New Enzyme Targets for Developing Liver Cancer Drugs

Certain cancers are mainly caused due to the lack of enzymes that are required to maintain cell growth. While some may be caused due to the enzyme over-activity that intensifies cell growth. A research team from the University of California San Diego School of Medicine have discovered that either the loss of enzymes or the over-activity of the enzymes are found to be the potential reasons for liver disease and cancer.

The deficiency of two enzymes called Shp2 and Pten in human liver cancer sample were found to be associated with poor prognosis.

The study, published December 13 by Cell Reports, provides a new understanding of how liver cancer develops, a new therapeutic approach and new mouse model for studying the disease.

"When it comes to liver cancer, I think we've been making strategic mistakes," said senior author Gen-Sheng Feng, PhD, professor of pathology and biological sciences at UC San Diego. "In cancer development, we always thought about two distinct families of enzymes -- one promotes cancer, one inhibits it. Many drugs have been developed to block the cancer-promoting pathways, but we and others are now finding that many classical pro-cancer proteins are actually inhibitors."

Based on Shp2's well-known role in promoting tumor formation, researchers have long assumed that drugs that block the enzyme would inhibit tumor formation. But Feng's team previously found the opposite to be true -- loss of the Shp2 enzyme can promote liver cancer. In contrast, in a study published last year , Feng and team discovered that removing both Shp2 and Pten, a tumor-suppressing enzyme, neutralized leukemia development.

"So the roles of tumor-promoting and tumor-suppressing enzymes are not as simple as we thought," Feng said. "This also explains many unwanted side effects with drugs that target these enzymes. Their consequences can differ depending on cell type."

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In this latest study, Feng and team found that Shp2 and Pten cooperate to suppress liver tumor formation in experimental mice. When the researchers deleted both the Shp2 and Pten genes specifically in the mice's liver cells, early-onset liver disease (non-alcoholic steatohepatitis, or NASH) was more severe and liver tumors occurred earlier and more frequently than in control mice with one or both enzymes functioning.

Normal mice did not experience any tumors. In mice lacking either Pten or Shp2, liver tumors began to appear after approximately seven or 12 months. But for mice lacking both enzymes, 80 percent spontaneously developed liver tumors in five months; 100 percent had tumors at seven months.

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The increased severity of liver disease and frequency of liver cancer in these models is likely because lack of Shp2 and Pten enzymes activates molecules involved in lipid metabolism, inflammation and fibrosis, the researchers said.

After their surprising results in mice, the researchers wondered if the same phenomenon occurs in human liver cancers. They analyzed 335 human liver tumor samples and found that approximately 52 percent of the tumors were low in both Shp2 and Pten enzyme levels. Those patients with low Shp2 and Pten enzyme levels in the tumors had a poorer prognosis than those with higher levels of one or both enzymes -- at 50 months after surgery, approximately 60 percent of patients with low Shp2 and Pten were alive, compared to approximately 90 percent of patients with high Shp2 and Pten levels.

These results provide new information about how liver cancer arises and a new target for drug development. But the findings also offer a new laboratory model for studying the disease. Previously, Feng's team and others would use chemical carcinogens to induce liver cancer in mouse models. Instead of taking this artificial approach, Feng said researchers can now generate more realistic mouse models of non-alcoholic fatty liver disease and liver cancer simply by removing the Pten and Shp2 enzymes.

"Liver cancer is more complicated than we thought. These pathways, when over-activated, stimulate tumor development, but so does inhibiting them," Feng said. "That's why we can't rush to conclusions like we have in the past. But now that we have a good model that mimics the human pathogenic process and we can use that to work out the mechanisms that lead to liver disease and cancer, and search for novel drug targets."



Source-Eurekalert