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Phenotypic changes induced by a novel benzophenone derivative and resultant suppression of cell proliferation in the human thymic acute lymphoblastic leukemia cell line HPB-ALL.

Abstract
A novel benzophenone derivative, 2-(2-benzoyl-4-chlorophenoxy)-N-methylpropionamide (Ch-13), induced phenotypic differentiation linked to the inhibition of cell proliferation in human thymic acute lymphoblastic leukemia cell line HPB-ALL cells. The Ch-13-induced morphological changes consist of a decrease in cell size, nucleolar disappearance, and an alteration in the chromatin distribution, resembling large or atypical lymphocytes. Treatment with Ch-13 brought about a remarkable reduction in OKT6-, OKT4/Leu3a-, and OKT9-positive cells. At the optimal differentiation-inducing dose (5 X 10(-5)M), Ch-13 inhibited the cell proliferation, de novo DNA synthesis, and specific antibody-induced cell surface antigen capping.
AuthorsY Nakao, S Matsuda, T Matsui, T Nakagawa, T Koizumi, T Saida, T Fujita
JournalCancer research (Cancer Res) Vol. 44 Issue 12 Pt 1 Pg. 5836-44 (Dec 1984) ISSN: 0008-5472 [Print] United States
PMID6594195 (Publication Type: Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Antigens, Surface
  • Benzophenones
  • 2-(2-benzoyl-4-chlorophenoxy)-N-methylpropionamide
Topics
  • Antigens, Surface (analysis)
  • Benzophenones (toxicity)
  • Cell Division (drug effects)
  • Cell Line
  • Humans
  • Kinetics
  • Leukemia, Lymphoid (pathology)
  • Phenotype
  • Structure-Activity Relationship
  • Thymus Neoplasms (pathology)

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