Cancer Research The Future of Cancer Research: Science and Patient Impact  Tumor Immunology: New Perspectives
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 47, 11-15, January 1, 1987]
© 1987 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 Chen, B. D-M.
Right arrow Articles by Chou, T.-h.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Chen, B. D-M.
Right arrow Articles by Chou, T.-h.

Induction of Prostaglandin Production by Hyperthermia in Murine Peritoneal Exudate Macrophages1

Ben D-M. Chen2, Stephen A. Sapareto and Ta-hsu Chou

Division of Hematology/Oncology, Department of Internal Medicine, Wayne State University School of Medicine, Detroit, Michigan 48201

In response to inflammatory stimuli, macrophages synthesize and secrete prostaglandins (PGE) along with other potent inflammatory mediators. We have studied the effect of hyperthermia on the production of PGE by murine mononuclear phagocytes. Exposure to high temperature induced PGE production by cultured C3H/HeJ exudate macrophages in a time- and temperature-dependent manner. Increase in PGE production was detected when macrophages were treated at 41°C and above for 1 h with a much greater increase at 42 and 43°C. The secretion of PGE into culture supernatants by heat-treated macrophages reached a maximum approximately 24 hr after heat treatment. The production of PGE by macrophages after hyperthermia was inhibited either by the addition of 5 x 10-7 M indomethacin or by the subsequent incubation at 4°C, suggesting that the elevated PGE production by macrophages is mediated through the activation of cyclooxygenase. Heat treatment under the same conditions failed to stimulate the production of PGE by either a human monocyte-like tumor cell line (U-937) or a mouse fibroblast cell line (L-929).

1 Supported in part by USPHS Grant AI-23499 awarded by the National Institute of Allergy and Infectious Diseases; by Grant CA-34935 awarded by the National Cancer Institute, Department of Health and Human Services; and by the Wayne State University Ben Kasle Trust for Cancer Research.

2 To whom requests for reprints should be addressed, at Division of Hematology/Oncology, Wayne State University, P. O. Box 02188, Detroit, MI 48201.

Received 3/27/86. Revised 7/22/86. Accepted 9/12/86.







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 © 1987 by the American Association for Cancer Research.