A new tool to observe cell behavior has revealed surprising clues about how cancer cells respond to therapy and may offer a way to further refine personalized cancer treatments.
The approach, developed by investigators at Vanderbilt-Ingram Cancer Center, shows that erlotinib a targeted therapy that acts on a growth factor receptor mutated in some lung, brain and other cancers doesn't simply kill tumor cells as was previously assumed. The drug also causes some tumor cells to go into a non-dividing (quiescent) state or to slow down their rate of division. This variability in cell response to the drug may be involved in cancer recurrence and drug resistance, the authors suggest.
The new tool, reported Aug. 12 in Nature Methods, may offer ways to improve personalized cancer therapy by predicting tumor response and testing combinations of targeted therapies in an individual patient's tumor.
In the personalized approach to cancer treatment, a patient's tumor is analyzed for a set of mutations to which there are matching drugs that act on those mutations.
This approach has worked rather well for many cancers that carry specific mutations, said senior author Vito Quaranta, M.D., professor of Cancer Biology.
"The genetics is well understood, the clinical effect is understood and the chemistry behind the therapy is understood. But there is a missing piece," said Quaranta. "Believe it or not, what is actually not understood is how cells respond to these drugs, what is actually happening."
The prevailing view has been that targeted therapies kill all the cells harboring a particular mutation.
But even if the tumor is composed entirely of genetically identical cells which is unlikely a drug will not affect all cells the same way, Quaranta explained.
"Some of these cells may die, some may just stop dividing and sit there (called quiescence), and some may keep dividing, but more slowly."
|Contact: Melissa Stamm|
Vanderbilt University Medical Center