Tumors grown in dishes could help
customize cancer treatment
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[March 24, 2015]
By Ben Gruber
Experiments conducted at an underground
laboratory at Vanderbilt University could prove vital in the fight
against cancer. Alex Walsh, a biomedical researcher, is using a laser to
make what she calls organoids glow.
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"Organoids are small pieces of a patients' tumor that are about
100 to 300 microns in diameter and they grow as kind of sphere like
shapes." said Walsh, who recently successfully defended her
dissertation on the topic of organoids.
A tiny sample is placed in dish filled with a collagen gel which
feeds the tiny tumor, allowing the different cell types that
comprise it to thrive as they would inside the human body. The
organoid is then dosed with a cocktail of cancer drugs and placed
under a microscope at which point it is blasted with a laser. The
laser is tuned to the frequencies that cause two enzymes in the
cells to glow or fluoresce. Measuring the variations in the
intensity of the resulting fluorescence provides a readout of
cellular metabolism which, Walsh says, is an accurate and speedy
biomarker of drug response.
"We're using these readouts of cellular metabolism to predict the
drug response that the sample came from," added Walsh.
The tumor-on-a-dish method has proven successful in mice and Melissa
Skala, an assistant professor of biomedical engineering at
Vanderbilt University, says the team are now trailing it on tumors
from breast cancer patients. She says everyone's cancer is unique,
which is why customizing treatment options is essential.
"So the idea here is to eliminate those drugs that don't work and if
needed replace them with drugs that do work so we are hoping to have
the smallest common denominator of drugs that achieve the lowest
toxicity yet achieve treatment efficacy," said Skala adding that the
method could prove a game changer for cancer patients.
Breast cancer is the second leading cause of cancer deaths in woman
in the United States. according to the American Cancer Society.
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Skala says that having the ability to customize a drug protocol for
patients before they start chemo may significantly improve the odds
for a successful treatment.
"Thirty to forty percent of patience that receive those therapies as
their first line therapy don't respond to those drugs ever. And so
they suffer toxicity from treatment that ultimately isn't going to
benefit them," she said.
"I think we can add to what's already been done and hopefully just
improve the experience of the patient so that they recover faster,"
she added.
Along with breast cancer, Skala and her team have also started
testing the organoids derived from pancreatic cancer patients. If
further trials prove successful, Skala estimates it will take 5 to
10 years to move tumor-on-dishes out of the lab and into the clinic.
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