The in vitro growth and characterization of the skeletal muscle component of Wilms' tumor.

Skeletal muscle differentiation within a Wilms' tumor is a well-documented histopathologic entity thought to occur at a relatively low incidence and influence prognosis. A serum-free hormonally defined growth medium has been developed, allowing the long-term growth of the skeletal muscle component of Wilms' tumors. Eight Wilms' tumors have been grown under these conditions. Three cases grew a homogeneous population of cells which ultrastructurally displayed all stages of myogenesis through myotubule formation. They also possessed immunoreactivity for skeletal muscle myosin and myoglobin and synthesized the M and B subunits of creatine kinase. Of interest was the finding that the ability to yield skeletal muscle cultures was limited to those cases which exhibited skeletal muscle fibers in vivo. This technique is also a very sensitive marker for identifying Wilms' tumors possessing a myoid component. A second serum-free hormonally defined medium has also been developed that supports the long-term culture of a unique cell type from Wilms' tumors which contain a myoid component. These cells are spindle-shaped and exhibit all of the characteristics of early myoblasts.

[1]  T. Seidal,et al.  The ultrastructure of alveolar and embryonal rhabdomyosarcoma. A correlative light and electron microscopic study of 17 cases. , 2009, Acta pathologica, microbiologica, et immunologica Scandinavica. Section A, Pathology.

[2]  D. Sens,et al.  Tissue culture as a diagnostic technique for soft-tissue sarcoma of childhood. , 1984, Archives of pathology & laboratory medicine.

[3]  D. Sens,et al.  Skeletal muscle differentiation in Wilms' tumor. Antibody identification and explant culture. , 1984, Archives of pathology & laboratory medicine.

[4]  M. Tsokos,et al.  Immunohistochemical study of alveolar and embryonal rhabdomyosarcoma. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[5]  W. Hsueh,et al.  Rhabdomyogenesis in renal neoplasia of childhood , 1981, The American journal of surgical pathology.

[6]  C. Clegg,et al.  Myogenic differentiation in permanent clonal mouse myoblast cell lines: regulation by macromolecular growth factors in the culture medium. , 1981, Developmental biology.

[7]  J. Schlessinger,et al.  Fibronectin delays the fusion of L6 myoblasts. , 1979, Experimental cell research.

[8]  L. R. Hill,et al.  Wilms' tumor: Prognostic factors for patients without metastases at diagnosis. Results of the national Wilms' tumor study , 1978, Cancer.

[9]  D. Nuss,et al.  Cultural characteristics of mesoblastic nephromas. , 1977, Journal of pediatric surgery.

[10]  M. Waghe,et al.  Studies of hydrolytic enzymes and isoenzymes of normal and neoplastic childhood renal tissues and their tissue cultured cells. , 1977, British journal of urology.

[11]  C. Nezelof,et al.  Limitation of the potentialities of nephroblastoma differentiation in vitro. , 1977, European journal of cancer.

[12]  H. Wigger Fetal rhabdomyomatous nephroblastoma-a variant of Wilms' tumor. , 1976, Human pathology.

[13]  J. Zucker,et al.  Wilms' tumor: Natural history and prognostic factors. A retrospective study of 248 cases treated at the institut Gustave‐Roussy 1952–1967 , 1976, Cancer.

[14]  E. Bernt,et al.  Creatine kinase in serum: 1. Determination of optimum reaction conditions. , 1976, Clinical chemistry.

[15]  C. Nezelof,et al.  Behaviour of Wilms tumour and normal metanephros in organ culture. , 1974, European journal of cancer.

[16]  W. Engel,et al.  ULTRASTRUCTURAL DEVELOPMENT OF EXPLANTED HUMAN SKELETAL MUSCLE IN TISSUE CULTURE , 1972, Journal of neuropathology and experimental neurology.