NIH-funded research R37 grant

Targeting mitochondrial energy in triple-negative breast cancer that remains after chemo

Official title: Metabolic adaptation in residual triple negative breast cancer following chemotherapy

Funded at Baylor College of Medicine · NIH-11238042 · Data updated 2026-11-12

This work looks at whether blocking a tumor's mitochondrial energy program can help people with triple-negative breast cancer whose tumors remain after chemotherapy.

More Breast Cancer research and trials

Quick facts

Grant typeR37 grant
Study typeNIH-funded research
Funding institutionBaylor College of Medicine
NIH-funded
Lab location1 site (Houston, United States)
Project startDecember 27, 2022
Project endNovember 30, 2027
Funding year2026
Award (this year)$650,936
NIH project number5R37CA269783-04
Project IDNIH-11238042 on NIH RePORTER

Who could benefit from this research

Could help

People with triple-negative breast cancer who still have measurable residual tumor after neoadjuvant (pre-surgery) chemotherapy, especially those without BRCA mutations, would be the best fit.

Less likely to help

Patients whose cancer is not triple-negative or who had a complete response to chemotherapy (no residual tumor) are unlikely to benefit from this work.

What this research studies

I would be asked to provide tumor biopsy samples taken before and after pre-surgery chemotherapy so researchers can compare energy-related changes. The team grows patient-derived tumors in models and measures mitochondrial proteins and structure, especially the fusion protein OPA1, to see how leftover cancer cells change after chemo. They test drugs and genetic approaches that shut down oxidative phosphorylation or alter mitochondrial fusion to see if resistant cells can be killed. The aim is to find ways to eliminate residual TNBC that puts patients at high risk of recurrence.

Why it matters

Potential benefit: If successful, this could lead to new treatments that kill chemotherapy-resistant triple-negative breast cancer cells and reduce the chance of the cancer coming back.

How similar studies have gone: Preclinical studies and patient-derived tumor models have shown that oxidative phosphorylation can drive resistance and may be targetable, but clinical testing of this exact approach is still limited.

Where this research is happening

  • Baylor College of Medicine
    Houston, United States
    Active

Researchers

  • Principal investigator: Echeverria, Gloria Vittone — Baylor College of Medicine
  • Study coordinator: Echeverria, Gloria Vittone

Related research

Other NIH-funded projects on the same topics.

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.
Last reviewed 2026-11-14 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.