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New Inhibitor Identified Can Treat Fibrosis Without Side Effects

by Hannah Joy on Sep 7 2017 12:19 PM

Fibrosis is accumulation and scarring of excessive connective tissue. Compounds have been identified to help in treating fibrosis without harmful side effects.

New Inhibitor Identified Can Treat Fibrosis Without Side Effects
A class of compounds has been identified as inhibitors of TGF-β1-induced responses in fibroblasts that target the cells causing fibrosis, reveals a new study.
Fibrosis describes the accumulation of excessive of connective tissue that occurs in response to organ injury or pathological states. Scars that replace injured skin are an example of external, visible fibrosis.

Progressive scarring of the lung, liver, and heart represent fibrotic diseases that are major drivers of mortality. The tissue stiffness that characterizes fibrosis is also known to play a role in cancer metastasis.

Fibrosis-initiating cells, or fibroblasts, respond to signaling by the growth factor TGF-β, but this molecule also acts on epithelial and immune cells to suppress inflammation and autoimmunity.

Global and chronic inhibition of TGF-β signaling has numerous adverse effects, necessitating a more specific approach to blocking fibrosis-initiating TGF-β pathways.

Using a high-throughout screen of small molecules, researchers in Harold Chapmanā€™s lab at UCSF School of Medicine identified a class of compounds called trihydroxyphenolics as inhibitors of TGF-β1-induced responses in fibroblasts. They observed that trihydroxyphenolics do not affect non-fibrogenic epithelial or immune cells.

Further studies determined that fibroblasts and fibroblast-like cancer cells produce a specific protein that generates an intermediate metabolite of trihydroxyphenolic compounds.

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As only fibrosis-initiating cells produce the metabolite, trihydroxyphenol treatment selectively affects fibrogenic cells.

As the group describes in a study published in the JCI, the identification of this class of compounds as TGF-β inhibitors with selective anti-fibrotic activity delineates a possible therapeutic approach to attenuate fibrosis without the harmful side effects of non-specific TGF-β inhibition.

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Source-Eurekalert


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