Abstract
The family history of breast cancer was studied in 1975 breast cancer patients of all ages. All the patients were found in an ongoing care program for breast cancer patients in the Stockholm area. One hundred and thirty-three families (6.7%) with hereditary breast cancer, 87 (4.4%) families with hereditary breast- and other cancers, and 14 (0.7%) families with the SBLA syndrome were found. There was no association between familiality and bilateral disease, but familial cases tended to be younger at the time of diagnosis. Determination of the parental origin of the disease gene among the index cases revealed twice as many cases where the disease was maternally transmitted. This might be due to a better prognosis when the predisposing gene is maternally transmitted, and could be explained by parental imprinting or environmental factors influencing the expression of the gene.
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Sattin RW, Rubin GL, Webster LA, Huezo CM, Wingo PA, Ory HW, Layde PM: The cancer and steroid hormone study: family history and the risk of breast cancer. JAMA 253: 1908–1913, 1985
Ottman R, Pike MC, King M-C, Casagrande JT, Henderson BE: Familial breast cancer in a population-based series. Am J Epidemiol 123: 15–21, 1986
Anderson DE: A genetic study of human breast cancer. J Natl Cancer Inst 48: 1029–1034, 1972
Anderson DE: Breast cancer in families. Cancer 40: 1855–1860, 1977
Anderson DE, Badzioch MD: Risk of familial breast cancer. Cancer 56: 383–387, 1985
Anderson DE, Badzioch MD: Bilaterality in familial breast cancer patients. Cancer 56: 2092–2098, 1985
Lynch HT, Guirgis H, Brodkey F, Maloney K, Lynch PM, Rankin L, Lynch J: Early age of onset in familial breast cancer. Arch Surg 111: 126–131, 1976
Lynch HT, Watson P, Conway T, Fitzsimmons ML, Lynch J: Breast cancer family history as a risk factor for early onset breast cancer. Breast Cancer Res Treat 11: 263–267, 1988
Claus EB, Risch N, Thompson WD: Genetic analysis of breast cancer in the cancer and steroid horomone study. Am J Human Genet 48: 232–242, 1991
Lynch HT, Conway T, Fitzgibbons R Jr, Schreiman J, Watson P, Marcus J, Fitzsimmons ML, Lynch JF: Age-of-onset heterogeneity in hereditary breast cancer: minimal clues for diagnosis. Breast Cancer Res Treat 12: 275–285, 1988
Lynch HT, Conway T, Watson P, Schreiman J, Fitzgibbons RJ Jr: Extremely early onset hereditary breast cancer: surveillance/management implications. Nebraska Med J 73: 97–100, 1988
Li FP, Fraumeni JF: Soft-tissue sarcomas, breast cancer and other neoplasms. Ann Int Med 71: 747–752, 1969
Lynch HT, Krush AJ: Carcinoma of the breast and ovary in three families. Surg Gynecol Obstet 133: 644–648, 1971
Lynch HT, Harris RE, Guirgis HA, Maloney K, Carmody LL, Lynch JF: Familial association of breast ovarian carcinoma. Cancer 41: 1543–1549, 1978
Phipps RF, Perry PM: Familial breast cancer and the association with colonic carcinoma. Eur J Surg Oncol 15: 109–111, 1989
Petritsch W, Pristautz H, Schreiber F, Stauber R, Kullnig P, Höfler H, Smolle J: Cowden-syndrom. Z Gastroenterol 28: 358–362, 1990
Børresen A-L, Ikdahl Andersen T, Tretli S, Heiberg A, Møller P: Breast cancer and other cancers in Norwegian families with ataxia-telangiectasia. Genes Chrom and Cancer 2: 339–340, 1990
Swift M, Morrell D, Massey RB, Chase CL: Incidence of cancer in 161 families affected by ataxia-telangiectasia. N Engl J Med 325: 1831–1836, 1992
Iselius L, Littler M, Morton N: Transmission of breast cancer — a controversy resolved. Clin Genet 41: 211–217, 1992
Goldstein AM, Amors CI: Segregation analysis of breast cancer from the cancer and steroid hormone study: histologic subtypes. J Natl Cancer Inst 82: 1911–1917, 1990
Hall JM, Lee MK, Newman B, Morrow JE, Andersson LA, Huey B, King M-C: Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250: 1684–1689, 1990
Malkin D, Li FP, Strong LC, Fraumeni JF Jr, Nelson CE, Kim DH, Kassel J, Gryka MA, Bischoff FZ, Tainsky MA, Friend SH: Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 259: 1233–1238, 1990
Srivastava S, Zou Z, Pirollo K, Blattner W, Chang EH: Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature 348: 747–749, 1990
Love RR, Evans AM,et al.: The accuracy of patient reports of a family history of cancer. J Chronic Dis 38: 289–293, 1985
Snedecor GW, Cochran WG: Statistical Methods, 6th ed., 1967, Iowa, p 246
Lynch HT, Fitzsimmons ML, Schreiman J, Conway T, Lynch JF: Breast cancer diagnosis in a putative obligate gene carrier. Cancer Genet Cytogenet 36: 205–210, 1988
Levine EG, King RA, Bloomfield CD: The role of heredity in cancer. J Clin Oncol 7: 527–540, 1989
Adami HO, Hansen J, Jung B, Rimsten Å: Familiality in breast cancer: a case-control study in a Swedish population. Br J Cancer 42: 71–77, 1980
Adami HO, Hansen J, Jung B, Rimsten Å: Characteristics of familial breast cancer in Sweden: absence of relation to age and unilateral versus bilateral disease. Cancer 48: 1688–1694, 1981
Penrose LS, Mackenzie HJ, Karn MN: A genetical study of human mammary cancer. Ann Eugen 14: 234–266, 1948
Langlands AO, Kerr GR, Bloomer SM: Familial breast cancer. Clin Oncol 2: 41–45, 1976
Lynch HT, Albano W, Recerbaren J, Lynch PM, Lynch JF, Elston R: Prolonged survival as a component of hereditary breast and nonpolyposis colon cancer. Med Hypothesis 7: 1201–1209, 1981
Anderson DE, Badzioch MD: Survival in familial breast cancer patients. Cancer 58: 360–365, 1986
Hall J: Genomic imprinting: review and relevance to human diseases. Am J Hum Genet 46: 857–873, 1990
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Lindblom, A., Rotstein, S., Larsson, C. et al. Hereditary breast cancer in sweden: a predominance of maternally inherited cases. Breast Cancer Res Tr 24, 159–165 (1992). https://doi.org/10.1007/BF01961248
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DOI: https://doi.org/10.1007/BF01961248