Regulation of cell proliferation: Late down-regulation of c-myb preceding myelo-monocytic cell differentiation

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Abstract
Expression of the c‐myb nuclear oncogene during the cell proliferation and differentiation of HL‐60 human promyelocytic leukemia cells was characterized and compared to the expression of c‐fos, another nuclear oncogene with transcriptional regulatory activity. During progression through the cell cycle, the amount of c‐myb protein increased. The increase was commensurate with total cell size, thus preserving the relative abundance of c‐myb protein present at the onset of the cell cycle. In HL‐60 cells, the induced metabolic cascade leading to terminal myeloid or monocytic differentiation segregates into two steps occuring over two division cycles. Expression of c‐myb did not diverge from the control until late in this metabolic cascade when it declined prior to onset of terminal differentiation. This course of expression was similar for both the retinoic acid induced myloid or the 1,25‐dihydroxy vitamin D2 induced monocytic terminal differentiation of the cells. Bromodeoxyuridine, which induces proliferative arrest but not phenotypic differentiation of these cells, induced the same course of c‐myb expression as the inducers of terminal differentiation. The same course of c‐myb expression with growth arrest induced by these three different means is consistent with a potential proliferation regulatory role for c‐myb in late but not early events leading to terminal differentiation. The dynamics of c‐myb expression during this process were qualitatively, out not quantitatively, similar to the course of c‐fos expression. Thus, taken with previous results, then amongst the nuclear oncogenes or tumor suppressor genes, c‐myc, RB, c‐fos, and c‐myb, only c‐myc and RB expression exhibit early regulation during induced HL‐60 cell differentiation.