Title : PI3K/AKT/mTOR pathway is activated after imatinib secondary resistance in gastrointestinal stromal tumors (GISTs).

Pub. Date : 2015 Apr

PMID : 25757539






8 Functional Relationships(s)
Download
Sentence
Compound Name
Protein Name
Organism
1 PI3K/AKT/mTOR pathway is activated after imatinib secondary resistance in gastrointestinal stromal tumors (GISTs). Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
2 Phosphatidylinositol-3-kinase (PI3K)/AKT/mammalian target of the rapamycin (mTOR) pathway activation may be related to imatinib resistance; however, no study has focused on whether signal conduction of this pathway will change after imatinib resistance. Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
3 Phosphatidylinositol-3-kinase (PI3K)/AKT/mammalian target of the rapamycin (mTOR) pathway activation may be related to imatinib resistance; however, no study has focused on whether signal conduction of this pathway will change after imatinib resistance. Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
4 The activation of AKT/mTOR was significantly higher in imatinib secondary resistant GIST (53.1 %) than in imatinib-sensitive (27.1 %) and primary resistant GIST (33.3 %) (P = 0.049). Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
5 The activation of AKT/mTOR was significantly higher in imatinib secondary resistant GIST (53.1 %) than in imatinib-sensitive (27.1 %) and primary resistant GIST (33.3 %) (P = 0.049). Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
6 AKT/mTOR status was inactivated in pre-imatinib and on-treatment samples in eight patients with effective imatinib; however, the status of six patients was changed from inactivated to activated in 12 patients at the time of tumor progression. Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
7 AKT/mTOR status was inactivated in pre-imatinib and on-treatment samples in eight patients with effective imatinib; however, the status of six patients was changed from inactivated to activated in 12 patients at the time of tumor progression. Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens
8 PI3K/AKT/mTOR pathway can be partly activated after imatinib secondary resistance in GIST. Imatinib Mesylate mechanistic target of rapamycin kinase Homo sapiens