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Sweet Treatment

24 Mar 2015
Guest Contributor
Off
cancer, sacchrin, Sweet 'N Low, Sweet Twin, Necta, sugar substitute, American Chemical Society, University of Floriday, Robert McKenna, anti-cancer drug, carbonic anhydrase IX, Jenna Driscoll, Brian Mahon

Sacchrin Could Lead to New Cancer Care

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, the popular sugar substitute could potentially lead to the development of drugs capable of combating aggressive, difficult-to-treat cancers with fewer side effects.

A form of saccharin could lead to the development of drugs that battle aggressive cancers. (Photo: Doug Dollemore/American Chemical Society)

A form of saccharin could lead to the development of drugs that battle aggressive cancers. (Photo: Doug Dollemore/American Chemical Society)

The finding was presented Monday at the 249th National Meeting & Exposition of the American Chemical Society.

“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 the University of Florida’s Robert McKenna, Ph.D. “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 spread to other parts of the body. Because of this finding, the researchers wanted to develop saccharin-based drugs 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 — once considered a possible carcinogen — comes in.

In earlier work, scientists 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 another team at an Australian university 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 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.

Article by the American Chemical Society

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This article was written by the guest columnist listed at the end of the article.

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This article was written by the guest columnist listed at the end of the article. 
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