[HTML][HTML] Insulin-like growth factor-I receptor signalling and acquired resistance to gefitinib (ZD1839; Iressa) in human breast and prostate cancer cells

HE Jones, L Goddard, JMW Gee… - Endocrine-related …, 2004 - erc.bioscientifica.com
De novo and acquired resistance to the anti-tumour drug gefitinib (ZD1839; Iressa), a
specific epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) has been …

Combined targeting of epidermal growth factor receptor and MDM2 by gefitinib and antisense MDM2 cooperatively inhibit hormone-independent prostate cancer

R Bianco, R Caputo, R Caputo, V Damiano… - Clinical cancer …, 2004 - AACR
Purpose: The epidermal growth factor receptor (EGFR) may play a relevant role in the
progression, hormone therapy resistance, and prognosis of prostate cancer patients. Also …

Inhibition of angiogenesis by the antiepidermal growth factor receptor antibody ImClone C225 in androgen-independent prostate cancer growing orthotopically in …

T Karashima, P Sweeney, JW Slaton, SJ Kim… - Clinical cancer …, 2002 - AACR
In human androgen-independent prostate cancer (PCa), epidermal growth factor receptor
(EGFR) regulates angiogenesis, tumor growth, and progression. In this study, we evaluated …

Gefitinib–trastuzumab combination on hormone-refractory prostate cancer xenograft

P Formento, JM Hannoun-Levi, F Gérard… - European Journal of …, 2005 - Elsevier
New drugs and new combinations of drugs have recently shown promising clinical activity in
hormone refractory prostate cancer. We studied the association of gefitinib with trastuzumab …

ZD1839, a selective epidermal growth factor receptor tyrosine kinase inhibitor, shows antimetastatic activity using a hepatocellular carcinoma model

M Matsuo, H Sakurai, I Saiki - Molecular cancer therapeutics, 2003 - AACR
The epidermal growth factor receptor (EGFR) is highly expressed in many human tumors
and provides a new target for anticancer drug development. EGFR-targeted agents have …

Non-genomic effects of the androgen receptor and vitamin D agonist are involved in suppressing invasive phenotype of prostate cancer cells

L Bonaccorsi, S Marchiani, P Ferruzzi, M Muratori… - Steroids, 2006 - Elsevier
Suppression of invasive phenotype is essential in developing new therapeutic tools to treat
prostate cancer (PC). Evidence indicates that androgen-dependent (AD) prostate cancer …

[HTML][HTML] Inhibition of androgen-independent prostate cancer cell growth is enhanced by combination therapy targeting Hedgehog and ErbB signalling

G Shaw, DM Prowse - Cancer cell international, 2008 - Springer
Background Prostate cancer is a leading cause of male cancer specific mortality. When cure
by radical prostatectomy is not possible the next line of prostate cancer treatment is …

EGF signalling in prostate cancer cell lines is inhibited by a high expression level of the endocytosis protein REPS2

JK Oosterhoff, LC Kühne… - … Journal of cancer, 2005 - Wiley Online Library
In advanced prostate cancer, cellular changes occur leading to a transition from androgen‐
dependent to androgen‐independent growth. During this transition, proliferation of …

[HTML][HTML] MP470, a novel receptor tyrosine kinase inhibitor, in combination with Erlotinib inhibits the HER family/PI3K/Akt pathway and tumor growth in prostate cancer

W Qi, LS Cooke, A Stejskal, C Riley, KD Croce… - BMC cancer, 2009 - Springer
Background Prostate cancer is a common disease in men and at present there is no
effective therapy available due to its recurrence despite androgen deprivation therapy. The …

Loss of EGFR induced autophagy sensitizes hormone refractory prostate cancer cells to adriamycin

S Xu, Z Weihua - The Prostate, 2011 - Wiley Online Library
BACKGROUND The epidermal growth factor receptor (EGFR), a receptor tyrosine kinase, is
over‐expressed in advanced prostate cancer but tyrosine kinase inhibitors are not clinically …