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| Monique Nilsson, Ph.D. | John Heymach, M.D., Ph.D. Photo Credit: Courtesy of University of Texas M. D. Anderson Cancer Center |
Researchers at The University of Texas MD Anderson Cancer Center have identified CD70 as being highly expressed on drug-resistant cancer cells in EGFR-mutant non-small cell lung cancer (NSCLC), highlighting a novel therapeutic target that could be used to eliminate resistant cells remaining after treatment with commonly used EGFR tyrosine kinase inhibitors (TKIs). The study published today in Cancer Cell.
The preclinical research was led by Monique Nilsson, Ph.D., and corresponding author John Heymach, M.D., Ph.D., chair of Thoracic/Head and Neck Medical Oncology. The researchers discovered that CD70, a cell surface protein normally found on immune cells, is highly overexpressed in resistant cells as well as in the residual cancer cells immediately following TKI treatment. They demonstrated that CD70 can be effectively used to target these cells with antibody-drug conjugates (ADCs) or cell therapies in laboratory models.
“Residual cancer cells left over from TKI treatment are essentially a reservoir from which future resistant cells eventually grow,” Heymach said. “These findings set the stage for a really promising approach in which we may give initial effective therapies and immediately follow them with these CD70-targeting drugs to eliminate the remaining residual cells.”


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