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PMID: 19502809 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Stromal caveolin-1 levels predict early DCIS progression to invasive breast cancer.

Cancer biology & therapy ·Vol. 8 ·No. 11 ·2009-06-00 ·Pages 1071-9

Witkiewicz AK, Dasgupta A, Nguyen KH, Liu C, Kovatich AJ, Schwartz GF, Pestell RG, Sotgia F, Rui H, Lisanti MP

Abstract

Here, we determined the possible association of stromal caveolin-1 (Cav-1) levels with DCIS recurrence and/or progression to invasive breast cancer. An initial cohort of 78 DCIS patients with follow-up data was examined. As ER-positivity was associated with recurrence, we focused our analysis on this subset of 56 patients. In this group, we observed that DCIS progressed to invasive breast cancer in approximately 14% of the patient population (8/56), in accordance with an expected progression rate of 12-15%. Nearly ninety percent of DCIS patients (7/8) that underwent recurrence to invasive breast cancer had reduced or absent levels of stromal Cav-1. Remarkably, an absence of stromal Cav-1 (score = 0) was specifically associated with early disease progression to invasive breast cancer, with reduced time to recurrence and higher recurrence rate. All DCIS patients with an absence of stromal Cav-1 underwent some form of recurrence (5/5) and the majority (4/5) underwent progression to invasive breast cancer. This represents an overall cumulative incidence rate of 100% for recurrence and 80% for progression. An absence of stromal Cav-1 in DCIS lesions was also specifically associated with the presence of inflammatory cells. Conversely, ninety-seven percent of ER(+) DCIS patients (35/36) with high levels of stromal Cav-1 (score = 2) did not show any invasive recurrence over the duration of follow-up (4-208 mo), and 89% of such patients are estimated to remain free of invasive recurrence, even after 15 y. Thus, determination of stromal Cav-1 levels may be a useful new biomarker for guiding the treatment of ER(+) DCIS patients.

MeSH Terms
Adult Aged Aged, 80 and over Biomarkers, Tumor/biosynthesis Breast Neoplasms/metabolism,pathology Breast Neoplasms, Male/metabolism,pathology Carcinoma, Ductal, Breast/metabolism,pathology Caveolin 1/biosynthesis Cohort Studies Disease Progression Female Humans Immunohistochemistry Kaplan-Meier Estimate Male Middle Aged Neoplasm Recurrence, Local/metabolism,pathology
Chemicals
Biomarkers, Tumor Caveolin 1
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Witkiewicz Agnieszka K
Stem Cell Biology and Regenerative Medicine Center, Department of Pathology, Thomas Jefferson University, Philadelphia, PA 19107, USA. agnieszka.witkiewicz@jefferson.edu
Dasgupta Abhijit
Nguyen Katherine H
Liu Chengbao
Kovatich Albert J
Schwartz Gordon F
Pestell Richard G
Sotgia Federica
Rui Hallgeir
Lisanti Michael P
Article Info
Journal
Cancer biology & therapy
Abbr.
Cancer Biol Ther
ISSN
1555-8576
Published
2009-06-00
Epub
2009-00-29
Pages
1071-9
Language
English
Region
United States
NLM ID
101137842
Subset
IM
Grants
NCI NIH HHS · R01-CA-120876 · United States
NCI NIH HHS · R01-CA-70896 · United States
NCI NIH HHS · R01-CA-098779 · United States
NCI NIH HHS · R01-CA-86072 · United States
NCI NIH HHS · R01-CA-75503 · United States
NCI NIH HHS · P30 CA056036 · United States
NCI NIH HHS · R01-CA-80250 · United States
NCI NIH HHS · P30-CA-56036 · United States
NCI NIH HHS · R01-CA-107382 · United States
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