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Controlled Release of Enzyme TrxR1 Can Help Treat 60 Types of Cancer

by Julia Samuel on Feb 16 2018 12:51 PM

Small molecules that specifically control a selenium-containing enzyme in the human body may become a tool to fight cancer.

Controlled Release of Enzyme TrxR1 Can Help Treat 60 Types of Cancer
Molecules that control the release of a selenium-containing enzyme in the human body may become a tool to fight cancer.
Scientists effectively treated over 60 different types of cancer cells under laboratory conditions with these molecules.

The study published in the US medical journal Science Translational Medicine said researchers at Karolinska Institute in Sweden treated cancer in mice with these molecules and observed rapid tumor-killing effects.

They have expressed hope that this new principle could be extended to treat cancer in humans, Xinhua news agency reported.

Selenium is a chemical element that is an essential micronutrient. A selenium-containing enzyme, called TrxR1, can be used to support the growth of various cells and protect them from oxidative stress.

Oxidative stress is the imbalance between the production of free radicals, which are highly reactive with other molecules, and the body's ability to counteract or to repair the resulting damage.

However, in several forms of cancer, raised levels of TrxR1 could be detected.

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Researchers analyzed almost 400,000 different molecules to find new ones that would more specifically control TrxR1 and found three different types which proved to be active as anti-cancer medicines.

"This effectiveness against cancer may be a result of cancer cells' seemingly greater sensitivity to oxidative stress when compared to normal cells, which in turn can be utilized in cancer therapy," Elias Arner, a professor at the Karolinska Institute, who led the study, said.

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"This seems to work in mouse models and we are therefore hopeful that this principle of treatment can be developed for humans, even if this will require many years of further research," he added.

Source-IANS


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