Journal of Clinical Pathology 2006;59:692-698
ORIGINAL ARTICLE
Relationship of p53, Bcl-2, Ki-67 index and E-cadherin expression in early invasive breast cancers with comedonecrosis as an accelerated apoptosis
1 Department of Clinical Pathology, Toyooka Hospital, Toyooka, Hyogo, Japan
2 First Department of Pathology, Kansai Medical University, Moriguchi, Osaka, Japan
Correspondence to:
Correspondence to:
Dr Susumu Ikehara
First Department of Pathology, Kansai Medical University, 1015 Fumizono-Cho, Moriguchi, Osaka 570-8506, Japan; ikehara{at}takii.kmu.ac.jp
Aims: To study the relationship between comedonecrosis formation and morphology, apoptosis, and p53, Bcl-2, Ki-67 index and E-cadherin expression in early invasive breast cancer.
Experimental design: Early invasive breast cancers were first divided into two groups according to the presence (CN+ tumours) or absence (CN tumours) of comedonecrosis. The histological grade, apoptosis, and expression of E-cadherin, Ki-67, p53 and Bcl-2 in the cancer-affected area, and in normal ducts from the specimen, were then examined.
Results: Less tubule and gland formation was seen in CN+ tumours than in CN tumours, although the histological grade between the groups was not different. During early comedonecrosis, cells undergo apoptosis and subsequent necrosis. p53 was higher in CN+ tumours than in CN tumours and normal ducts, whereas Bcl-2 was lower in CN+ tumours than in CN tumours and normal ducts. Both tumours had higher Ki-67 than in normal ducts, but no difference was evident between the tumours. CN+ tumours had slightly higher E-cadherin than that in CN tumours, but lower than that in normal ducts. The level of comedonecrosis was positively correlated with p53, but inversely correlated with Bcl-2 in all tumours, and p53 and Bcl-2 were inversely correlated with each other. Furthermore, comedonecrosis and p53 were correlated with Ki-67 in CN+ tumours, and Bcl-2 was correlated with Ki-67 in CN tumours.
Conclusion: Comedonecrosis may be actively regulated through an apoptotic procedure in massive cancers for their survival and progression, and the above proteins may be associated cooperatively in this process. CN+ and CN tumours may have opposite proliferative systems under the p53Bcl-2 pathway.
Abbreviations: HER2, human epidermal growth factor receptor 2; TUNEL, terminal deoxynucleotidyl transferase-mediated 2'-deoxyuridine 5'-triphosphate-biotin nick end-labelling; ssDNA, single-strand DNA
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
