Ontology highlight
ABSTRACT:
SUBMITTER: Saintas E
PROVIDER: S-EPMC5305101 | biostudies-literature | 2017
REPOSITORIES: biostudies-literature
Saintas Emily E Abrahams Liam L Ahmad Gulshan T GT Ajakaiye Anu-Oluwa M AM AlHumaidi Abdulaziz S H A M AS Ashmore-Harris Candice C Clark Iain I Dura Usha K UK Fixmer Carine N CN Ike-Morris Chinedu C Mato Prado Mireia M Mccullough Danielle D Mishra Shishir S Schöler Katia M U KM Timur Husne H Williamson Maxwell D C MD Alatsatianos Markella M Bahsoun Basma B Blackburn Edith E Hogwood Catherine E CE Lithgow Pamela E PE Rowe Michelle M Yiangou Lyto L Rothweiler Florian F Cinatl Jindrich J Zehner Richard R Baines Anthony J AJ Garrett Michelle D MD Gourlay Campbell W CW Griffin Darren K DK Gullick William J WJ Hargreaves Emma E Howard Mark J MJ Lloyd Daniel R DR Rossman Jeremy S JS Smales C Mark CM Tsaousis Anastasios D AD von der Haar Tobias T Wass Mark N MN Michaelis Martin M
PloS one 20170213 2
The formation of acquired drug resistance is a major reason for the failure of anti-cancer therapies after initial response. Here, we introduce a novel model of acquired oxaliplatin resistance, a sub-line of the non-MYCN-amplified neuroblastoma cell line SK-N-AS that was adapted to growth in the presence of 4000 ng/mL oxaliplatin (SK-N-ASrOXALI4000). SK-N-ASrOXALI4000 cells displayed enhanced chromosomal aberrations compared to SK-N-AS, as indicated by 24-chromosome fluorescence in situ hybridis ...[more]