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Increased level of Oct-1 protein in tumor cells modulates cellular response to anticancer drugs.

Abstract
The effect of overexpression of Oct-1 protein isoforms on the cell response to two anticancer drugs camptothecin and dexamethasone was studied. The effect of Oct-1 isoforms on regulated gene transcription was estimated by the difference in the level of mRNA in Burkitt's lymphoma cells (Namalwa line) untransfected and stably transfected with Oct-1 isoforms. The response to anticancer drugs of the Oct-1 target genes involved in the development of apoptosis depended, firstly, on the type of drug, secondly, on the concentration of Oct-1 in cells. and, thirdly, on the Oct-1 isoform with which these cells were transfected.
AuthorsT N Portseva, E V Pankratova, A G Stepchenko, S G Georgieva
JournalDoklady. Biochemistry and biophysics (Dokl Biochem Biophys) Vol. 469 Issue 1 Pg. 269-72 (Jul 2016) ISSN: 1608-3091 [Electronic] United States
PMID27599509 (Publication Type: Journal Article)
Chemical References
  • Antineoplastic Agents
  • Biomarkers, Tumor
  • MYC protein, human
  • Octamer Transcription Factor-1
  • POU2F1 protein, human
  • Protein Isoforms
  • Proto-Oncogene Proteins c-myc
  • RNA, Messenger
  • Dexamethasone
  • Camptothecin
Topics
  • Antineoplastic Agents (pharmacology)
  • Apoptosis (drug effects, physiology)
  • Biomarkers, Tumor (genetics, metabolism)
  • Burkitt Lymphoma (drug therapy, genetics, metabolism)
  • Camptothecin (pharmacology)
  • Cell Line, Tumor
  • Dexamethasone (pharmacology)
  • Gene Expression Regulation, Neoplastic (drug effects, physiology)
  • Humans
  • Octamer Transcription Factor-1 (genetics, metabolism)
  • Protein Isoforms
  • Proto-Oncogene Proteins c-myc (genetics, metabolism)
  • RNA, Messenger (metabolism)
  • Transfection

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