Skip to main content
  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

AACR logo

  • Register
  • Log in
  • My Cart
Advertisement

Main menu

  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
    • CME
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CCR Focus Archive
    • Meeting Abstracts
    • Collections
      • COVID-19 & Cancer Resource Center
      • Breast Cancer
      • Clinical Trials
      • Immunotherapy: Facts and Hopes
      • Editors' Picks
      • "Best of" Collection
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • Editors' Picks
    • OnlineFirst
    • Citation
    • Author/Keyword
    • RSS Feeds
    • My Alert Summary & Preferences
  • News
    • Cancer Discovery News
  • COVID-19
  • Webinars
  • Search More

    Advanced Search

  • AACR Publications
    • Blood Cancer Discovery
    • Cancer Discovery
    • Cancer Epidemiology, Biomarkers & Prevention
    • Cancer Immunology Research
    • Cancer Prevention Research
    • Cancer Research
    • Clinical Cancer Research
    • Molecular Cancer Research
    • Molecular Cancer Therapeutics

User menu

  • Register
  • Log in
  • My Cart

Search

  • Advanced search
Clinical Cancer Research
Clinical Cancer Research
  • Home
  • About
    • The Journal
    • AACR Journals
    • Subscriptions
    • Permissions and Reprints
    • Reviewing
    • CME
  • Articles
    • OnlineFirst
    • Current Issue
    • Past Issues
    • CCR Focus Archive
    • Meeting Abstracts
    • Collections
      • COVID-19 & Cancer Resource Center
      • Breast Cancer
      • Clinical Trials
      • Immunotherapy: Facts and Hopes
      • Editors' Picks
      • "Best of" Collection
  • For Authors
    • Information for Authors
    • Author Services
    • Best of: Author Profiles
    • Submit
  • Alerts
    • Table of Contents
    • Editors' Picks
    • OnlineFirst
    • Citation
    • Author/Keyword
    • RSS Feeds
    • My Alert Summary & Preferences
  • News
    • Cancer Discovery News
  • COVID-19
  • Webinars
  • Search More

    Advanced Search

Regular Articles

Reduced Nuclear Expression of Transcription Factor AP-2 Associates with Aggressive Breast Cancer

Johanna Pellikainen, Vesa Kataja, Kirsi Ropponen, Jari Kellokoski, Timo Pietiläinen, Jan Böhm, Matti Eskelinen and Veli-Matti Kosma
Johanna Pellikainen
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Vesa Kataja
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Kirsi Ropponen
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jari Kellokoski
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Timo Pietiläinen
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jan Böhm
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Matti Eskelinen
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Veli-Matti Kosma
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
DOI:  Published November 2002
  • Article
  • Figures & Data
  • Info & Metrics
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • Fig. 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 1.

    A, ductal carcinoma, grade I. Nuclear staining (arrow). B, strong nuclear (arrows) AP-2 staining in ductal carcinoma, grade II. C, ductal carcinoma, grade III. Nuclear (arrow) and cytoplasmic (asterisk) expressions. D, cytoplasmic expression (asterisk) with a few positive nuclei in ductal carcinoma, grade III. E1–E2, lobular carcinoma, nuclear staining. F1–F2, negative control slides of samples B and C, respectively. A–D, E2–F2: bar, 40 μm; E1: bar, 80 μm.

  • Fig. 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 2.

    Western blot analysis for AP-2. Four representative AP-2-positive tumor samples (T) and one benign AP-2 positive breast sample (N) were included in the analysis. All of the samples showed a band Mr about 50,000, which is the same as given for AP-2α. Trial Mix Protein marker (M) was used as a size marker. kDa, Mr in thousands.

  • Fig. 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 3.

    The P of RFS according to nuclear AP-2 expression (median as a cutoff value). A, in all of the patients; B, in the lymph node-positive patients.

  • Fig. 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Fig. 4.

    Probability of RFS according to combined (nuclear/cytoplasmic) expression of AP-2. The group “nuclear” contains those patients with high nuclear AP-2 expression without cytoplasmic involvement. The group titled as “others” contains all of the patients with low nuclear AP-2 expression and those with positive cytoplasmic staining. A, all of the patients; B, the lymph node-positive patients.

Tables

  • Figures
  • Table 1

    The clinicopathological data of the patients

    Characteristicn%
    No. of patients420100
    Age, yr
     Mean (range)59.1 (23.3–91.6)
    Tumor size
     T121852
     T216840
     T3246
     T4102
    Lymph node status
     Negative24458
     Positive16840
     Unknown82
    Stage
     I16038
     II21351
     III399
     Unknown82
    Histological type
     Ductal27064
     Lobular6816
     Other8220
    Histological grade
     I11026
     II19246
     III11828
    ER status
     Positive32678
     Negative9322
     Data not available1<1
    PR status
     Positive26162
     Negative15737
     Data not available21
    Menopausal status
     Premenopausal13131
     Postmenopausal28969
    Recurrence at 5 yr
     No34482
     Yes7618
    Cause of death at 5 yr
     Alive33379
     Breast cancer5012
     Other379
  • Table 2

    Relationships between nuclear AP-2 expression and clinicopathological variables

    VariableSample nAP-2 expression (%)χ2dfP
    LowaHigha
    Stage41212.420.002
     I1603961
     II2135743
     III395941
    Lymph node status4126.410.012
     Negative2444555
     Positive1685842
    Histological type4206.120.048
     Ductal2705248
     Lobular683763
     Other825545
    Histological grade42014.120.001
     I1103961
     II1924852
     III1186436
    ER-status419<0.110.927
     Positive3265050
     Negative935149
    PR-status418<0.110.860
     Positive2615149
     Negative1575050
    Recurrence at 5 yr4209.010.003
     No3444753
     Yes766634
    • a Median as a cutoff value.

  • Table 3

    Statistically significant variables of BCRS and RFS in univariate analysis

    VariableSurviving breast cancer at 5 yearsRecurrence-free at 5 yr
    n%Pn%P
    Stage412<0.0001412<0.0001
     I1609216086
     II2138621377
     III39553955
    Lymph node status412<0.0001412<0.0001
     Negative2449224486
     Positive1687716868
    Histological grade4200.03144200.0498
     I1109211085
     II1928519278
     III1188011873
    ER status419<0.00014190.0910
     Positive3268932680
     Negative93719374
    PR status4180.00124180.1884
     Positive2618926180
     Negative1577815776
    Nuclear AP-24200.09644200.0028
     Low < 80%2118321173
     High ≥ 80%2098820985
  • Table 4

    Results of Cox’s multivariate analysis for BCRS and RFS

    Category (variable)β (SE)Relative risk (95% CI)aP
    BCRS
     Stage<0.0001
      IReference
      II0.88 (0.41)2.41 (1.08–5.39)0.0323
      III2.25 (0.45)9.45 (3.92–22.77)<0.0001
     ER status
      Negative0.87 (0.41)2.39 (1.08–5.32)0.0321
      PositiveReference
    RFS
     Stage0.0001
      IReference
      II0.56 (0.29)1.74 (0.99–3.08)0.0560
      III1.53 (0.36)4.60 (2.26–9.37)<0.0001
     Nuclear AP-2
      Low < 80%0.54 (0.25)1.71 (1.06–2.78)0.0292
      High ≥ 80%Reference
    RFS in the lymph node-positive patients
     Stage
      IIReference
      III0.78 (0.31)2.17 (1.19–3.95)0.0110
     Nuclear AP-2
      Low < 80%0.79 (0.32)2.20 (1.16–4.14)0.0151
      High ≥ 80%Reference
    • a CI, confidence interval.

PreviousNext
Back to top
November 2002
Volume 8, Issue 11
  • Table of Contents

Sign up for alerts

View this article with LENS

Open full page PDF
Article Alerts
Sign In to Email Alerts with your Email Address
Email Article

Thank you for sharing this Clinical Cancer Research article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Reduced Nuclear Expression of Transcription Factor AP-2 Associates with Aggressive Breast Cancer
(Your Name) has forwarded a page to you from Clinical Cancer Research
(Your Name) thought you would be interested in this article in Clinical Cancer Research.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Citation Tools
Reduced Nuclear Expression of Transcription Factor AP-2 Associates with Aggressive Breast Cancer
Johanna Pellikainen, Vesa Kataja, Kirsi Ropponen, Jari Kellokoski, Timo Pietiläinen, Jan Böhm, Matti Eskelinen and Veli-Matti Kosma
Clin Cancer Res November 1 2002 (8) (11) 3487-3495;

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Share
Reduced Nuclear Expression of Transcription Factor AP-2 Associates with Aggressive Breast Cancer
Johanna Pellikainen, Vesa Kataja, Kirsi Ropponen, Jari Kellokoski, Timo Pietiläinen, Jan Böhm, Matti Eskelinen and Veli-Matti Kosma
Clin Cancer Res November 1 2002 (8) (11) 3487-3495;
del.icio.us logo Digg logo Reddit logo Twitter logo CiteULike logo Facebook logo Google logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • INTRODUCTION
    • PATIENTS AND METHODS
    • RESULTS
    • DISCUSSION
    • Acknowledgments
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • PDF
Advertisement

Related Articles

Cited By...

More in this TOC Section

Regular Articles

  • Lactoferrin Down-Regulates G1 Cyclin-Dependent Kinases during Growth Arrest of Head and Neck Cancer Cells
  • ZD6474, a Potent Inhibitor of Vascular Endothelial Growth Factor Signaling, Combined With Radiotherapy
  • Oral Silibinin Inhibits Lung Tumor Growth in Athymic Nude Mice and Forms a Novel Chemocombination with Doxorubicin Targeting Nuclear Factor κB–Mediated Inducible Chemoresistance
Show more Regular Articles

Molecular Oncology, Markers, Clinical Correlates

  • Prognostic Impact of Hypoxia-Inducible Factors 1α and 2α in Colorectal Cancer Patients
  • Loss of Heterozygosity and Immunohistochemistry of Adenocarcinomas of the Esophagus and Gastric Cardia
  • Impact of Vascular Endothelial Growth Factor-C and -D Expression in Human Pancreatic Cancer
Show more Molecular Oncology, Markers, Clinical Correlates
  • Home
  • Alerts
  • Feedback
  • Privacy Policy
Facebook  Twitter  LinkedIn  YouTube  RSS

Articles

  • Online First
  • Current Issue
  • Past Issues
  • CCR Focus Archive
  • Meeting Abstracts

Info for

  • Authors
  • Subscribers
  • Advertisers
  • Librarians

About Clinical Cancer Research

  • About the Journal
  • Editorial Board
  • Permissions
  • Submit a Manuscript
AACR logo

Copyright © 2021 by the American Association for Cancer Research.

Clinical Cancer Research
eISSN: 1557-3265
ISSN: 1078-0432

Advertisement