A faster way to recover from chemotherapy and marrow transplant

Jun 20, 2007

Researchers at Children’s Hospital Boston report finding a new way to increase stem cells in blood, suggesting a possible treatment to help patients who undergo chemotherapy or bone marrow transplant for leukemia and other cancers recover their immune function more quickly. In the June 21 issue of Nature, they demonstrate that a stable analog of prostaglandin can enhance the blood-forming system, both during embryonic development and after it’s been damaged.

The discovery, made possible through high-volume drug screening in zebrafish, marks the first time stem-cell production has been induced by a small-molecule drug, says the study’s senior author, Leonard Zon, MD, of the Children’s Hospital Boston Stem Cell Program and Division of Hematology/Oncology. Other studies, including one from Zon's own lab, have identified ways of increasing formation of blood stem cells, which give rise to each of the body’s various blood cell types. However, the methods are technically complex and haven’t lent themselves to broad medical use.

The hospital now hopes to conduct a clinical trial of the drug, a long-active derivative of prostaglandin E2 known as dmPGE2. This compound was originally tested more than 20 years ago for patients with gastritis, but was never marketed as a drug.

Currently, patients undergoing bone marrow transplant must wait for marrow from a matched donor to replenish their stem cells and reproduce the full array of blood cell types, including all the cells of the immune system. When there’s no suitable donor for a marrow match, patients can receive umbilical cord blood, which also contains blood stem cells. But the number of stem cells in one cord of blood is often not adequate for older children and adults, leaving them with diminished immune function and high risk for infections.

Zon and colleagues Trista North, PhD, and Wolfram Goessling, MD, PhD, both also of Children’s Stem Cell Program, zeroed in on dmPGE2 by screening more than 2,500 chemicals in zebrafish. Knowing that two genes, runx1 and cmyb, are required for blood stem cells to develop in vertebrate embryos, they looked for compounds that altered the expression (activation) of these genes. North spent six months placing 15,000+ tiny embryos in wells, each containing a different chemical – five embryos to a well, 48 wells to a plate – then checking each embryo 24 hours later to monitor its development and count its blood stem cells.

The screen identified 82 chemicals that markedly increased or decreased gene activity. Of these, 10 turned out to affect the prostaglandin pathway: five increased the formation of blood stem cells, and five decreased it. “We weren’t specifically looking for prostaglandins,” says Zon, a Howard Hughes Medical Institute investigator who is also a member of the Harvard Stem Cell Institute. “This was a surprise finding.”

A variety of experiments confirmed that prostaglandins, particularly dmPGE2, promote blood stem cell formation, while chemicals that block prostaglandin synthesis (such as aspirin or ibuprofen), suppress blood stem cell formation. Finally, in zebrafish whose marrow was depleted by irradiation, those given dmPGE2 recovered blood cell populations more quickly.

Prostaglandins are known to be released by the body when inflammation is present – such as after an injury – and may be among the compounds that aid recovery. “So it makes some sense that prostaglandins would have the ability to enhance regrowth of cells,” Zon says.

“The zebrafish is ideal for investigating blood formation,” says North. “It reproduces quickly and in large number and has a blood-forming system that shares many similarities with that of mammals.” Zebrafish embryos develop outside the mother’s body and can take up chemicals through their skin, making it easy to test the developmental effects of large numbers of compounds very rapidly, while their transparent skin makes it possible to visualize the blood stem cells in live fish.

The researchers also confirmed their observations in mammalian models. When dmPGE2 was added to mouse embryonic stem cells in the lab, production of blood stem cells increased. In mice that underwent bone marrow transplant, treatment with dmPGE2 led to enhanced blood-stem-cell formation, and the stem cells remained present in the marrow more than six months after transplantation, indicating long-term engraftment. “The fact that we confirmed the zebrafish discovery in a mammalian system suggests it may also be applicable in humans,” says Goessling.

The clinical trial, projected to begin in 2008 at Children’s Hospital Boston in conjunction with the Dana-Farber/Harvard Cancer Center, will recruit patients undergoing cord blood transplant for leukemia. Patients will receive cord blood to replenish their blood systems, some of it treated with dmPGE2 to enhance blood-stem-cell formation. “Having more stem cells should help the blood system to regrow faster and minimize complications, such as infections,” says North.

Source: Children's Hospital Boston

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