Results 101 to 110 of about 2,224,846 (160)

Erlotinib completely reverses topotecan-resistance in multidrug resistant cancer cells overexpressing breast cancer resistant protein 1

open access: yes, 2019
[[abstract]]Erlotinib inhibits the ATP-binding site of the tyrosine kinase associated with the epidermal growth factor receptor. We have recently demonstrated that gefitinib, a structurally similar receptor tyrosine kinase inhibitor, inhibited functions ...
Yang, CH;Yang, CS;Huang, CJ;Cheng, AL;Whang-Peng, J;Yang, PC
core  

M6A associated TSUC7 inhibition contributed to Erlotinib resistance in lung adenocarcinoma through a notch signaling activation dependent way. [PDF]

open access: yesJ Exp Clin Cancer Res, 2021
Li K   +10 more
europepmc   +1 more source

Erratum: Overcoming erlotinib resistance in EGFR mutation-positive lung adenocarcinomas through repression of phosphoglycerate dehydrogenase: Erratum. [PDF]

open access: yesTheranostics, 2021
Dong JK   +13 more
europepmc   +1 more source

Axl mediates acquired resistance of head and neck cancer cells to the epidermal growth factor receptor inhibitor erlotinib

open access: yes, 2013
Elevated expression and activity of the epidermal growth factor receptor (EGFR) is associated with development and progression of head and neck cancer (HNC) and a poor prognosis. Clinical trials with EGFR tyrosine kinase inhibitors (e.g., erlotinib) have
Stuart, L.   +8 more
core   +1 more source

Summary of thirteen patients acquired resistance to erlotinib.

open access: yes, 2013
Time on erlotinib*, Time to progression after erlotinib therapy; Response#, Response to erlotinib; del,deletion; Adeno, adenocarcinoma. CR: Complete response; PR: Partial response; SD: Stable disease; PD: Progressive disease.
Xiaoju Zhang (387133)   +5 more
core   +1 more source

Re-use of erlotinib in a patient using osimertinib after erlotinib, case report

open access: yes, 1995
Introduction Most patients with non-small-cell lung cancer tumors that have epidermal growth factor receptor (EGFR) mutations have deletion mutations in exon 19 or exon 21, or both.In recent years, targeted therapies in lung cancer have increased ...
Ünal, Vahdet, Gursoy, Pinar
core   +1 more source

Home - About - Disclaimer - Privacy