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

[Genetic instability and cancer]

A Sarasin1

  • 1Laboratoire de génétique moléculaire, UPR 42, CNRS, Villejuif.

La Revue Du Praticien
|October 1, 1995
PubMed
Summary
This summary is machine-generated.

Most human tumors have multiple mutations, driven by genotoxic agents or inherited DNA repair gene defects. This genetic instability leads to a mutator phenotype, accelerating cancer development and progression.

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

The Iberian legacy into a young genetic xeroderma pigmentosum cluster in central Brazil.

Mutation research. Genetic toxicology and environmental mutagenesis·2020
Same author

Xeroderma pigmentosum in South Africa: Evidence for a prevalent founder effect.

The British journal of dermatology·2019
Same author

A genetic cluster of patients with variant xeroderma pigmentosum with two different founder mutations.

The British journal of dermatology·2016
Same author

Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type C.

The British journal of dermatology·2013
Same author

Transmembrane diffusion of gemcitabine by a nanoparticulate squalenoyl prodrug: an original drug delivery pathway.

Journal of controlled release : official journal of the Controlled Release Society·2010
Same author

DNA repair pathways and human metastatic malignant melanoma.

Current molecular medicine·2010

Area of Science:

  • Oncology
  • Genetics
  • Molecular Biology

Context:

  • Human tumors accumulate multiple genetic mutations essential for tumor progression.
  • Genotoxic agents or inherited defects in DNA repair pathways can drive this mutation accumulation.
  • Hereditary conditions affecting DNA repair, mismatch repair, or tumor suppressor genes increase cancer incidence.

Purpose:

  • To explore the role of multiple mutations in cancer development.
  • To understand the mechanisms leading to a mutator phenotype.
  • To investigate the link between genetic instability and cancer progression.

Summary:

  • Multiple mutations are a hallmark of human tumors, crucial for the selection of pre-tumoral, tumoral, and metastatic clones.
  • These mutations arise sequentially, induced by genotoxic agents or by inherited defects in genes controlling genetic stability.

Related Experiment Videos

  • Defective DNA repair mechanisms and tumor suppressor genes result in a 'mutator phenotype,' promoting rapid cancer cell evolution.
  • Impact:

    • Highlights the critical role of genetic instability in oncogenesis.
    • Provides insight into hereditary cancer syndromes.
    • Underscores the importance of DNA repair pathways in preventing cancer.