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

Centrosome function in normal and tumor cells.

Satish Sankaran1, Jeffrey D Parvin

  • 1Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.

Journal of Cellular Biochemistry
|July 4, 2006
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

Identification of TAP2 protein variants resistant to inhibition by the HSV1 ICP47 protein.

bioRxiv : the preprint server for biology·2024
Same author

ILT2 and ILT4 Drive Myeloid Suppression via Both Overlapping and Distinct Mechanisms.

Cancer immunology research·2024
Same author

Tumor histoculture captures the dynamic interactions between tumor and immune components in response to anti-PD1 in head and neck cancer.

Nature communications·2024
Same author

Multiplexed assay of variant effect reveals residues of functional importance in the BRCA1 coiled-coil and serine cluster domains.

PloS one·2023
Same author

DNA repair function scores for 2172 variants in the BRCA1 amino-terminus.

PLoS genetics·2023
Same author

DNA Repair Function Scores for 2172 Variants in the BRCA1 Amino-Terminus.

bioRxiv : the preprint server for biology·2023

Centrosome amplification, common in cancer, leads to abnormal cell division. This review explores regulatory factors, including the Breast Cancer 1 (BRCA1) ubiquitin ligase, that cause errors in centrosome duplication and mitosis.

Area of Science:

  • Cell Biology
  • Cancer Biology
  • Genetics

Background:

  • Centrosomes are critical for organizing microtubules and ensuring accurate chromosome segregation during cell division.
  • Aberrant centrosome numbers, particularly amplification (more than two per cell), are a hallmark of many cancers.
  • Cancer cells with amplified centrosomes often exhibit aneuploidy, a condition of abnormal chromosome numbers.

Purpose of the Study:

  • To review the cellular mechanisms governing centrosome duplication.
  • To elucidate how disruptions in these regulatory pathways contribute to abnormal centrosome numbers.
  • To highlight the emerging role of the Breast Cancer 1 (BRCA1) ubiquitin ligase in centrosome regulation.

Main Methods:

  • This review synthesizes existing research on centrosome duplication and cell cycle regulation.

Related Experiment Videos

  • It integrates findings from molecular biology, cell biology, and cancer research.
  • Focus is placed on genetic and biochemical studies investigating centrosome components and their regulators.
  • Main Results:

    • Proper centrosome duplication is tightly controlled by cell cycle machinery.
    • Dysregulation of key factors, such as the BRCA1 ubiquitin ligase, can lead to centrosome amplification.
    • Abnormal centrosome numbers correlate with mitotic errors and genomic instability in cancer cells.

    Conclusions:

    • Understanding centrosome duplication regulation is crucial for comprehending cancer development.
    • The BRCA1 ubiquitin ligase represents a significant factor in maintaining centrosome homeostasis.
    • Targeting pathways that control centrosome number may offer novel therapeutic strategies for cancer.