Development of patient-derived orthotopic xenografts from metastatic colorectal cancer in nude mice.
Bruno Roque-LimaCaroline Correa de Tulio Augusto RoqueMaria Dirlei BegnamiPatricia PeresiEduardo Nobrega Pereira LimaCelso Abdon Lopes de MelloFelipe JoséFernandez CoimbraRubens ChojniakTiago Goss Dos SantosPublished in: Journal of drug targeting (2018)
Liver metastasis is the major cause of death for patients with colorectal cancer. Despite treatment with surgery and chemotherapy, patient outcomes are quite unfavourable. Thus, there is an urgent need to develop new treatment strategies with the associated establishment of good animal models. Metastatic disease can be modelled using patient-derived orthotopic xenografts, which accurately replicate intra-tumoral heterogeneity so that various chemotherapeutic agents can be tested on individual tumours to aid in clinical decision-making. The objective of this study was to develop metastatic colorectal tumours in athymic nude mice by implanting fresh tumour fragments into mouse liver parenchyma. Metastatic tumours were successfully propagated in mice following transplantation from human patients, then serially implanted in second and third-generation mice. Morphologic and immunohistochemical characteristics indicate that xenografts recreate the tumour architecture and mismatch repair gene expression for MLH1, MSH2, MSH1, and PMS2. After tumour implantation during the first passage, the time of tumour growth decreased without loss of tumour identity. Post-transplantation lymphoproliferative disease was observed in one case. This pilot study was successful in establishing the institutional PDX preclinical platform to study new therapeutic strategies, disease progression biomarkers, and treatment responsiveness.
Keyphrases
- gene expression
- high fat diet induced
- squamous cell carcinoma
- small cell lung cancer
- endothelial cells
- metastatic colorectal cancer
- minimally invasive
- cell therapy
- dna methylation
- ejection fraction
- newly diagnosed
- metabolic syndrome
- skeletal muscle
- type diabetes
- wild type
- adipose tissue
- single cell
- insulin resistance
- mesenchymal stem cells
- locally advanced
- bone marrow
- acute coronary syndrome
- replacement therapy
- pluripotent stem cells