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

Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

15.5K
Cancer arises from mutations in the critical genes that allow healthy cells to escape cell cycle regulation and acquire the ability to proliferate indefinitely. Though originating from a single mutation event in one of the originator cells, cancer progresses when the mutant cell lines continue to gain more and more mutations, and finally, become malignant. For example, chronic myelogenous leukemia (CML) develops initially as a non-lethal increase in white blood cells, which progressively...
15.5K
Cancers Originate from Somatic Mutations in a Single Cell02:21

Cancers Originate from Somatic Mutations in a Single Cell

3.3K
3.3K
Cancer-Critical Genes I: Proto-oncogenes01:33

Cancer-Critical Genes I: Proto-oncogenes

11.9K
Genes usually encode proteins necessary for the proper functioning of a healthy cell. Mutations can often cause changes to the gene expression pattern, thereby altering the phenotype.
When the function of certain critical genes, especially those involved in cell cycle regulation and cell growth signaling cascades, gets disrupted, it upsets the cell cycle progression. Such cells with unchecked cell cycles start proliferating uncontrollably and eventually develop into tumors.
Such genes that act...
11.9K
Cancer-Critical Genes I: Proto-oncogenes01:33

Cancer-Critical Genes I: Proto-oncogenes

6.1K
6.1K
Abnormal Proliferation02:23

Abnormal Proliferation

5.4K
Under normal conditions, most adult cells remain in a non-proliferative state unless stimulated by internal or external factors to replace lost cells. Abnormal cell proliferation is a condition in which the cell's growth exceeds and is uncoordinated with normal cells. In such situations, cell division persists in the same excessive manner even after cessation of the stimuli, leading to persistent tumors. The tumor arises from the damaged cells that replicate to pass the damage to the...
5.4K
Mutations01:35

Mutations

45.4K
Mutations are changes in the sequence of DNA. These changes can occur spontaneously or they can be induced by exposure to environmental factors. Mutations can be characterized in a number of different ways: whether and how they alter the amino acid sequence of the protein, whether they occur over a small or large area of DNA, and whether they occur in somatic cells or germline cells.
Chromosomal Alterations Are Large-Scale Mutations
While point mutations are changes in a single nucleotide in...
45.4K

You might also read

Related Articles

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

Sort by
Same author

Chromosome aberration in typical biological systems under exposure to low- and high-intensity magnetic fields.

Electromagnetic biology and medicine·2020
Same author

Ancient Food Habits Dictate that Food Can Be Medicine but Medicine Cannot Be "Food"!!

Medicines (Basel, Switzerland)·2017
See all related articles

Related Experiment Video

Updated: Mar 26, 2026

Rapid Analysis of Chromosome Aberrations in Mouse B Lymphocytes by PNA-FISH
07:54

Rapid Analysis of Chromosome Aberrations in Mouse B Lymphocytes by PNA-FISH

Published on: August 19, 2014

17.6K

Cells With Chromosomal Aberrations Trigger Neoplastic Transformations in Humans.

Hit Kishore Goswami

    Twin Research and Human Genetics : the Official Journal of the International Society for Twin Studies
    |January 27, 2016
    PubMed
    Summary

    Marker dots (MDs), chromatin bodies found in humans prone to cancer, may indicate early neoplastic transformation. These 2-3 micron structures originate from specific chromosomes, suggesting potential as early cancer indicators.

    Keywords:
    MDsearly detection of malignancy by chromosomesmarker dotsspecific chromosomal attenuation releases marker dots

    More Related Videos

    Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae
    09:40

    Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae

    Published on: September 23, 2011

    15.3K
    Chromosome Preparation From Cultured Cells
    07:42

    Chromosome Preparation From Cultured Cells

    Published on: January 28, 2014

    84.4K

    Related Experiment Videos

    Last Updated: Mar 26, 2026

    Rapid Analysis of Chromosome Aberrations in Mouse B Lymphocytes by PNA-FISH
    07:54

    Rapid Analysis of Chromosome Aberrations in Mouse B Lymphocytes by PNA-FISH

    Published on: August 19, 2014

    17.6K
    Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae
    09:40

    Quantitation and Analysis of the Formation of HO-Endonuclease Stimulated Chromosomal Translocations by Single-Strand Annealing in Saccharomyces cerevisiae

    Published on: September 23, 2011

    15.3K
    Chromosome Preparation From Cultured Cells
    07:42

    Chromosome Preparation From Cultured Cells

    Published on: January 28, 2014

    84.4K

    Area of Science:

    • Human cytogenetics
    • Cancer research
    • Cell biology

    Background:

    • Cytogenetic studies in human populations identify specific cellular markers.
    • Certain individuals prone to malignancy exhibit unique chromatin structures.

    Purpose of the Study:

    • To investigate the nature and origin of marker dots (MDs) in individuals predisposed to cancer.
    • To determine if MDs can serve as early indicators of neoplastic transformation.

    Main Methods:

    • Analysis of human population cytogenetic data.
    • Microscopic examination of chromatin bodies (marker dots).
    • Identification of chromosomal origins of MDs.

    Main Results:

    • A majority of individuals prone to malignant features possess marker dots (MDs).
    • MDs measure approximately 2 to 3 microns in size.
    • MDs are observed emanating from specific chromosomes.

    Conclusions:

    • Marker dots (MDs) are associated with a predisposition to developing malignant features.
    • The chromosomal origin of MDs suggests their potential role as early indicators of neoplastic transformation.