Sahmyook University Study Repurposes Meclofenamate to Treat Abnormal Respiratory Mucus
2023-07-17 2,305
Korean researchers have shown that meclofenamate is a promising drug for controlling mucin levels in the respiratory mucus
The inner lining of our respiratory system is coated with mucus, the gel-like nature of which is controlled by mucin proteins. Abnormal secretion of mucins can lead to various respiratory diseases. Since many of the available drugs used to treat this condition cause unnecessary side effects, a group of Korean researchers have successfully repurposed an existing anti-inflammatory drug called meclofenamate, thus providing new hope for patients with related respiratory diseases.
![](https://www.syu.ac.kr/eng/wp-content/uploads/sites/81/2023/07/SYOOK_3_3_Infographic_final.png)
Our respiratory system is lined with a thin fluid layer called mucus on the inside. The mucus protects us from inhaling harmful and unwanted airborne agents from germs to pollutants; it achieves this feat due to its unique gel-like texture imparted by proteins called mucins. By extension, over- or under-secretion of mucins can lead to abnormal respiratory mucus—a pathological manifestation in many respiratory diseases like chronic bronchitis, cystic fibrosis, and asthma, among others. Although multiple clinically approved drugs are available that can combat abnormal respiratory mucus, many of them cause unwanted and potentially serious side effects. This calls for an alternative solution to provide relief to patients having respiratory diseases.
In a recent study, a group of researchers from Korea repurposed an available drug called meclofenamate to understand its effects on the respiratory mucus. Meclofenamate had been traditionally used as a nonsteroidal anti-inflammatory drug for treating arthritis, parasitic infections, and prostate cancer, among other diseases. The researchers have now found that meclofenamate can also treat abnormal respiratory mucus by controlling mucin secretion. Their study was made available online on April 7, 2023, and was published in Volume 31 Issue 3 of the journal, Biomolecules & Therapeutics, in March 13, 2023.
Speaking about the clinical potential of the results of the study, Dr. Hyun-Jae Lee, who is an associate professor at Smith Liberal Arts College and Department of Addiction Science, Graduate School, Sahmyook University, and one of the lead researchers exclaims, “Compared to conventional drug development strategies, our strategy of discovering new therapeutic effects from existing drugs saves a lot of time and costs.” How indeed did Dr. Lee and his team go about this landmark study?
The researchers tested the meclofenamate in a cell line called NCI-H292 that mimicked the respiratory cells, replete with the secretion of mucus with mucins. Specifically, they checked for the expression of a gene responsible for secreting a key mucin, MUC5AC. Further, they explored the molecular pathways involved in the action of meclofenamate on the mucin. Their findings hit the bull’s eye, to say the least.
Their results suggested that meclofenamate markedly reduced the gene and, additionally, the protein expression of MUC5AC. The drug was found to achieve this by influencing a biomolecular pathway that is extensively involved in the immune response, namely the nuclear factor kappa light chain enhancer of activated B (or NF-kB) cell signaling pathway; it reduced the degradation of a biomolecular component called ‘inhibitory kappa Bα’ and the movement of another such component called ‘p65’ into the nucleus of the respiratory cells. The gist of these findings is clear—meclofenamate is capable of controlling mucin secretion, and in turn, the characteristics of respiratory mucus.
Without doubt, meclofenamate has emerged as a novel therapeutic agent for abnormal respiratory mucus, with this study. These findings not only succeed in repurposing a readily available and clinically approved drug for a new disease condition, but also sets an example for ongoing efforts related to drug development and research.
“Discovering the unknown therapeutic effects of existing drugs against different diseases and related symptoms is more promising than de novo drug discovery and development. While the former requires only 3 to 12 years of intense research and investment of resources, the latter requires at least 10 to 17 years.” concludes Dr. Lee. This study is indeed a valuable lesson in drug discovery research.
Reference
Title of original paper: Meclofenamate Suppresses MUC5AC Mucin Gene Expression by Regulating the NF-kB Signaling Pathway in Human Pulmonary Mucoepidermoid NCI-H292 Cells
Journal: Biomolecules & Therapeutics
DOI: 10.4062/biomolther.2023.035
About Sahmyook University
Sahmyook University is situated in metropolitan Seoul, South Korea. The university is renowned for its pristine campus, earning the title of "Korea's most beautiful university." Its commitment to environmental sustainability is reflected in its eco-friendly construction. The university prides itself on its unique holistic academic counselling system in which students and professors organically work together in receiving and giving guidance. Comprising six colleges, including the College of Theology, Humanities & Social Science, and Health Science & Social Welfare, as well as four graduate schools, Sahmyook University provides a comprehensive educational experience.
Website: https://www.syu.ac.kr/eng/
About Associate Professor Hyun-Jae Lee
Prof. Hyun-Jae Lee is an associate professor at Smith Liberal Arts College and the Department of Addiction Science, Graduate School, Sahmyook University. His research centers around the regulation of excessive airway mucus secretion and production, crucial for the management and prognosis of respiratory diseases. By exploring the mechanisms of action of natural products, he aims to develop effective treatments for conditions such as asthma, pneumonia, bronchitis, and pulmonary fibrosis, among others. Previously, he served as a postdoctoral research professor at Chungnam National University School of Medicine. He obtained his doctoral degree in natural products pharmacology from the Graduate School of Chungnam National University in 2011.
The inner lining of our respiratory system is coated with mucus, the gel-like nature of which is controlled by mucin proteins. Abnormal secretion of mucins can lead to various respiratory diseases. Since many of the available drugs used to treat this condition cause unnecessary side effects, a group of Korean researchers have successfully repurposed an existing anti-inflammatory drug called meclofenamate, thus providing new hope for patients with related respiratory diseases.
![](https://www.syu.ac.kr/eng/wp-content/uploads/sites/81/2023/07/SYOOK_3_3_Infographic_final.png)
Our respiratory system is lined with a thin fluid layer called mucus on the inside. The mucus protects us from inhaling harmful and unwanted airborne agents from germs to pollutants; it achieves this feat due to its unique gel-like texture imparted by proteins called mucins. By extension, over- or under-secretion of mucins can lead to abnormal respiratory mucus—a pathological manifestation in many respiratory diseases like chronic bronchitis, cystic fibrosis, and asthma, among others. Although multiple clinically approved drugs are available that can combat abnormal respiratory mucus, many of them cause unwanted and potentially serious side effects. This calls for an alternative solution to provide relief to patients having respiratory diseases.
In a recent study, a group of researchers from Korea repurposed an available drug called meclofenamate to understand its effects on the respiratory mucus. Meclofenamate had been traditionally used as a nonsteroidal anti-inflammatory drug for treating arthritis, parasitic infections, and prostate cancer, among other diseases. The researchers have now found that meclofenamate can also treat abnormal respiratory mucus by controlling mucin secretion. Their study was made available online on April 7, 2023, and was published in Volume 31 Issue 3 of the journal, Biomolecules & Therapeutics, in March 13, 2023.
Speaking about the clinical potential of the results of the study, Dr. Hyun-Jae Lee, who is an associate professor at Smith Liberal Arts College and Department of Addiction Science, Graduate School, Sahmyook University, and one of the lead researchers exclaims, “Compared to conventional drug development strategies, our strategy of discovering new therapeutic effects from existing drugs saves a lot of time and costs.” How indeed did Dr. Lee and his team go about this landmark study?
The researchers tested the meclofenamate in a cell line called NCI-H292 that mimicked the respiratory cells, replete with the secretion of mucus with mucins. Specifically, they checked for the expression of a gene responsible for secreting a key mucin, MUC5AC. Further, they explored the molecular pathways involved in the action of meclofenamate on the mucin. Their findings hit the bull’s eye, to say the least.
Their results suggested that meclofenamate markedly reduced the gene and, additionally, the protein expression of MUC5AC. The drug was found to achieve this by influencing a biomolecular pathway that is extensively involved in the immune response, namely the nuclear factor kappa light chain enhancer of activated B (or NF-kB) cell signaling pathway; it reduced the degradation of a biomolecular component called ‘inhibitory kappa Bα’ and the movement of another such component called ‘p65’ into the nucleus of the respiratory cells. The gist of these findings is clear—meclofenamate is capable of controlling mucin secretion, and in turn, the characteristics of respiratory mucus.
Without doubt, meclofenamate has emerged as a novel therapeutic agent for abnormal respiratory mucus, with this study. These findings not only succeed in repurposing a readily available and clinically approved drug for a new disease condition, but also sets an example for ongoing efforts related to drug development and research.
“Discovering the unknown therapeutic effects of existing drugs against different diseases and related symptoms is more promising than de novo drug discovery and development. While the former requires only 3 to 12 years of intense research and investment of resources, the latter requires at least 10 to 17 years.” concludes Dr. Lee. This study is indeed a valuable lesson in drug discovery research.
Reference
Title of original paper: Meclofenamate Suppresses MUC5AC Mucin Gene Expression by Regulating the NF-kB Signaling Pathway in Human Pulmonary Mucoepidermoid NCI-H292 Cells
Journal: Biomolecules & Therapeutics
DOI: 10.4062/biomolther.2023.035
About Sahmyook University
Sahmyook University is situated in metropolitan Seoul, South Korea. The university is renowned for its pristine campus, earning the title of "Korea's most beautiful university." Its commitment to environmental sustainability is reflected in its eco-friendly construction. The university prides itself on its unique holistic academic counselling system in which students and professors organically work together in receiving and giving guidance. Comprising six colleges, including the College of Theology, Humanities & Social Science, and Health Science & Social Welfare, as well as four graduate schools, Sahmyook University provides a comprehensive educational experience.
Website: https://www.syu.ac.kr/eng/
About Associate Professor Hyun-Jae Lee
Prof. Hyun-Jae Lee is an associate professor at Smith Liberal Arts College and the Department of Addiction Science, Graduate School, Sahmyook University. His research centers around the regulation of excessive airway mucus secretion and production, crucial for the management and prognosis of respiratory diseases. By exploring the mechanisms of action of natural products, he aims to develop effective treatments for conditions such as asthma, pneumonia, bronchitis, and pulmonary fibrosis, among others. Previously, he served as a postdoctoral research professor at Chungnam National University School of Medicine. He obtained his doctoral degree in natural products pharmacology from the Graduate School of Chungnam National University in 2011.