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Cytogenetic Studies of Human Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma Cell Lines


Affiliations
1 Dept. of Radiobiology, Research Institute for Environmental Sciences, Hachazawa 2-121, Takahoko, Rokkasho, Kamikita, Aomori 039-3213, Japan
2 Department of Surgery, Research Institute for Radiation Biology and Medicine, Hiroshima University, Kasumi 1-1-1, Minami-ku, Hiroshima 734-8552, Japan
 

Esophagus and gastric cancer are one of the most common in Asian countries, but molecular event in the carcinogenesis remains as largely unidentified associated oncogenes. Detailed karyotypic analyses were performed on 4 cell lines derived from malignant cells of a patient with esophagus carcinoma of both diagnosis and metastasis stages and 2 cell lines from 2 independent patients with gastric cancer of metastasis stages. Most of these cells examined were near triploid with modal chromosome number of 59-73. These cells had a complex karyotype with more than 10 rearrangements. The karyotypic pattern was relatively stable; consistent alterations involved long arm of chromosomes 2, 9 and 12 and short arm of chromosomes 3 in both diagnosis and metastasis stages in esophagus cell lines. Those alterations of gastric cancer involved chromosomes 7 and 11. Higher rearrangements associated with translocations and deletions were observed at 2q23 of chromosome2, 3p14 of chromosome 3, 4q11 of chromosome 4 and 11q25 of chromosome 11 in esophagus cancer; while 7p13 of chromosome 7 and 11p15 of chromosome 11 in gastric cancer. The overall chromosome pattern was not similar between these cancers, although these tumors arise from anatomically or biologically related site. Unknown oncogenes localizing on these chromosome breakpoints for translocation or deletion region might be associated with the pathogenesis of esophagus or gastric cancer. These newly established cell lines will be useful tools in the study of the molecular pathogenesis and for testing new therapeutic reagents for these cancers in the future.

Keywords

Esophagus Cancer, Gastric Adenocarcinoma, Karyotypic Analyses, Metastasis, Human Cell Line
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  • Akagi T, Ito T, Kato M, Jin Z, Cheng Y, Kan T, Yamamoto N, Boult J, Soukiasian HJ, Miller CW, Ogawa S, Meltzer SJ and Koeffler HP (2009) Chromosomal abnormalities and novel diseaserelated regions in progression from Barrett’s esophagus to esophageal adenocarcinoma. Int. J. Cancer. 125(10), 2349-2359.
  • Asaoka Y, Tada M, Ikenoue T, Seto M, Imai M, Miyabayashi K, Yamamoto K, Yamamoto S, Kudo Y, Mohri D, Isommura Y, Ijiri H, Tateishi K, Kanai F, Ogawa S, Omata M and Koike K (2010) Gastric cancer cell line Hs746T harbors a splice site mutation of c-Met causing juxtamembrane domain deletion. Biochem. Biophys. Res. Commun. 394(4), 1042-1046.
  • Barrett MT, Sanchez CA, Prevo LJ, Wong DJ, Galipeau PC, Paukson TG, Rabinovitch PS and Reid BJ (1999) Evolution of neoplastic cell lineage in Barret esophagus. Nature Genet. 22(1), 106-109.
  • Blount PL, Meltzer SJ, Yin J, Krasna MJ and Reid BJ (1993) Clonal ordering of 17p and 5q allelic losses in Barrett dysplasia and adenocarcinoma. Proc. Natl. Acad. Sci, USA. 90(8), 3221-3225.
  • Buffart TE, Grieken NC, Tjissen M, Coffa J, Ylstra B, Grabsch HI, van de Velde CJ, Carvalho B and Meijer GA (2009) High resolution analysis of DNA copynumber aberrations of chromosomes 8, 13 and 20 in gastric cancers. Virchows Arch. 455(3), 213-223.
  • Ferti-Passantonopoulou AD, Panani AD, Viachos JD and Raptis SA (1987) Common cytogenetic findings in gastric cancer. Cancer Genet. Cytogenet. 24, 63-73.
  • Galipeau PC, Prevo LJ, Sanchez CA, Longton GM and Reid BJ (1999) Clonal expression and loss of heterozygosity at chromosomes 9p and 17p in premalignant esophageal (Barret's) tissues. J. Natl. Cancer Inst. 91(24), 2087-2095.
  • Hu N, Wang C, Su H, Li WJ, Emmert-Buck MR, Roth MJ, Tang ZZ, Lu N, Giffen C, Albert PS, Taylor PR and Goldstein AM (2004) High frequency of CDKN2A alterations in esophageal squamous cell carcinoma from a high-risk Chinese population. Genes Chromosome Cancer. 39(3), 205-216.
  • ISCN (2005) An international system for human cytogenetic nomenclature. Shaffer LG & Tommerrup N (ed.), also in cytogenetics and genome research, Karger, Basel.
  • Ito H, Oda N, Ito M, Nakayama H and Tahara E (1989) Cytogenetic analysis of the human gastric carcinoma cell line TMK-1. Hiroshima J. Med. Sci. 38(3), 121- 124
  • Jin Y, Jin C, Law S, Chu KM, Zhang H, Storobeck B, Yuen AP and Kwong YL (2004) Cytogenetic and fluorescence in situ hybridization characterization of clonal chromosomal aberrations and CCND1 amplification in esophageal carcinoma. Cancer Genet. Cytogenet. 148(1), 21-28.
  • Kamitani S, Sugihara H, Shimi H, Tani T and Hattori T (2002) Intratumoral regional variations in copy number of the chromosomal part revealed by microdissection and combined ploidy and comparative genomic hybridization analyses in esophageal squamous cell carcinoma. Cancer Genet. Cytogenet. 132(1), 30-35.
  • Kimura Y, Noguchi T, Kawahara K, Kashima K, Daa T and Ypkoyama S (2004) genetic alterations in 102 primary gastric cancers by comparative genomic hybridization: gain of 20q and loss of 18q are associated with tumor progression. Mol. Pathol. 17(11), 1328-1337.
  • Kokkola A, Monni O, Puolakkainen P, Larramendy ML, Victorzon M, Nordling S, Haapianen R, Kivillakso Eand Knuutila S (1997) 17q12-21 amplicon, a novel recurrent genetic change in intestinal type of gastric carcinoma: a comparative genomic hybridization study. Genes Chrom. Cancer 20(1), 38-43.
  • Kokkola A, Monni O, Puolakkainen P, Nordliong S, Haapianen R, Kivilaakso E and Knuutila S (1998) Presence of high-level DNA copy number gains in gastric carcinoma and severity dyspastic adenomas but not in moderately dysplastic adenomas. Cancer Genet. Cytogenet. 107(1), 32-36.
  • Lima EM, Rissino JD, Harada ML, Assumpço PP, Demachki S, Guimarães, AC, Casartelli C, Smith MA and Burbano RR (2004) Conventional cytogenetic characterization of a new cell line, ACP01, established from a primary human gastric tumor. Braz. J. Med. Biol. Res. 37(12), 1831-1818.
  • Maesawa C, Tamura G, Nishizuka S, Iwata T, Ogasawara S, Oshida K, Sakata K, Sato N, Ikeda K, Kimura Y, Saito K and Satodate R (1997) MAD-related genes on 18q21.1, Smad2 and Smad4, are altered infrequently in esophageal squamous carcinoma. Jpn. J. Cancer Res. 88(4), 340-343.
  • Manoel-Caetano Fda S, Borim AA, Caetano A, Cury PM and Silva AE (2004) Cytogenetic alterations in chagasic achalasia compared to esopahageal carcinoma. Cancer Genet. Cytogenet. 149(1), 17-22.
  • Menke-Pluymers MB, van Drunen E, Vissers KJ, Mulder AH, Tilanus HW and Hagemeijer A (1996) Cytogenetic analysis of Barrett’s mucosa and adenocarcinoma of the distal esophagus and cardia. Cancer Genet. Cytogent. 90(2), 109-117.
  • Mita H, Toyota M, Aoki F, Akahsi H, Maruyama R, Sasaki Y, Suzuki H, Idogawa M, Kahsima L, Yanagihara K, Fujita M, Hosokawa M, Kusano M, Sabau SV, Tatsumi H, Imai K, Shinomura Y and Tokino T (2009) A novel method, digital genome scanning detects KRAS gene amplification in gastric cancers: involvement of overexpressed wild-type KRAS in downstream signaling and cancer cell growth. BMC Cancer .23(9), 198.
  • Montesano R, Hollistein M and Hainaut P (1996) Genetic alterations in esophageal cancer and their relevance to etiology and pathogenesis: a review. Int. J. Cancer. 69(3), 225-235.
  • Moskaluk CA, Hu J and Perlman EJ (1998) Comparative genomic hybridization of esophageal and gastroesophageal adenocarcinomas shows consensus area of DNA. Genes Chrom. Cancer.22(4), 305-311.
  • Noguchi T, Wirtz HC, Michaelis S, Gabbert HE and Mueller W (2001) Chromosome imbalances in gastric cancer. Correlation with histological subtypes and tumor progression. Am. J. Clin. Pathol. 115(6), 828- 834.
  • Ochi H, Dauglass Jr HO and Sandberg AA (1986) Cytogenetic studies in primary gastric cancer. Cancer Genet. Cytogenet. 22, 295-307.
  • Pack SD, Karkera JD, Zhuang Z, Pak ED, Balan KV, Hwu P, Park WS, Pham T, Ault DO, Glaser M, Liotta L, Detera-Wadleigh SD and Wadleigh RG (1999) Molecular cytogenetic finding of esophageal squamous cell carcinoma by comparative genomic hybridization reveals a consistent pattern of chromosomal alterations. Genes Chrom. Cancer 25(2), 160-168.
  • Park JG, Frucht H, LaRocca RV, Bliss DP Jr, Kurita Y, Chen TR, Henslee JG, Trepel JB, Jensen RT, Johnsen RT, Johnson BE, Bang YJ, Kim JP and Gazdar AF (1990) Characteristics of cell lines established from human gastric carcinoma. Cancer Res. 50(9), 2773-2780.
  • Petty EM, Kalikin LM, Orringer MB and Beer DG (1998) Distal chromosome 17q loss in Barrett’s esophageal and gastric cardia adenocarcinomas: implications for tumorigenesis. Mol. Carcinog. 22(4), 222-228.
  • Rao PH, Mathew S, Kelsen DP and Chaganti RS (1995) Cytogenetics of gastric and esophageal adenocarcinomas: 3q deletion as a possible primary chromosomal change. Cancer Genet. Cytogenet. 81(2), 139-143.
  • Rodriguez E, Rao PH, Ladanyi M, Altorki N, Albino AP, Kelsen DP, Jhanwar SC and Chaganti RS (1990) 11p13-15 is a specific region of chromosomal rearrangement in gastric and esophageal adenocarcinima. Cancer Res. 50(1), 6410-6416.
  • Rosenblum-Vos LS, Meltzer SJ, Leana-CoX J and Schwartz S (1993) Cytogentic studies of primary cultures of esophageal squamous cell carcinoma. Cancer Genet. Cytogent. 70(2), 127-131.
  • Rumpel CA, Powell SM and Moskaluk CA (1999) Mapping of genetic deletions on the long arm of chromosome 4 in human esophageal adenocarcinomas. Am. J. Pathol. 154(5), 129-1334.
  • Rygiel AM, Milano F, Ten Kate FJ, Schaap A, Wang KK, Peppelenbosch MP, Bergman JJ and Krishnadath KK (2008) Gains and amplifications of c-myc, EGFR, and 20.q13 loci in the no dysplasia-dysplasiaadenocarcinoma sequence of Barrett’s esophagus. Cancer Epidemiol. Biomarkers Prev. 17(6), 1380-1385.
  • Sakakura C, Mori T, Sakabe T, Ariyama Y, Shinomiya T, Date K, Hagiwara A, Yamaguchi T, Takahashi T, Nakamura Y, Abe T and Inazawa J (1999) gains, losses, and amplifications of genomic materials in primary gastric cancers analyzed by comparative genomic hybridization. Genes Chrom. Cancer. 24(4), 299-305.
  • Shimada M, Yanagisawa A, Kato Y, Inoue M, Shiozaki H, Monden M and Nakamura Y (1996) Genetic mechanisms in esophageal carcinogenesis: frequent deletion of 3p and 17p in premalignant lesions. Genes Chromosome Cancer. 15(3), 165-169.
  • Tarmin L, Yin J, Zhou X, Suzuki H, Jiang HY, RhyuMG, Abraham JM, Krasna MJ, Cottrel J and Meltzer SJ (1994) Frequent loss of heterozygosity on chromosome 9 in adenocarcinoma and squamous cell carcinoma of the esophagus. Cancer Res. 54(23), 6094-6096.
  • Tomioka N, Morita K, Kobayashi N, Tada M, Itoh T, Saitoh S, Kondo M, Takahashi N, Kataoka A, Nakanishi K, Takahashi M, Kamiyama T, Ozaki M, Hirano T and Todo S (2010) Array comparative genomic hybridization analysis revealed four genomic prognostic biomarkers for primary cancers. Cancer Genet. Cytogenet. 201(1), 6-14.
  • Van Dekken H, Geelen E, Dinjens WN, Winjnhoven BP, Tilanus HW, Tanke HJ and Rosenberg C (1999) Comparative genomic hybridization of cancer of the gastroesophageal junction: deletion of 14Q31-32.1 discriminates between esophageal (Barrett’s) and gastric cardia adenocarcinomas. Cancer Res. 59(3), 748-752.
  • Van der Riet-Fox MF, Reitief AE and Von Niekert WA (1979) Chromosome changes in 17 human neoplasms studied with banding. Cancer. 44, 2108-2119.
  • Wagata T, Ishizaki K, Imamura M, Shimada Y, Ikenaga M and Tobe T (1991) Deletion of 17p and amplification of the int-2 gene in esophageal carcinomas. Cancer Res. 51(8), 2113-2117.
  • Wang-Peng J, Banks-Schlegel SP and Lee EC (1990) Cytogenetic studies of esophageal carcinoma cell lines. Cancer Genet. Cytogenet. 45(1), 101-120.
  • Wu YP, Yang YL, Yang GZ, Wang XY, Luo ML, Zhang Y, Feng YB, Han X, Han YL, Cai Y, Zhan QM, Dong JT and Wang MR (2006) Identification of chromosome aberrations in esophageal cancer cell line KYSE180 by multicolour fluorescence in situ hybridization. Cancer Genet. Cytogent. 170(2), 102-107.
  • Wuu K-D, Cheng M, Wang - Woo S, Hu CP and Chang O (1986) Chromosome analysis on a cell line (CE48T/VGH) derived from a human esophageal carcinoma. Cancer Genet. Cytogenet. 20, 279-285.
  • Xiao S, Feng XL, Geng JS, Yan FC, Liu QZ and Li P (1991) Cytogenetic studies of five primary esophageal cancers. Cancer Genet. Cytogenet. 55(2), 197-205.
  • Yang L, Leung AC, Ko JM, Lo PH, Tang JC, Srivastava G, Oshimura M, Stanbridge EJ, Daigo Y, Nakamura Y, Tang CM, Lau KW, Law S and Lung ML (2005) Tumor suppressive role of a 2.4 Mb 9q33-q34 critical region and DEC1 in esophgeal squamous cell carcinoma. Oncogene. 24(4), 697-705.
  • Yang Y, Chu J, Wu Y, Luo M, Xu X, Han Y, Cai Y, Zhan Q and Wang M (2008) Chromosome analysis of esophageal squamous cell carcinoma cell line KYSE 410-4 by repetitive multicolor fluorescence in situ hybridization. J. Genet. Genomics. 35(1), 11-16.

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  • Cytogenetic Studies of Human Esophageal Squamous Cell Carcinoma and Gastric Adenocarcinoma Cell Lines

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Authors

Kimio Tanaka
Dept. of Radiobiology, Research Institute for Environmental Sciences, Hachazawa 2-121, Takahoko, Rokkasho, Kamikita, Aomori 039-3213, Japan
Naoki Hirabayashi
Department of Surgery, Research Institute for Radiation Biology and Medicine, Hiroshima University, Kasumi 1-1-1, Minami-ku, Hiroshima 734-8552, Japan

Abstract


Esophagus and gastric cancer are one of the most common in Asian countries, but molecular event in the carcinogenesis remains as largely unidentified associated oncogenes. Detailed karyotypic analyses were performed on 4 cell lines derived from malignant cells of a patient with esophagus carcinoma of both diagnosis and metastasis stages and 2 cell lines from 2 independent patients with gastric cancer of metastasis stages. Most of these cells examined were near triploid with modal chromosome number of 59-73. These cells had a complex karyotype with more than 10 rearrangements. The karyotypic pattern was relatively stable; consistent alterations involved long arm of chromosomes 2, 9 and 12 and short arm of chromosomes 3 in both diagnosis and metastasis stages in esophagus cell lines. Those alterations of gastric cancer involved chromosomes 7 and 11. Higher rearrangements associated with translocations and deletions were observed at 2q23 of chromosome2, 3p14 of chromosome 3, 4q11 of chromosome 4 and 11q25 of chromosome 11 in esophagus cancer; while 7p13 of chromosome 7 and 11p15 of chromosome 11 in gastric cancer. The overall chromosome pattern was not similar between these cancers, although these tumors arise from anatomically or biologically related site. Unknown oncogenes localizing on these chromosome breakpoints for translocation or deletion region might be associated with the pathogenesis of esophagus or gastric cancer. These newly established cell lines will be useful tools in the study of the molecular pathogenesis and for testing new therapeutic reagents for these cancers in the future.

Keywords


Esophagus Cancer, Gastric Adenocarcinoma, Karyotypic Analyses, Metastasis, Human Cell Line

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DOI: https://doi.org/10.17485/ijst%2F2011%2Fv4i5%2F30044