The Stanford Institute for Stem Cell Body and Regenerative Medicine released a study about a cancer cell antibody, which may send a signal to cancer cells to essentially eat themselves.
The molecule named CD47 is the molecule that tells cancer not to eat itself. These researchers found an antibody that will deaden the CD47 signal; they are unsure as to how to control it, and how it will ultimately help fight cancer.
Findings also show that although CD47 is found in other molecular cells within the body, the anti-CD47 doesn’t affect all of them. The link may be due to the presence of calreticulin an agent that gives off the signal to cancer cells to be attacked an eaten. Director of the Stanford Institute, Dr. Irving Weissman reports, that although the calreticulin shows up in many cancer cells, it does not in most normal cells structures. “The research also shows that most normal cell populations don’t display calreticulin and are, therefore, not depleted when we expose them to a blocking anti-CD47 antibody.”
The institute will continue to study the effects of the calreticulin on cell communities and how its discovery can assist in the fight against cancer.
Many cancer cells found to have an ‘eat me’ signal in Stanford study
STANFORD, Calif. — Researchers at the Stanford University School of Medicine have discovered that many cancer cells carry the seeds of their own destruction — a protein on the cell surface that signals circulating immune cells to engulf and digest them. On cancer cells, this “eat me” signal is counteracted by a separate “don’t eat me” signal that was described in an earlier study. The two discoveries may lead to better cancer therapies, and also solve a mystery about why a previously reported cancer therapy is not more toxic.
In the study to be published Dec. 22 in Science Translational Medicine, the researchers discovered that many forms of cancer display the protein calreticulin, or CRT, which invites immune cells called macrophages to engulf and destroy them. The reason most cancer cells are not destroyed by macrophages is that they also display another molecule, a “don’t eat me” signal, called CD47, which counteracts the CRT signal.
The characterization of the function of CD47 protein in cancer was previously published by the Stanford scientists. In the earlier work, they reported that an antibody that blocks CD47 could be a potent anti-cancer therapy. They demonstrated that the anti-CD47 antibody could eliminate disease in mice transplanted with human acute myeloid leukemia and cure a large proportion of mice with human non-Hodgkin’s lymphoma when combined with a second antibody.
Although the result was exciting, it presented a couple mysteries. “Many normal cells in the body have CD47, and yet those cells are not affected by the anti-CD47 antibody,” said Mark Chao, a Stanford MD/PhD candidate who is first author of the new paper. “At that time, we knew that anti-CD47 antibody treatment selectively killed only cancer cells without being toxic to most normal cells, although we didn’t know why.”
The researchers also questioned whether simply blocking CD47 would be enough to bring on a cell’s destruction. “It wouldn’t be likely that killing cells was the default action of the immune system,” said Ravindra Majeti, MD, PhD, assistant professor of hematology and co-principal investigator on the project. “We postulated that there had to be an ‘eat me’ signal that the cancer cells were also carrying in addition to CD47.” CRT became the leading candidate for this signal because other researchers had previously shown that CRT and CD47 work together to govern a process of programmed cell death called apoptosis.
Indeed, when the scientists looked for CRT they found it on a variety of cancers, including several leukemias, non-Hodgkin’s lymphoma and bladder, brain and ovarian cancers. “This research demonstrates that the reason that blocking the CD47 ‘don’t eat me’ signal works to kill cancer is that leukemias, lymphomas and many solid tumors also display a calreticulin ‘eat me’ signal,” said Irving Weissman, MD, director of the Stanford Institute for Stem Cell Biology and Regenerative Medicine and the study’s other co-principal investigator. “The research also shows that most normal cell populations don’t display calreticulin and are therefore not depleted when we expose them to a blocking anti-CD47 antibody.”
The researchers also found that the most aggressive cancers were the ones making the most CRT. This raises hopes that some of the worst cancers may be the most vulnerable to therapies targeting CD47 and CRT.
But it also raises new mysteries: Why would cancer cells carry a protein that invites their own destruction, and why would the worst cancers make more of this protein? One possibility is that CRT is a part of the cell’s regulatory system that cancers have figured a way around. When normal cells become damaged, CRT protein gets exposed on the cell surface, which marks the cell to be eaten and ultimately destroyed. This is one of many ways the immune system keeps abnormal cells in check. “In cancer, CRT expression may be a marker of this process, requiring cancer cells to make more CD47 to avoid getting eaten,” said Chao. “It’s also possible that CRT confers some unknown advantage on cancer, which is an area we are actively investigating.”
One next step for the researchers will be to understand how CRT and CD47 dynamically balance each other’s influence in patients undergoing chemotherapy, the standard treatment for most cancers. This may provide greater chances of success as they move toward a clinical trial of the anti-CD47 antibody in cancer patients.
The scientists also want to learn more about the biology of CRT in cancer. “We want to know how it contributes to the disease process and what is happening in the cell that causes the protein to move to the cell surface,” Majeti said. “Any of these mechanisms offer potential new ways to treat the disease by interfering with those processes.”