Tumor angiogenesis and bone metastasis - Correlation in invasive breast carcinoma

Chong Sun, Jianmin Li*, Bin Wang, Junjie Shangguan, Matteo Figini, Na Shang, Liang Pan, Zhuoli Zhang

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Purpose To test the hypotheses that pathological biomarkers including CD34 positive endothelial cell and microvessel density (MVD) of the primary breast tumor can be used to predict the probability of occurrence for bone metastases and provide information for appropriate therapeutic strategies at an early stage. Methods Three groups of CD34 immunohistochemical stained slices (n = 60) were acquired from surgical specimens of sixty patients including non-metastasis (group 1), only lymph node metastasis (group 2), and bone metastasis (group 3). MVD was measured by TissueGnostics system. Results The MVD measurement results were 57.14 ± 23.00 in group 1, 86.44 ± 21.13 in group 2, and 126.85 ± 47.89 in group 3. There were statistical differences between group 1 and group 2 (P = 0.0002), between group 2 and group 3 (P = 0.0014) and between group 1 and group 3 (P < 0.0001). The strong correlations were found between CD34 positive cell measurement and its percentage (group 1, r = 0.74, P = 0.0002; group 2, r = 0.62, P = 0.0034; group 3, r = 0.84, P < 0.0001), and between CD34 positive endothelial cell measurement and MVD (r = 0.61, P < 0.0001). Conclusions Quantitative CD34 positive endothelial cell and MVD measurements of the primary breast tumor have a strong correlation with the occurrence rate of bone metastases, which predicts the probability of occurrence for bone metastases at an early stage.

Original languageEnglish (US)
Pages (from-to)46-52
Number of pages7
JournalJournal of Immunological Methods
Volume452
DOIs
StatePublished - Jan 2018

Keywords

  • Bone metastasis
  • Breast carcinoma
  • Pathological biomarkers
  • Tumor angiogenesis

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

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