Although EGFR-targeted therapy significantly prolongs the survival of NSCLC patients with EGFR kinase domain activating mutations, acquired resistance to EGFR tyrosine kinase inhibitors (TKIs) poses a significant clinical problem. Recent clinical studies demonstrated that an increasing number of these resistant NSCLCs undergo epithelial to mesenchymal transition (EMT); however, the molecular basis of acquired EGFR TKI with an EMT phenotype remains elusive. Consequently, patients with the acquired resistance do not benefit from effective therapies. We have demonstrated that the inhibition of mutant EGFR in NSCLC promotes TGF?1-mediated EMT. In patient specimens, C-X-C chemokine receptor type 7 (CXCR7) is significantly upregulated in acquired EGFR TKI resistant NSCLC cells with an EMT phenotype. Prolonged depletion of CXCR7 with shRNA in the resistant cells not only restores epithelial phenotype but also sensitivity to EGFR TKIs. Our central hypothesis is that CXCR7 is a novel therapeutic target which promotes an EMT phenotype in EGFRmutant NSCLC and provides alternate survival/proliferation pathways when mutated-EGFR is inhibited. The overall objective is to determine the mechanism by which CXCR7 promotes EMT and thus resistance to EGFR TKI and determine whether CXCR7 is a superior drug target for NSCLC therapy.
In Aim 1, we will determine the mechanism by which CXCR7 promotes survival of EGFR TKI resistant NSCLC. For this aim, we will investigate if a ligand activation of CXCR7 is required for the engagement of the resistant phenotype. Additionally, we will evaluate therapeutic approaches using in vitro and in vivo models to suppress CXCR7 signaling to specifically target EMT-associated NSCLC cells with EGFR-TKI resistance.
In Aim 2, we will determine mechanisms responsible for EMT regulation by CXCR7 in NSCLC. To this end, we will investigate how CXCR7 activates downstream transcription factors to support EMT in EGFR mutant NSCLC by using genomics and proteomics approaches, cell culture and complementary transgenic murine EGFR mutant NSCLC models.
In Aim 3, we will determine the therapeutic efficacy of targeting CXCR7 to eliminate EGFR TKI resistant cells with EMT. For this aim, we will investigate if EGFR TKI resistant cells with an EMT phenotype emerge through evolution from drug tolerant cells with increase expression of CXCR7 using PDX models and CXCR7 inhibitors. The results obtained from this proposal will facilitate the discovery of prognostic and therapeutic tools to inhibit CXCR7 expression leading to EGFR TKI resistance, to prevent the induction of EMT upon EGFR inhibition, and to provide a rationale to stratify NSCLC patients who become refractory to EGFR TKI with mesenchymal biomarkers for CXCR7-targeted therapeutics.

Public Health Relevance

SIGNIFICANCE Although non-small cell lung cancer (NSCLC) patients with an activating EGFR mutation initially respond to EGFR tyrosine kinase inhibitors (TKIs), many patients succumb to acquired resistance, underscoring the need for improved therapeutic strategies especially for the increasing number of patients presenting with an epithelial- to-mesenchymal transition (EMT) phenotype. CXCR7 is a molecule that regulates both survival and an EMT phenotype of NSCLC cells resistant to EGFR TKIs. This proposal will uncover previously unknown activities of CXCR7 in NSCLC, which could lead to improved treatment options for patients with drug resistance with an EMT phenotype.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA230778-02
Application #
9989086
Study Section
Tumor Cell Biology Study Section (TCB)
Program Officer
Ault, Grace S
Project Start
2019-08-05
Project End
2024-07-31
Budget Start
2020-08-01
Budget End
2021-07-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Illinois at Chicago
Department
Surgery
Type
Schools of Medicine
DUNS #
098987217
City
Chicago
State
IL
Country
United States
Zip Code
60612