Project Details
Description
Project Summary
The rapid increase in the incidence of Barrett’s esophagus (BE), its malignant form esophageal adenocarcinoma
(EAC), and junctional gastric cancer has produced serious health and financial burdens in the U.S. Thus far,
effective treatment options for these diseases are limited in part due to an incomplete understanding of the
molecular mechanisms driving the initial metaplasia and subsequent neoplastic progression. This application, by
two PIs with complementary expertise, seeks to address the issue through combining scRNA-sequencing analysis,
innovative BE mouse models and organoid modeling. We previously demonstrated that gastric cardia progenitor
cells and transitional basal cell (TBCs) contribute to BE in the transitional zone of the gastro-esophageal junction
(GEJ). However, how these progenitor cells behave in BE-dysplasia-EAC progression remains unclear.
Additionally, the molecular mechanism driving the disease progression is also unknown. Our preliminary data
suggest GEJ metaplasia and its progression towards EAC involves progenitor plasticity facilitated by p53 loss,
an early genetic lesion in BE. Furthermore, we found that Barrett’s metaplasia and EAC is associated with the
enrichment of tuft cells. Therefore we hypothesize that Barrett’s metaplasia and dysplasia originate from GEJ
progenitor cells, modulated by the presence of p53 mutation and tuft cell expansion. Three specific aims are
formulated to test the hypothesis: Aim 1 is to determine the origins and evolution of BE metaplasia from
progenitor cells at the EGJ. Aim 2 is to elucidate the mechanisms by which p53 mutation promotes BE
progression, and Aim 3 is to clarify the role of tuft cells in BE pathogenesis and progression. Combining our joint
expertise on mouse genetics, cell biology, chromatin biology and epigenomics, this work will provide novel
mechanistic insights into the mechanisms underlying Barrett’s metaplasia and its malignant progression, offering
new approaches to treat these diseases.
Status | Finished |
---|---|
Effective start/end date | 9/1/22 → 8/31/23 |
Funding
- National Cancer Institute: US$972,000.00
ASJC Scopus Subject Areas
- Biotechnology
- Cancer Research
- Oncology
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