A form of saccharin, an artificial sweetener, could lead to the development of drugs that battle aggressive cancers. Credit: Doug Dollemore, American Chemical Society
Saccharin, the artificial sweetener that is the main ingredient in Sweet 'N Low, Sweet Twin and Necta, could do far more than just keep our waistlines trim. According to new research, this popular sugar substitute could potentially lead to the development of drugs capable of combating aggressive, difficult-to-treat cancers with fewer side effects.
The finding will be presented today at the 249th National Meeting & Exposition of the American Chemical Society (ACS).
"It never ceases to amaze me how a simple molecule, such as saccharin—something many people put in their coffee everyday—may have untapped uses, including as a possible lead compound to target aggressive cancers," says Robert McKenna, Ph.D., who is at the University of Florida. "This result opens up the potential to develop a novel anti-cancer drug that is derived from a common condiment that could have a lasting impact on treating several cancers."
The new work examines how saccharin binds to and deactivates carbonic anhydrase IX, a protein found in some very aggressive cancers. It is one of many driving factors in the growth and spread of such cancers in the breast, lung, liver, kidney, pancreas and brain. Carbonic anhydrase IX helps regulate pH in and around cancer cells, allowing tumors to thrive and potentially metastasize to other parts of the body. Because of this finding, the researchers wanted to develop saccharin-based drug candidates that could slow the growth of these cancers and potentially make them less resistant to chemo or radiation therapies.
Except for in the gastrointestinal tract, carbonic anhydrase IX is normally not found in healthy human cells. According to McKenna, this makes it a prime target for anti-cancer drugs that would cause little or no side effects to healthy tissue surrounding the tumor.
Unfortunately, there's a catch.
Carbonic anhydrase IX is similar to other carbonic anhydrase proteins that our bodies need to work properly. So far, finding a substance that blocks carbonic anhydrase IX without affecting the other ones has been elusive. And that's where saccharin—ironically, once considered a possible carcinogen— comes in.
In earlier work, scientists from a group led by Claudiu T. Supuran, Ph.D., at the University of Florence, Italy, discovered that saccharin inhibits the actions of carbonic anhydrase IX, but not the 14 other carbonic anhydrase proteins that are vital to our survival. Building on this finding, a team led by Sally-Ann Poulsen, Ph.D., at Griffith University, Australia, created a compound in which a molecule of glucose was chemically linked to saccharin. This small change had big effects. Not only did it reduce the amount of saccharin needed to inhibit carbonic anhydrase IX, the compound was 1,000 times more likely to bind to the enzyme than saccharin.
Using X-ray crystallography, McKenna and his students Jenna Driscoll and Brian Mahon have taken this work a step further by determining how saccharin binds to carbonic anhydrase IX, and how it or other saccharin-based compounds might be tweaked to enhance this binding and boost its anti-cancer treatment potential.
McKenna's team is currently testing the effects of saccharin and saccharin-based compounds on breast and liver cancer cells. If successful, these experiments could lead to animal studies.
Explore further: How spiders spin silk
More information: Saccharin and its carbohydrate-conjugate shows promise for isoform selective inhibition of Carbonic Anhydrase IX: a lead approach to anti-cancer drug development, 249th National Meeting & Exposition of the American Chemical Society (ACS).
Abstract
Carbonic anhydrase IX (CA IX) is a zinc metalloenzyme that is highly expressed in several aggressive cancer types and its expression has been linked to a poorer prognosis in patients. Inhibition of CA IX has shown to be advantageous in terms of reducing tumor cell proliferation, growth, and inducing chemo- and radiosensitivity in solid tumors. As such, CA IX has been characterized as an ideal anti-cancer target due to its minimal expression in normal human tissue and its physiochemical properties. Despite inhibition of CA IX showing great therapeutic promise, designing selective CA IX inhibitors has been challenging due to its high homology with other ubiquitously expressed human isoforms. Here we demonstrate that saccharin, the main additive in "Sweet N' Low", can be used as a lead compound for structure-based drug design of CA IX selective inhibitors. Furthermore we show how the linkage of a carbohydrate fragment to saccharin enhances CA IX inhibition by >1000-fold over other isoforms and provide insights into the structure-activity relationships of such compounds. This data presents a new class of CA IX inhibitors that will potentially aide in the treatment of several cancers.
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A form of saccharin, an artificial sweetener, could lead to the development of drugs that battle aggressive cancers. Credit: Doug Dollemore, American Chemical Society
Saccharin, the artificial sweetener that is the main ingredient in Sweet 'N Low, Sweet Twin and Necta, could do far more than just keep our waistlines trim. According to new research, this popular sugar substitute could potentially lead to the development of drugs capable of combating aggressive, difficult-to-treat cancers with fewer side effects.
The finding will be presented today at the 249th National Meeting & Exposition of the American Chemical Society (ACS).
"It never ceases to amaze me how a simple molecule, such as saccharin—something many people put in their coffee everyday—may have untapped uses, including as a possible lead compound to target aggressive cancers," says Robert McKenna, Ph.D., who is at the University of Florida. "This result opens up the potential to develop a novel anti-cancer drug that is derived from a common condiment that could have a lasting impact on treating several cancers."
The new work examines how saccharin binds to and deactivates carbonic anhydrase IX, a protein found in some very aggressive cancers. It is one of many driving factors in the growth and spread of such cancers in the breast, lung, liver, kidney, pancreas and brain. Carbonic anhydrase IX helps regulate pH in and around cancer cells, allowing tumors to thrive and potentially metastasize to other parts of the body. Because of this finding, the researchers wanted to develop saccharin-based drug candidates that could slow the growth of these cancers and potentially make them less resistant to chemo or radiation therapies.
Except for in the gastrointestinal tract, carbonic anhydrase IX is normally not found in healthy human cells. According to McKenna, this makes it a prime target for anti-cancer drugs that would cause little or no side effects to healthy tissue surrounding the tumor.
Unfortunately, there's a catch.
Carbonic anhydrase IX is similar to other carbonic anhydrase proteins that our bodies need to work properly. So far, finding a substance that blocks carbonic anhydrase IX without affecting the other ones has been elusive. And that's where saccharin—ironically, once considered a possible carcinogen— comes in.
In earlier work, scientists from a group led by Claudiu T. Supuran, Ph.D., at the University of Florence, Italy, discovered that saccharin inhibits the actions of carbonic anhydrase IX, but not the 14 other carbonic anhydrase proteins that are vital to our survival. Building on this finding, a team led by Sally-Ann Poulsen, Ph.D., at Griffith University, Australia, created a compound in which a molecule of glucose was chemically linked to saccharin. This small change had big effects. Not only did it reduce the amount of saccharin needed to inhibit carbonic anhydrase IX, the compound was 1,000 times more likely to bind to the enzyme than saccharin.
Using X-ray crystallography, McKenna and his students Jenna Driscoll and Brian Mahon have taken this work a step further by determining how saccharin binds to carbonic anhydrase IX, and how it or other saccharin-based compounds might be tweaked to enhance this binding and boost its anti-cancer treatment potential.
McKenna's team is currently testing the effects of saccharin and saccharin-based compounds on breast and liver cancer cells. If successful, these experiments could lead to animal studies.
Explore further: How spiders spin silk
More information: Saccharin and its carbohydrate-conjugate shows promise for isoform selective inhibition of Carbonic Anhydrase IX: a lead approach to anti-cancer drug development, 249th National Meeting & Exposition of the American Chemical Society (ACS).
Abstract
Carbonic anhydrase IX (CA IX) is a zinc metalloenzyme that is highly expressed in several aggressive cancer types and its expression has been linked to a poorer prognosis in patients. Inhibition of CA IX has shown to be advantageous in terms of reducing tumor cell proliferation, growth, and inducing chemo- and radiosensitivity in solid tumors. As such, CA IX has been characterized as an ideal anti-cancer target due to its minimal expression in normal human tissue and its physiochemical properties. Despite inhibition of CA IX showing great therapeutic promise, designing selective CA IX inhibitors has been challenging due to its high homology with other ubiquitously expressed human isoforms. Here we demonstrate that saccharin, the main additive in "Sweet N' Low", can be used as a lead compound for structure-based drug design of CA IX selective inhibitors. Furthermore we show how the linkage of a carbohydrate fragment to saccharin enhances CA IX inhibition by >1000-fold over other isoforms and provide insights into the structure-activity relationships of such compounds. This data presents a new class of CA IX inhibitors that will potentially aide in the treatment of several cancers.
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Preparation and characterization of gas-phase carbonic acid and its monomethyl ester
(Phys.org) —Until fairly recently, scientists were convinced that carbonic acid (H2CO3) does not exist as a stable molecule. In the journal Angewandte Chemie, German researchers have now introduced a simple ...
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New potential for personalized treatments in bowel cancer
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A new study provides the first evidence that the mediator complex subunit 15 (MED15) may play a crucial role in the pathophysiology of head and neck squamous cell carcinoma (HNSCC). MED15 overexpression was found to be associated ...
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