Rhabdomyosarcoma is the most common soft-tissue sarcoma occurring in children and young adults. These tumors are unique among sarcomas in that they are thought to derive from skeletal muscle tissue. Tumors express myogenic markers, but fail to undergo terminal differentiation. Two subclasses of rhabdomyosarcomas exist, the embryonal and alveolar. Whereas the embryonal form compromises the majority of cases and is more responsive to multi-modal therapy, alveolar rhabdomyosarcoma is a more primitive malignant neoplasm where prognosis for children with advanced disease remains dismal. Therefore, effective therapies will likely hinge on our abilities to better resolve the underlying mechanisms of alveolar rhabdomyosarcoma. NF-?B is a transcription factor whose signaling pathway has been implicated in a variety of cancers. In skeletal muscle, NF-?B functions in immature cells to negatively regulate terminal differentiation. Recently we discovered that NF-?B functions in this capacity by participating in a regulatory circuit with the Polycomb group protein, YY1, and the microRNA, miR-29. In undifferentiated myoblasts, NF-?B stimulates YY1 production, which epigenetically silences miR-29. However, as differentiation ensues, NF-?B activity decreases causing a concomitant reduction of YY1 and a derepression of miR-29. This microRNA in turn feeds back on YY1 to further reduce its expression and favor a differentiation state. Significantly, in rhabdomyosarcoma cell lines and primary tumors NF-?B - YY1 - miR-29 circuitry becomes deregulated as a result of elevated levels of NF-?B that cause silencing of miR-29. Further results indicate that NF-?B activation in rhabdomyosarcoma is mediated through the NF-?B classical pathway that switches from the alternative pathway found in normal differentiated muscle. Inhibition of classical NF-?B signaling in rhabdomyosarcoma cells restores the regulatory circuit and promotes a muscle differentiation phenotype. Based on these results we hypothesize that NF-?B contributes to rhabdomyosarcoma by blocking terminal differentiation through deregulation of the NF-?B - YY1 - miR-29 circuit. To test this hypothesis, specific aims will 1) determine the relevance of the NF-?B classical versus alternative signaling pathway in rhabdomyosarcomagenesis, and 2) determine the requirement of NF-?B in the initiation and progression of alveolar rhabdomyosarcoma. Results from these studies are likely to yield significant mechanistic insight into the role of NF-?B signaling in alveolar rhabdomyosarcoma, which may prove useful for treatment of this lethal childhood cancer.

Public Health Relevance

Rhabdomyosarcoma is a common soft-tissue cancer in children and adolescents that in its advanced form produces an unfavorable outcome. The tumors are related to the skeletal muscle lineage, but lack the ability to undergo terminal differentiation. NF-?B is part of a signaling pathway that in immature muscle cells functions to inhibit differentiation. Since NF-?B is activated in rhabdomyosarcoma, this proposal will examine how NF-?B signals in these tumor cells and whether NF-?B activity is required for tumor development by acting as a negative regulator of the myogenic differentiation program. .

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA143082-01A1
Application #
8042024
Study Section
Tumor Cell Biology Study Section (TCB)
Program Officer
Yassin, Rihab R,
Project Start
2011-01-01
Project End
2015-12-31
Budget Start
2011-01-01
Budget End
2011-12-31
Support Year
1
Fiscal Year
2011
Total Cost
$335,221
Indirect Cost
Name
Ohio State University
Department
Microbiology/Immun/Virology
Type
Schools of Medicine
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
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