To date, the lack of chemo-naive cell models limited exploratory studies to define novel therapies for Burkitt lymphoma (BL). To obtain a useful tool for biological and translational studies for this tumor, we established the RALE051 cell line from the malignant ascitic fluid cells of a patient at initial diagnosis, not previously exposed to any treatment. The cell line was characterized by karyotyping, fluorescence in situ hybridization (FISH), single nucleotide polymorphism (SNP) array, immunohistochemistry, and RNA-Seq, revealing the persistence of biological and molecular features observed in the primary ascitic fluid, such as the cell morphology and immunophenotype, the occurrence of a t(8;22) translocation deregulating MYC, knock-out ID3 mutations in a compound homozygous state, and a mutated TP53. Moreover, additional alterations characterizing the ex vivo transformation included the emergence of three novel fusion transcripts and a nonsense mutation affecting TP53. The establishment of this cell line would be beneficial for future biological and therapeutic studies of BL.
L'Abbate, A., Iacobucci, I., Lonoce, A., Turchiano, A., Ficarra, E., Paciello, G., et al. (2018). RALE051: a novel established cell line of sporadic Burkitt lymphoma. LEUKEMIA & LYMPHOMA, 59(5), 1252-1255 [10.1080/10428194.2017.1372580].
RALE051: a novel established cell line of sporadic Burkitt lymphoma
Iacobucci, Ilaria;Ficarra, Elisa;Cattina, Federica;Ferrari, Anna;Imbrogno, Enrica;Agostinelli, Claudio;Zinzani, Pier Luigi;Martinelli, Giovanni;Derenzini, Enrico;Storlazzi, Clelia Tiziana
2018
Abstract
To date, the lack of chemo-naive cell models limited exploratory studies to define novel therapies for Burkitt lymphoma (BL). To obtain a useful tool for biological and translational studies for this tumor, we established the RALE051 cell line from the malignant ascitic fluid cells of a patient at initial diagnosis, not previously exposed to any treatment. The cell line was characterized by karyotyping, fluorescence in situ hybridization (FISH), single nucleotide polymorphism (SNP) array, immunohistochemistry, and RNA-Seq, revealing the persistence of biological and molecular features observed in the primary ascitic fluid, such as the cell morphology and immunophenotype, the occurrence of a t(8;22) translocation deregulating MYC, knock-out ID3 mutations in a compound homozygous state, and a mutated TP53. Moreover, additional alterations characterizing the ex vivo transformation included the emergence of three novel fusion transcripts and a nonsense mutation affecting TP53. The establishment of this cell line would be beneficial for future biological and therapeutic studies of BL.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.