FOXM1 (Forkhead box M1) in tumorigenesis: overexpression in human cancer, implication in tumorigenesis, oncogenic functions, tumor-suppressive properties, and …

I Wierstra - Advances in cancer research, 2013 - Elsevier
Abstract FOXM1 (Forkhead box M1) is a typical proliferation-associated transcription factor
and is also intimately involved in tumorigenesis. FOXM1 stimulates cell proliferation and cell …

EGFR targeting therapies: monoclonal antibodies versus tyrosine kinase inhibitors: similarities and differences

O Dassonville, A Bozec, JL Fischel, G Milano - Critical reviews in oncology …, 2007 - Elsevier
Current development of targeted therapy in oncology is particularly active and concerns
principally two types of agents which are monoclonal antibodies (Mabs) and tyrosine kinase …

Co-delivery of oxygen and erlotinib by aptamer-modified liposomal complexes to reverse hypoxia-induced drug resistance in lung cancer

F Li, H Mei, Y Gao, X Xie, H Nie, T Li, H Zhang, L Jia - Biomaterials, 2017 - Elsevier
Tumor hypoxia is a common feature of the tumor microenvironment and has been regarded
as one of the key factors in driving the emergence of drug resistance in solid tumors. To …

Differential metabolism of gefitinib and erlotinib by human cytochrome P450 enzymes

J Li, M Zhao, P He, M Hidalgo, SD Baker - Clinical Cancer Research, 2007 - AACR
Purpose: To examine the enzyme kinetics of gefitinib and erlotinib metabolism by individual
cytochrome P450 (CYP) enzymes, and to compare their effects on CYP3A activity, with the …

MUC1 induces acquired chemoresistance by upregulating ABCB1 in EGFR-dependent manner

W Jin, X Liao, Y Lv, Z Pang, Y Wang, Q Li, Y Liao… - Cell death & …, 2017 - nature.com
Chemoresistance contributes to cancer relapse and increased mortality in a variety of
cancer types, raising a pressing need to better understand the underlying mechanism …

Gefitinib for non-small-cell lung cancer patients with epidermal growth factor receptor gene mutations screened by peptide nucleic acid-locked nucleic acid PCR …

A Sutani, Y Nagai, K Udagawa, Y Uchida… - British journal of …, 2006 - nature.com
This study was prospectively designed to evaluate a phase II study of gefitinib for non-small-
cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutations …

Metabolism considerations for kinase inhibitors in cancer treatment

DR Duckett, MD Cameron - Expert opinion on drug metabolism & …, 2010 - Taylor & Francis
Importance of the field: A concerted effort by the pharmaceutical industry over the last
decade has led to the successful clinical development of protein kinase inhibitors as …

Women and lung cancer: epidemiology, tumor biology, and emerging trends in clinical research

CP Belani, S Marts, J Schiller, MA Socinski - Lung cancer, 2007 - Elsevier
Lung cancer is the leading cause of cancer-related death in both men and women.
Environmental carcinogens, particularly tobacco smoke, play a dominant role in the …

Where next for gefitinib in patients with lung cancer?

F Blackhall, M Ranson, N Thatcher - The lancet oncology, 2006 - thelancet.com
Gefitinib belongs to the small-molecule class of epidermal growth factor receptor (EGFR)
tyrosine-kinase inhibitors. It was given conditional approval by the US Food and Drug …

Comparison of the drug-drug interactions potential of erlotinib and gefitinib via inhibition of UDP-glucuronosyltransferases

Y Liu, J Ramírez, L House, MJ Ratain - Drug Metabolism and Disposition, 2010 - ASPET
We aimed to investigate and compare the effects of erlotinib and gefitinib on UDP-
glucuronosyltransferase (UGT) activities and to quantitatively evaluate their drug-drug …