2003
DOI: 10.1038/sj.leu.2403052
|View full text |Cite
|
Sign up to set email alerts
|

Differential effects of kinase cascade inhibitors on neoplastic and cytokine-mediated cell proliferation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
37
0

Year Published

2004
2004
2015
2015

Publication Types

Select...
6
4

Relationship

3
7

Authors

Journals

citations
Cited by 51 publications
(39 citation statements)
references
References 59 publications
2
37
0
Order By: Relevance
“…UO126 inhibited MEK1/2 and ERK1/2 activity to a significant extent in cells, but this was not enough to lower infection to zero suggesting a possible role for signaling emanating from Raf kinase, other than the traditional MEK1/24ERK1/2 pathway. Such situations have been documented where Raf signaling may transmit its signaling through more than one intermediate (Janssen et al, 1998;Baumann et al, 2000;Shelton et al, 2003). Further, MEK inhibitors cannot suppress all the effects of Raf signaling.…”
Section: Inhibition Of Mek Suppresses Hhv-8 Infectionmentioning
confidence: 99%
“…UO126 inhibited MEK1/2 and ERK1/2 activity to a significant extent in cells, but this was not enough to lower infection to zero suggesting a possible role for signaling emanating from Raf kinase, other than the traditional MEK1/24ERK1/2 pathway. Such situations have been documented where Raf signaling may transmit its signaling through more than one intermediate (Janssen et al, 1998;Baumann et al, 2000;Shelton et al, 2003). Further, MEK inhibitors cannot suppress all the effects of Raf signaling.…”
Section: Inhibition Of Mek Suppresses Hhv-8 Infectionmentioning
confidence: 99%
“…It has been known for quite some time now, that treatment with certain inhibitors (for example, Raf inhibitors), can result in hyper-activation of wildtype (WT) Raf. 8,[146][147][148] It has recently become clear that it will be essential to determine the genetic status at both BRAF and RAS before treatment with B-Raf selective inhibitors proceeds. 149 Class I B-Raf inhibitors (active conformation inhibitors) such as PLX4720 and 885-A (a close analog of SB590885) will inhibit BRAF mutants, however, these ATP-competitive B-Raf inhibitors will not inhibit WT BRAF or mutant RAS.…”
Section: Pecularities Of Raf Kinase Inhibitorsmentioning
confidence: 99%
“…Raf inhibitors have been developed [47][48][49][50][51] Figure 2 Genes mutated in hematopoietic cells, which result in sensitivity to targeted therapy. Activation of these molecules often results in dependence ('oncogene addiction') of the cells on the mutated gene for proliferation.…”
Section: Aberrant Regulation Of Apoptosis and Drug Resistancementioning
confidence: 99%