Approaching tumour therapy beyond platinum drugs: status of the art and perspectives of ruthenium drug candidates
A Bergamo, C Gaiddon, JHM Schellens… - Journal of inorganic …, 2012 - Elsevier
The study of metal complexes for the treatment of cancer diseases has resulted in the
identification of some unique properties of ruthenium-based compounds. Among these inorganic-…
identification of some unique properties of ruthenium-based compounds. Among these inorganic-…
Photodynamic therapy in oncology
M Triesscheijn, P Baas, JHM Schellens… - The oncologist, 2006 - academic.oup.com
Learning Objectives After completing this course, the reader will be able to: Discuss the safety
and side effects of PDT. Identify appropriate indications for PDT. Explain the choice of PDT …
and side effects of PDT. Identify appropriate indications for PDT. Explain the choice of PDT …
An update on in vitro test methods in human hepatic drug biotransformation research: pros and cons
EFA Brandon, CD Raap, I Meijerman… - Toxicology and applied …, 2003 - Elsevier
The liver is the predominant organ in which biotransformation of foreign compounds takes
place, although other organs may also be involved in drug biotransformation. Ideally, an in …
place, although other organs may also be involved in drug biotransformation. Ideally, an in …
Role of breast cancer resistance protein in the bioavailability and fetal penetration of topotecan
JW Jonker, JW Smit, RF Brinkhuis… - Journal of the …, 2000 - academic.oup.com
Background and Methods: Breast cancer resistance protein (BCRP/MXR/ABCP) is a
multidrug-resistance protein that is a member of the adenosine triphosphate-binding cassette family …
multidrug-resistance protein that is a member of the adenosine triphosphate-binding cassette family …
[HTML][HTML] Inhibition of Poly(ADP-Ribose) Polymerase in Tumors from BRCA Mutation Carriers
Background The inhibition of poly(adenosine diphosphate [ADP]–ribose) polymerase (PARP)
is a potential synthetic lethal therapeutic strategy for the treatment of cancers with specific …
is a potential synthetic lethal therapeutic strategy for the treatment of cancers with specific …
Increased oral bioavailability of topotecan in combination with the breast cancer resistance protein and P-glycoprotein inhibitor GF120918
CMF Kruijtzer, JH Beijnen, H Rosing… - Journal of Clinical …, 2002 - ascopubs.org
PURPOSE: We discovered that breast cancer resistance protein (BCRP), a recently identified
adenosine triphosphate–binding cassette drug transporter, substantially limits the oral …
adenosine triphosphate–binding cassette drug transporter, substantially limits the oral …
Subcellular localization and distribution of the breast cancer resistance protein transporter in normal human tissues
M Maliepaard, GL Scheffer, IF Faneyte… - Cancer research, 2001 - AACR
… DD, van der Valk P., Dalton WS, Schellens JHM, Scheper RJ BCRP is localized at the plasma
… Meerum Terwogt JM, Beijnen JH, ten Bokkel Huinink WW, Rosing H., Schellens JHM Co-…
… Meerum Terwogt JM, Beijnen JH, ten Bokkel Huinink WW, Rosing H., Schellens JHM Co-…
[HTML][HTML] Encorafenib, Binimetinib, and Cetuximab in BRAF V600E–Mutated Colorectal Cancer
Background Patients with metastatic colorectal cancer with the BRAF V600E mutation have
a poor prognosis, with a median overall survival of 4 to 6 months after failure of initial therapy…
a poor prognosis, with a median overall survival of 4 to 6 months after failure of initial therapy…
[PDF][PDF] Poly(ADP)-Ribose Polymerase Inhibition: Frequent Durable Responses in BRCA Carrier Ovarian Cancer Correlating With Platinum-Free Interval
PC Fong, TA Yap, DS Boss, CP Carden… - Journal of clinical …, 2010 - researchgate.net
Purpose Selective tumor cell cytotoxicity can be achieved through a synthetic lethal strategy
using poly (ADP)-ribose polymerase (PARP) inhibitor therapy in BRCA1/2 mutation carriers …
using poly (ADP)-ribose polymerase (PARP) inhibitor therapy in BRCA1/2 mutation carriers …
A Phase I and Pharmacological Study with Imidazolium-trans-DMSO-imidazole-tetrachlororuthenate, a Novel Ruthenium Anticancer Agent
JM Rademaker-Lakhai, D Van Den Bongard… - Clinical Cancer …, 2004 - AACR
Purpose: NAMI-A {H 2 Im[trans-RuCl 4 (DMSO)HIm] or imidazolium-trans-DMSO-imidazole-tetrachlororuthenate}
is a novel ruthenium-containing compound that has demonstrated …
is a novel ruthenium-containing compound that has demonstrated …