Study Identifies Mechanism Behind Genetic Abnormality That Accelerates Growth of Ewing Sarcoma
The genetic abnormality that drives the bone cancer Ewing sarcoma operates through two distinct processes, both activating genes that stimulate tumor growth and suppressing those that should keep cancer from developing. The findings by Riggi et al, published in Cancer Cell, may lead to new therapies targeting these aberrant mechanisms.
The second most common bone cancer in children and young adults, Ewing sarcoma is caused by a chromosomal translocation in which the chromosome 22 gene EWS is fused to the chromosome 11 gene FLI1. Exactly how that abnormality, which produces a fusion protein called EWS-FLI1, leads to tumor development was not known, although it had been recognized that FLI1 and related proteins were transcription factors that regulate the expression of other genes.
Study Details
Led by Miguel Rivera, MD, and Bradley Bernstein, MD, PhD, of the Massachusetts General Hospital Department of Pathology and Center for Cancer Research, the investigators analyzed how regulatory changes resulting from the EWS-FLI1 fusion alter the activation and repression of regions across the genome. This approach, called chromatin profiling, is a powerful tool for determining how transcription factors act in cancer and revealed that EWS-FLI1 acts through two different mechanisms.
First the fusion protein converts common repetitive elements within the genome into active enhancing elements that stimulate the expression of other genes. This ‘pioneer’ function is remarkable, Dr. Rivera noted, because while these repeat segments have no known function outside the setting of Ewing sarcoma, they are critical for the development of the tumor.
The second property of the EWS-FLI1 fusion is to turn off factors that regulate gene transcription at a different group of sites. In essence the abnormal protein both stimulates the abnormal cellular growth that leads to tumor formation and turns off factors that should keep that growth in check.
“Uncovering the molecular functions of EWS-FLI1 points to processes that may be targeted therapeutically” said Dr. Rivera, Assistant Professor of Pathology at Harvard Medical School. “In addition, some of the genes directly turned on by EWS-FLI1 may themselves be therapeutic targets. One such gene, the kinase VRK1, is regulated by an EWS-FLI1–dependent enhancer that is active in Ewing sarcoma cell lines, and we found that its expression is essential for the survival of Ewing sarcoma cells. These studies also underscore the importance of performing epigenetic analysis to understand the biological pathways that are altered in cancer.”
Drs. Bernstein and Rivera are the corresponding authors for the Cancer Cell article.
The study was supported by grants from the Burroughs Wellcome Fund, Howard Hughes Medical Institute, Hyundai Hope on Wheels, National Human Genome Research Institute.
The content in this post has not been reviewed by the American Society of Clinical Oncology, Inc. (ASCO®) and does not necessarily reflect the ideas and opinions of ASCO®.
