Skip to main content
British Journal of Cancer logoLink to British Journal of Cancer
. 1999 Dec 8;82(1):65–73. doi: 10.1054/bjoc.1999.0878

Chromosomal alterations in the clonal evolution to the metastatic stage ofquamous cell carcinomas of the lung

S Petersen 1, M Aninat-Meyer 1, K Schlüns 1, K Gellert 2,2, M Dietel 1, I Petersen 1
PMCID: PMC2363206  PMID: 10638968

Abstract

Comparative genomic hybridization (CGH) was applied to squamous cellcarcinomas (SCC) of the lung to define chromosomal imbalances that are associated with the metastatic phenotype. In total, 64 lung SCC from 50 patients were investigated, 25 each with or without evidence of metastasis formation. The chromosomal imbalances summarized by a CGH histogram of the 50 cases revealed deletions most frequently on chromosomes 1p21–p31, 2q34–q36, 3p, 4p, 4q, 5q, 6q14–q24, 8p, 9p, 10q, 11p12–p14, 13q13–qter, 18q12–qter and 21q21. DNA over-representations were most pronounced for chromosomes 1q11–q25, 1q32–q41, 3q, 5p, 8q22–qter, 11q13, 12p, 17q21–q22, 17q24–q25, 19, 20q and 22q. In ten cases, paired samples of primaries and at least one metastasis were analysed. The comparison revealed a considerable chromosomal instability and genetic heterogeneity; however, the CGH pattern indicated a clonal relationship in each case. The difference in histograms from the metastatic and non-metastatic tumour groups was most useful in pinpointing chromosomal imbalances associated with the metastatic phenotype, indicating that the deletions at 3p12–p14, 3p21, 4p15–p16, 6q24–qter, 8p22–p23, 10q21–qter and 21q22, as well as the over-representations at 1q21–q25, 8q, 9q34, 14q12 and 15q12–q15, occurred significantly more often in the metastatic tumour group. The comparison of the paired samples confirmed these findings in individual cases and suggested distinct genetic changes, in particular the extension of small interstitial deletions, during tumour progression. Importantly, metastasis-associated lesions were frequently detectable in the primary tumour providing a method of identifying patients at risk for tumour dissemination. Individual profiles and histograms are accessible at our web site http://amba.charite.de/cgh. © 2000 Cancer Research Campaign

Keywords: lung cancer, tumor progression, CGH

Full Text

The Full Text of this article is available as a PDF (348.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Alers J. C., Krijtenburg P. J., Rosenberg C., Hop W. C., Verkerk A. M., Schröder F. H., van der Kwast T. H., Bosman F. T., van Dekken H. Interphase cytogenetics of prostatic tumor progression: specific chromosomal abnormalities are involved in metastasis to the bone. Lab Invest. 1997 Nov;77(5):437–448. [PubMed] [Google Scholar]
  2. Bockmühl U., Petersen S., Schmidt S., Wolf G., Jahnke V., Dietel M., Petersen I. Patterns of chromosomal alterations in metastasizing and nonmetastasizing primary head and neck carcinomas. Cancer Res. 1997 Dec 1;57(23):5213–5216. [PubMed] [Google Scholar]
  3. Brison O. Gene amplification and tumor progression. Biochim Biophys Acta. 1993 May 25;1155(1):25–41. doi: 10.1016/0304-419x(93)90020-d. [DOI] [PubMed] [Google Scholar]
  4. Gronwald J., Störkel S., Holtgreve-Grez H., Hadaczek P., Brinkschmidt C., Jauch A., Lubinski J., Cremer T. Comparison of DNA gains and losses in primary renal clear cell carcinomas and metastatic sites: importance of 1q and 3p copy number changes in metastatic events. Cancer Res. 1997 Feb 1;57(3):481–487. [PubMed] [Google Scholar]
  5. Hung J., Kishimoto Y., Sugio K., Virmani A., McIntire D. D., Minna J. D., Gazdar A. F. Allele-specific chromosome 3p deletions occur at an early stage in the pathogenesis of lung carcinoma. JAMA. 1995 Feb 15;273(7):558–563. [PubMed] [Google Scholar]
  6. Ichikawa T., Nihei N., Kuramochi H., Kawana Y., Killary A. M., Rinker-SchaefferCW, Barrett J. C., Isaacs J. T., Kugoh H., Oshimura M. Metastasis suppressor genes for prostate cancer. Prostate Suppl. 1996;6:31–35. [PubMed] [Google Scholar]
  7. Isola J., DeVries S., Chu L., Ghazvini S., Waldman F. Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples. Am J Pathol. 1994 Dec;145(6):1301–1308. [PMC free article] [PubMed] [Google Scholar]
  8. Joos S., Bergerheim U. S., Pan Y., Matsuyama H., Bentz M., du Manoir S., Lichter P. Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization. Genes Chromosomes Cancer. 1995 Dec;14(4):267–276. doi: 10.1002/gcc.2870140405. [DOI] [PubMed] [Google Scholar]
  9. Kirchhoff M., Gerdes T., Rose H., Maahr J., Ottesen A. M., Lundsteen C. Detection of chromosomal gains and losses in comparative genomic hybridization analysis based on standard reference intervals. Cytometry. 1998 Mar 1;31(3):163–173. [PubMed] [Google Scholar]
  10. Kohno T., Kawanishi M., Matsuda S., Ichikawa H., Takada M., Ohki M., Yamamoto T., Yokota J. Homozygous deletion and frequent allelic loss of the 21q11.1-q21.1 region including the ANA gene in human lung carcinoma. Genes Chromosomes Cancer. 1998 Mar;21(3):236–243. doi: 10.1002/(sici)1098-2264(199803)21:3<236::aid-gcc8>3.0.co;2-0. [DOI] [PubMed] [Google Scholar]
  11. Kuukasjärvi T., Karhu R., Tanner M., Kähkönen M., Schäffer A., Nupponen N., Pennanen S., Kallioniemi A., Kallioniemi O. P., Isola J. Genetic heterogeneity and clonal evolution underlying development of asynchronous metastasis in human breast cancer. Cancer Res. 1997 Apr 15;57(8):1597–1604. [PubMed] [Google Scholar]
  12. Levin N. A., Brzoska P. M., Warnock M. L., Gray J. W., Christman M. F. Identification of novel regions of altered DNA copy number in small cell lung tumors. Genes Chromosomes Cancer. 1995 Jul;13(3):175–185. doi: 10.1002/gcc.2870130307. [DOI] [PubMed] [Google Scholar]
  13. Levin N. A., Brzoska P., Gupta N., Minna J. D., Gray J. W., Christman M. F. Identification of frequent novel genetic alterations in small cell lung carcinoma. Cancer Res. 1994 Oct 1;54(19):5086–5091. [PubMed] [Google Scholar]
  14. Moore D. H., 2nd, Pallavicini M., Cher M. L., Gray J. W. A t-statistic for objective interpretation of comparative genomic hybridization (CGH) profiles. Cytometry. 1997 Jul 1;28(3):183–190. doi: 10.1002/(sici)1097-0320(19970701)28:3<183::aid-cyto1>3.0.co;2-f. [DOI] [PubMed] [Google Scholar]
  15. Paredes-Zaglul A., Kang J. J., Essig Y. P., Mao W., Irby R., Wloch M., Yeatman T. J. Analysis of colorectal cancer by comparative genomic hybridization: evidence for induction of the metastatic phenotype by loss of tumor suppressor genes. Clin Cancer Res. 1998 Apr;4(4):879–886. [PubMed] [Google Scholar]
  16. Petersen I., Bujard M., Petersen S., Wolf G., Goeze A., Schwendel A., Langreck H., Gellert K., Reichel M., Just K. Patterns of chromosomal imbalances in adenocarcinoma and squamous cell carcinoma of the lung. Cancer Res. 1997 Jun 15;57(12):2331–2335. [PubMed] [Google Scholar]
  17. Petersen I., Langreck H., Wolf G., Schwendel A., Psille R., Vogt P., Reichel M. B., Ried T., Dietel M. Small-cell lung cancer is characterized by a high incidence of deletions on chromosomes 3p, 4q, 5q, 10q, 13q and 17p. Br J Cancer. 1997;75(1):79–86. doi: 10.1038/bjc.1997.13. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Petersen S., Rudolf J., Bockmühl U., Gellert K., Wolf G., Dietel M., Petersen I. Distinct regions of allelic imbalance on chromosome 10q22-q26 in squamous cell carcinomas of the lung. Oncogene. 1998 Jul 30;17(4):449–454. doi: 10.1038/sj.onc.1201949. [DOI] [PubMed] [Google Scholar]
  19. Petersen S., Wolf G., Bockmühl U., Gellert K., Dietel M., Petersen I. Allelic loss on chromosome 10q in human lung cancer: association with tumour progression and metastatic phenotype. Br J Cancer. 1998;77(2):270–276. doi: 10.1038/bjc.1998.43. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Pisani P., Parkin D. M., Ferlay J. Estimates of the worldwide mortality from eighteen major cancers in 1985. Implications for prevention and projections of future burden. Int J Cancer. 1993 Dec 2;55(6):891–903. doi: 10.1002/ijc.2910550604. [DOI] [PubMed] [Google Scholar]
  21. Ried T., Petersen I., Holtgreve-Grez H., Speicher M. R., Schröck E., du Manoir S., Cremer T. Mapping of multiple DNA gains and losses in primary small cell lung carcinomas by comparative genomic hybridization. Cancer Res. 1994 Apr 1;54(7):1801–1806. [PubMed] [Google Scholar]
  22. Roth K., Wolf G., Dietel M., Petersen I. Image analysis for comparative genomic hybridization based on a karyotyping program for windows. Anal Quant Cytol Histol. 1997 Dec;19(6):461–474. [PubMed] [Google Scholar]
  23. Schwendel A., Langreck H., Reichel M., Schröck E., Ried T., Dietel M., Petersen I. Primary small-cell lung carcinomas and their metastases are characterized by a recurrent pattern of genetic alterations. Int J Cancer. 1997 Feb 20;74(1):86–93. doi: 10.1002/(sici)1097-0215(19970220)74:1<86::aid-ijc15>3.0.co;2-g. [DOI] [PubMed] [Google Scholar]
  24. Sekido Y., Fong K. M., Minna J. D. Progress in understanding the molecular pathogenesis of human lung cancer. Biochim Biophys Acta. 1998 Aug 19;1378(1):F21–F59. doi: 10.1016/s0304-419x(98)00010-9. [DOI] [PubMed] [Google Scholar]
  25. Tarkkanen M., Karhu R., Kallioniemi A., Elomaa I., Kivioja A. H., Nevalainen J., Böhling T., Karaharju E., Hyytinen E., Knuutila S. Gains and losses of DNA sequences in osteosarcomas by comparative genomic hybridization. Cancer Res. 1995 Mar 15;55(6):1334–1338. [PubMed] [Google Scholar]
  26. Welch D. R., Chen P., Miele M. E., McGary C. T., Bower J. M., Stanbridge E. J., Weissman B. E. Microcell-mediated transfer of chromosome 6 into metastatic human C8161 melanoma cells suppresses metastasis but does not inhibit tumorigenicity. Oncogene. 1994 Jan;9(1):255–262. [PubMed] [Google Scholar]
  27. Wick W., Petersen I., Schmutzler R. K., Wolfarth B., Lenartz D., Bierhoff E., Hümmerich J., Müller D. J., Stangl A. P., Schramm J. Evidence for a novel tumor suppressor gene on chromosome 15 associated with progression to a metastatic stage in breast cancer. Oncogene. 1996 Mar 7;12(5):973–978. [PubMed] [Google Scholar]
  28. Wu C. L., Roz L., Sloan P., Read A. P., Holland S., Porter S., Scully C., Speight P. M., Thakker N. Deletion mapping defines three discrete areas of allelic imbalance on chromosome arm 8p in oral and oropharyngeal squamous cell carcinomas. Genes Chromosomes Cancer. 1997 Dec;20(4):347–353. doi: 10.1002/(sici)1098-2264(199712)20:4<347::aid-gcc5>3.0.co;2-1. [DOI] [PubMed] [Google Scholar]

Articles from British Journal of Cancer are provided here courtesy of Cancer Research UK

RESOURCES