Fluorescence in Situ Hybridization (FISH)

 

Fluorescence in SituFrom the Latin, Hybridization

FISH is a technique that measures geneA stretch of DNA that leads to the production of an RNA. The RNA is produced during the process of transcription. This RNA can be used to guide the formation of a protein via translation or can be used directly in the cell. amplificationAlso: gene amplification. An abnormal process in which many copies of the same chromosome region are produced via DNA replication. The result can be a small 'microsatellite' chromosome or a region of DNA within a chromosome with many contiguous copies of a small set of genes. using fluorescently labeled DNAAbbreviation for deoxyribonucleic acid. Composed of very long strings of nucleotides, which are abbreviated as A, C, G and T. DNA is the storage form of our genetic material. All of the instructions for the production of proteins are encoded in our DNA. (probe). The sample of breast tumor tissue is prepared for FISH by heating it. This heating process breaks the DNA into two strands; this produces two single strands of DNA and is called denaturing. The labeled probe is added to the denatured DNA mixture. The fluorescently labeled DNA matches certain regions of the denatured DNA and when the matching regions come in contact with each other they stick together. The mixture is washed so any unbound labeled DNA is removed. The washed mixture is viewed using a special microscope that can detect the color emitted by the probe. The probe marks the areas of DNA (genes) that code for the proteinOne of the four basic types of biomolecule. Proteins are polymers made up of strings of amino acids. Proteins serve many functions in organisms including transport of molecules, structure, cell adhesion and as signaling molecules such as hormones. Many transcription factors, including p53 and Rb are proteins. of interest, thus the amount of probe bound to the DNA is an indirect indicator of the number of genes present coding for the protein.1, 2, 3

In the video above, chromosomes from the cells of a patient are mixed with test DNA. The test DNA is linked to a protein that binds to a colored dye. If the test DNA finds and binds similar sequences in the patient's DNA, it can be identified by adding the dye to the chromosomes.

FISH is a fast and highly sensitive technique that provides an objective scoring system. It is more expensive than IHC and requires a fluorescence microscope for interpretation, so it is not available in all areas.1, 2, 3

FISH for determination of HER2 status in breast cancer

In the case of HER2 status of breast cancer, the labeled DNA probe is  binds to the DNA region coding for the HER2 protein. Pathologists can determine the number of HER2 genes present by measuring the amount of probe in the sample. A tumor is considered HER2 positive if a sample has over 2 copies of the HER2 gene per chromosomeA long DNA molecule containing genetic information (genes). Humans have 46 chromosomes. One set of 23 is inherited from each parent. A full set of chromosomes is present in the nucleus of each human cell. 17.1

A sample of an entire set of chromosomes that has been labeled with different colored dyes using a variation of the FISH technique is shown below:

 

  • 1.a. b. c. DG Hicks, RR Tubbs. Assessment of the HER2 status in breast cancer by fluorescence in situ hybridization: a technical review with interpretive guidelines. Human Pathology. 2005 Mar;36(3):250-61. [PUBMED]
  • 2.a. b. DG Hicks, RR Tubbs. Assessment of the HER2 status in breast cancer by fluorescence in situ hybridization: a technical review with interpretive guidelines. Human Pathology. 2005; 36:250-261. [PUBMED]
  • 3.a. b. M Bilous, M Dowsett, et al. Current Perspectives on HER2 Testing: A Review of National Testing Guidelines. Modern Pathology. 2003; 16(2):173-182. [PUBMED]