Skip to main content
Log in

Karyotype pecularities of human colorectal adenocarcinomas

  • Original investigations
  • Published:
Human Genetics Aims and scope Submit manuscript

Summary

The data of the chromosome abnormalities in 15 colorectal tumors are presented. Rearrangements of the short arm of chromosome 17, leading to deletions of this arm or its part were noted in 12 tumors; in 2 other cases, one of the homologs of pair 17 was lost. The losses of at least one homolog of other chromosomal pairs were also found: chromosome 18, in 12 out of 13 cases with fully identified numerical abnormalities; chromosome 5, in 6 tumors; chromosome 21, in 5 cases; chromosomes 4, 15, and 22, in 4 cases each. Additional homologs of pair 20 were observed in 6 tumors, extra 8q was found in 5 tumors, and extra 13q in 6 cases. Rearrangements of the short arm of chromosome 1 and the long arm of chromosome 11 characterized 6 tumors each. The data recorded in our series differ from the data of other authors in two respects: the high incidence of the loss of sex chromosomes and the rearrangements of the long arm of chromosome 9. X chromosomes were missing in 4 out of 7 tumors in females, and Y chromosomes were absent in 5 out of 8 tumors in males. The long arm of chromosome 9 was rearranged in 8 cases, in 5 of them the breakpoint being at 9q22. Cytological manifestations of gene amplification (double minutes or multiple microchromosomes) were noted in 6 tumors.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Atkin NB, Baker MC (1989) Chromosome 17p loss in carcinoma of the cervix uteri. Cancer Genet Cytogenet 37:229–233

    Google Scholar 

  • Baker SJ, Fearon ER, Nigro JM, Hamilton SR, Preisinger AC, Jessap JM, Tuinen P van, Ledbetter DH, Baker DF, Nakamura Y, White R, Vogelstein B (1989) Chromosome 17p deletions and p53 gene mutations in colorectal carcinomas. Science 244:217–221

    Google Scholar 

  • Bale SJ, Dracopoli NC, Tucker MA, Clark WH, Fraser MC, Stanger BZ, Green P, Donis-Keller P, Housman DE, Greene MH (1989) Mapping the gene for hereditary cutaneous malignant melanoma — dysplastic nevus to chromosome 1p. N Engl J Med 320:1367–1372

    Google Scholar 

  • Bodmer WT, Bailey CJ, Bodmer J, Bussey HJ, Ellis A, Gorman P, Lucibello FC, Murday VA, Rider SH, Scambler P, Sheer D, Solomon E, Spurr NK (1987) Localization of the gene for familial adenomatous polyposis on chromosome 5. Nature 328:614–616

    Google Scholar 

  • Chumakov PM, Fleischman EW, Kopnin BP, Jenkins JR (1991) p53 gene is not necessary mutated in human colorectal carcinomas with 17p chromosomal abnormalities. Proc Natl Acad Sci USA 88 (submitted)

  • Couturier-Turpin MH, Couturier D, Nepveux P, Louvel A, Chapuis Y, Guerre J (1982) Human chromosome analysis in 24 cases of primary carcinoma of the large intestine: contribution of the G-banding technique. Br J Cancer 46:856–869

    Google Scholar 

  • Croce CM (1987) Role of chromosome translocations in human neoplasia. Cell 49:155–156

    Google Scholar 

  • Dracopoli NC, Marnett P, Bale SJ, Stanger BZ, Tucker MA, Housman DE, Kefford KF (1989) Loss of alleles from the distal short arm of chromosome 1 occurs late in melanoma tumor progression. Proc Natl Acad Sci USA 86:4614–4618

    Google Scholar 

  • Erisman MD, Litwin S, Keidan RD, Comis RL, Astrin SM (1988) Non correlation of the expression of the c-myc oncogene in colorectal carcinomas with recurrence of disease or patient survival. Cancer Res 48:1350–1355

    Google Scholar 

  • Erisman MD, Scott JK, Astrin SM (1989) Evidence that the familial adenomatous polyposis gene is involved in a subset of colon cancers with a complementable defect in c-myc regulation. Proc Natl Acad Sci USA 86:4264–4268

    Google Scholar 

  • Fearon ER, Hamilton SR, Vogelstein B (1987) Clonal analysis of human colorectal tumors. Science 238:193–197

    Google Scholar 

  • Ferti AD, Panani AD, Raptis S (1988) Cytogenetic study of rectosigmoidal adenocarcinomas. Cancer Genet Cytogenet 34:101–109

    Google Scholar 

  • Fitzgerald PH, Morris CM (1989) The variable hematologic expression of the BCR/ABL genomic mutation and its possible determinants. Cancer Genet Cytogenet 42:9–25

    Google Scholar 

  • Fong C, Dracopoli NC, White PS, Merril PT, Griffith RC, Housman DE, Brodeur GM (1989) Loss of heterozygosity for the short arm of chromosome 1 in human neuroblastomas: correlation with N-myc amplification. Proc Natl Acad Sci USA 86:3753–3757

    Google Scholar 

  • Goyns MH, Hann JM, Stewart J, Gegonne A, Birnie GD (1987) The c-ets-1 proto-oncogene is rearranged in some cases of acute lymphoblastic leukemia. Br J Cancer 56:611–613

    Google Scholar 

  • Hinrichs SH, Jaramillo MA, Gumerlock PH, Garden MB, Lewis IP, Freeman AE (1985) Myxoid chondrosarcoma with a translocation involving chromosomes 9 and 22. Cancer Genet Cytogenet 14:219–226

    Google Scholar 

  • Klein G (1988) Oncogenes and tumor supressor genes. Acta Oncol 27:427–437

    Google Scholar 

  • Klein G (1989) Multiple phenotypic consequences of the Ig/Myc translocation in B-cell derived tumors. Genes Chromosomes Cancer 1:3–8

    Google Scholar 

  • Lathe RA, Nakamura Y, Woodward S, Gedde-Dahl T, White R (1988) VNTR (variable number of tandem repeats) markers show loss of chromosome 17p sequences in human colorectal carcinomas. Cytogenet Cell Genet 48:167–169

    Google Scholar 

  • Levine AJ (1990) Tumor supressor genes. Bioessays 12:60–66

    Google Scholar 

  • Martin P, Levin B, Golomb HM, Riddel RH (1979) Chromosome analysis of primary large bowel tumors: a new method for improving the yield of analyzable metaphases. Cancer 44:1656–1664

    Google Scholar 

  • Mitelman F (1985) Catalog of chromosome aberration in cancer, 2nd edn. Liss, New York

    Google Scholar 

  • Monpezant J-P, Delattre O, Bernard A, Grunwald D, Remvicos Y, Muleris M, Salmon RJ, Frelat G, Dutrillaux B, Thomas G (1988) Loss of the alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas. Int J Cancer 41:404–408

    Google Scholar 

  • Muleris M, Salmon RJ, Zafrani B, Girodet J, Dutrillaux B (1985) Consistent deficiences of chromosome 18 and of the short arm of chromosome 17 in eleven cases of human large bowel cancer: a possible recessive determinism. Ann Génét (Paris) 28:206–213

    Google Scholar 

  • Muleris M, Salmon RJ, Girodet J, Zafrani B, Dutrillaux B (1987a) Recurrent deletions of chromosomes 11q and 3p in anal canal carcinoma. Int J Cancer 39:595–598

    Google Scholar 

  • Muleris M, Salmon RJ, Dutrillaux B (1987b) Characteristic chromosomal pattern in colorectal carcinoma. 2nd International Workshop on Chromosomes in Solid Tumors, Tucson, Arizona, 1987. Cancer Genet Cytogenet 29:34

    Google Scholar 

  • Muleris M, Salmon RJ, Dutrillaux B (1988) Existence of two distinct processes of chromosomal evolution in near-diploid colorectal tumors. Cancer Genet Cytogenet 32:43–50

    Google Scholar 

  • Reichman A, Riddel RH, Martin P, Levin B (1980) Double minutes in human large bowel cancer. Gastroenterology 79:334–339

    Google Scholar 

  • Reichman A, Martin P, Levin B (1981) Chromosomal banding patterns in human large bowel cancer. Int J Cancer 28:431–440

    Google Scholar 

  • Reichman A, Martin P, Levin B (1984) Chromosomes in human large bowel tumors. A study of chromosome 1. Cancer Genet Cytogenet 12:295–301

    Google Scholar 

  • Reichman A, Martin P, Levin B (1985) Marker chromosomes in direct preparations of human large bowel tumors. Cancer Genet Cytogenet 16:229–233

    Google Scholar 

  • Rovigatti U, Watson DK, Yunis YY (1986) Amplification and rearrangement of Hu-ets-1 in leukemia and lymphoma with involvement of 11q23. Science 232:398–400

    Google Scholar 

  • Sandberg AA (1980) The chromosomes in human cancer and leukemia. Elsevier, New York Amsterdam

    Google Scholar 

  • Solomon E, Voss R, Hall V, Bodmer WF, Yass Y-R, Jeffreys AJ, Lucibello FC, Patel I, Rider SH (1987) Chromosome 5 allele loss in human colorectal carcinomas. Nature 328:616–619

    Google Scholar 

  • Sreekantaiah C, Baer MR, Preisler HD, Sandberg AA (1989) Involvement of bands 9q21–22 in five cases of acute nonlymphocytic leukemia. Cancer Genet Cytogenet 39:55–64

    Google Scholar 

  • Tal M, Wetzler M, Josefberg Z, Deutch A, Gutman M, Assaf D, Kris R, Shiloh Y, Givol D, Sclessinger J (1985) Sporadic amplification of the HER2/neu protooncogene in adenocarcinomas of various tissues. Cancer Res 48:1517–1520

    Google Scholar 

  • Untwale S, Blick M, Pathak S (1987) Karyotype and molecular analysis of colon cancer. 2nd International Workshop on Chromosomes in Solid Tumors, Tucson, Arizona, 1987. Cancer Genet Cytogenet 28:34

    Google Scholar 

  • Vogelstein B, Fearon ER, Hamilton SR, Kern SE, Preisinger AC, Lepher M, Nakamura Y, White R, Smits AM, Boss JL (1988) Genetic alterations during colorectal tumor development. N Engl J Med 319:525–532

    CAS  PubMed  Google Scholar 

  • Vogelstein B, Fearon ER, Kern SE, Hamilton SR, Preisinger AC, Nakamura Y, White R (1989) Allelotype of colorectal carcinomas. Science 244:207–211

    Google Scholar 

  • Yokota J, Tsunetsugu-Yokota Y, Battifora H, LeFevre C, Cline MJ (1986) Alterations of myc, myb, and ras-HA proto-on-cogenes in cancers are frequent and show clinical correlation. Science 231:261–265

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Konstantinova, L.N., Fleischman, E.W., Knisch, V.I. et al. Karyotype pecularities of human colorectal adenocarcinomas. Hum Genet 86, 491–496 (1991). https://doi.org/10.1007/BF00194640

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00194640

Keywords

Navigation