Frozen tissue array

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Frozen tissue array is a laboratory technique used in the field of pathology and molecular biology to analyze multiple tissue samples simultaneously. This method involves embedding small cores of fresh-frozen tissue from various sources into a single array block. This technique allows for high-throughput analysis of gene expression, protein expression, and DNA alterations across multiple tissue specimens.

Overview[edit | edit source]

Frozen tissue arrays are created by extracting cylindrical cores from fresh-frozen tissues using a biopsy punch. These cores are then carefully arranged in a predefined pattern in a recipient paraffin block. Once assembled, the block can be sectioned using a microtome, producing thin slices that can be transferred to microscope slides for further analysis. This approach enables the simultaneous analysis of multiple samples under identical experimental conditions, significantly increasing the efficiency of immunohistochemistry (IHC), in situ hybridization (ISH), and other molecular assays.

Applications[edit | edit source]

Frozen tissue arrays are particularly useful in the fields of oncology and cancer research, where they are employed to study the expression of oncogenes, tumor suppressor genes, and other markers of tumor progression and response to therapy. They are also used in biomarker discovery and validation, allowing researchers to quickly assess the clinical relevance of potential diagnostic, prognostic, and therapeutic markers across a wide range of tissue types and disease states.

Advantages[edit | edit source]

The primary advantage of frozen tissue arrays over traditional single-tissue analysis is the ability to perform high-throughput comparative studies. This not only conserves valuable research resources but also ensures that experimental conditions are uniform across all samples, reducing variability and improving the reliability of the results. Additionally, because the tissues are frozen rather than fixed in formalin and embedded in paraffin, they better preserve the native proteins, RNA, and DNA, facilitating more accurate molecular analyses.

Limitations[edit | edit source]

Despite their advantages, frozen tissue arrays also have some limitations. The quality of the results can be affected by the heterogeneity of the tissue samples and the precision of the core extraction and placement process. Furthermore, the need for specialized equipment and expertise can limit their use to well-equipped laboratories. Finally, the preservation of tissue integrity and molecular fidelity requires stringent storage and handling protocols, which can be challenging to maintain.

Conclusion[edit | edit source]

Frozen tissue arrays represent a powerful tool for the simultaneous analysis of multiple tissue samples, offering significant advantages in terms of efficiency and reliability for molecular pathology and cancer research. Despite their limitations, the continued refinement of this technique and its applications holds great promise for advancing our understanding of disease mechanisms and improving the development of targeted therapies.


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Contributors: Prab R. Tumpati, MD