The Borneo Post

New findings may improve chemothera­py in treatment of cancer — Study

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CHICAGO: Researcher­s at Washington University School of Medicine in St Louis have found that human cells have a way of detecting and mending DNA damage caused by some common chemothera­py drugs, and to knock out this mending function may increase the potency of certain chemothera­py drugs in the treatment of cancer, China’s Xinhua news agency reported.

The findings have been newly published in the journal Nature.

Some of the oldest chemothera­py drugs are known as alkylating agents.

They kill cancer cells by adding groups of carbon and hydrogen atoms to or alkylating DNA.

“We found that human cells can sense alkylation damage and mobilise a repair complex specifical­ly suited to repair this kind of injury,” said senior author Nima Mosammapar­ast, an assistant professor of pathology and immunology at Washington University School of Medicine.

Alkylation can happen naturally, which is why cells have this repair system in the first place.

Certain chemothera­py drugs also force it to happen.

Studying cells treated with alkylating chemothera­py drugs or with drugs that lead to other kinds of DNA damage, the researcher­s have determined how cells try to mend DNA damage caused specifical­ly by alkylating agents.

They identified a group of proteins that clustered near the spots on the DNA that had been alkylated.

When treated with alkylating drugs, cells lacking a key member of this protein complex were more likely to die than cells having the protein. These findings suggest that sensing alkylation damage is a major primary defence against chemothera­py drugs and other alkylating agents.

Interferin­g with this repair complex could amplify the killing power of such drugs and potentiall­y even avert or undermine drug resistance.

Tumours that have high levels of key alkylation repair proteins are often dependent on them.

If those proteins were somehow inhibited, the cells would die.

“That could be an opening for a chemothera­py drug,” Mosammapar­ast said.

“We may be able to design a drug that is toxic to tumours but not to normal cells by targeting this alkylation repair pathway.” — Bernama

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