Retraction: CD133 and DNA-PK regulate MDR1 via the PI3K- or Akt-NF-κB pathway in multidrug-resistant glioblastoma cells in vitro (Oncogene (2016) 35 (241-250) DOI: 10.1038/onc.2015.78);CD133 and DNA-PK regulate MDR1 via the PI3K- or Akt-NF-κB pathway in multidrug-resistant glioblastoma cells in vitro

Oncogene

Volumn 35, Issue 2, 2016, Pages 241-250

  Xi, G ^a   Hayes, E ^a   Lewis, R ^a   Ichi, S ^a,c   Mania Farnell, B ^b   Shim, K ^a,d   Takao, T ^a,e   Allender, E ^a   Mayanil, C S ^a   Tomita, T ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

^b PURDUE UNIVERSITY CALUMET   (United States)

^c JAPANESE RED CROSS MEDICAL CENTER   (Japan)

^d Yonsei University College of Medicine   (South Korea)

^e UNIVERSITY OF TSUKUBA   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CD133 ANTIGEN; DNA DEPENDENT PROTEIN KINASE; DOXORUBICIN; IMMUNOGLOBULIN ENHANCER BINDING PROTEIN; MULTIDRUG RESISTANCE PROTEIN 1; PHOSPHATIDYLINOSITOL 3 KINASE; SMALL INTERFERING RNA; ABCB1 PROTEIN, HUMAN; ANTINEOPLASTIC AGENT; ENZYME INHIBITOR; GLYCOPROTEIN; LEUKOCYTE ANTIGEN; MULTIDRUG RESISTANCE PROTEIN; NUCLEAR PROTEIN; PEPTIDE; PRKDC PROTEIN, HUMAN; PROTEIN KINASE B;

ARTICLE; CANCER CHEMOTHERAPY; CANCER RESISTANCE; CONTROLLED STUDY; DOWN REGULATION; ENZYME INHIBITION; GLIOBLASTOMA CELL LINE; HUMAN; HUMAN CELL; IN VITRO STUDY; MULTIDRUG RESISTANCE; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN FUNCTION; PROTEIN PROTEIN INTERACTION; PROTEIN TARGETING; REGULATORY MECHANISM; SIGNAL TRANSDUCTION; ANTAGONISTS AND INHIBITORS; DRUG EFFECTS; DRUG RESISTANCE; GENETICS; GLIOBLASTOMA; METABOLISM; TUMOR CELL LINE;

ANTIGENS, CD; ANTINEOPLASTIC AGENTS; CELL LINE, TUMOR; DNA-ACTIVATED PROTEIN KINASE; DOXORUBICIN; DRUG RESISTANCE, NEOPLASM; ENZYME INHIBITORS; GLIOBLASTOMA; GLYCOPROTEINS; HUMANS; NF-KAPPA B; NUCLEAR PROTEINS; P-GLYCOPROTEINS; PEPTIDES; PHOSPHATIDYLINOSITOL 3-KINASES; PROTO-ONCOGENE PROTEINS C-AKT; SIGNAL TRANSDUCTION;

EID: 84955207765     PISSN: 09509232     EISSN: 14765594     Source Type: Journal    
DOI: 10.1038/onc.2016.64     Document Type: Erratum

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