Genetic and cell-level changes in endometriosis across diverse women

Functional Genomics Across an Ethnically and Racially Diverse Endometriosis Population

NIH-funded research University of Texas Hlth Science Center · NIH-11242059

This work looks for genetic changes and cell-level differences in endometriosis tissues from women of different racial and ethnic backgrounds to find new treatment targets.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionUniversity of Texas Hlth Science Center NIH-funded
Lab location1 site (San Antonio, United States)
Project IDNIH-11242059 on NIH RePORTER

What this research studies

Researchers will analyze tissue and data from more than 1,400 people with endometriosis, sequencing lesion DNA to catalogue somatic mutations across White, Asian, Black, and Hispanic patients. They will use single-cell RNA and epigenomic profiling plus spatial transcriptomics to see how those mutations change specific cell types and tissue organization. Findings from patient samples will be tested in an orthotopic mouse model to explore how mutations affect disease behavior and treatment responses. The combined approach aims to reveal molecular targets that could guide more effective or ancestry-informed therapies.

Who could benefit from this research

Good fit: Women with a confirmed diagnosis of endometriosis who can provide tissue samples and clinical information are the ideal candidates, with emphasis on enrolling Black, Hispanic, Asian, and White participants.

Not a fit: People without endometriosis or those unable or unwilling to provide tissue samples and medical information are unlikely to benefit directly from this project.

Why it matters

Potential benefit: If successful, this work could identify molecular targets that lead to more precise or new treatments for endometriosis, especially tailored for diverse populations.

How similar studies have performed: Previous studies have found driver mutations such as KRAS, PIK3CA, and ARID1A in endometriosis lesions, and applying single-cell and spatial genomics is a promising but still emerging path toward treatment targets.

Where this research is happening

San Antonio, United States

Researchers

About this research

  1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
  2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
  3. For full project details, budget, and progress reports, visit the official NIH RePORTER page below.
Last reviewed 2026-06-13 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.