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 Concept Videos

Overview of Cell Death01:30

Overview of Cell Death

Cell death is an essential process where the body gets rid of old or damaged cells. Cell proliferation and death need to be balanced, as an imbalance between the two may lead to cancer or autoimmune diseases.
Cell death was observed in the early 19th century, but there was no experimental evidence to prove it. In 1842, Carl Vogt first discovered cell death in a metamorphic toad; however, it was not termed ‘cell death.’ Scientists discovered different cell death pathways only in the 20th century...
Necrosis01:16

Necrosis

Necrosis is considered as an “accidental” or unexpected form of cell death that ends in cell lysis. The first noticeable mention of “necrosis” was in 1859 when Rudolf Virchow used this term to describe advanced tissue breakdown in his compilation titled “Cell Pathology”.
Morphological Manifestations of Necrosis
Necrotic cells show different types of morphological appearance depending on the type of tissue and infection. In coagulative necrosis, cells become anucleated and die, but their...
Cellular Injury IlI: Cellular Death01:11

Cellular Injury IlI: Cellular Death

Cell death is the irreversible loss of cellular structure and function, representing the final stage of severe injury. It plays a key role in both normal physiology and disease.Types of Cell DeathThe two main types are necrosis and apoptosis, though others like necroptosis and pyroptosis also exist.Necrosis:Necrosis is an unregulated form of cell death caused by severe injury such as trauma, toxins, or ischemia. It is characterized by cell swelling, membrane loss, rupture, and leakage of...
Cellular Injury V: Apoptosis and Autophagy01:22

Cellular Injury V: Apoptosis and Autophagy

Cells respond to damage and stress through highly coordinated processes that decide whether they survive or undergo controlled self-destruction. Two major pathways involved in this regulation are apoptosis, a type of programmed cell death, and autophagy, a survival mechanism that helps cells adapt to adverse conditions.ApoptosisApoptosis removes aged or injured cells to maintain tissue balance. During this process, the cell shrinks, chromatin condenses and fragments, and membrane-bound...
Determination01:51

Determination

During embryogenesis, cells become progressively committed to different fates through a two-step process: specification followed by determination. Specification is demonstrated by removing a segment of an early embryo, “neutrally” culturing the tissue in vitro—for example, in a petri dish with simple medium—and then observing the derivatives. If the cultured region gives rise to cell types that it would normally generate in the embryo, this means that it is specified. In contrast, determination...
Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...

You might also read

Related Articles

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

Sort by
Same author

Surveillance adherence and clinical findings in children with confirmed or familial TP53 variants: the Swedish multicenter constitutional TP53 study (SWEP53).

Genetics in medicine : official journal of the American College of Medical Genetics·2026
Same author

Dual epigenetic targeting in neuroblastoma: a new paradigm from synergistic lethality to clinical translation.

Epigenomics·2026
Same author

Local application of otoprotective compounds other than sodium thiosulfate to prevent cisplatin-induced hearing loss: a systematic review.

Drug delivery·2026
Same author

Ribosomal modifications are associated with mesenchymal fate selection in the neural crest lineage.

Nature communications·2026
Same author

Systemic Immune Alterations in Paediatric Classical Hodgkin Lymphoma With CCL17 and MCP-4 as Diagnostic and Predictive Biomarkers.

EJHaem·2026
Same author

Mitoxantrone alters CD24/Siglec-10 expression in malignant brain tumor models.

Scientific reports·2026

Related Experiment Video

Updated: Jun 25, 2026

Neurogenesis Using P19 Embryonal Carcinoma Cells
07:46

Neurogenesis Using P19 Embryonal Carcinoma Cells

Published on: April 27, 2019

Embryonal neural tumours and cell death.

John Inge Johnsen1, Per Kogner, Ami Albihn

  • 1Department of Woman and Child Health, Karolinska Institutet, Astrid Lindgren Children's Hospital, Childhood Cancer Research Unit, Karolinska University Hospital, Stockholm, Sweden.

Apoptosis : an International Journal on Programmed Cell Death
|March 5, 2009
PubMed
Summary

Childhood brain tumors like medulloblastoma and neuroblastoma resist chemotherapy due to faulty apoptosis. This review explores their development and identifies new therapeutic targets for these embryonal tumors.

More Related Videos

Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress
09:51

Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress

Published on: May 7, 2014

Related Experiment Videos

Last Updated: Jun 25, 2026

Neurogenesis Using P19 Embryonal Carcinoma Cells
07:46

Neurogenesis Using P19 Embryonal Carcinoma Cells

Published on: April 27, 2019

Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress
09:51

Assessing Cell Cycle Progression of Neural Stem and Progenitor Cells in the Mouse Developing Brain after Genotoxic Stress

Published on: May 7, 2014

Area of Science:

  • Pediatric Oncology
  • Neuro-oncology
  • Cancer Biology

Background:

  • Medulloblastoma and neuroblastoma are aggressive embryonal tumors affecting the central and peripheral nervous systems in children.
  • These childhood cancers often exhibit poor prognosis, largely due to resistance to conventional chemotherapy.
  • Both tumor types share a common characteristic: deficient apoptotic (programmed cell death) pathways, inherited from their progenitor cells.

Purpose of the Study:

  • To review the specific developmental origins of medulloblastoma and neuroblastoma.
  • To highlight key biological pathways implicated in the pathogenesis of these embryonal tumors.
  • To identify potential molecular targets for novel therapeutic strategies against these challenging childhood cancers.

Main Methods:

  • Literature review focusing on embryonal tumor development.
  • Analysis of biological pathways involved in medulloblastoma and neuroblastoma.
  • Identification of potential therapeutic targets based on pathway dysregulation.

Main Results:

  • Understanding the embryonal origin provides context for tumor biology.
  • Deficient apoptosis is a critical factor in treatment resistance for both tumor types.
  • Specific molecular pathways are implicated in tumor initiation and progression.

Conclusions:

  • Targeting deficient apoptotic machinery and related pathways offers promise for new treatments.
  • Novel therapeutic approaches are needed to overcome chemotherapy resistance in pediatric embryonal tumors.
  • Further research into these biological pathways could lead to improved clinical outcomes for children with medulloblastoma and neuroblastoma.