Short-term starvation reduces IGF-1 levels to sensitize lung tumors to PD-1 immune checkpoint blockade
- Nat Cancer. 2020 Jan;1(1):75-85. doi: 10.1038/s43018-019-0007-9.
- 1. Program in Solid Tumors, Center for Applied Medical Research (CIMA), University of Navarra, Pamplona, Spain. [email protected].
- 2. Navarra Institute for Health Research (IdISNA), Pamplona, Spain. [email protected].
- 3. Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain. [email protected].
- 4. Department of Biochemistry and Genetics, School of Sciences, University of Navarra, Pamplona, Spain. [email protected].
- 5. Program in Solid Tumors, Center for Applied Medical Research (CIMA), University of Navarra, Pamplona, Spain.
- 6. Department of Biochemistry and Genetics, School of Sciences, University of Navarra, Pamplona, Spain.
- 7. Navarra Institute for Health Research (IdISNA), Pamplona, Spain.
- 8. Program in Immunology and Immunotherapy, CIMA, University of Navarra, Pamplona, Spain.
- 9. Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain.
- 10. Department of Pathology, Anatomy and Physiology, School of Medicine, University of Navarra, Pamplona, Spain.
- 11. Cytometry Platform, CIMA, University of Navarra, Pamplona, Spain.
- 12. Department of Oncology, Clínica Universidad de Navarra, Pamplona, Spain.
- 13. Clinical Chemistry Department, Clínica Universidad de Navarra, Pamplona, Spain.
- 14. Department of Pathology, Clínica Universidad de Navarra, Pamplona, Spain.
Harnessing the immune system by blocking the programmed cell death protein 1 (PD-1) pathway has been a major breakthrough in non-small-cell lung Cancer treatment. Nonetheless, many patients fail to respond to PD-1 inhibition. Using three syngeneic models, we demonstrate that short-term starvation synergizes with PD-1 blockade to inhibit lung Cancer progression and metastasis. This antitumor activity was linked to a reduction in circulating insulin-like growth factor 1 (IGF-1) and a downregulation of IGF-1 receptor (IGF-1R) signaling in tumor cells. A combined inhibition of IGF-1R and PD-1 synergistically reduced tumor growth in mice. This effect required CD8 cells, boosted the intratumoral CD8/Treg ratio and led to the development of tumor-specific immunity. In patients with non-small-cell lung Cancer, high plasma levels of IGF-1 or high IGF-1R expression in tumors was associated with resistance to anti-PD-1-programmed death-ligand 1 immunotherapy. In conclusion, our data strongly support the clinical evaluation of IGF-1 modulators in combination with PD-1 blockade.