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Eur J Cancer. 1990;26(6):733-7.

Differential expression of the oncoproteins c-myc and c-myb in human lymphoproliferative disorders.

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Medizinische Klinik und Poliklinik, Universitätsklinikum Rudolf Virchow, Berlin, F.R.G.


Altered regulation of oncogene expression has been described in a variety of hematopoietic malignancies. In this study we analyzed the protein level of c-myc and c-myb in 15 established cell lines derived from lymphopoietic disorders and in 45 samples from patients with acute or chronic lymphatic leukemias. Oncoproteins were assayed by radioimmuno-precipitation with polyclonal rabbit antibodies. In B-cell derived lines, such as Burkitt lymphoma and plasmocytoma lines, we found high amounts of c-myc and no or low amounts of c-myb. In contrast, all T-cell-derived lines revealed high levels of c-myb. In addition, T-lymphoma cell lines of low malignancy also exhibited high levels of c-myc, while T-cell lines of high malignancy (acute T-lymphoblastic leukemias) exhibited moderate levels of c-myc. Of the 45 patient samples analyzed, only three (one B-prolymphocytic and two acute T-lymphoblastic leukemias) contained detectable amounts of myc or myb protein. Corresponding to the results found in established cell lines, the B-cell sample revealed a high level of c-myc but no c-myb, while the T-cell samples revealed high levels of c-myb and no or low levels of c-myc. We therefore conclude that the predominance of c-myc or c-myb expression in malignant lymphoproliferative disorders may be associated to the B-cell or T-cell lineage, respectively. Further, regarding the T-cell lines, there is a possible correlation between cell maturation and the level of c-myc found together with a consistently elevated c-myb.

[Indexed for MEDLINE]

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