RUNX3

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RUNX3[edit | edit source]

RUNX3 is a transcription factor that plays a crucial role in the regulation of gene expression and cell differentiation. It belongs to the Runt-related transcription factor (RUNX) family, which also includes RUNX1 and RUNX2. RUNX3 is primarily expressed in epithelial tissues and has been found to be involved in various biological processes, including development, cell cycle control, and tumor suppression.

Structure and Function[edit | edit source]

The RUNX3 gene is located on chromosome 1p36 and consists of nine exons. The protein encoded by this gene contains several functional domains, including a Runt domain, a transactivation domain, and a C-terminal repression domain. The Runt domain is responsible for DNA binding and heterodimerization with other transcription factors, while the transactivation domain regulates the expression of target genes.

RUNX3 acts as a transcriptional regulator by binding to specific DNA sequences in the promoter regions of target genes. It can either activate or repress gene expression depending on the context and interacting partners. Through its interactions with co-regulatory proteins and other transcription factors, RUNX3 influences the expression of genes involved in cell fate determination, cell cycle progression, and immune response.

Role in Development[edit | edit source]

During embryonic development, RUNX3 is essential for the formation and differentiation of various tissues and organs. Studies in mice have shown that loss of RUNX3 function leads to defects in skeletal development, hematopoiesis, and neurogenesis. In particular, RUNX3 is crucial for the development of the gastrointestinal tract, where it regulates the differentiation of gastric epithelial cells and controls the balance between proliferation and differentiation.

Tumor Suppressor[edit | edit source]

RUNX3 has been identified as a tumor suppressor in various types of cancer, including gastric cancer, colorectal cancer, and lung cancer. Its tumor-suppressive function is mainly attributed to its ability to induce cell cycle arrest, promote apoptosis, and inhibit cell migration and invasion. Loss of RUNX3 expression or inactivation of its function is frequently observed in cancer cells, and this is often associated with poor prognosis and advanced disease stages.

Clinical Significance[edit | edit source]

The dysregulation of RUNX3 has been implicated in several human diseases. In addition to its role in cancer, altered expression of RUNX3 has been linked to autoimmune disorders, such as rheumatoid arthritis and systemic lupus erythematosus. Furthermore, RUNX3 has been identified as a potential therapeutic target for the treatment of certain diseases, including gastric cancer and osteoporosis.

See Also[edit | edit source]

References[edit | edit source]

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Contributors: Prab R. Tumpati, MD