Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1993;423(1):51-5.
doi: 10.1007/BF01606432.

Immunocytochemical detection of DNA topoisomerase type II in primary breast carcinomas: correlation with clinico-pathological features

Affiliations

Immunocytochemical detection of DNA topoisomerase type II in primary breast carcinomas: correlation with clinico-pathological features

G Tuccari et al. Virchows Arch A Pathol Anat Histopathol. 1993.

Abstract

DNA topoisomerase type II (DT-II) is a major component of interphase nuclear matrix fractions, present in S-phase of the cell cycle. A series of 80 carcinomatous breast surgical samples was evaluated by immunohistochemistry, using a polyclonal antibody in a comparison with Ki-67 antiserum. A correlation with clinico-pathological data was also performed. Infiltrating ductal and lobular carcinomas constantly express DT-II with varying intensity of nuclear staining; a similar immunohistochemical pattern is observed with Ki-67. A frequent co-expression of DT-II and Ki-67 is encountered with double immunostaining; accordingly to these data, a linear relationship is evident when linear regression is employed. In addition, significant relationships between DT-II values and tumour size, histological grade and node involvement are shown, while an inverse correlation is appreciable between DT-II and oestrogen receptors and progesterone receptors. DT-II may be considered to be an additional operational marker for the proliferating fraction of cells in breast carcinomas.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Cancer Res. 1989 Mar 1;49(5):1118-24 - PubMed
    1. Proc Natl Acad Sci U S A. 1985 Jun;82(12):4142-6 - PubMed
    1. Annu Rev Biochem. 1989;58:351-75 - PubMed
    1. Biochemistry. 1986 Apr 22;25(8):2248-56 - PubMed
    1. EMBO J. 1982;1(11):1353-8 - PubMed

MeSH terms

LinkOut - more resources