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This Year’s Modeling: 3-D organoids

Posted November 3, 2015

The development of a new method to grow three-dimensional organoid cultures of pancreatic tumors directly from patients’ surgical tissue offers a promising opportunity for testing targeted therapies and drug responses and personalizing treatments in a rapid, cost-effective manner, according to a report published today in Nature Medicine.

“These 3-D organoids are, essentially, ‘mini tumors’ in a culture dish,” explained the study’s corresponding author Senthil Muthuswamy, director of the cell biology program in the Cancer Research Institute at Beth Israel Deaconess Medical Center and visiting professor at Harvard Medical School. “The organoids have the same properties or traits that are seen in the patient tumor from which they came and, therefore, can serve as an innovative platform for both cancer research and cancer treatment.”

Pancreatic cancer organoid. Image credit: Senthil Muthuswamy.

Pancreatic cancer organoid. Image credit: Senthil Muthuswamy.

Scientists have been growing cells in 3-D culture for decades. These models are used to help understand various biological processes such as tissue development and cancer growth. Muthuswamy’s laboratory has spent the past 15 years growing normal and cancer-derived cells from human breast tissue as 3-D organoids.

The new paper provides an innovative direction for this technology. “We have now developed a new methodology to grow human pancreatic tumor cells from surgical tissues and have demonstrated that these tumor organoids recreate both morphology and biology of the cancer tissue in the patient,” said Muthuswamy, who conducted this research while at the University of Toronto.

The research team also demonstrated that these clonally derived organoids could be used to identify patient-specific sensitivities to novel therapeutic agents.

“From a research point of view, this organoid approach now provides us with a ‘live’ biobank of tissue for discovery and validation of new drugs and targets and modeling resistance to therapy,” said Muthuswamy. “By using a cohort of patient samples from which we can screen for drugs and mutations, we can begin to understand why some patients respond to a treatment while others do not, and can thereby avoid giving patients unnecessary or ineffective treatments. And from a clinical point of view, this approach could help assist patients and their oncologists in making treatment decisions.”

“Pancreatic cancer is a terrible disease,” said Pier Paolo Pandolfi, the HMS George C. Reisman Professor of Medicine and director of the Cancer Center at Beth Israel Deaconess, who was not involved in the study. “Patients diagnosed with locally advanced or metastatic pancreatic cancer have a survival rate of less than three percent. Early detection methods and new treatment strategies are desperately needed. These new pancreatic progenitor organoids and tumor organoids can be used to model pancreatic cancer and for drug screening to identify precision therapy strategies.”

Source: HMS

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