U01CA294536
Cooperative Agreement
Overview
Grant Description
Pre-cancer atlas of skin cancer - The overarching goal of our proposal is to develop a pre-cancer atlas of skin cancer.
Skin is an ideal model to study the early phases of tumorigenesis because it is easily accessible for monitoring and non-invasive sampling.
As the primary barrier against the environment, skin cells acquire large numbers of somatic mutations during each person’s life, fueling the growth of a diverse set of tumors from the various cell types in the organ.
Our atlas will focus on the evolution of melanoma and cutaneous squamous cell carcinoma, which respectively arise from melanocytes and keratinocytes, because these are the deadliest forms of skin cancer, responsible for an estimated 20,000 deaths per year in the United States.
Skin is also an immunologically active organ, providing opportunities to study the role of the immune system in cancer development.
The role of immune surveillance in restraining skin cancers is illustrated by the dramatic increase of skin cancers in immunosuppressed individuals and the therapeutic successes of immune-based therapies.
There is a major, unmet need to understand how the immune system interacts with tumors early in their development.
To address this need, we designed an atlas to deduce how the immune system shapes tumor evolution during the transition from the pre-cancerous to cancerous stage.
This will be accomplished through a series of molecular assays, performed on precursor-associated cancers (i.e., skin cancers with an adjacent pre-cursor lesion).
Specifically, we will perform:
1. Bulk-cell DNA-sequencing,
2. T-cell and B-cell receptor clonotyping,
3. Bulk-cell RNA-sequencing,
4. Spatial transcriptomics (10X Visium),
5. Spatial transcriptomics (10X Xenium), and
6. Spatial proteomics (IBEX) and compare the individual progression stages of each precursor-associated tumor.
Collectively, these assays will reveal the key genetic and immunological events occurring at the transition from pre-cancer to cancer.
Completion of these studies will reveal candidate diagnostic and prognostic biomarkers and possibly novel targets for therapeutic intervention.
Our team has a collaborative track record of studying the evolution of skin cancers with clinical impact.
Our work has contributed to the World Health Organization’s classification of melanoma, and we have discovered multiple biomarkers that have entered routine use in clinical practice to diagnose melanocytic neoplasms.
As another major component of our center, we will establish a core, with dedicated personnel, charged with the goal of engaging with the HTAN network, the broader scientific community, and the lay public.
Skin is an ideal model to study the early phases of tumorigenesis because it is easily accessible for monitoring and non-invasive sampling.
As the primary barrier against the environment, skin cells acquire large numbers of somatic mutations during each person’s life, fueling the growth of a diverse set of tumors from the various cell types in the organ.
Our atlas will focus on the evolution of melanoma and cutaneous squamous cell carcinoma, which respectively arise from melanocytes and keratinocytes, because these are the deadliest forms of skin cancer, responsible for an estimated 20,000 deaths per year in the United States.
Skin is also an immunologically active organ, providing opportunities to study the role of the immune system in cancer development.
The role of immune surveillance in restraining skin cancers is illustrated by the dramatic increase of skin cancers in immunosuppressed individuals and the therapeutic successes of immune-based therapies.
There is a major, unmet need to understand how the immune system interacts with tumors early in their development.
To address this need, we designed an atlas to deduce how the immune system shapes tumor evolution during the transition from the pre-cancerous to cancerous stage.
This will be accomplished through a series of molecular assays, performed on precursor-associated cancers (i.e., skin cancers with an adjacent pre-cursor lesion).
Specifically, we will perform:
1. Bulk-cell DNA-sequencing,
2. T-cell and B-cell receptor clonotyping,
3. Bulk-cell RNA-sequencing,
4. Spatial transcriptomics (10X Visium),
5. Spatial transcriptomics (10X Xenium), and
6. Spatial proteomics (IBEX) and compare the individual progression stages of each precursor-associated tumor.
Collectively, these assays will reveal the key genetic and immunological events occurring at the transition from pre-cancer to cancer.
Completion of these studies will reveal candidate diagnostic and prognostic biomarkers and possibly novel targets for therapeutic intervention.
Our team has a collaborative track record of studying the evolution of skin cancers with clinical impact.
Our work has contributed to the World Health Organization’s classification of melanoma, and we have discovered multiple biomarkers that have entered routine use in clinical practice to diagnose melanocytic neoplasms.
As another major component of our center, we will establish a core, with dedicated personnel, charged with the goal of engaging with the HTAN network, the broader scientific community, and the lay public.
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
San Francisco,
California
941153006
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 409% from $1,019,013 to $5,182,743.
San Francisco Regents Of The University Of California was awarded
Skin Cancer Pre-Cancer Atlas: Immune System Interaction Study
Cooperative Agreement U01CA294536
worth $5,182,743
from National Cancer Institute in September 2024 with work to be completed primarily in San Francisco California 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 Pre-Cancer Atlas (PCA) 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 U01CA294536
Additional Detail
Award ID FAIN
U01CA294536
SAI Number
U01CA294536-1242759639
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Public/State Controlled Institution Of Higher Education
Awarding Office
75NC00 NIH National Cancer Institute
Funding Office
75NC00 NIH National Cancer Institute
Awardee UEI
KMH5K9V7S518
Awardee CAGE
4B560
Performance District
CA-11
Senators
Dianne Feinstein
Alejandro Padilla
Alejandro Padilla
Modified: 9/24/25