^
Association details:
Evidence:
Evidence Level:
Sensitive: D – Preclinical
New
Source:
Title:

A synthetic-lethality RNAi screen reveals an ERK-mTOR co-targeting pro-apoptotic switch in PIK3CA+ oral cancers

Excerpt:
Combination of rapamycin with trametinib, a MEK1/2 inhibitor, demonstrated strong synergism in HNSCC-derived cells in vitro and in vivo, including HNSCC cells expressing the HRAS and PIK3CA oncogenes….We used UM-SCC-17B, which has a HRAS Q61L mutant and Detroit 562 cells exhibiting the PIK3CA H1047R mutation. The combination of rapamycin and trametinib demonstrated strong synergism in growth inhibition of these cells (Figure ​(Figure2A,2A, Supplementary Figure S1A).
Secondary therapy:
nanoparticle albumin-bound rapamycin
DOI:
10.18632/oncotarget.7372
Evidence Level:
Sensitive: D – Preclinical
New
Title:

Response of Head and Neck Squamous Cell Carcinoma Cells Carrying PIK3CA Mutations to Select Targeted Therapies

Excerpt:
CONTRADICTED EVIDENCE...we also tested the response of our engineered cell lines to trametinib, which is a selective inhibitor of MEK 1/MEK2 activation and kinase activity. Similar to the trends with 17-AAG and GDC-0941, E545K- and H1047R-SCC25 cells exhibited decreased sensitivity to trametinib
DOI:
10.1001/jamaoto.2015.0471