부산대학교 도서관

Expression of hyper-active RAF kinases, such as the oncogenic B-RAF-V600E mutant, in normal human cells triggers a proliferative arrest that blocks tumor formation. We discovered that glucocorticoids delay the entry into senescence induced by B-RAF-V600E in human fibroblasts, and allow bypass when the cells are regularly passaged, but they do not allow proliferation of cells that were already senescent. Transcriptome and siRNA analyses revealed that the EGR1 gene is one target of glucocorticoid action. Transcription of the EGR1 gene is activated by the RAF-MEK-ERK MAP kinase pathway and acts as a sensor of hypermitogenic pathway activity. The EGR1 transcription factor regulates the expression of p15-CDKN2B and p21-CDKN1A that are redundantly required for the proliferative arrest of BJ fibroblasts upon expression of B-RAF-V600E. Our results highlight the need to evaluate glucocorticoid action on cancer progression in melanoma, thyroid and colon carcinoma in which B-RAF-V600E is a frequent oncogene, and cancers in which evasion from senescence has been shown. [ABSTRACT FROM AUTHOR]