Medical Journals

Dormancy of Solitary Metastatic Cells.

Authors:
  • Townson Jason L
  • Chambers Ann F

From: Department of Medical Biophysics, University of Western Ontario and the London Regional Cancer Program, London, Ontario, Canada.

Cell cycle (Georgetown, Tex.)

  • Publish Date: Aug 2006
  • ISSN: 1551-4005
  • Volume: 5
  • Issue: 16
  • Pages: 1744-50
  • Medium: Internet
  • Language: English
  • Citation (JAMA): Townson Jason L, Chambers Ann F, et al. Dormancy of Solitary Metastatic Cells.. Cell Cycle Aug 2006;5:1744-50

Abstract

After arriving in a secondary site metastatic cells may begin proliferating, undergo apoptosis or remain as solitary dormant cells. The process of metastasis, although dangerous, is extremely inefficient with the majority of the cells undergoing apoptosis and thus becoming clinically irrelevant. Of the cells that begin proliferating, the few that make it past the micrometastasis stage may be of immediate clinical relevance. Dormant cells, while not of immediate clinical concern, are believed to be at least in part responsible for cancer recurrence that can occur decades after apparently successful initial treatment. Dormant solitary cells are different from “dormant” micrometastases, in which active proliferation is balanced by apoptosis. The mechanisms of cell cycle regulation and the function of the molecules regulating this process are well understood. However, there is relatively little known about the mechanisms controlling cell cycle regulation and dormancy of solitary metastatic cells. There are several inherent difficulties impeding the study of solitary cells. This review paper will examine the models used in the study of dormant solitary metastatic cells, methods of imaging and studying these cells, the molecular mechanisms believed to be responsible for solitary cell dormancy, and finally the unique treatment challenges posed by these cells.

Mesh Headings (Keywords): Animals, Antineoplastic Agents, Apoptosis, Cell Cycle Proteins, Cell Line, Tumor, Cell Proliferation, Cell Survival, Humans, Mice, Microscopy, Mitogen-Activated Protein Kinases, Neoplasm Metastasis, Neoplasms, Experimental, Neoplastic Stem Cells, Staining and Labeling


Check for Full Text / PubMed Unique Identifier (PMID): 16861927


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

Linked medical terms appearing on this page are added by Healia to help readers find more information and are not part of the original PubMed document.

The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


Advertisements

About | Privacy Policy | Business Solutions | Advertise | Contact | Add Healia to your site

©2012. Healia / Meredith Corporation  

Use of this site constitutes acceptance of our Terms of Service and Privacy Policy. All content on this Web site, including medical opinion and any other health-related information, is for informational purposes only and should not be used for a specific diagnosis or individual treatment plan for any situation. Use of this site and the information contained herein does not create a doctor-patient relationship. Always seek the direct advice of your doctor in connection with any questions or issues you may have regarding your own health or the health of others.