Abstract

Many human tumors show significant changes in their signal transduction pathways and, thus, the way the cells interact with their environment. Often caused by chromosomal rearrangements, including gene amplifications, translocations or deletions, the altered levels of gene expression may provide a tumor-specific signature that can be exploited for diagnostic or therapeutic purposes. We investigated the utility of multiplexed fluorescence in situ hybridization (FISH) using non-isotopically labeled cDNA probes detected by Spectral Imaging as a sensitive and rapid procedure to measure tumor-specific gene expression signatures. We used a commercially available system to acquire and analyze multicolor FISH images. Initial investigations used panels of fluorescent calibration standards to evaluate the system. These experiments were followed by hybridization of five-to-six differently labeled cDNA probes, which target the transcripts of tyrosine kinase genes known to be differently expressed in normal cells and tumors of the breast or thyroid gland. The relatively simple, yet efficient, molecular cytogenetic method presented here may find many applications in characterization of solid tumors or disseminated tumor cells. Addressing tumor heterogeneity by means of multi-parameter single cell analyses is expected to enable a wide range of investigations in the areas of tumor stem cells, tumor clonality and disease progression.

Highlights

  • The field of molecular cytogenetic technology is comprised of various approaches to determine the chromosomal make-up of diploid cells, spermatocytes or polar bodies in research and clinical practice.While the chromosomal analysis using fluorescence in situ hybridization (FISH) has dominated the field for many years, DNA microarray-based assays have gained popularity in recent years due to the fact that they are relatively easy to automate and offer superb resolution

  • Results indicated that the spectral imaging software delivers virtually identical results when repeatedly analyzing the same image

  • Analyzing beads located in the center of the images, we found relative standard deviations ranging from 2%–5%

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Summary

Introduction

The field of molecular cytogenetic technology is comprised of various approaches to determine the chromosomal make-up of diploid cells, spermatocytes or polar bodies in research and clinical practice. Chromosome-specific DNA repeat probes and single copy DNA probes labeled with combinations of six reporter molecules allowed the routine enumeration of 10 different chromosome types in single blastomere cells from human preimplantation embryos [28]. The analysis using such ‘combinatorial labeled probes’ [35], becomes much more difficult when hybridization domains overlap spatially [32]. With the measurement of intratumoral heterogeneity in mind, we decided to develop a SIm-based analytical technology platform for single cell gene expression profiling that uses gene-specific cDNA probes labeled with individual, distinguishable reporter molecules. We describe the principle components of our SPECTRA system and demonstrate its application for the semi-quantitative analysis of five-to-six tyrosine kinase (tk) RNA species in breast or thyroid epithelial cells

System Evaluation Using Fluorescent Beads
Gene Expression Analysis of Cancer Cell Lines
Fluorescent Beads
Tissue Specimens
Fluorescence in situ Hybridization
Image Acquisition
Digital Image Analysis
Conclusions
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