A research team from the Technical University of Munich (TUM) has recently explained the molecular fundamentals of additional effects for Imiquimod drug which is been successfully used for the treatment of skin diseases.
The findings of the study indicate new approach for the treatment of inflammatory conditions.
‘Discovering novel mechanisms of action for Imiquimod (Skin cancer drug) might indicate new approaches to treat inflammatory illness.’
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PD Dr. Olaf Groß, group leader at the TUM Institute for Clinical Chemistry and Pathobiochemistry , has been working together with his team to investigate Imiquimod. This medication has been successfully used to treat viral skin infections and certain types of skin cancer since 1997. The scientists have now published their results in the journal Immunity.
Imiquimod is an immunomodulatory agent, which means it triggers an immune reaction which causes the body's immune system to attack modified cells. For several years, this process was the medication's only known mechanism of action. However, in the meantime it has been shown that imiquimod also triggers other processes in the body. On one hand, imiquimod directly impairs the growth of cancer cells. On the other hand, Imiquimod activates a complex within cells of the immune system termed the inflammasome. While the inflammasome is very important for our body's ability to defend against infection, uncontrolled activation of the inflammasome can lead to inflammatory diseases. "We think that these other mechanisms of action of Imiquimod might contribute to the efficacy or adverse side effects of the medication," says Olaf Groß.
Intervention in the mitochondria
Imiquimod specifically activates the NLRP3 inflammasome, which is a special type of inflammasome that responds to tissue stress and cellular damage. Olaf Groß and his team were able to show that NLRP3 is activated because Imiquimod impairs the respiratory chain in mitochondria. The respiratory chain is a series of mitochondrial protein complexes that generates the energy, in the form of a molecule called adenosine triphosphate, or ATP for short, that cells need to survive.
"Inhibition of the respiratory chain by imiquimod not only impairs ATP production, but also results in the production of toxic oxygen radicals," explains Dr. Ritu Mishra, one of the two primary authors of the study. "Imiquimod causes an especially large amount of radicals to be released. In contrast to other substances that intervene in the respiratory chain but generate a lower amount of radicals, here a threshold value is exceeded that results in the activation of NLRP3."
Implications for anti-inflammatory medications
"There is a lot of excitement about generating new anti-inflammatory medications by targeting the NLRP3 inflammasome," says Dr. Christina J. Groß, also one of the study's primary authors. "We hope that our research will lead to the design of medications that can prevent dangerous hyperactivation of the NLRP3 inflammasome that may occur in diseases like gout and multiple sclerosis." Olaf Groß and his team are following-up on this study by investigating whether the effect of imiquimod on the mitochondria is the mechanism behind the unexplained finding that imiquimod directly inhibits growth of cancer cells. After that, they plan to investigate new chemical substances related to Imiquimod in order to find out how the various effects of the medication can be uncoupled.
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