It’s the cancer version of “mini-me.” Cold Spring Harbor Laboratory (CSHL) Professor David Spector, among others, has developed organoids, which are miniature, three-dimensional copies of cancers.
Organoids can be derived from cancer or healthy cells. They allow scientists to study the basic biology of particular types of tumours, then test specific drugs on those cancers in a dish, instead of in a patient. Recently, Spector, postdoctoral researcher Sonam Bhatia, and collaborators from CSHL and Northwell Health created a biobank of 87 triple-negative breast cancer organoids. The researchers published their work in the journal Cancer Research.
The research team, which plans to expand the biobank to over 100 patient-derived samples, conducted extensive tests to ensure the organoids had the same characteristics as the tumours when they were in the patient. They tested that organoids and tumours: (1) had similar genetic variation in their DNA; (2) had similar RNA profiles; and (3) produced tumours, similar to the patients’ tumours, when implanted into mice. As Spector explained:
“That was our rationale for approaching this from many different directions, to really develop a comprehensive analysis as to whether these breast tumour organoid models would be good model systems.”
Spector’s lab is testing various treatments to find weaknesses specific to each tumour. They are developing a library of therapeutics known as antisense oligonucleotides to target RNA molecules active in cancer cells, but not in healthy cells. Spector and his team already have 200 potential targets and will prioritize RNA molecules that are made in the largest amounts.
Spector, whose efforts to improve organoid science might one day allow doctors to use them in a clinic, credited a team of researchers for this effort. He described Bhatia as the “key driver” who brought this “massive undertaking” together.
For her part, Bhatia believed this research would have practical applications.
“This biobank opens up an exciting avenue to use this cutting-edge class of therapeutics with better patient-specific models,” Bhatia said. “In the longer term, these patient-derived organoids can be used to test therapy options outside of the patients, in a dish, and can provide information on what treatments the patient does or does not respond to.”
Source: CSHL