-4) Organoid Omics To Detect And Defeat Ductal Pancreatic Cancer
(PQA-4) 类器官组学检测和战胜导管胰腺癌
- 批准号:
8930940 - 财政年份:2014
- 资助金额:
$ 55.27万 - 项目类别:
Mutant mouse models of exocrine pancreatic cancer
外分泌胰腺癌突变小鼠模型
- 批准号:
7498542 - 财政年份:2004
- 资助金额:
$ 55.27万 - 项目类别:
Mutant mouse models of exocrine pancreatic cancer
外分泌胰腺癌突变小鼠模型
- 批准号:
6916463 - 财政年份:2004
- 资助金额:
$ 55.27万 - 项目类别:
Mutant mouse models of exocrine pancreatic cancer
外分泌胰腺癌突变小鼠模型
- 批准号:
7227182 - 财政年份:2004
- 资助金额:
$ 55.27万 - 项目类别:
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