Absence of mutations in the NBS1 gene in B-cell malignant lymphoma patients

Anticancer Research

Volumn 20, Issue 3 B, 2000, Pages 1897-1900

  Hama, Seiji ^a,b,c   Matsuura, Shinya ^a   Tauchi, Hiroshi ^a   Sawada, Jyunko ^a   Kato, Chikage ^a   Yamasaki, Fumiyuki ^b   Yoshioka, Hiroyuki ^b   Sugiyama, Kazuhiko ^b   Arita, Kazunori ^b   Kurisu, Kaoru ^b   Kamada, Nanao ^a   Heike, Yuji ^c   Komatsu, Kenshi ^a  

^a HIROSHIMA UNIVERSITY   (Japan)

^b HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

^c NATIONAL HOSPITAL ORGANIZATION SHIKOKU CANCER CENTER   (Japan)

Author keywords

B cell malignant lymphoma; NBS1

Indexed keywords

COMPLEMENTARY DNA; DNA;

ARTICLE; B CELL LYMPHOMA; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; GENE MUTATION; HUMAN; HUMAN TISSUE; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; TUMOR SUPPRESSOR GENE;

ADOLESCENT; ADULT; BRAIN NEOPLASMS; CHILD; CHILD, PRESCHOOL; CODON; DNA MUTATIONAL ANALYSIS; DNA, NEOPLASM; GENES, RECESSIVE; GENES, TUMOR SUPPRESSOR; HUMANS; INFANT; LYMPHOMA, B-CELL; NEOPLASM PROTEINS; NEOPLASTIC SYNDROMES, HEREDITARY; NUCLEAR PROTEINS; POLYMORPHISM, GENETIC; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RADIATION TOLERANCE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

EID: 0033869097     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. The International Nijmegen Breakage Syndrome Study Group: Nijmegen Breakage Syndrome, on submission.
2. Hall J, and Angele S: Radiation, DNA damage and cancer. Mol Med 5: 157-164, 1999.
3. Matsuura S, Tauchi H, Nakamura A, Kondo N, Sakamoto S, Endo S, Smeets D, Solder B, Belohradsky BH, Kaloistian VMD, Oshimura M, Isomura M, Nakamura Y, and Komatsu K: Positional cloning of the gene for Nijmegen breakage syndrome. Nat genet 19: 179-181, 1998.
4. Varon R, Visssinga C, Platzer M, Cerosaletti KM, Chrzanowska KH, Saar K, Beckmann G, Seemanova E, Cooper PR, Nowak NJ, Stumm M, Weemaes CMR, Gatti RA, Wilson RK, Digweed M, Rosenthal A, Sperling K, Concannon P, and Reis A: Nibrin, a novel DNA double-strand break repair protein, is mutated in Nijmegen breakage syndrome. Cell 93: 467-476, 1998.
5. Carney JP, Maser RS, Olivares H, Davis EM, Beau ML, Yates III JR, Hays L, Morgan WF, and Petrini JHJ: The hMre11/hRad50 protein complex and Nijmegen breakage syndrome: linkage of double-strand break repair to the cellular DNA damage response. Cell 93: 477-486, 1998.
6. Hochberg FH, and Miller D: Primary central nervous system lymphoma. J Neurosurg 68: 835-853, 1988.
7. Kawakami Y, Tabuchi K, Ohnishi R, Asari S, and Nishimoto A: Primary central nervous system lymphoma. J Neurosurg 62: 522-527, 1985.
8. Larocca LM, Capello D, Rinelli A, Nori S, Antinori A, Gloghini A, Cingolani A, Migliazza A, Saglio G, Cammilleri-Broet S, Raphael M, Carbone A, and Gaidano G: The molecular and phenotypic profile of primary central nervous system lymphoma identifies distinct categories of the disease and is consistent with histogenetic derivation from germinal center-related B cell. Blood 92: 1011-1019, 1998.
9. The non-Hodgkin's Lymphoma Pathologic Classification Project: National Cancer Institute sponsored study of classifications of non-Hodgkin's lymphomas: sammary and description of a Working Formulation for clinical usage. Cancer 49: 2112-2135, 1982.
10. Zhong O, Chen CF, Li S, Chen Y, Wang CC, Xiao J, Chen PL, Sharp ZD, and Lee WH: Association of BRCA1 with the hRAD50-hMre11-p95 complex and the DNA damage response. Science 285: 747-750, 1999.
11. Hall J, Lee MK, Newman B, Morrow JE, Anderson LA, Huey B, and King MC: Linkage of early-onset familial breast cancer to chromosome 17q21. Science 250: 1684-1689, 1990.
12. Brown MA, and Solomon E: Towards cloning the familial breast-ovarian gene on chromosome 17. Curr Opin Genes Dev 4: 439-445, 1994.
13. Easton DF, Bishop DT, Ford D, and Crockford GP: Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. Am J Hum Genet 52: 678-701, 1993.
14. Hiramoto T, Nakanishi T, Sumiyoshi T, Fukuda T, Matsuura S, Tauchi H, Komatsu K, Shibasaki Y, Inui H, Watatani M, Sumii K, Kajiyama G, Kamada N, Miyagawa K, and Kamiya K: Mutations of a novel human RAD54 homologue, RAD54B, in primary cancer. Oncogene 18: 3422-3426, 1999.
15. Matsuda M, Miyagawa K, Takahashi M, Fukuda T, Kataoka T, Asahara T, Inui H, Watatani M, Yasutomi M, Kamada N, Dohi K, and Kamiya K: Mutations in the RAD54 recombination gene in primary cancers. Oncogene 18: 3427-3430, 1999.