Higher frequencies of numerical aberrations of chromosome 17 in primary gastric cancers are associated with lymph node metastasis

Journal of Gastroenterology

Volumn 34, Issue 1, 1999, Pages 11-17

  Terada, Ryusuke ^a   Yasutake, Toru ^a   Yamaguchi, Eiichirou ^a   Hisamatsu, Takashi ^a   Nakamura, Shirou ^a   Ayabe, Hiroyoshi ^a   Tagawa, Yutaka ^b  

^a NAGASAKI UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b NAGASAKI UNIVERSITY   (Japan)

Author keywords

Chromosome 17; Fluorescence in situ hybridization (FISH); Gastric cancer; Lymph node metastasis

Indexed keywords

ADULT; AGED; ARTICLE; CANCER INVASION; CHROMOSOME 17; CHROMOSOME ABERRATION; CHROMOSOME LOSS; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN TISSUE; LYMPH NODE METASTASIS; MAJOR CLINICAL STUDY; MALE; MULTIPLE REGRESSION; PATHOLOGY; PRIORITY JOURNAL; STOMACH CANCER;

ADULT; AGED; AGED, 80 AND OVER; CHROMOSOME ABERRATIONS; CHROMOSOMES, HUMAN, PAIR 17; DISEASE PROGRESSION; DNA, NEOPLASM; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; LYMPHATIC METASTASIS; MALE; MIDDLE AGED; NEOPLASM INVASIVENESS; NEOPLASM STAGING; RETROSPECTIVE STUDIES; STOMACH NEOPLASMS;

EID: 0033064243     PISSN: 09441174     EISSN: None     Source Type: Journal    
DOI: 10.1007/s005350050210     Document Type: Article

References (29)

1. Isobe M, Emanuel BS, Givol D, et al. Localization of gene for human p53 tumour antigen to band 17pl3. Nature 1986;320:84-5.
2. Leone A, McBride OW, Weston A, et al. Somatic allelic deletion of nm23 in human cancer. Cancer Res 1991;51:2490-3.
3. Semba K, Kamata N, Toyoshima K, et al. A v-erbB-related protooncogene, c-erbB-2, is distinct from the c-erbB-1/epidermal growth factor-receptor gene and is amplified in a human salivary gland adenocarcinoma. Proc Natl Acad Sci USA 1985;82:6497-501.
4. Tagawa Y, Sawai T, Nakagoe T, et al. Numerical aberrations of chromosome 11 and 17 in colorectal adenocarcinomas. Jpn J Surg 1996;26:869-74.
5. Gomyo Y, Osaki M, Kaibara N, et al. Numerical aberration and point mutation of the p53 gene in human gastric intestinal metaplasia and well-differentiated adenocarcinoma: Analysis by fluorescence in situ hybridization (FISH) and PCR-SSCP. Int J Cancer 1996;66:594-9.
6. Kobayashi M, Kawashima A, Mai M, et al. Analysis of chromosome 17p13 (p53 locus) alterations in gastric carcinoma cells by dual-color fluorescence in situ hybridization. Am J Pathol 1996;149:1575-84.
7. Ichikawa D, Hashimoto N, Hoshima M, et al. Analysis of numerical aberrations of specific chromosomes by fluorescent in situ hybridization as a diagnostic tool in breast cancer. Cancer 1996;77:2064-9.
8. Watatani M, Nagayama K, Imanishi Y, et al. Genetic alterations on chromosome 17 in human breast cancer. Breast Cancer Res Tr 1993;28:231-9.
9. Uchina S, Tuda H, Noguchi M, et al. p53 mutation in gastric cancer: a genetic model for carcinogenesis is common to gastric and colorectal cancer. Int J Cancer 1993;54:759-64.
10. Shiao YH, Rugge M, Correa P, et al. p53 alteration in gastric precancerous lesions. Am J Pathol 1994;144:511-7.
11. Lemoine NR, Jain S, Silvestre F, et al. Amplification and overexpression of the EGF receptor and c-erbB-2 protooncogenes in human stomach cancer. Br J Cancer 1991;64:79-83.
12. Hattori Y, Odagiri H, Nakatani H, et al. K-sam, an amplified gene in stomach cancer, is a member of the heparin-binding growth factor receptor genes. Proc Natl Acad Sci 1990;87:5983-7.
13. Hiki Y, Shimano H, Mieno H, et al. Modified treatment of early gastric cancer: evaluation of endoscopic treatment of early gastric cancers with respect to treatment indication groups. World J Surg 1995;19:517-22.
14. Seto Y, Nagawa H, Muto T. Impact of lymph node metastasis on survival with early gastric cancer. World J Surg 1997;21:186-9.
15. Japanese Research Society for Gastric Cancer. The general rules of the gastric cancer study. 12th ed. (in Japanese). Tokyo: Kanehara, 1993.
16. Pinkel D, Straume T, Gray JW. Cytogenic analysis using quantitative, high-sensitivity, fluorescence hybridization. Proc Natl Acad Sci USA 1986;83:2934-8.
17. Hopman AHN, Moesker O, Smeets WGB, et al. Numerical chromosome 1, 7, 9, and 11 aberrations in bladder cancer detected by in situ hybridization. Cancer Res 1991;51:644-51.
18. Hopman AHN, Ramaekers FCS, Raap AK, et al. In situ hybridization as a tool to study numerical chromosome aberrations in solid bladder tumors. Histochemistry 1988;89:307-16.
19. Bishop JM. Molecular themes in oncogenesis. Cell 1991;64:235-48.
20. Solomon E, Borrow J, Goddard AD. Chromosome aberrations and cancer. Science 1991;254:1153-60.
21. Baker SJ, Fearon ER, Nigro JM, et al. Chromosome 17 deletions and p53 gene mutations in colorectal carcinomas. Science 1989;244:217-21.
22. Baker SJ, Preisinger AC, Jessup JM, et al. p53 mutations occur in combination with 17p allelic deletions as late events in colorectal tumorigenesis. Cancer Res 1990;50:7717-22.
23. Lichter P, Cremer T, Borden J, et al. Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Hum Genet 1988;80:224-34.
24. Matsumura K, Kallioniemi A, Kallioniemi O, et al. Deletion of chromosome 17p loci in breast cancer cells detected by fluorescence in situ hybridization. Cancer Res 1992;52:3474-7.
25. Matsuyama H, Pan Y, Skoog L, et al. Deletion mapping of chromosome 8p in prostate cancer by fluorescence in situ hybridization Oncogene 1994;9:3071-6.
26. Kovach JS, McGovern RM, Cassady JD, et al. Direct sequencing from touch preparations of human carcinomas. J Natl Cancer Inst 1991;83:1004-9.
27. Kurtin PJ, Pinkus GS. Leukocyte common antigen, a diagnostic discriminant between hematopoietic and non hematopoietic neoplasms in paraffin sections using monoclonal antibodies: correlation with immunologic studies and ultrastructual localization. Hum Pathol. 1985;16:353-65.
28. Hopman AHN, van Hooren E, van de Kaa CA, et al. Detection of numerical chromosome aberrations using in situ hybridization in paraffin sections of routinely processed bladder cancers. Mod Pathol 1991;4:503-13.
29. Devilee P, Thierry RF, Kievitus T, Kolluri R, et al. Detection of chromosome aneuploidy in interphase nuclei from primary breast tumors using chromosome-specific repetitive DNA probes. Cancer Res 1988;48:5825-30.