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Loss of PTEN Expression Is Associated With IGFBP2 Expression, Younger Age, and Late Stage in Triple-Negative Breast Cancer.

Authors :
Dean, Sarah J. R.
Perks, Claire M.
Holly, Jeff M. P.
Bhoo-Pathy, Nirmala
Lai-Meng Looi
Taib Mohammed, Nur Aishah
Koobotse, Moses O.
Soo-Hwang Teo
Kein-Seong Mun
Cheng-Har Yip
Rhodes, Anthony
Source :
American Journal of Clinical Pathology. Mar2014, Vol. 141 Issue 3, p323-333. 11p. 5 Color Photographs, 5 Charts, 2 Graphs.
Publication Year :
2014

Abstract

Objectives: To investigate the association between PTEN loss and IGFBP2 expression in a series of triple-negative breast cancers and to relate this expression to basal cytokeratin expression and clinicopathologic features. Methods: One hundred and one formalin-fixed and paraffin-processed triple-negative breast cancer cases from the University of Malaya Medical Centre were tested immunohistochemically for cytokeratins 5/6 and 14, PTEN, and IGFBP2. The resulting slides were scored for proportion and intensity of staining. Results: Loss of tumor nuclear and cytoplasmic staining for PTEN occurred in 48.3% of cases and was significantly associated with younger age at diagnosis (47 years compared with 57 years in those without PTEN loss; P = .005). Independent predictors of PTEN loss were late stage at presentation ( P = .026), cytokeratin 5/6 positivity ( P = .028), and IGFBP2 expression ( P = .042). High levels of IGFBP2 expression were seen in 32% of cases; an independent predictor of high levels was cytokeratin 14 negativity ( P = .005). PTEN loss and high levels of IGFBP2 expression were associated with poorer survival, but neither of these trends was significant. Conclusions: PTEN loss is a frequent event in triple-negative breast cancers and is significantly associated with younger age at onset of breast cancer, late stage, and IGFBP2 expression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00029173
Volume :
141
Issue :
3
Database :
Academic Search Index
Journal :
American Journal of Clinical Pathology
Publication Type :
Academic Journal
Accession number :
94403733
Full Text :
https://doi.org/10.1309/AJCPR11DEAYPTUSL