795
Views
5
CrossRef citations to date
0
Altmetric
Brief Report

Targeting oncogenic protein kinase Cι for treatment of mutant KRAS LADC

, Ph.D, , &
Pages 58-64 | Received 14 May 2016, Accepted 24 May 2016, Published online: 06 Jul 2016

Figures & data

Figure 1. Clinically relevant PKCɩ-targeted combination therapies for treatment of KRAS LADC. “Vertical Blockade” of the PKCɩ-ELF3-Notch3 signaling axis and “Horizonal Blockade” of PKCɩ and mTOR signaling pathways are denoted.

Figure 1. Clinically relevant PKCɩ-targeted combination therapies for treatment of KRAS LADC. “Vertical Blockade” of the PKCɩ-ELF3-Notch3 signaling axis and “Horizonal Blockade” of PKCɩ and mTOR signaling pathways are denoted.

Figure 2. ATM and rapamycin exhibit synergistic growth inhibitory activity against KRAS LADC. (A) Combination Index (CI) analysis of ATM combined with Erlotinib, rapamycin and sorafenib for inhibition of anchorage independent growth of KRAS LADC cells. (B) Combined ATM and rapamycin significantly inhibits growth of H460 KRAS LADC xenograft tumors. Mice were treated with ATM (60 mg/kg/day) and/or rapamycin (5 mg/kg/day) or diluent alone (control). Mean +/− SE is plotted. n = 8–9/group. *p < 0.05 versus control; **p < 0.05 vs. rapamycin or ATM alone.

Figure 2. ATM and rapamycin exhibit synergistic growth inhibitory activity against KRAS LADC. (A) Combination Index (CI) analysis of ATM combined with Erlotinib, rapamycin and sorafenib for inhibition of anchorage independent growth of KRAS LADC cells. (B) Combined ATM and rapamycin significantly inhibits growth of H460 KRAS LADC xenograft tumors. Mice were treated with ATM (60 mg/kg/day) and/or rapamycin (5 mg/kg/day) or diluent alone (control). Mean +/− SE is plotted. n = 8–9/group. *p < 0.05 versus control; **p < 0.05 vs. rapamycin or ATM alone.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.