Literature DB >> 2545806

Do aggressive subclones within primary colorectal cancer give rise to liver metastases?

J R Jass1, K Mukawa, P I Richman, P A Hall.   

Abstract

Primary colorectal cancers and hepatic metastases from 24 patients have been compared according to type, grade, DNA content as measured by flow cytometry, and expression of two differentiation antigens and carcinoembryonic antigen (CEA). The primary and secondary tumours were histologically indistinguishable in 23 out of 24 cases. DNA content differed between primary and metastasis in only six cases. Immunohistochemical profiles were usually the same in the primary and metastasis. In particular, heterogeneous expression by the primary was mirrored in the metastasis. In 17 out of 24 (70.1%) patients the primary and metastasis were indistinguishable by all six parameters. In one of these, the liver metastasis had been removed 14 years 10 months after the primary tumour. It is concluded that DNA content as measured by flow cytometry may remain stable for long periods and that the differences shown in this study may simply be due to inadequate sampling of the primary tumour. Phenotypic heterogeneity may be epigenetic and not indicative of genetic instability and cannot be used to track the progression of subclones.

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Year:  1989        PMID: 2545806     DOI: 10.1007/BF01646869

Source DB:  PubMed          Journal:  Int J Colorectal Dis        ISSN: 0179-1958            Impact factor:   2.571


  40 in total

1.  Existence of two distinct processes of chromosomal evolution in near-diploid colorectal tumors.

Authors:  M Muleris; R J Salmon; B Dutrillaux
Journal:  Cancer Genet Cytogenet       Date:  1988-05

2.  Value of flow cytometric determination of ploidy as a guide to prognosis in operable rectal cancer: a multivariate analysis.

Authors:  H S Goh; J R Jass; W S Atkin; J Cuzick; J M Northover
Journal:  Int J Colorectal Dis       Date:  1987-02       Impact factor: 2.571

Review 3.  The implications of tumor heterogeneity for studies on the biology of cancer metastasis.

Authors:  I R Hart; I J Fidler
Journal:  Biochim Biophys Acta       Date:  1981-08-31

4.  The selection and characterization of an invasive variant of the B16 melanoma.

Authors:  I R Hart
Journal:  Am J Pathol       Date:  1979-12       Impact factor: 4.307

5.  Differences in lectin reactivities of cellular glycoconjugates between primary human colorectal carcinomas and their metastases.

Authors:  I H Kellokumpu
Journal:  Cancer Res       Date:  1986-09       Impact factor: 12.701

6.  Prognostic significance of DNA aneuploidy and cell proliferation in rectal adenocarcinomas.

Authors:  P Quirke; M F Dixon; A D Clayden; P Durdey; J E Dyson; N S Williams; C C Bird
Journal:  J Pathol       Date:  1987-04       Impact factor: 7.996

7.  Plasma carcinoembryonic antigen concentrations and immunohistochemical patterns of epithelial marker antigens in patients with large bowel carcinoma.

Authors:  T Rognum; K Elgjo; P Brandtzaeg; H Orjasaeter; A Bergan
Journal:  J Clin Pathol       Date:  1982-09       Impact factor: 3.411

8.  Increasing metastatic potential is associated with increasing genetic instability of clones isolated from murine neoplasms.

Authors:  M A Cifone; I J Fidler
Journal:  Proc Natl Acad Sci U S A       Date:  1981-11       Impact factor: 11.205

9.  Do metastases arise from pre-existing subpopulations of cancer cells?

Authors:  L Weiss; J C Holmes; P M Ward
Journal:  Br J Cancer       Date:  1983-01       Impact factor: 7.640

10.  Murine melanoma: a model for intracranial metastasis.

Authors:  A Raz; I R Hart
Journal:  Br J Cancer       Date:  1980-08       Impact factor: 7.640

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  1 in total

1.  Current concepts in metastasis.

Authors:  J R Jass
Journal:  Gut       Date:  1995-01       Impact factor: 23.059

  1 in total

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