Title : Potential biomarkers for the therapeutic efficacy of sorafenib, sunitinib and everolimus.

Pub. Date : 2017 Jan

PMID : 27840968






5 Functional Relationships(s)
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1 Sorafenib inhibited the expression of phospho-ERK and -4EBP1 in 769-P cells; sunitinib, phospho-ERK and -4EBP1 in 786-O and 769-P cells; and everolimus, phospho-p70 in 786-O and 769-P cells. Sorafenib mitogen-activated protein kinase 1 Homo sapiens
2 Knockdown of ERK reduced sensitivity to sorafenib in both cell lines, knockdown of ERK and 4EBP1 reduced sensitivity to sunitinib in 769-P cells, and knockdown of 4EBP1 and p70 reduced sensitivity to everolimus in 786-O cells. Sorafenib mitogen-activated protein kinase 1 Homo sapiens
3 High expression of phospho-ERK, -4EBP1 and -p70 correlated with better progression-free survival in patients treated with sorafenib, sunitinib and everolimus, respectively. Sorafenib mitogen-activated protein kinase 1 Homo sapiens
4 Our results indicate that phospho-ERK, -4EBP1 and/or -ERK, and phospho-p70 can be used as biomarkers for the therapeutic efficacy of sorafenib, sunitinib and everolimus, respectively. Sorafenib mitogen-activated protein kinase 1 Homo sapiens
5 Our results indicate that phospho-ERK, -4EBP1 and/or -ERK, and phospho-p70 can be used as biomarkers for the therapeutic efficacy of sorafenib, sunitinib and everolimus, respectively. Sorafenib mitogen-activated protein kinase 1 Homo sapiens