grant

Cancer Biology and Cancer Stem Cells

Organization STANFORD UNIVERSITYLocation STANFORD, UNITED STATESPosted 4 Jun 2007Deadline 31 May 2027
NIHUS FederalResearch GrantFY2025ATAC sequencingATAC-seqATACseqAreaAssay for Transposase-Accessible Chromatin using sequencingBasic ResearchBasic ScienceBiologic ModelsBiologicalBiological ModelsBreast CancerCancer BiologyCancer InductionCancer TreatmentCancersCarcinomaCell BodyCell Communication and SignalingCell Culture SystemCell SignalingCellsChromatinClinicalClinical InvestigatorClinical TrialsCollaborationsDevelopmentDoctor of PhilosophyDrugsEatingEngineeringEpithelial cancerEpitheliumErinaceidaeFaculty RecruitmentFocus GroupsFood IntakeFundingFutureGEM modelGEMM modelGene ExpressionGeneralized GrowthGeneticGenetically Engineered MouseGenomicsGoalsGrantGroup MeetingsGrowthHedgehogsHepatic CancerHumanitiesInfrastructureInstitutionIntracellular Communication and SignalingJournalsLungLung Respiratory SystemMacrophageMagazineMalignant Breast NeoplasmMalignant CellMalignant Epithelial NeoplasmsMalignant Epithelial TumorsMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant Pancreatic NeoplasmMalignant TumorMalignant Tumor of the LungMalignant lymphoid neoplasmMalignant neoplasm of liverMalignant neoplasm of lungMalignant neoplasm of pancreasManuscriptsMedicationMetastasisMetastasizeMetastatic LesionMetastatic MassMetastatic NeoplasmMetastatic TumorModel SystemModelingNational Institutes of HealthNeoplasm MetastasisNormal TissueNormal tissue morphologyOncogenesisOrganoidsPancreasPancreas CancerPancreaticPancreatic CancerPathway interactionsPeer ReviewPh.D.PhDPharmaceutical PreparationsProteomicsPublishingPulmonary CancerPulmonary malignant NeoplasmRegulationResearchResearch Peer ReviewResource SharingRoleScienceSecondary NeoplasmSecondary TumorSignal PathwaySignal TransductionSignal Transduction SystemsSignalingSolid NeoplasmSolid TumorSourceStructureTherapeuticTissue GrowthTranslatingTranslational ResearchTranslational ScienceTumor CellTumor Suppressor ProteinsUnited States National Institutes of HealthWomanWorkanti-cancer therapyassay for transposase accessible chromatin followed by sequencingassay for transposase accessible chromatin seqassay for transposase accessible chromatin sequencingassay for transposase-accessible chromatin with sequencingbiologicbiological signal transductioncancer cellcancer diagnosiscancer initiationcancer metastasiscancer microenvironmentcancer progenitorcancer progenitor cellscancer progressioncancer stem cellcancer stem like cellcancer therapycancer-directed therapycarcinogenesisdevelopmentaldrug developmentdrug/agentepithelial carcinomagenetically engineered mouse modelgenetically engineered murine modelimprovedinhibitorinsightliver cancerliver malignancylung cancerlymphoid cancerslymphoid malignancymalignancymalignant breast tumormalignant liver tumormalignant progenitormalignant stem cellmedical collegemedical schoolsmembermouse modelmurine modelnative protein drugneoplasm progressionneoplasm/cancerneoplastic cellneoplastic progressionnew approachesnew drug targetnew drug treatmentsnew druggable targetnew drugsnew pharmacological therapeuticnew pharmacotherapy targetnew technologynew therapeutic targetnew therapeuticsnew therapynew therapy targetnext generation therapeuticsnovelnovel approachesnovel drug targetnovel drug treatmentsnovel druggable targetnovel drugsnovel pharmaco-therapeuticnovel pharmacological therapeuticnovel pharmacotherapy targetnovel strategiesnovel strategynovel technologiesnovel therapeutic targetnovel therapeuticsnovel therapynovel therapy targetoncogenic progenitoroncogenic stem cellsontogenypancreatic malignancypathwaypeer supportpharmaceutical proteinpre-clinical studypreclinical studyprogenitor like cancer cellprogramsprotein drug agentprotein-based drugrecruit teachersresponse to therapyresponse to treatmentschool of medicineself-renewself-renewalsmall moleculesocial rolestem like cancer cellteacher recruitmenttherapeutic proteintherapeutic responsetherapeutic targettherapy responsetissue progenitortissue specific progenitor cellstissue specific stem cellstissue stem cellstranslation researchtranslational impacttranslational investigationtreatment responsetreatment responsivenesstumortumor cell metastasistumor growthtumor microenvironmenttumor progressiontumor suppressortumorigenesiswork groupworking group
Sign up free to applyApply link · pipeline · email alerts
— or —

Get email alerts for similar roles

Weekly digest · no password needed · unsubscribe any time

Full Description

PROJECT SUMMARY
The Cancer Biology and Cancer Stem Cells (CB) Program is a basic and translational science program that aims

to understand the fundamental mechanisms underlying cancer development. From these insights, we aspire to

improve cancer diagnosis and treatment through the following specific aims: (1) understand the regulation and

function of normal and cancer stem cells, (2) understand the mechanisms of initiation and progression of

epithelial cancers, and (3) identify potential new therapeutic targets.

The program is co-led by Laura Attardi, PhD, and Roeland Nusse, PhD. In 2019, the former Cancer Biology

Program and Cancer Stem Cells Program merged with the approval of the EAB to become the current Cancer

Biology and Cancer Stem Cells Program. In the current funding period, program members have made substantial

progress in understanding the self-renewal pathways of cancer stem cells and in elucidating signaling pathways

of high cancer relevance, including most prominently the Wnt and Hedgehog pathways. They have also

pioneered a new technology, ATAC-seq, that enables a more fundamental understanding of the role of chromatin

in gene expression and used organoid and mouse model systems to discover the mechanisms of tumor

suppressors and progression and to uncover new therapeutic targets. The 53 members of the current program

represent 16 departments within the Schools of Medicine (SOM), Humanities and Sciences, and Engineering.

Members are supported by peer-reviewed research totaling $25.6M, including 34 R01s, 12 R35s, 6 U01s, and

3 T32s. Peer-reviewed cancer-focused research funding consists of $7M from the NCI, $12M from other NIH

sources, and $6.6M from other peer-reviewed sources. The members of this program are highly motivated and

interactive in their goal to use basic science approaches to understand cancer initiation and progression, with

the ultimate aim of improving cancer diagnosis and treatment. Since 2015, members of the CB Program have

published 668 manuscripts. Of these, 16% represent intra-programmatic, 31% represent inter-programmatic,

and 95% multi-institutional collaborations, 43% and 33% are in journals with IF>10 and IF>20, respectively. The

Stanford Cancer Institute (SCI) enhances the program’s goals by providing state-of-the-art shared resources,

seed grant support for new projects, programmatic funds, retreats, special seminars, support for new faculty

recruitments, and clinical trial infrastructure for translation of research findings. The support from the SCI has

also been instrumental in promoting both intra- and inter-programmatic collaborations through organizing

programmatic and working group meetings and providing the means to interface with the more clinically oriented

programs to enhance our translational impact. Future plans incluce to further enhance intra- and inter-

progammtic collaborations by enhance cancer focused working groups.

Grant Number: 5P30CA124435-17
NIH Institute/Center: NIH

Principal Investigator: LAURA ATTARDI

Sign up free to get the apply link, save to pipeline, and set email alerts.

Sign up free →

Agency Plan

7-day free trial

Unlock procurement & grants

Upgrade to access active tenders from World Bank, UNDP, ADB and more — with email alerts and pipeline tracking.

$29.99 / month

  • 🔔Email alerts for new matching tenders
  • 🗂️Track tenders in your pipeline
  • 💰Filter by contract value
  • 📥Export results to CSV
  • 📌Save searches with one click
Start 7-day free trial →