Folate receptor 1: Difference between revisions

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File:Brainsci-10-00762-g004-550.png|Folate receptor 1
File:Identification_of_ovarian_cancer_metastases_using_fluorescence_imaging_of_folate_receptor_alpha.jpg|Identification of ovarian cancer metastases using fluorescence imaging of folate receptor alpha
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Latest revision as of 04:18, 18 February 2025

Folate Receptor 1 (FOLR1) is a protein that in humans is encoded by the FOLR1 gene. It is a member of the folate receptor (FR) family, which also includes Folate Receptor 2 (FOLR2) and Folate Receptor 3 (FOLR3). Folate receptors are involved in the cellular uptake of folate, a vitamin essential for numerous bodily functions, including DNA synthesis and repair, cell division, and amino acid synthesis. Folate Receptor 1 is particularly important in mediating the uptake of folate in tissues with high metabolic demand such as in the placenta and in various cancer cells.

Function[edit]

Folate Receptor 1 binds to folate and reduced folic acid derivatives, facilitating their transport across the cell membrane through a process known as receptor-mediated endocytosis. This receptor is attached to the cell membrane by a glycosylphosphatidylinositol (GPI) anchor, which allows it to capture folate from the extracellular environment and deliver it into the cell. The high affinity of Folate Receptor 1 for folate makes it a critical component in maintaining folate homeostasis, especially in situations where folate demand is increased or in tissues with limited access to folate.

Clinical Significance[edit]

The expression of Folate Receptor 1 is elevated in several types of cancers, including ovarian cancer, breast cancer, and lung cancer, making it a potential target for cancer therapy. Drugs and immunotherapeutic agents targeting Folate Receptor 1 are being developed to deliver toxic agents specifically to cancer cells, minimizing damage to normal tissues. Additionally, alterations in the expression or function of Folate Receptor 1 have been implicated in various diseases and conditions, including neural tube defects and autoimmune diseases, highlighting its importance in human health and disease.

Genetics[edit]

The FOLR1 gene is located on chromosome 11 in humans. Variants and mutations in this gene can affect the expression and function of Folate Receptor 1, potentially leading to altered folate uptake and associated health issues. Genetic studies are ongoing to better understand the role of FOLR1 gene variants in disease and to develop personalized medical approaches based on an individual's genetic makeup.

Research Directions[edit]

Research on Folate Receptor 1 continues to explore its role in health and disease, with a particular focus on its potential as a therapeutic target in cancer. Studies are also investigating the impact of genetic variations in the FOLR1 gene on the risk of developing certain diseases and on the efficacy of folate-based therapies. Understanding the molecular mechanisms regulating the expression and function of Folate Receptor 1 is crucial for developing new and more effective treatments for diseases associated with folate metabolism.

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