A University of Alberta researcher in the Faculty of Medicine & Dentistry may have found a new target for cancer therapy.
One of the most important genes in the human genome is called p53 and its function is to suppress tumors, says Roger Leng (pictured), a researcher in the Department of Laboratory Medicine and Pathology. Leng has discovered the mechanism by which p53 is inactivated in cancerous cells, allowing tumors to grow.
“Successful completion of the proposed experiments could lead to novel anti-cancer therapies that could potentially improve the prognosis for cancer patients and reduce the public-health burden from cancer,” said Leng.
It has long been known by scientists that another protein, MDM2, lowers p53 in the body but in cancerous cells p53 is inactivated in more than 50 per cent of all human tumors. MDM2 does not have the ability to functionally silence the tumor-suppressing protein on its own, leaving scientists wondering what molecule in the body is helping MDM2 to nearly eliminate p53 in cancerous cells.
Leng’s lab has answered that question and the culprit is called UBE4B. Leng made the discovery because he found that UBE4B binds with both p53 and MDM2. From there his lab was able to discover the relationship between the proteins.
Paired with MDM2, also known as HDM2 in humans, the two proteins completely degrade p53 in a laboratory model. This is a process known as poly-ubiquitination, which means a specific protein completely disappears in a cell.
They also did experiments on several cancerous human brain tissues and found the same results.
“They have the same function,” said Leng. “The idea now is you can target UBE4B and MDM2 won’t function.”
“We want to understand how it regulates MDM2,” said Leng. “We also want to see, if you get DNA damage, what happens in UBE4B and p53.”
Illustration: University of Alberta.
University of Alberta News Release (02/14/11)
e! Science News (02/14/11)
Abstract (Nature Medicine; 17, 347-355 (02/13/11))