U01CA294527
Cooperative Agreement
Overview
Grant Description
A Multimodal 3D Atlas of Colorectal Cancer Across Ages of Onset - Project Summary
We propose the construction of a three-dimensional (3D) multimodal molecular atlas of colorectal cancer (CRC) across different ages of onset of the disease.
We aim to address the emerging clinical challenge of rising early-onset CRC cases by exploring molecular differences between early-onset and later-onset CRCS.
We hypothesize that aberrant interactions between the carcinogenic microbes, tumor metabolic niche, and the tumor microenvironment lead to accelerated transitions of precancerous cell states to malignant states.
Our atlas will focus on spatially mapping transitions from precancerous to cancerous components within the same tumor, utilizing a "phylogeographic" mapping approach to create individualized and global progression trajectories between tumor subtypes (early onset CRCS, later-onset microsatellite stable CRCS, later-onset microsatellite unstable CRCS).
We employ cutting-edge technologies, such as customized spatial transcriptomics, co-detection by indexing highly multiplexed immunofluorescence microscopy, untargeted imaging mass spectrometry, and histological and autofluorescence imaging, to comprehensively characterize CRC tissue at various molecular levels and spatial scales.
We employ a 3D multimodal strategy by reconstructing volumes from interleaving serial tissue sections evaluated by different technologies.
Paired whole exome sequencing and single-cell RNA-sequencing data will anchor our spatial analyses to our previous Human Tumor Atlas Network (HTAN) data.
We leverage our previous success in building colorectal atlases within the HTAN and ensure that data are released for open-access use to the research community.
We have a strong team with expertise in genomic profiling, multi-omic spatial analysis, biostatistics, and artificial intelligence.
Our proposal emphasizes our team's extensive track record in CRC research, with active programs in CRC, gut epithelial biology, CRC microbiome, epidemiology, and pathology.
Our goal is to provide unprecedented insights into the genetic, transcriptomic, metabolomic, microbial, and architectural features of CRC in a spatially resolved manner to better understand CRCS across various age groups.
We propose the construction of a three-dimensional (3D) multimodal molecular atlas of colorectal cancer (CRC) across different ages of onset of the disease.
We aim to address the emerging clinical challenge of rising early-onset CRC cases by exploring molecular differences between early-onset and later-onset CRCS.
We hypothesize that aberrant interactions between the carcinogenic microbes, tumor metabolic niche, and the tumor microenvironment lead to accelerated transitions of precancerous cell states to malignant states.
Our atlas will focus on spatially mapping transitions from precancerous to cancerous components within the same tumor, utilizing a "phylogeographic" mapping approach to create individualized and global progression trajectories between tumor subtypes (early onset CRCS, later-onset microsatellite stable CRCS, later-onset microsatellite unstable CRCS).
We employ cutting-edge technologies, such as customized spatial transcriptomics, co-detection by indexing highly multiplexed immunofluorescence microscopy, untargeted imaging mass spectrometry, and histological and autofluorescence imaging, to comprehensively characterize CRC tissue at various molecular levels and spatial scales.
We employ a 3D multimodal strategy by reconstructing volumes from interleaving serial tissue sections evaluated by different technologies.
Paired whole exome sequencing and single-cell RNA-sequencing data will anchor our spatial analyses to our previous Human Tumor Atlas Network (HTAN) data.
We leverage our previous success in building colorectal atlases within the HTAN and ensure that data are released for open-access use to the research community.
We have a strong team with expertise in genomic profiling, multi-omic spatial analysis, biostatistics, and artificial intelligence.
Our proposal emphasizes our team's extensive track record in CRC research, with active programs in CRC, gut epithelial biology, CRC microbiome, epidemiology, and pathology.
Our goal is to provide unprecedented insights into the genetic, transcriptomic, metabolomic, microbial, and architectural features of CRC in a spatially resolved manner to better understand CRCS across various age groups.
Awardee
Funding Goals
TO PROVIDE SUPPORT FOR INITIATIVES FUNDED UNDER THE 21ST CENTURY CURES ACT TO SUPPORT CANCER RESEARCH, SUCH AS THE DEVELOPMENT OF CANCER VACCINES, THE DEVELOPMENT OF MORE SENSITIVE DIAGNOSTIC TESTS FOR CANCER, IMMUNOTHERAPY AND THE DEVELOPMENT OF COMBINATION THERAPIES, AND RESEARCH THAT HAS THE POTENTIAL TO TRANSFORM THE SCIENTIFIC FIELD, THAT HAS INHERENTLY HIGHER RISK, AND THAT SEEKS TO ADDRESS MAJOR CHALLENGES RELATED TO CANCER.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
Nashville,
Tennessee
37203
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 385% from $1,063,411 to $5,159,940.
Vanderbilt University was awarded
3D Multimodal Atlas of Colorectal Cancer Across Ages - SEO Grant Title
Cooperative Agreement U01CA294527
worth $5,159,940
from National Cancer Institute in September 2024 with work to be completed primarily in Nashville Tennessee United States.
The grant
has a duration of 5 years and
was awarded through assistance program 93.353 21st Century Cures Act - Beau Biden Cancer Moonshot.
The Cooperative Agreement was awarded through grant opportunity Human Tumor Atlas (HTA) Research Centers (U01 Clinical Trial Not Allowed).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
9/1/24
Start Date
8/31/29
End Date
Funding Split
$5.2M
Federal Obligation
$0.0
Non-Federal Obligation
$5.2M
Total Obligated
Activity Timeline
Transaction History
Modifications to U01CA294527
Additional Detail
Award ID FAIN
U01CA294527
SAI Number
U01CA294527-24415268
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NC00 NIH National Cancer Institute
Awardee UEI
GTNBNWXJ12D5
Awardee CAGE
5E694
Performance District
TN-05
Senators
Marsha Blackburn
Bill Hagerty
Bill Hagerty
Modified: 9/24/25