Scientists reverse #PancreaticCancer cells to normal cells in lab

Pancreatic cancer cells can be reversed back into normal cells by introducing a protein called E47 that controls genes involved in growth and differentiation, a U.S. study suggested Monday.

The findings may lead to a potential new treatment for pancreatic cancer, one of the deadliest and most aggressive forms of cancer, which killed Apple co-founder Steve Jobs.

“For the first time, we have shown that over expression of a single gene can reduce the tumor-promoting potential of pancreatic adenocarcinoma cells and reprogram them toward their original cell type,” said Pamela Itkin-Ansari, adjunct professor at the Sanford- Burnham Medical Research Institute and lead author of the study published in the journal Pancreas.

“Thus, pancreatic cancer cells retain a genetic memory which we hope to exploit.”

For the study, Itkin-Ansari and colleagues generated human pancreatic ductal adenocarcinoma cell lines to make higher than normal levels of E47, which caused cells to stall in the early growth phase, and differentiate back toward an acinar cell phenotype.

When the reprogrammed cancer cells were introduced into mice, their ability to form tumors was greatly diminished compared to untreated adenocarcinoma cells, the researchers found.

Currently, pancreatic adenocarcinoma, the most common form of pancreatic cancer, is treated with cytotoxic agents, yet the average survival for patients post-diagnosis is merely six months, and the improvements in therapies are measured in days, according to co-author Andrew Lowy, professor of surgery at the University of California San Diego.

(click here to continue reading this article)

*credit verbatim via*


Leave a Reply

Fill in your details below or click an icon to log in: Logo

You are commenting using your account. Log Out /  Change )

Google photo

You are commenting using your Google account. Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. Log Out /  Change )

Connecting to %s