Dehydroepiandrosterone and 16 alpha-Br-epiandrosterone inhibit 12-O-tetradecanoylphorbol-13-acetate stimulation of superoxide radical production by human polymorphonuclear leukocytes.

Abstract:

:Both dehydroepiandrosterone (DHEA) and the synthetic steroid 16 alpha-Br-epiandrosterone (Br-Epi), a more potent inhibitor of glucose-6-phosphate dehydrogenase (G6PDH) than DHEA, inhibit the 12-O-tetradecanoylphorbol-13-acetate (TPA) stimulation of superoxide anion (O2-) formation by human neutrophils. DHEA has previously been shown to inhibit the development of spontaneous breast cancer and chemically induced tumors of the lung and colon as well as TPA promoted skin tumors in the mouse. The inhibition of TPA stimulated O2- formation by DHEA may contribute to the cancer preventive activity of this steroid.

journal_name

Carcinogenesis

journal_title

Carcinogenesis

authors

Whitcomb JM,Schwartz AG

doi

10.1093/carcin/6.3.333

subject

Has Abstract

pub_date

1985-03-01 00:00:00

pages

333-5

issue

3

eissn

0143-3334

issn

1460-2180

journal_volume

6

pub_type

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