Tumor suppressor protein targets liver cancer
Tumor suppressor protein targets liver cancer. Credit: © blueringmedia - Depositphotos
Salk Institute scientists, together with researchers from Switzerland’s University of Basel and University Hospital Basel, discovered a protein called LHPP that acts as a molecular switch to turn off the uncontrolled growth of cells in liver cancer. The tumor suppressor, which could be useful as a biomarker to help diagnose and monitor treatment for liver cancer, could also be relevant for other cancer types. The work appeared in print in the journal Nature on March 21, 2018, and adds to the growing body of knowledge about cellular processes that either promote or prevent cancer.
“I think we’ve discovered a new control mechanism for cell proteins that, when disrupted, could be a driver for cancer,” says Tony Hunter, Salk’s American Cancer Society Professor and an author on the new paper. “It’s exciting because it offers the possibility of new therapeutics or new diagnostics for a cancer that’s basically untreatable–liver cancer–and potentially others, as well.”
Hunter is known for his 1979 discovery of a molecular signaling process called tyrosine phosphorylation. In this process, proteins called kinases attach the chemical phosphate–like a sticky note–to the amino acid tyrosine in target proteins. But, when dysfunctional, tyrosine phosphorylation can also turn on the uncontrolled cell growth that leads to cancer. Hunter’s breakthrough opened the door to the development of a new class of anti-cancer pharmaceuticals called tyrosine kinase inhibitors, including the life-saving leukemia drug Gleevec.
Since then, Hunter’s lab has continued to study the process of phosphorylation, not only in terms of adding phosphates (via kinases or “on switches”) but also removing them (via proteins called phosphatases or “off switches”). In 2015, his team developed an antibody to identify and study phosphates bonded to another amino acid called histidine.
In the new work, the international team, led by Professor Michael Hall of the Biozentrum, University of Basel, examined these switches in a mouse model of the most common form of primary liver cancer–hepatocellular carcinoma. To compare tumor cells with normal cells, the team analyzed more than 4,000 proteins in healthy and diseased liver tissue. By the end, three proteins stood out: the histidine kinases NME1 and NME2 were elevated in tumor cells, and the suspected histidine phosphatase LHPP was deficient.
“It is striking that LHPP is present in healthy tissue and completely absent in tumor tissue,” says Sravanth Hindupur, a postdoctoral researcher at the University of Basel and the paper’s first author. That gave the researchers a clue to explore histidine phosphorylation as a potential cancer target. Indeed, they found that the levels of protein phosphorylated in histidine were significantly higher in the tumor tissue than in normal liver tissue.
NME1 and NME2 are known histidine kinases and LHPP had been suspected to be a histidine phosphatase. With further experiments, the team verified that not only is LHPP a histidine phosphatase, but it is also a tumor suppressor–essentially an “off” switch for cancer. Reintroducing LHPP into the liver of the model mice destined to develop tumors prevented the formation of tumors.
When the researchers next examined samples from human liver tumors, they found a similar pattern: NME1 and 2 levels were high and LHPP was low compared to healthy liver tissue. Furthermore, the Cancer Genome Atlas database, a collection of RNA sequences obtained from different human cancers, showed that a significant fraction of human liver cancers have low levels of LHPP, and that both disease severity and life expectancy are correlated with LHPP levels.
“The parallels between tyrosine phosphorylation and histidine phosphorylation are what really got me interested in the project,” adds Hunter. “Whether this can be used as a therapeutic avenue, I don’t know. But the fact that it could be so disease-relevant motivates me.”
Materials provided by the Salk Institute. Content may be edited for clarity, style, and length.