Glypican 1

From WikiMD's Food, Medicine & Wellness Encyclopedia

Glypican 1 (GPC1) is a protein that in humans is encoded by the GPC1 gene. It is a member of the glypican family, a group of heparan sulfate proteoglycans that are attached to the membrane by a glycosylphosphatidylinositol (GPI) anchor. Glypicans are involved in the regulation of cell growth, cell division, and cell differentiation. GPC1 plays a significant role in cell signaling pathways, particularly those involving growth factors and their receptors.

Function[edit | edit source]

GPC1 is integral to the modulation of Wnt, Hedgehog, and fibroblast growth factor (FGF) signaling pathways, which are critical for embryonic development and in various processes in adults. By interacting with these pathways, GPC1 influences cell proliferation, apoptosis (programmed cell death), and angiogenesis (formation of new blood vessels). This makes it a key player in tissue regeneration and repair, as well as in the development of certain diseases, including cancer.

Clinical Significance[edit | edit source]

The expression of GPC1 has been found to be upregulated in several types of cancers, including pancreatic cancer, breast cancer, and glioma. Its presence in exosomes—small vesicles released by cells—has been studied as a potential biomarker for the early detection of cancer, particularly pancreatic cancer. Elevated levels of GPC1-positive exosomes in the bloodstream have been associated with the presence of tumor, offering a non-invasive diagnostic tool.

Moreover, due to its role in cell signaling pathways that are often dysregulated in cancer, GPC1 is being explored as a target for cancer therapy. Inhibiting GPC1 function has shown promise in reducing tumor growth and metastasis in preclinical models.

Genetics[edit | edit source]

The GPC1 gene is located on the long (q) arm of chromosome 7 at position 21.1, specifically from base pair 76,117,763 to 76,144,976. The gene consists of multiple exons that encode the GPC1 protein. Mutations in this gene, although rare, have been associated with certain developmental disorders and diseases.

See Also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD