Autologous cell lines from circulating colon cancer cells captured from sequential liquid biopsies as model to study therapy-driven tumor changes

被引:68
作者
Soler, Alexandra [1 ]
Cayrefourcq, Laure [1 ]
Mazard, Thibault [2 ]
Babayan, Anna [3 ]
Lamy, Pierre-Jean [4 ]
Assou, Said [5 ]
Assenat, Eric [6 ]
Pantel, Klaus [3 ]
Alix-Panabieres, Catherine [1 ]
机构
[1] Univ Med Ctr Montpellier, Lab Rare Human Circulating Cells, EA2415, Montpellier, France
[2] Canc Inst Montpellier, Dept Med Oncol, Montpellier, France
[3] Univ Med Ctr Hamburg Eppendorf, Dept Tumor Biol, Hamburg, Germany
[4] Labosud, Imagenome, Montpellier, France
[5] Montpellier Univ, Univ Med Ctr Montpellier, IRMB, INSERM,U1183, Montpellier, France
[6] Univ Med Ctr Montpellier, Dept Med Oncol, Montpellier, France
关键词
BREAST-CANCER; COLORECTAL-CANCER; EXPRESSION; METASTASIS; SURVIVAL; METAANALYSIS; PROGRESSION; PD-L1;
D O I
10.1038/s41598-018-34365-z
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Circulating tumor cells (CTCs) are important clinical indicators for prognosis and treatment efficacy. However, CTC investigation is hampered by their low number, making the establishment of permanent CTC lines very challenging. We derived and characterized nine CTC lines using blood samples from a patient with metastatic colorectal cancer collected before and after chemotherapy and targeted therapy, and during cancer progression. These cell lines displayed an intermediate epithelial/ mesenchymal phenotype, stem-cell like characteristics, angiogenesis potential, an osteomimetic signature and the capacity to escape from the immune system. Moreover, they showed changes in mRNA and protein expression (e.g., DEFA6, ABCB1 and GAL), whereas analysis of chromosomal copy number aberrations revealed no significant variation overtime. These data indicate that although CTC lines derived from sequential blood samples during therapy have common traits, treatment-resistant CTC clones with distinct phenotypic characteristics are selected over time.
引用
收藏
页数:12
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