NIH-funded research P01 program project

Replication Stress Sensing Defects in Small Cell Lung Cancer

Official title: Replication Stress Sensing and Signaling Defects in SCLC

Funded at New York University School of Medicine · NIH-11390984 · Data updated 2026-11-12

A study in people might not be involved directly, but it aims to understand why a common lung cancer responds poorly to therapy over time by examining how cancer cells handle replication stress.

Quick facts

Grant typeP01 program project
Study typeNIH-funded research
Funding institutionNew York University School of Medicine
NIH-funded
Lab location1 site (New York, United States)
Project startAugust 16, 2024
Project endJuly 31, 2029
Funding year2026
Award (this year)$350,490
NIH project number5P01CA288368-03
Project IDNIH-11390984 on NIH RePORTER

Who could benefit from this research

Could help

Ideal candidates are patients with small cell lung cancer whose tumors could be modeled or whose tumor biology aligns with SLFN11-related replication stress pathways.

Less likely to help

Patients whose cancer biology does not involve SLFN11 pathways or replication stress responses may derive little direct benefit.

What this research studies

This project looks at why small cell lung cancer (SCLC) is initially sensitive to chemotherapy but later becomes resistant, focusing on replication stress and DNA damage responses. Researchers will study SLFN11, a gene linked to sensitivity to DNA damage, and how its expression affects early replication stress responses by using cell models with mutant SLFN11 proteins. The work will distinguish immediate effects of SLFN11 from longer-term changes in the cell by examining protein levels and replication fork dynamics. Findings could reveal new ways to overcome resistance to chemotherapy in SCLC. The grant uses cell-based experiments to illuminate mechanisms that could guide future therapies.

Why it matters

Potential benefit: If successful, the research could identify new targets to prevent or delay chemotherapy resistance in SCLC, potentially improving treatment effectiveness.

How similar studies have gone: Prior studies have linked SLFN11 expression to chemotherapy sensitivity across several cancers, supporting potential translational impact.

Where this research is happening

  • New York University School of Medicine
    New York, United States
    Active

Researchers

  • Principal investigator: Huang, Tony Tung — New York University School of Medicine
  • Study coordinator: Huang, Tony Tung

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.