Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Cellular signaling in cell death

D J McConkey1

  • 1Dana-Farber Cancer Institute, Department of Pathology, Harvard Medical School, Boston, MA 02115.

New Horizons (Baltimore, Md.)
|February 1, 1993
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Marizomib, a proteasome inhibitor for all seasons: preclinical profile and a framework for clinical trials.

Current cancer drug targets·2011
Same author

Proteasome inhibitors activate autophagy as a cytoprotective response in human prostate cancer cells.

Oncogene·2009
Same author

Measuring soluble forms of extracellular cytokeratin 18 identifies both apoptotic and necrotic mechanisms of cell death produced by adenoviral-mediated interferon alpha: possible use as a surrogate marker.

Cancer gene therapy·2009
Same author

Phase II trial of imatinib mesylate in patients with metastatic melanoma.

British journal of cancer·2008
Same author

Early RB94-produced cytotoxicity in cancer cells is independent of caspase activation or 50 kb DNA fragmentation.

Cancer gene therapy·2008
Same author

Adenoviral-mediated interferon alpha overcomes resistance to the interferon protein in various cancer types and has marked bystander effects.

Cancer gene therapy·2006
Same journal

Palliative care in the intensive care unit.

New horizons (Baltimore, Md.)·2001
Same journal

An international perspective on the treatment of pediatric shock: the Brazilian experience.

New horizons (Baltimore, Md.)·1998
Same journal

Nutrition and shock in pediatric patients.

New horizons (Baltimore, Md.)·1998
Same journal

Recent advances in pediatric cardiopulmonary resuscitation and advanced life support.

New horizons (Baltimore, Md.)·1998
Same journal

Potential protective role of the heat shock response in sepsis.

New horizons (Baltimore, Md.)·1998
Same journal

Molecular biology of septic shock.

New horizons (Baltimore, Md.)·1998
See all related articles

Apoptosis, a form of programmed cell death, involves specific molecular pathways regulated by intracellular signals and gene expression. Understanding these mechanisms is crucial for both normal physiology and disease states.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Biochemistry

Background:

  • Apoptosis is programmed cell death mediated by endogenous endonuclease activation.
  • It is a fundamental process for normal development and tissue homeostasis.
  • Dysregulation of apoptosis is implicated in various diseases.

Purpose of the Study:

  • To elucidate the molecular regulation of apoptosis.
  • To identify key signaling pathways and genetic factors involved in cell death.
  • To explore the role of apoptosis in both physiologic and pathologic conditions.

Main Methods:

  • Analysis of signal transduction pathways.
  • Investigation of protein kinase A and C activation.
  • Assessment of poly(adenosine 5'-diphosphate-ribose) polymerase activity.

Related Experiment Videos

  • Examination of oncogene, tumor suppressor gene, and transcription factor roles.
  • Main Results:

    • Apoptosis regulation involves increased cytosolic calcium and activation of protein kinases A and C.
    • The nuclear enzyme poly(adenosine 5'-diphosphate-ribose) polymerase is stimulated during apoptosis.
    • Gene expression, including oncogenes and tumor suppressor genes, influences cell death induction.

    Conclusions:

    • Apoptosis is a highly regulated process involving complex intracellular signaling.
    • Biochemical mechanisms in pathologic cell death often mirror those in normal apoptosis.
    • Further research into these pathways can inform therapeutic strategies for diseases involving cell death.