# Project 3: Contribution of inflammation and DNA damaging factors to clonal expansion and malignant transformation in a community cohort of older adults

> **NIH NIH P01** · BAYLOR COLLEGE OF MEDICINE · 2024 · $636,666

## Abstract

Project Summary/Abstract
Project 3 will test the hypothesis that modifiable risk factors, including inflammation and DNA-damaging factors,
influence expansion of hematopoietic stem and progenitor cell (HSPC) clones with certain genetic mutations and
their transformation to hematologic malignancy. We will identify modifiable risk factors associated with HSPC
clonal expansion and malignant transformation in a prospective epidemiologic study of 9,513 persons (Black
27%, female 55%) now all >75 years old from ARIC, a long-standing community cohort study. We will use stored
buffy coat for single cell DNA sequencing, and leverage completed peripheral blood leukocyte (PBL) whole
exome sequencing (WES), methylation, and proteomic profiling. Aim 1 will determine long-term changes in clonal
composition at the single-cell level with resources from Core A and identify inflammation and DNA damage-
related factors associated with those changes. For 250 ARIC participants with ³1 clonal variant by WES at Time
1 or at Time 2 (20 years later) and/or hematologic malignancy after Time 2, we will measure individual leukocyte
variant profiles at both times by single cell-DNA sequencing. By tracking individual clones at unprecedented
resolution, we will assess clonal fitness and identify modifiable risk factors for expansion of clones with specific
variants. Our study is the first to address change in clonal composition with hematologic malignancy in a
community cohort. In Aim 2, we will evaluate the association of clonal composition, variant allele frequencies
(VAFs), and changes of known myeloid malignancy driver genes and novel recurrent variants with hematologic
malignancy risk over the span of two decades. In 9,513 participants, we will interrogate WES data at Time 1 and
2 (20 years apart) to identify novel recurrent variants with changing VAFs and classify participants by clonal
composition and VAFs of known driver genes. For driver genes, we will estimate associations of change in clonal
composition and VAF over time with hematologic malignancy risk. We project 341 first and 66 second primary
hematologic malignancies within our cohort. Aim 3 will evaluate the association of inflammation- and DNA
damage-related factors with hematologic malignancy risk in persons with detectable clonal variants. By Time 2,
we expect >10% of participants will have clonal variants detectable by WES in driver and novel genes. We will
estimate the association of modifiable factors with hematologic malignancy in persons with and without specific
clonal variants over 30 years. Project 3 will identify drugs to test as interventions for clonal expansion and
malignant transformation in mice in Projects 1 and 2. We also will test associations between altered cytokines
and CpG methylation identified in Project 1 and determine whether mutations identified in Project 2 are observed
in participants with DNA-damaging exposures. This Project will extensively utilize Core A for single-cell analysi...

## Key facts

- **NIH application ID:** 10833505
- **Project number:** 5P01CA265748-03
- **Recipient organization:** BAYLOR COLLEGE OF MEDICINE
- **Principal Investigator:** ELIZABETH A. PLATZ
- **Activity code:** P01 (R01, R21, SBIR, etc.)
- **Funding institute:** NIH
- **Fiscal year:** 2024
- **Award amount:** $636,666
- **Award type:** 5
- **Project period:** 2022-04-08 → 2027-03-31

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10833505

## Citation

> US National Institutes of Health, RePORTER application 10833505, Project 3: Contribution of inflammation and DNA damaging factors to clonal expansion and malignant transformation in a community cohort of older adults (5P01CA265748-03). Retrieved via AI Analytics 2026-05-26 from https://api.ai-analytics.org/grant/nih/10833505. Licensed CC0.

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