NIH-funded research R01 grant

Blocking a key amino acid transporter (SLC6A14) to fight pancreatic cancer

Official title: SLC6A14 as a unique drug target to treat pancreatic cancer

Funded at Texas Tech University Health Scis Center · NIH-11308259 · Data updated 2026-11-12

This research tests whether stopping a protein that brings amino acids into pancreatic cancer cells can slow tumor growth for people with pancreatic ductal adenocarcinoma.

More Pancreatic Cancer research and trials

Quick facts

Grant typeR01 grant
Study typeNIH-funded research
Funding institutionTexas Tech University Health Scis Center
NIH-funded
Lab location1 site (Lubbock, United States)
Project startMay 12, 2023
Project endApril 30, 2028
Funding year2026
Award (this year)$349,640
NIH project number5R01CA262420-04
Project IDNIH-11308259 on NIH RePORTER

Who could benefit from this research

Could help

People with pancreatic ductal adenocarcinoma—especially those whose tumors show high SLC6A14 levels—would be the most likely candidates for future therapies developed from this work.

Less likely to help

Patients with other cancer types, tumors that do not express SLC6A14, or those who cannot tolerate drugs that block autophagy/macropinocytosis are less likely to benefit from this approach.

What this research studies

Researchers are focusing on SLC6A14, a protein often turned up in pancreatic tumors that helps cancer cells import many amino acids they need to grow. In the lab they use human pancreatic cancer cell lines and mouse models to remove or block SLC6A14 and watch how tumors respond. They are also studying how cancer cells switch on survival pathways like autophagy and macropinocytosis when SLC6A14 is blocked. The team plans to test combinations that block both SLC6A14 and these compensatory nutrient-scavenging pathways to try to get a stronger anti-tumor effect.

Why it matters

Potential benefit: If successful, this work could lead to new drugs or drug combinations that slow tumor growth and improve outcomes for people with pancreatic cancer.

How similar studies have gone: Preclinical studies by this group and others have shown that removing or blocking SLC6A14 can slow pancreatic tumor growth in cell and mouse models, while combination approaches targeting compensatory pathways are a newer, still-developing idea.

Where this research is happening

  • Texas Tech University Health Scis Center
    Lubbock, United States
    Active

Researchers

  • Principal investigator: Bhutia, Yangzom Doma — Texas Tech University Health Scis Center
  • Study coordinator: Bhutia, Yangzom Doma

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.