Proliferation marker

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Proliferation Marker

A proliferation marker is a type of biomarker used in the field of cell biology and oncology to identify and measure the degree of cell proliferation. Cell proliferation is a fundamental process in which cells grow and divide to create new cells. This process is crucial for the growth and development of organisms, tissue repair, and immune response. However, uncontrolled cell proliferation can lead to diseases such as cancer.

Types of Proliferation Markers[edit | edit source]

There are several types of proliferation markers, each with its unique characteristics and applications. Some of the most commonly used proliferation markers include:

  • Ki-67: Ki-67 is a nuclear protein that is associated with cellular proliferation. It is present during all active phases of the cell cycle (G1, S, G2, and mitosis), but is absent in resting cells (G0). Therefore, Ki-67 is a reliable marker for determining the growth fraction of a given cell population.
  • PCNA (Proliferating Cell Nuclear Antigen): PCNA is a protein that acts as a processivity factor for DNA polymerase δ in eukaryotic cells and is essential for replication. PCNA is often used as a marker of proliferation due to its role in DNA synthesis.
  • Cyclins: Cyclins are a family of proteins that control the progression of cells through the cell cycle by activating cyclin-dependent kinase (CDK) enzymes.

Applications[edit | edit source]

Proliferation markers are widely used in both research and clinical settings. In research, they are used to study the effects of various factors on cell proliferation, such as drugs, radiation, and environmental conditions. In clinical settings, proliferation markers are used to diagnose and prognose various diseases, particularly cancer. For example, a high proliferation index, as indicated by a high percentage of Ki-67-positive cells, often correlates with a more aggressive tumor and a poorer prognosis.

Limitations[edit | edit source]

While proliferation markers are valuable tools in cell biology and oncology, they also have limitations. For instance, they cannot distinguish between cell proliferation and cell cycle arrest, as both processes can result in an increase in marker expression. Furthermore, the expression of proliferation markers can vary between different cell types and under different conditions, which can complicate their interpretation.

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Contributors: Prab R. Tumpati, MD