NIH-funded research R01 grant

Why some triple-negative breast cancers resist chemotherapy

Official title: Investigating mechanisms of chemoresistance in triple-negative breast cancer

Funded at Tufts University Medford · NIH-11251640 · Data updated 2026-11-12

This research explores whether changes in the tumor’s surrounding support tissue (the extracellular matrix) and a protein called Cathepsin B change how chemotherapy works for people with triple-negative breast cancer.

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionTufts University Medford
NIH-funded
Lab location1 site (Boston, UNITED STATES)
Project startJanuary 11, 2022
Project endDecember 31, 2026
Funding year2026
Award (this year)$347,067
NIH project number5R01CA255742-05
Project IDNIH-11251640 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are people with triple-negative breast cancer or patients willing to donate tumor tissue or participate in related translational studies.

Less likely to help

People with non–triple-negative breast cancers or those seeking immediate treatment changes should not expect direct, immediate benefit from this primarily lab-based project.

What this research studies

As someone affected by triple-negative breast cancer (TNBC), this project looks at why chemotherapy sometimes fails to kill tumor cells and can even promote later spread. Researchers will use 3-D tumor models and tumor samples to study specific extracellular matrix (ECM) proteins and the protease Cathepsin B (CTSB) that breaks them down. They will test how these ECM changes and CTSB levels affect response to the chemotherapy drug paclitaxel and tumor cell movement. The work aims to connect tumor microenvironment changes to chemoresistance and chemotherapy-induced metastasis.

Why it matters

Potential benefit: If successful, this work could point to new ways to make chemotherapy more effective for people with TNBC or identify markers that predict who will respond.

How similar studies have gone: Prior studies have linked ECM remodeling and cell migration to chemoresistance, but targeting ECM components and CTSB in TNBC is a relatively new and mostly preclinical approach.

Where this research is happening

  • Tufts University Medford
    Boston, United States
    Active

Researchers

  • Principal investigator: Oudin, Madeleine Julie — Tufts University Medford
  • Study coordinator: Oudin, Madeleine Julie

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.