The discovery is significant - and could eventually contribute to development of new cancer therapies, researchers said.
"More than 20 per cent of human cancers - as well as a number of other diseases - are linked to chronic viral infections," said Xiaonan Dong from University of Texas Southwestern Medical Centre (UTSW).
The study found that the autophagy-related protein beclin 2 - also discovered by researchers - can help break down the key oncogenic viral protein associated with Kaposi's sarcoma, a type of cancer most commonly found in people with HIV infection or transplant-related suppression of their immune systems.
The findings showed that in addition to mediating autophagy, beclin 2 is also involved in a novel immune pathway that suppresses viral infection and virus-caused cancer.
"We found that beclin 2 can promote the degradation of Kaposi's sarcoma-associated herpesvirus G protein-coupled receptor (GPCR), and thereby suppress its cancer-causing signalling," said Dong.
"Transgenic mice deficient in beclin 2 are more prone to viral GPCR-driven oncogenesis that resembles human Kaposi's sarcoma," he said.
This response is part of an endolysolomal trafficking process in which microbes and their constituent proteins are delivered to enzyme-filled cellular components called lysosomes.
Kaposi's sarcoma can affect the skin and internal organs. It is most often seen in people infected with HIV, but also has an incidence of about 1 in 200 transplant patients, researchers said.
"These findings deepen understanding of the mechanisms that our immune system uses to protect against cancer and potentially against other serious diseases caused by pathogenic viral proteins," said Beth Levine from UTSW.
The findings were published in the journal Proceedings of the National Academy of Sciences.
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