Caspase-3 is not essential for DNA fragmentation in MCF-7 cells during apoptosis induced by the pyrrolo-1,5-benzoxazepine, PBOX-6

FEBS Lett. 2002 Mar 27;515(1-3):66-70. doi: 10.1016/s0014-5793(02)02440-7.

Abstract

Effector caspases-3, -6 and -7 are responsible for producing the morphological features associated with apoptosis, such as DNA fragmentation. The present study demonstrates that a member of a novel series of pyrrolo-1,5-benzoxazepines, PBOX-6, induces apoptosis in MCF-7 cells, which lack caspase-3. Apoptosis was accompanied by DNA fragmentation and the activation of caspase-7, but not caspases-3 and -6. Inhibition of caspase-7 activity reduced the extent of apoptosis induced, indicating that activation of caspase-7 is involved in the mechanism by which PBOX-6 induces apoptosis in MCF-7 cells. This study suggests that caspase-3 is not necessarily essential for DNA fragmentation and the morphological changes associated with apoptosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Agents / pharmacology*
  • Apoptosis*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • Carcinoma / drug therapy*
  • Carcinoma / metabolism
  • Carcinoma / pathology
  • Caspase 3
  • Caspase 7
  • Caspases / metabolism*
  • DNA Fragmentation / drug effects
  • DNA Fragmentation / physiology*
  • Enzyme Activation / drug effects
  • Female
  • Flow Cytometry
  • Humans
  • In Situ Nick-End Labeling
  • Oxazepines / pharmacology*
  • Pyrroles / pharmacology*
  • Tumor Cells, Cultured

Substances

  • Antineoplastic Agents
  • Oxazepines
  • Pyrroles
  • CASP3 protein, human
  • CASP7 protein, human
  • Caspase 3
  • Caspase 7
  • Caspases
  • PBOX-6