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DOI 10.1016/j.leukres.2005.08.016

Медицинская библиотека · Leukemia research · 2005

Four human t(11;14)(q13;q32)-containing cell lines having classic and variant features of Mantle Cell Lymphoma.

Tucker Catherine A, Bebb Gwyn, Klasa Richard J, Chhanabhai Mukesh, Lestou Valia, Horsman Douglas E, Gascoyne Randy D, Wiestner Adrian, Masin Dana, Bally Marcel, Williams Michael E

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

The objectives of this study were foremost to further characterize pre-existing cell lines containing the t(11;14)(q13;q32) translocation. This translocation along with cyclin D1 overexpression is characteristic of Mantle Cell Lymphoma (MCL), an aggressive B cell neoplasm. Considerable variation in the abundance of cyclin D1 expression was observed. mRNA levels were examined by RT-PCR as differences in cyclin D1 mRNA abundance have been shown to synergize with INK4A/Arf deletions to dictate proliferation rate and survival in MCL patient samples. In this study, the cell lines, Z-138 and HBL-2, which exhibited the fastest growth rates and the shortest survival times in Rag2-M mice, had high expression of either one or both cyclin D1 mRNA isoforms and had negligible expression of p16. On the other hand, NCEB-1 and JVM-2 had low expression of both mRNA isoforms, retained p16 expression, and had slower growth rates and exhibited longer survival times in Rag2-M mice. Furthermore, JVM-2, which was found to have the lowest expression of cyclin D1, was the only cell line that expressed cyclin D2. The results of the characterization of Z-138, HBL-2, NCEB-1 and JVM-2 reveal that this group of cell lines represents both classic and variant features of MCL.

Для цитирования: Tucker Catherine A, Bebb Gwyn, Klasa Richard J, Chhanabhai Mukesh, Lestou Valia, Horsman Douglas E, Gascoyne Randy D, Wiestner Adrian, Masin Dana, Bally Marcel, Williams Michael E. Four human t(11;14)(q13;q32)-containing cell lines having classic and variant features of Mantle Cell Lymphoma.. Leukemia research. 2005. DOI: 10.1016/j.leukres.2005.08.016.

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