Novel mechanism described by which glioblastoma tumors resist targeted therapies


Glioblastoma (GBM) tumor cells can evade targeted therapies, as shown recently, by essentially hiding the signaling molecule targeted by such therapies. This may affect new treatment strategies.
Furthermore, new developments could suggest alternative approaches that could improve outcomes for cancer patients.

This study was conducted at the Ludwig Cancer Research center in San Diego, California.

GBM tumors (the most common kind of brain cancer) typically carry mutant forms of the EGF receptor. The gene for the most common of these mutant receptors, EGFRvIII, lies on small fragments of DNA known as double minute chromosomes and promotes uncontrolled cell proliferation. "You would expect that drugs that block EGF receptor signaling would devastate GBM tumors," says Paul Mischel, MD, Ludwig scientist based at the University of California, San Diego School of Medicine. Mischel led the multi-institutional study in close collaboration with Ludwig colleagues Web Cavenee, PhD, and Frank Furnari, PhD. "Yet such targeted drugs have not worked in GBM, and that has raised some serious questions among cancer researchers."

Only about 60 percent of cells express the aberrant receptor. To probe how this heterogeneity contributes to drug resistance, Mischel and his colleagues treated tumors taken from patients with targeted therapies. They found, to their surprise, that this prompted GBM cells to almost completely shut down their expression of EGFRvIII. But were the two cell types this yielded - those that expressed the EGFRvIII mutant, and those that did not - equally cancerous?

The answer: An unequivocal yes. The findings showed that GBM tumors don't survive targeted therapy by replacing susceptible cells with mutants unaffected by the drugs in question - a classical mechanism of resistance - but by hiding the target of those drugs. And they did this, surprisingly, by depleting the double minute chromosomes themselves. "Those DNA double minutes seem to hide out in a reservoir," says Mischel, "and when the drug is removed, the tumors come screaming back. When they return, the cells become susceptible once again to targeted therapy."

"Our research might have significant implications for how we dose patients," says Mischel. "A high-dose regimen of EGF receptor-targeting drugs, given in pulses, might be more effective than the continuous, lower-dose regimen employed today. That is a study that needs to be done."

The findings also amend a second prevailing model of drug resistance in cancer. Double minute chromosomes are thought to contribute to drug resistance mainly by encoding multiple copies of proteins that detoxify chemotherapy or drive cancer in other ways. But in GBM, tumors actually shut down a cancer-promoting gene to evade drug targeting. "Many kinds of tumors have extra-chromosomal DNA fragments that carry cancer-promoting genes," says Mischel. "So this new mechanism could be a far more common phenomenon in cancer than we've realized."

Mischel and his colleagues are now exploring that possibility.


Source: Medical News Today:

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