Cancer Research Research Funding  CR Podcast
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 57, 5406-5409, December 1, 1997]
© 1997 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Carbone, A.
Right arrow Articles by Ranelletti, F. O.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Carbone, A.
Right arrow Articles by Ranelletti, F. O.

Methyl-p-hydroxyphenyllactate-esterase Activity in Breast Cancer: A Potentially New Prognostic Factor in Short-Term Follow-up1

Arnaldo Carbone2, Fabio Giosuè Serra, Gabriella Ferrandina, Giovanni Scambia, Daniela Terribile, Rocco Bellantone, Mauro Piantelli and Franco Oreste Ranelletti

Departments of Pathology [A. C., F. G. S.], Gynecology [G. F., G. S.], Surgery [D. T., R. B.], and Histology [F. O. R.], Catholic University, 00168 Rome, and Department of Human Pathology, University of Chieti, 66100 Chieti [M. P.], Italy

We assayed methyl-p-hydroxyphenyllactate esterase (MeHPLAase) activity in 48 cases of primary breast cancer. MeHPLAase activity did not show significant correlation with estrogen receptor and progesterone receptor levels. No significant relationship was found between enzymatic activity and tumor diameter, lymph node status, mitotic activity, degree of nuclear differentiation, and proportion of the S-phase fraction. During the follow-up period (median, 18.8 months; range, 6–69 months), recurrences were observed in 18 of 48 (37%) cases. The Weibull survival regression model using the enzymatic activity as a continuous covariate showed that levels of enzymatic activity were directly associated with the risk of recurrence (P = 0.02). Assuming the mean value of enzymatic activity as the cutoff value, we found a statistically significant relationship between high MeHPLAase activity and shorter recurrence-free survival. On multivariate analysis, MeHPLAase activity proved to be an independent factor for predicting a short period of recurrence-free survival.

1 Partially supported by Ministero dell'Università e della Ricerca Scientifica e Tecnologica, grant 40 and 60%, and by Associazione Italiana per la Ricerca sul Cancro.

2 To whom requests for reprints should be addressed, at Department of Pathology, Catholic University, Largo F. Vito 1, 00168 Rome, Italy.

Received 6/20/97. Accepted 10/ 3/97.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1997 by the American Association for Cancer Research.