Mutation of the multiple endocrine neoplasia type 1 gene in nonfamilial, malignant tumors of the endocrine pancreas

Cancer Research

Volumn 58, Issue 3, 1998, Pages 377-379

  Hessman, Ola ^a   Lindberg, Daniel ^a   Skogseid, Britt ^a   Carling, Tobias ^a   Hellman, Per ^a   Rastad, Jonas ^a   Åkerström, Göran ^a   Westin, Gunnar ^a  

^a UPPSALA UNIVERSITY HOSPITAL   (Sweden)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CANCER GENETICS; CHROMOSOME 11Q; CLINICAL ARTICLE; DNA DETERMINATION; FEMALE; GENE MUTATION; GLUCAGONOMA; HETEROZYGOSITY LOSS; HUMAN; HYPOTHESIS; MALE; MULTIPLE ENDOCRINE NEOPLASIA; PANCREAS ISLET CELL CARCINOMA; PRIORITY JOURNAL;

ADULT; AGED; CHROMOSOMES, HUMAN, PAIR 11; DNA, NEOPLASM; FEMALE; GLUCAGONOMA; HUMANS; LOSS OF HETEROZYGOSITY; MALE; MIDDLE AGED; NEOPLASM PROTEINS; PANCREATIC NEOPLASMS; POLYMERASE CHAIN REACTION; PROTO-ONCOGENE PROTEINS;

EID: 0032005227     PISSN: 00085472     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Skogseid, B. Multiple endocrine neoplasia type 1. Clinical genetics and diagnosis. In: A. Arnold (ed.) Endocrine Neoplasms, pp. 383-406. Boston: Kluwer Academic Publishers, 1997.
2. Larsson, C., Skogseid, B., Öberg, K., Nakamura, Y., and Nordenskjöld, M. Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma. Nature (Lond.), 332: 85-87, 1988.
3. Byström, C., Larsson, C., Blomberg, C., Sandelin, K., Falkmer, U., Skogseid, B., Öberg, K., Werner, S., and Nordenskjöld, M. Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors. Proc. Natl. Acad. Sci. USA, 87: 1968-1972, 1990.
4. Lubensky, I. A., Debelenko, L. V., Zhuang, Z., Emmert-Buck, M. R., Dong, Q., Chandrasekharappa, S. C., Guru, S. C., Manickam, P., Olufemi, S-E., Mark, S. J., Speigel, A. M., Collins, F. S., and Liotta, L. A. Allelic deletions on chromosome 11q13 in multiple tumors from individual MEN1 patients. Cancer Res., 56: 5272-5278, 1996.
5. Chandrasekharappa, S. C., Guru, S. C., Manickam, P., Olufemi, S-E., Collins, F. S., Emmert-Buck, M. R., Debelenko, L. V., Zhuang, Z., Lubensky, I. A., Liotta, L. A., Crabtree, J. S., Wang, Y., Roe, B. A., Weisemann, J., Boguski, M. S., Agarwal, S. K., Kester, M. B., Kim, Y. S., Heppner, C., Dong, Q., Speigel, A. M., Burns, A. L., and Mark, S. J. Positional cloning of the gene for multiple endocrine neoplasia-type 1. Science (Washington DC), 276: 404-407, 1997.
6. Agarwal, S. K., Kester, M. B., Debelenko, L. V., Heppner, C., Emmert-Buck, M. R., Skarulis, M. C., Doppman, J. L., Kim, Y. S., Lubensky, I. A., Zhuang, Z., Green, J. S., Guru, S. C., Manickam, P., Olufemi, S-E., Liotta, L. A., Chandrasekharappa, S. C., Collins, F. S., Spiegel, A. M., Burns, A. L., and Mark, S. J. Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states. Hum. Mol. Genet., 6: 1169-1175, 1997.
7. The European Consortium on MEN1. Identification of the multiple endocrine neoplasia type 1 (MEN1) gene. Hum. Mol. Genet., 6: 1177-1183, 1997.
8. Heppner, C., Kester, M. B., Agarwal, S. K., Debelenko, L. V., Emmert-Buck, M. R., Guru, S. C., Manickam, P., Olufemi, S-E., Skarulis, M. C., Doppman, J. L., Alexander, R. H., Kim, Y. S., Saggar, S K., Lubensky, I. A., Zhuang, Z., Liotta, L. A., Chandrasekharappa, S. C., Collins, F. S., Speigel, A. M., Bums, A. L., and Mark, S. J. Somatic mutations of the MEN1 gene in parathyroid tumours. Nat. Genet., 16: 375-378, 1997.
9. Sandford, A. J., Shirakawa, T., Moffatt, M. F., Daniels, S. E., Ra, C., Faux, J. A., Young, R. P., Nakamura, Y., Lathrop, G. M., Cookson, W. O. C., and Hopkin, J. M. Localisation of atopy and beta subunit of high-affinity IgE receptor (Fc∈RI) on chromosome 11q. Lancet, 341: 332-334, 1993.
10. Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. The -94 Généthon human genetic linkage map, Nat. Genet., 7: 246-339, 1994, 1993.
11. Giraud, S., Choplin, H., Teh, B. T., Lespinasse, J., Jouvet, A., Labat-Moleur, F., Lenoir, G., Hamon, B., Hamon, P., and Calender, A. A large multiple endocrine neoplasia type 1 family with clinical expression suggestive of anticipation. J. Clin. Endocrinol. Metab., 82: 3487-3492, 1997.
12. Teh, B. T., Hayward, N. K., Wilkinson, S., Woods, G. M., Cameron, D., and Shepherd, J. J. Clonal loss of INT-2 alleles in sporadic and familial pancreatic endocrine tumours. Br. J. Cancer, 62: 253-254, 1990.
13. Sawicki, M. P., Wan, Y-J. Y., Johnson, C. L., Berenson, J., Gatti, R., and Passaro, E., Jr. Loss of heterozygosity on chromosome 11 in sporadic gastrinomas. Hum. Genet., 89: 445-449, 1992.
14. Debelenko, L. V., Zhuang, Z., Emmert-Buck, M. R., Chandrasekharappa, S. C., Manickam, P., Guru, S. C., Marx, S. J., Skarulis, M. C., Spiegel, A. M., Collins, F. S., Jensen, R. T., Liotta, L. A., and Lubensky, I. A. Allelic deletions on chromosome 11q13 in multiple endocrine neoplasia type 1-associated and sporadic gastrinomas and pancreatic endocrine tumors. Cancer Res., 57: 2238-2243, 1997.
15. Young, D. C., Smith, A. P., Louis, D. N., Graeme-Cook, F., Warshaw, A. L., and Arnold, A. A novel pancreatic endocrine tumor suppressor gene locus on chromosome 3p with clinical prognostic implications. J. Clin. Invest., 100: 404-410, 1997.