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

Altered angiogenesis underlying age-dependent changes in tumor growth

R Pili1, Y Guo, J Chang

  • 1Cell Biology Unit, National Institute of Aging, National Institutes of Health, Baltimore, Md 21224.

Journal of the National Cancer Institute
|September 7, 1994
PubMed
Summary

Tumor growth and vascularization are impaired in older mice due to reduced angiogenic factors and increased extracellular matrix. Targeting tumor vascularization may offer a strategy to reduce tumor growth and progression in elderly patients.

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

An in vivo angiogenesis assay to study positive and negative regulators of neovascularization.

Methods in molecular medicine·2011
Same author

Beta-platelet-derived growth factor receptor mediates motility and growth of Ewing's sarcoma cells.

Oncogene·2003
Same author

Extracellular matrix-derived angiogenic factor(s) inhibit endothelial cell proliferation, enhance differentiation, and stimulate angiogenesis in vivo.

Endothelium : journal of endothelial cell research·2002
Same author

Bcl-2 overexpression attenuates resveratrol-induced apoptosis in U937 cells by inhibition of caspase-3 activity.

Carcinogenesis·2001
Same author

Runt-related gene 2 in endothelial cells: inducible expression and specific regulation of cell migration and invasion.

Cancer research·2001
Same author

Telomerized human microvasculature is functional in vivo.

Nature biotechnology·2001

Area of Science:

  • Oncology
  • Aging Research
  • Vascular Biology

Background:

  • Tumor growth and spread slow in the elderly, with murine models showing reduced tumor growth and spread in older animals.
  • Neovascularization is critical for tumor growth, and age-related alterations in vascular response may impact tumor progression.

Purpose of the Study:

  • To investigate age-related differences in tumor growth and vascularization using transplantable tumor cells, tumors, and extracts.
  • To understand how host age influences tumor biology and angiogenesis.

Main Methods:

  • Englebreth-Holm-Swarm (EHS) carcinoma and B16-F10 melanoma cells were implanted in C57BL mice of varying ages.
  • Tumor growth, histology, DNA synthesis, and vascularization (using basic fibroblast growth factor and in vivo angiogenesis assay) were assessed.

Related Experiment Videos

  • Tumor extracts were tested for their effects on endothelial cell differentiation in vitro and tumor growth in vivo.
  • Main Results:

    • EHS tumors grew larger in young mice than in old mice, with rapid growth resuming upon transfer to young hosts.
    • Tumors from old mice showed a higher extracellular matrix to tumor cell ratio and fewer, larger blood vessels compared to tumors from young mice.
    • Young mice exhibited a stronger angiogenic response; tumor extracts from old mice impaired endothelial cell differentiation and reduced tumor growth in vivo.

    Conclusions:

    • Tumor growth and morphology are age-dependent, influenced by reduced vascularization capacity due to diminished angiogenic factors or presence of host inhibitors.
    • Age-related changes in host factors may affect tumor growth and tissue repair, suggesting that reducing tumor vascularization is a potential therapeutic target.