MED12
MDA-7 | |||||||
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Identifiers | |||||||
Symbol | ? | ||||||
NCBI gene | 11009 | ||||||
HGNC | 5983 | ||||||
OMIM | 605401 | ||||||
RefSeq | NM_006850 | ||||||
UniProt | Q13007 | ||||||
|
MDA-7, also known as IL-24 (Interleukin-24), is a member of the IL-10 family of cytokines. It was originally identified as a gene induced during terminal differentiation in human melanoma cells, hence the name Melanoma Differentiation Associated gene-7 (MDA-7). MDA-7/IL-24 has been studied extensively for its role in cancer biology, particularly its ability to induce apoptosis selectively in cancer cells while sparing normal cells.
Structure[edit | edit source]
MDA-7/IL-24 is a secreted protein that is encoded by the IL24 gene located on chromosome 1q32. The protein consists of 206 amino acids and contains several glycosylation sites that are important for its stability and function. The structure of MDA-7/IL-24 is characterized by a typical cytokine fold, which is crucial for its interaction with specific receptors on target cells.
Function[edit | edit source]
MDA-7/IL-24 functions primarily as a cytokine with multiple biological activities. It is known for its ability to:
- Induce apoptosis in a wide range of cancer cell types, including melanoma, breast cancer, lung cancer, and prostate cancer.
- Inhibit angiogenesis, the process of new blood vessel formation, which is essential for tumor growth and metastasis.
- Modulate immune responses by affecting the activity of various immune cells, including macrophages, T cells, and natural killer cells.
Mechanism of Action[edit | edit source]
The pro-apoptotic effects of MDA-7/IL-24 are mediated through multiple pathways. It binds to specific receptors, such as IL-20R1/IL-20R2 and IL-22R1/IL-20R2 heterodimers, on the surface of target cells. This binding activates the JAK/STAT signaling pathway, leading to the transcription of genes involved in apoptosis and cell cycle arrest. Additionally, MDA-7/IL-24 can induce endoplasmic reticulum stress and reactive oxygen species (ROS) production, further promoting cancer cell death.
Therapeutic Potential[edit | edit source]
Due to its selective cytotoxicity towards cancer cells, MDA-7/IL-24 has been explored as a potential therapeutic agent in cancer treatment. Gene therapy approaches using adenoviral vectors to deliver the IL-24 gene directly into tumors have shown promising results in preclinical and early clinical trials. These studies have demonstrated significant tumor regression and minimal side effects, highlighting the potential of MDA-7/IL-24 as a novel anticancer therapy.
Research and Development[edit | edit source]
Ongoing research is focused on understanding the detailed molecular mechanisms of MDA-7/IL-24 action, optimizing delivery methods, and evaluating its efficacy in combination with other cancer therapies. Researchers are also investigating its role in other diseases, such as autoimmune disorders and inflammatory diseases, given its immunomodulatory properties.
Also see[edit | edit source]
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Contributors: Prab R. Tumpati, MD