BRAF

From WikiMD's Wellness Encyclopedia

BRAF[edit | edit source]

BRAF is a gene that encodes a protein known as B-Raf, which is involved in sending signals inside cells and directing cell growth. The B-Raf protein is a part of the MAPK/ERK signaling pathway, which helps regulate cell division, differentiation, and secretion. Mutations in the BRAF gene can lead to uncontrolled cell growth and are implicated in various cancers.

Structure and Function[edit | edit source]

The BRAF gene is located on chromosome 7q34 and encodes a protein that is part of the serine/threonine protein kinase family. The B-Raf protein is composed of three conserved domains:

  • The N-terminal regulatory domain
  • The kinase domain
  • The C-terminal domain

The kinase domain is responsible for the protein's enzymatic activity, which involves the phosphorylation of target proteins on serine and threonine residues. This activity is crucial for the transmission of signals from the cell surface to the nucleus, influencing gene expression and cell behavior.

Role in Cancer[edit | edit source]

Mutations in the BRAF gene are found in a variety of cancers, including:

The most common mutation is the V600E mutation, which results in a substitution of valine (V) with glutamic acid (E) at position 600. This mutation leads to constitutive activation of the B-Raf protein, promoting continuous cell proliferation and survival.

Diagnostic and Therapeutic Implications[edit | edit source]

The presence of BRAF mutations, particularly V600E, has significant implications for diagnosis and treatment. Testing for BRAF mutations is a standard part of the diagnostic workup for certain cancers, such as melanoma.

Targeted Therapies[edit | edit source]

Targeted therapies have been developed to inhibit the activity of mutant B-Raf proteins. These include:

These drugs specifically target the B-Raf V600E mutation and have shown efficacy in treating patients with BRAF-mutant cancers. However, resistance to these therapies can develop, often due to additional mutations in the MAPK/ERK pathway.

Research and Future Directions[edit | edit source]

Ongoing research is focused on understanding the mechanisms of resistance to BRAF inhibitors and developing combination therapies to overcome this challenge. Additionally, the role of BRAF mutations in other diseases and their potential as therapeutic targets continues to be an area of active investigation.

See Also[edit | edit source]

References[edit | edit source]

External Links[edit | edit source]

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Contributors: Prab R. Tumpati, MD