Expression of the SEPT9-i4 isoform confers resistance to microtubule-interacting drugs

Cellular Oncology

Volumn 35, Issue 2, 2012, Pages 85-93

  Chacko, Alex D ^a   McDade, Simon S ^a   Chanduloy, Severine ^a   Church, Stewart W ^a   Kennedy, Richard ^a   Price, John ^b   Hall, Peter A ^c,d   Russell, S E Hilary ^a  

^a QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^b BELFAST CITY HOSPITAL   (United Kingdom)

^c KING FAISAL SPECIALIST HOSPITAL AND RESEARCH CENTER   (Saudi Arabia)

^d ALFAISAL UNIVERSITY   (Saudi Arabia)

Author keywords

Drug resistance; Microtubules; SEPT9; Septin

Indexed keywords

CISPLATIN; ETOPOSIDE; ISOPROTEIN; NAVELBINE; PACLITAXEL; PROTEIN SEPTIN 9 I4; SEPTIN; TUBULIN; UNCLASSIFIED DRUG; DRUG DERIVATIVE; ICE; SEPT9 PROTEIN, HUMAN; VINBLASTINE;

ARTICLE; BREAST CANCER; CANCER CHEMOTHERAPY; CANCER RESISTANCE; CELL CULTURE; CELL SURVIVAL; CONTROLLED STUDY; GENE; GENE OVEREXPRESSION; HUMAN; HUMAN CELL; MICROTUBULE; OVARY CANCER; PRIORITY JOURNAL; PROTEIN EXPRESSION; SEPTIN9 I4 GENE; DNA DAMAGE; DRUG EFFECT; DRUG RESISTANCE; FLOW CYTOMETRY; METABOLISM; POLYMERIZATION; TUMOR CELL LINE;

CELL LINE, TUMOR; DNA DAMAGE; DRUG RESISTANCE, NEOPLASM; FLOW CYTOMETRY; HUMANS; ICE; MICROTUBULES; PACLITAXEL; POLYMERIZATION; PROTEIN ISOFORMS; SEPTINS; VINBLASTINE;

EID: 84866772542     PISSN: 22113428     EISSN: 22113436     Source Type: Journal    
DOI: 10.1007/s13402-011-0066-0     Document Type: Article

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