IRGD

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IRGD


IRGD (iRGD) is a tumor-homing peptide that has been extensively studied for its potential in cancer therapy. It was first identified in 2009 by a team of researchers led by Erkki Ruoslahti, a distinguished professor at the Sanford Burnham Prebys Medical Discovery Institute. The peptide is known for its ability to penetrate tumor tissues and deliver drugs or other therapeutic agents directly to the cancer cells.

Structure and Function[edit | edit source]

IRGD is a 9-amino acid peptide with the sequence CRGDKGPDC. The peptide has a unique Retro-Inverso configuration, which means that the sequence of amino acids is reversed and each amino acid is replaced by its mirror image. This configuration enhances the stability of the peptide and its ability to bind to specific receptors on the surface of tumor cells.

The function of IRGD is to bind to neuropilin-1 (NRP-1), a receptor that is overexpressed on the surface of many types of cancer cells. Upon binding to NRP-1, IRGD is cleaved to produce a smaller peptide, RGD, which can then bind to integrins on the surface of the cancer cells. This binding triggers a process called endocytosis, in which the cancer cell engulfs the peptide and any attached therapeutic agents.

Therapeutic Applications[edit | edit source]

The ability of IRGD to penetrate tumor tissues and deliver drugs directly to the cancer cells has led to its exploration as a potential tool in cancer therapy. In preclinical studies, IRGD has been shown to enhance the delivery and efficacy of a variety of anticancer drugs, including doxorubicin, paclitaxel, and cisplatin. It has also been used to deliver nanoparticles and gene therapy vectors to tumor tissues.

In addition to its potential in drug delivery, IRGD has also been studied for its ability to enhance the delivery of radiation therapy and immunotherapy to tumor tissues. These studies suggest that IRGD could be used to improve the efficacy of these treatments and reduce their side effects.

Future Directions[edit | edit source]

While the results of preclinical studies are promising, further research is needed to determine the safety and efficacy of IRGD in humans. Clinical trials are currently underway to evaluate the use of IRGD in combination with various anticancer drugs. If these trials are successful, IRGD could become a valuable tool in the fight against cancer.


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