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PMID: 9722729 Published · ppublish English Comparative Study Journal Article

Tumor vascularity, proliferation, and apoptosis in human melanoma micrometastases and macrometastases.

Archives of dermatology ·Vol. 134 ·No. 8 ·1998-08-00 ·Pages 991-4

Barnhill RL, Piepkorn MW, Cochran AJ, Flynn E, Karaoli T, Folkman J

Abstract

Clinically undetectable or dormant metastases (micrometastases) probably account for disease recurrence, ie, clinically evident metastases, in patients after disease-free intervals of variable length. Recently developed animal models have shown that dormancy may potentially be explained by the fact that these micrometastases are not vascularized and have comparable rates of cellular proliferation and programmed cell death (apoptosis), enabling them to remain viable indefinitely but not to show progressive growth. We report for the first time that melanoma micrometastases from humans are similarly not vascularized (mean number of microvessels, 10.2), have significantly lower rates of tumor cell proliferation (mean, 2.4%), comparable rates of proliferation and apoptosis (means, 2.4.% and 0.2%, respectively), compared with melanoma macrometastases, which have significantly greater tumor vascularity (mean number of microvessels, 18.7), higher rates of proliferation (mean, 18%), and higher rates of proliferation relative to apoptosis (means, 18% vs 1.6%). Tumor vascularity was quantified using the lectin Ulex europaeus agglutinin I to identify the number of microvessels per unit area (microscope ocular grid with an area of 7.84 x 10(-2) mm2 at x400 magnification). Melanoma cell proliferation rate was assessed with the MIB-1 antibody (Ki-67) as the number of positive nuclei per total number of tumor nuclei counted at x400 magnification. Apoptosis was quantified using the method of terminal deoxynucleotidyl transferase-medicated deoxyuridine triphosphate-biotin nick end labeling. The number of positive nuclei were quantified per total number of tumor nuclei; usually 200 tumor nuclei were counted at x400 magnification. We report, for the first time, that human micrometastases demonstrate attributes, ie, the lack of significant tumor vascularity and low but comparable rates of proliferation and apoptosis, that may explain the dormant state.

MeSH Terms
Apoptosis/genetics Cell Division Cell Nucleus/ultrastructure Cell Survival Coloring Agents DNA Nucleotidylexotransferase Deoxyuracil Nucleotides Disease-Free Survival Humans Ki-67 Antigen/analysis Lectins Melanoma/blood supply,pathology,secondary Microcirculation/pathology Neoplasm Recurrence, Local/pathology Plant Lectins Skin Neoplasms/blood supply,pathology
Chemicals
Coloring Agents Deoxyuracil Nucleotides Ki-67 Antigen Lectins Plant Lectins Ulex europaeus lectins deoxyuridine triphosphate DNA Nucleotidylexotransferase
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Barnhill R L
Department of Pathology, Brigham and Women's Hospital, Boston, Mass, USA.
Piepkorn M W
Cochran A J
Flynn E
Karaoli T
Folkman J
Article Info
Journal
Archives of dermatology
Abbr.
Arch Dermatol
ISSN
0003-987X
Published
1998-08-00
Pages
991-4
Language
English
Region
United States
NLM ID
0372433
Subset
IM
Corrections
CommentIn
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