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

Karyotypic evolution in human malignant melanoma.

G B Balaban, M Herlyn, W H Clark

    Cancer Genetics and Cytogenetics
    |January 1, 1986
    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

    A slow-cycling subpopulation of melanoma cells with highly invasive properties.

    Oncogene·2017
    Same author

    Long-term 2007-2013 monitoring of reproductive disturbance in the dun sentinel Assiminea grayana with regard to polymeric materials pollution at the coast of Lower Saxony, North Sea, Germany.

    Environmental science and pollution research international·2016
    Same author

    A stress-induced early innate response causes multidrug tolerance in melanoma.

    Oncogene·2015
    Same author

    A stress-induced early innate response causes multidrug tolerance in melanoma.

    Oncogene·2014
    Same author

    Periostin cooperates with mutant p53 to mediate invasion through the induction of STAT1 signaling in the esophageal tumor microenvironment.

    Oncogenesis·2013
    Same author

    MEK inhibition affects STAT3 signaling and invasion in human melanoma cell lines.

    Oncogene·2013
    Same journal

    Letter to the editor regarding the article "Chromosome abnormalities additional to the Philadelphia chromosome at the diagnosis of chronic myelogenous leukemia: pathogenic and prognostic implications".

    Cancer genetics and cytogenetics·2010
    Same journal

    A novel t(10;12)(q21;p13) involving ETV6 in a patient with acute myeloid leukemia.

    Cancer genetics and cytogenetics·2010
    Same journal

    A case of acute myeloid leukemia initially treated as chronic lymphocytic leukemia: what do we know about t(4;12)(q12;p13)?

    Cancer genetics and cytogenetics·2010
    Same journal

    Myelodysplastic syndrome with isochromosome 5p and trisomy 8 after treatment of a multiple myeloma.

    Cancer genetics and cytogenetics·2010
    Same journal

    Chromosomal imbalances in urinary bladder paraganglioma.

    Cancer genetics and cytogenetics·2010
    Same journal

    A pericentric inv(9)(p22q34) of the der(9)t(9;22)(q34;q11.2) is a recurrent secondary anomaly in Ph-positive leukemia.

    Cancer genetics and cytogenetics·2010
    See all related articles

    Genetic abnormalities in melanoma increase with disease progression. Common nevi show normal chromosomes, while advanced melanomas exhibit multiple cytogenetic changes, particularly involving chromosomes 1, 6, and 7.

    Area of Science:

    • Cytogenetics
    • Dermatology
    • Cancer Biology

    Background:

    • Melanocytic lesions range from benign nevi to metastatic melanoma.
    • Understanding the genetic underpinnings of melanoma progression is crucial for developing targeted therapies.

    Purpose of the Study:

    • To investigate chromosomal abnormalities in various stages of melanocytic lesions.
    • To correlate cytogenetic changes with the clinical progression of melanoma.

    Main Methods:

    • Karyotype analysis of direct preparations, early passage cultures, and cell lines from 37 patients.
    • Analysis included common nevi, dysplastic nevi, primary melanomas (radial and vertical growth phases), and metastases.

    Main Results:

    • Common nevi had normal karyotypes.

    Related Experiment Videos

  • Dysplastic nevi showed occasional single chromosomal alterations.
  • All melanomas, including early and advanced stages, displayed multiple cytogenetic changes, frequently involving chromosomes 1, 6, and 7.
  • Metastases shared common alterations with primary tumors but acquired additional genetic changes.
  • Conclusions:

    • Somatic genetic abnormalities accumulate and increase in severity with melanoma progression.
    • Specific nonrandom chromosomal alterations, particularly on chromosomes 1, 6, and 7, are characteristic of melanoma.
    • Further research is needed to elucidate the role of specific genetic changes in melanoma evolution.