Scientists have used 3D models to break down the DNA behaviour of cancer cells, in a breakthrough new study which could revolutionise treatment for the disease.
In what is a first for science, a research team led by Dr Manel Esteller, Director of the Josep Carreras Leukaemia Research Institute (IJC), demonstrated how 3D models (known as organoids) can now be used to develop a characterisation of the DNA make-up - or the epigenetic fingerprint - of human cancer.
Pubished in Epigenetics, the research validates the use of these 3D samples for cancer research that could deliver new oncology treatments.
Dr Esteller, who is also Chaiman of Genetics at the University of Barcelona, explains: "Frequently, promising cancer therapies fail when applied to patients in the real clinical setting. This occurs despite many of these new treatments demonstrating promising results at the preclinical stage in the lab. One explanation is that many of the tumour models used in early research phases are established cell lines that have been growing for many decades and in two dimension (2D) culture flasks. These cancer cells might not completely resemble the features of real tumours from patients that expand into three dimensions (3D). Very recently, it has been possible to grow cancers in the laboratories but respecting the 3D structure: these models are called 'organoids'. We know very little about these cells and if they actually mimic the conformation of the tumour within the body, particularly the chemical behaviours (known as modifications) of DNA that are called epigenetics ("beyond the genetics"), such as DNA methylation."
"What our article solves is this unmet biomedical need in the cancer research field: the characterisation of the epigenetic fingerprint of human cancer organoids. The developed study shows that these tumour models can be very useful for the biomedical research community and the pharmaceutical companies developing anti-cancer drugs."
Specifically looking at 25 human cancer organoids, made available from the American Type Culture Collection (ATTC), Dr Esteller, an ICREA Research Professor, states that during their research the team made some interesting findings around the properties of the cancer cells.
"First, we found that every cancer organoid retains the properties of the tissue of origin, so this shows that if the samples were obtained from the surgery of a colon or pancreatic cancer, the organoid closely resembles the original primary tumour."
"Second, we discovered that there is no contamination of normal cells, thus, the malignant pure transformed cells can be analysed without interferences. And finally, the 3D organoid cancers are closer to the patient tumours than the commonly used 2D cell lines."
The study will now be used to help form Big Data, as the team's samples will be shared in easily accessible public databases between researchers to promote more collaborative studies.
"This will enable further data mining to produce new cancer discoveries using different biometric approaches or focusing on particular genes," explains Dr Esteller.
"And most importantly, the characterised cancer organoids can be readily obtainable from a reliable provider (the ATCC) researchers around the world can use the epigenetic information of these sharable samples to develop their own investigations."
Source: Taylor and Francis Group
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