High matrix metalloproteinase-to-E-cadherin ratio measured by bicolor fluorescent in situ hybridization is associated with lymphangiogenesis and lymph node metastasis in prostate cancer

Urol Oncol. 2012 May-Jun;30(3):306-13. doi: 10.1016/j.urolonc.2010.05.001. Epub 2010 Sep 16.

Abstract

Objective: The colorimetric in situ hybridization (CISH)-based matrix metalloproteinase (MMP)-to-E-cadherin (ECD) ratio (MER) has been revealed as an excellent marker for the disease stage in prostate cancer. The one aim of this study was investigating a new method for estimation of MER by bicolor fluorescent ISH (bicolor FISH) with a computerized fluorescence detector-based system. Another aim was examination of relation of MER by bicolor FISH with expression of vascular endothelial growth factor-C (VEGF-C).

Methods: The bicolor FISH technique used cyanin 5 (cy5)-labeled MMP-2 and -9 probes, and a cyanin 3 (cy3)-labeled ECD probe on needle biopsy specimens from 67 prostate cancer cases. The ISH was followed by computerized detection of the signal intensities and cy5-to-cy3 ratios using a fluorescence detector. VEGF-C expression was examined using cy5-labeled VEGF-C by computerized detection.

Results: The bicolor FISH-based MER was well correlated with CISH-based MER (P < 0.0001). The bicolor FISH-based MER correlated with Gleason score and pathologic stage of the cases. VEGF-C mRNA expression was associated with the pathologic stage and maximum lymph vessel density (LVD). The LVD was associated with VEGF-C expression at the tumor area where the maximum MER was detected (P < 0.0001).

Conclusion: The MER was correlated with the VEGF-C expression and LVD, indicating lymph node metastasis of prostate cancer. Therefore, this computer-assisted MER is a useful marker for preoperative prediction of disease stage, especially lymph node metastasis, of prostate cancer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy / methods
  • Biopsy, Needle / methods
  • Cadherins / biosynthesis*
  • Carbocyanines / pharmacology
  • Disease Progression
  • Humans
  • In Situ Hybridization, Fluorescence
  • Lymphangiogenesis*
  • Lymphatic Metastasis
  • Male
  • Matrix Metalloproteinase 2 / biosynthesis*
  • Matrix Metalloproteinase 9 / biosynthesis*
  • Medical Oncology / methods
  • Neoplasm Metastasis
  • Oligonucleotide Probes / pharmacology
  • Prostatic Neoplasms / diagnosis*
  • Prostatic Neoplasms / pathology
  • Vascular Endothelial Growth Factor C / metabolism

Substances

  • Cadherins
  • Carbocyanines
  • Oligonucleotide Probes
  • Vascular Endothelial Growth Factor C
  • cyanine dye 3
  • Matrix Metalloproteinase 2
  • Matrix Metalloproteinase 9