Patient Derived Xenografts for Genome-Driven Therapy of Osteosarcoma.
Lorena LanduzziMaria Cristina ManaraPier-Luigi LolliniKatia ScotlandiPublished in: Cells (2021)
Osteosarcoma (OS) is a rare malignant primary tumor of mesenchymal origin affecting bone. It is characterized by a complex genotype, mainly due to the high frequency of chromothripsis, which leads to multiple somatic copy number alterations and structural rearrangements. Any effort to design genome-driven therapies must therefore consider such high inter- and intra-tumor heterogeneity. Therefore, many laboratories and international networks are developing and sharing OS patient-derived xenografts (OS PDX) to broaden the availability of models that reproduce OS complex clinical heterogeneity. OS PDXs, and new cell lines derived from PDXs, faithfully preserve tumor heterogeneity, genetic, and epigenetic features and are thus valuable tools for predicting drug responses. Here, we review recent achievements concerning OS PDXs, summarizing the methods used to obtain ectopic and orthotopic xenografts and to fully characterize these models. The availability of OS PDXs across the many international PDX platforms and their possible use in PDX clinical trials are also described. We recommend the coupling of next-generation sequencing (NGS) data analysis with functional studies in OS PDXs, as well as the setup of OS PDX clinical trials and co-clinical trials, to enhance the predictive power of experimental evidence and to accelerate the clinical translation of effective genome-guided therapies for this aggressive disease.
Keyphrases
- copy number
- clinical trial
- high frequency
- genome wide
- mitochondrial dna
- data analysis
- dna methylation
- single cell
- stem cells
- emergency department
- gene expression
- transcranial magnetic stimulation
- bone mineral density
- body composition
- smoking cessation
- open label
- phase iii
- room temperature
- phase ii
- circulating tumor cells
- ionic liquid
- drug induced