[HTML][HTML] Gluconeogenesis in cancer cells–repurposing of a starvation-induced metabolic pathway?

G Grasmann, E Smolle, H Olschewski… - Biochimica et Biophysica …, 2019 - Elsevier
Cancer cells constantly face a fluctuating nutrient supply and interference with adaptive
responses might be an effective therapeutic approach. It has been discovered that in the …

Preclinical overview of sorafenib, a multikinase inhibitor that targets both Raf and VEGF and PDGF receptor tyrosine kinase signaling

SM Wilhelm, L Adnane, P Newell, A Villanueva… - Molecular cancer …, 2008 - AACR
Although patients with advanced refractory solid tumors have poor prognosis, the clinical
development of targeted protein kinase inhibitors offers hope for the future treatment of many …

A randomized trial of bevacizumab, an anti–vascular endothelial growth factor antibody, for metastatic renal cancer

JC Yang, L Haworth, RM Sherry, P Hwu… - … England Journal of …, 2003 - Mass Medical Soc
Background Mutations in the tumor-suppressor gene VHL cause oversecretion of vascular
endothelial growth factor by clear-cell renal carcinomas. We conducted a clinical trial to …

Sorafenib (BAY 43-9006) inhibits tumor growth and vascularization and induces tumor apoptosis and hypoxia in RCC xenograft models

YS Chang, J Adnane, PA Trail, J Levy… - Cancer chemotherapy …, 2007 - Springer
Purpose New research findings have revealed a key role for vascular endothelial growth
factor (VEGF) in the stimulation of angiogenesis in clear cell renal carcinoma (RCC) which is …

Sunitinib: from rational design to clinical efficacy

LQM Chow, SG Eckhardt - Journal of clinical oncology, 2007 - ascopubs.org
Sunitinib (SU011248) is an oral small molecular tyrosine kinase inhibitor that exhibits potent
antiangiogenic and antitumor activity. Tyrosine kinase inhibitors such as SU6668 and …

Bevacizumab: an angiogenesis inhibitor for the treatment of solid malignancies

T Shih, C Lindley - Clinical therapeutics, 2006 - Elsevier
BACKGROUND:: Bevacizumab is a recombinant humanized monoclonal antibody that was
approved by the US Food and Drug Administration (FDA) in February 2004 for use as part of …

Randomized phase II study of multiple dose levels of CCI-779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced refractory renal cell …

MB Atkins, M Hidalgo, WM Stadler, TF Logan… - Journal of clinical …, 2004 - ascopubs.org
Purpose To evaluate the efficacy, safety, and pharmacokinetics of multiple doses of CCI-
779, a novel mammalian target of rapamycin kinase inhibitor, in patients with advanced …

The ubiquitin-proteasome pathway and its role in cancer

A Mani, EP Gelmann - Journal of clinical oncology, 2005 - ascopubs.org
Critical cellular processes are regulated, in part, by maintaining the appropriate intracellular
levels of proteins. Whereas de novo protein synthesis is a comparatively slow process …

[HTML][HTML] HIF-α effects on c-Myc distinguish two subtypes of sporadic VHL-deficient clear cell renal carcinoma

JD Gordan, P Lal, VR Dondeti, R Letrero, KN Parekh… - Cancer cell, 2008 - cell.com
Summary von Hippel-Lindau (VHL) tumor suppressor loss results in hypoxia-inducible factor
alpha (HIF-α) stabilization and occurs in 70% of sporadic clear cell renal carcinomas …

Von hippel-lindau disease

WG Kaelin Jr - Annu. Rev. Pathol. Mech. Dis., 2007 - annualreviews.org
Abstract von Hippel-Lindau disease, which is characterized by an increased risk of
hemangioblastomas, clear cell renal carcinomas, and pheochromocytomas, is caused by …