A research team led by St. Jude Children's Research Hospital scientists has discovered details of how the abnormal breakage and rearrangement of chromosomes in white blood cells triggers a particularly aggressive form of acute lymphoblastic leukemia (ALL). Such leukemias are cancers of white blood cells, in which genetic mutations trigger overproduction of immature cells, called lymphoblasts.
The discoveries of the malfunction underlying the type called "Ph-like ALL" will aid in designing treatments for the leukemia, researchers said, and also offer useful lessons for investigators studying similar leukemias and other types of cancer.
The researchers, led by corresponding author Charles Mullighan, M.B.B.S., M.D., a member of the St. Jude Department of Pathology, published their findings in the February 8 issue of the journal Cancer Cell. First authors on the paper were Ilaria Iacobucci, Ph.D., a postdoctoral fellow in Mullighan's laboratory, and Yongjin Li, Ph.D., in the laboratory of author Jinghui Zhang, Ph.D., chair of the St. Jude Department of Computational Biology.
Although the investigators had previously identified an abnormal chromosome rearrangement in Ph-like ALL, little was known about the biological effects of that rearrangement. Iacobucci and colleagues set out to pinpoint those effects by studying human leukemic cells and mouse cells engineered to mimic the disorder.
Genomic analysis revealed the details of four distinctly different chromosomal rearrangements in the leukemia. All resulted in a truncated version of a gene called the erythropoietin receptor (EPOR) gene, and all produced the same outcome--driving the white blood cells to proliferate out of control. Li developed and applied the genomic analytical method used to define the truncations.
"To our knowledge, this is a previously unknown mechanism for leukemia," Mullighan said. "Our search of cancer genomic data has shown that there are many other examples of chromosomal rearrangements that alter genes' structure, but this type--where a truncating rearrangement leads to activation--is new."
In analysis of cells from patients with ALL, Iacobucci found the characteristic rearrangements in all the leukemic cells, suggesting these changes were fundamental to the development of cancer. And in experiments with mice, Iacobucci also showed that introducing the mutant receptor in blood cells gave rise to leukemia.
Importantly, Iacobucci and collaborators found the chromosomal alterations arise early in the development of the leukemia and persist as the disease progresses.
"That finding was important because it suggests that treatments for this leukemia targeting this receptor won't just impact a subset of the leukemia cells, allowing others to keep proliferating," Iacobucci said.
Mullighan said the group's findings will significantly aid design and testing of treatments for Ph-like ALL, including trials being developed by the Children's Oncology Group (COG) and St. Jude. The researchers expect that these trials will commence in the near future, because drugs that inhibit the over-activated biological pathway in the leukemia already exist and are widely used to treat other cancers. In fact, Iacobucci's experiments with both engineered mouse cells and human leukemic cells showed that using one of these drugs, ruxolitinib, inhibited the out-of-control machinery.
The researchers also cited the case of an adult patient at MD Anderson Cancer Research Center, Houston, whose genetic analysis revealed EPOR-rearranged ALL. That patient had not responded significantly to other chemotherapy drugs, but when given ruxolitinib, showed a major drop in leukemia cells.
In experiments with leukemic cells, Iacobucci also found that ruxolitinib worked synergistically to enhance the effectiveness of three widely used traditional chemotherapy drugs--dexamethasone, vincristine and daunorubicin.
"We think these findings provide a useful road map for planning more accurate testing of combination chemotherapies," Mullighan said.
Of the potential for aiding clinical trials, co-author Stephen Hunger, M.D., of Children's Hospital of Philadelphia, said: "These findings expand the number of ALL patients who should be amenable to precision medicine therapies that add targeted inhibitors to chemotherapy for ALL patents with specific genetic changes in the leukemia cells."
Hunger said COG has developed a clinical trial testing this strategy with ruxoltitinib, which will begin treating patients in mid-2016. Based on the results of this St. Jude-led study, he said, the trial will include children with ALL and EPOR rearrangements. COG is a federally supported clinical trials group focused exclusively on childhood cancer.
More broadly, Mullighan said the findings highlight the complexity of the chromosomal rearrangements underlying the many types of ALL.
"These findings drive home the point that we are dealing with a complex genomic landscape. Each one of these rearrangements is potentially its own entity, and each one merits its own detailed study. You can't just map a rearrangement and assume that it will produce the same mechanism in all patients that will yield to the same treatment," Mullighan said, adding that "meticulous, detailed genetic sequencing of the cancer cell genomes is required to tease apart the subtle differences among closely related cancers. Such sequencing is also critical for definitive diagnosis of the cancers."
Mullighan emphasized the importance of such detailed analysis in all cancers. "Often a lot of that data generated by whole-genome sequencing may not have been mined comprehensively, because such rigorous analysis is very difficult. But to fully understand these tumors, you have to look at large numbers to make correlations; and to really understand the driving mechanism, you have to find the recurrent biological changes in the tumors."
St. Jude co-authors included Kathryn Roberts, Debbie Payne-Turner, Marcus Valentine, Kelly McCastlain, John Easton, Donald Yergeau, Laura Janke, Ying Shao, Michael Rusch, Ching-Hon Pui, Zhaohui Gu and James Downing, all of St. Jude; Stephanie Dobson, Sasan Zandi and John Dick, all of the University of Toronto; Jaeseung Kim and John McPherson, both of the Ontario Institute of Cancer Research; I-Ming Chen and Cheryl Willman, both of the University of New Mexico, Albuquerque; Steven Kornblau, Marina Konopleva and Elias Jabbour, all of MD Anderson Cancer Center; Elisabeth Paietta and Janis Racevskis, both of Montefiore Medical Center, Bronx, N.Y.; Jacob Rowe, Shaare Zedek Medicak Center, Jerusalem; Julie Gastier-Foster, Nationwide Children's Hospital, Columbus, Ohio; Shalini Reshmi and Mignon Loh, both of University of California, San Francisco; Martin Tallman, Memorial Sloan-Kettering Cancer Center, New York; Peter Wiernik, Cancer Research Foundation of New York, Bronx; and Mark Litzow, Mayo Clinic, Rochester, Minn.
This work was supported in part by grants (CA211765, CA157937, CA114737, CA21115, CA14958, CA101140, CA145707, CA98543, CA98413, CA114766) from the National Cancer Institute, part of the National Institutes of Health; a Stand Up to Cancer Innovative Research Grant; the St. Baldrick's Foundation; the Leukemia and Lymphoma Society; the Lady Tata Memorial Trust Award; Alex's Lemonade Stand Foundation; and ALSAC.