Genetics and the Etiology of Childhood Cancer

A consideration of the world-wide incidences of childhood cancer and of hereditary subgroups leads to the conclusion that two successive mutations can initiate cancer cells and that such cells usually proceed to develop into detectable cancers in a period of time which is short compared with the time required for most adult cancers. Environmental carcinogens could hypothetically increase the rates at which these mutations occur, but they probably, in fact, contribute little to the incidences. Certain exceptions, notably leukemia and lymphoma, are noteworthy, and a viral origin for them has been widely hypothesized. If most solid tumors of childhood are indeed correctly attributable to mutations in germ and/or somatic cells, then the prospect for the prevention of childhood cancer becomes very dim. In fact, the incidence of the germinal forms may increase as treatment improves (18). In theory, one might be able to identify individuals harboring cancer genes germinally and even to identify them prenatally. But even if the burden of cancer attributable to the hereditary subgroups were elimanted, there would still remain the larger nonhereditary group resulting from somatic mutations. If this hypothesis is correct, then childhood cancer cannot be prevented. With this conclusion goes the admonition, however, that environmental mutagens might significantly increase the burden of childhood cancer. One such mutagen, therapeutic radiation, is known to increase the prospect that second tumors will occur in patients who carry a germinal cancer mutation. The major effort to reduce the incidence of childhood cancer by prevention should be spent in examining the possibility that leukemia and lymphoma are viral in origin. If the arguments presented are correct, then the main effort against childhood cancer must be that of early diagnosis and treatment. I realize that many have already argued for that strategy in the approach to cancer generally, but I now believe that it is particularly relevant to any program against cancer in children.

[1]  A. Knudson,et al.  Mutation and childhood cancer: a probabilistic model for the incidence of retinoblastoma. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[2]  R. W. Miller,et al.  U.S. childhood cancer deaths by cell type, 1960-68. , 1974, The Journal of pediatrics.

[3]  A. Knudson Heredity and human cancer. , 1974, The American journal of pathology.

[4]  E. Creagan,et al.  Epidemiology of selected sarcomas in children. , 1974, Journal of the National Cancer Institute.

[5]  R. Ellsworth,et al.  Pleiotropic effects of the gene for retinoblastoma , 1974, Journal of medical genetics.

[6]  P. Neurath,et al.  Computer-Assisted Analysis of Chromosomal Abnormalities: Detection of a Deletion in Aniridia/ Wilms' Tumor Syndrome , 1974, Science.

[7]  J. Parker,et al.  Defective DNA repair in Fanconi's anaemia , 1974, Nature.

[8]  M. Delbeke,et al.  Retinoblastoma and long arm deletion of chromosome 13. Attempts to define the deleted segment , 1974, Clinical genetics.

[9]  W. Baxt,et al.  Leukemia-specific DNA sequences in leukocytes of the leukemic member of identical twins. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[10]  R. Pruett,et al.  Retinoblastoma: chromosome banding in patients with heritable tumour. , 1973, Lancet.

[11]  B. Ames,et al.  Carcinogens are mutagens: a simple test system combining liver homogenates for activation and bacteria for detection. , 1973, Proceedings of the National Academy of Sciences of the United States of America.

[12]  A. Knudson,et al.  Mutation and cancer: neuroblastoma and pheochromocytoma. , 1972, American journal of human genetics.

[13]  A. Knudson,et al.  Mutation and cancer: a model for Wilms' tumor of the kidney. , 1972, Journal of the National Cancer Institute.

[14]  T. Waltz,et al.  Neurological involvement in the nevoid basal cell carcinoma syndrome. , 1971, Journal of neurosurgery.

[15]  M. Swift Fanconi's Anaemia in the Genetics of Neoplasia , 1971, Nature.

[16]  A. Knudson Mutation and cancer: statistical study of retinoblastoma. , 1971, Proceedings of the National Academy of Sciences of the United States of America.

[17]  J. Fraumeni,et al.  Soft-tissue sarcomas, breast cancer, and other neoplasms. A familial syndrome? , 1969, Annals of internal medicine.

[18]  R. W. Miller Deaths from childhood cancer in sibs. , 1968, The New England journal of medicine.

[19]  J. Chatten,et al.  Familial neuroblastoma. Report of a kindred with multiple disorders, including neuroblastomas in four siblings. , 1967, The New England journal of medicine.

[20]  B. Macmahon,et al.  PRENATAL ORIGIN OF CHILDHOOD LEUKEMIA. EVIDENCE FROM TWINS. , 1964, The New England journal of medicine.

[21]  J. Fraumeni,et al.  ASSOCIATION OF WILMS'S TUMOR WITH ANIRIDIA, HEMIHYPERTROPHY AND OTHER CONGENITAL MALFORMATIONS. , 1964, The New England journal of medicine.

[22]  D. Hewitt,et al.  A Survey of Childhood Malignancies , 1958, Public health reports.

[23]  E. Lewis Possible genetic consequences of irradiation of tumors in childhood. , 1975, Radiology.

[24]  A. Evans,et al.  Oncogenesis and other late effects of cancer treatment in children. , 1975, Radiology.

[25]  C. Koop,et al.  Wilms's tumor in three children of a woman with congenital hemihypertrophy. , 1974, The New England journal of medicine.

[26]  J. Davies Childhood tumours. , 1973, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

[27]  Nephroblastoma: an index reference cancer. , 1973, Lancet.

[28]  A. Knudson Mutation and Human Cancer , 1973 .

[29]  J. Cassady,et al.  Radiation induced neoplasia following external beam therapy for children with retinoblastoma. , 1969, The American journal of roentgenology, radium therapy, and nuclear medicine.

[30]  A. Knudson,et al.  [Heredity and cancer in man]. , 1953, Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke.