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
Carcinogenesisjournal_title
Carcinogenesisauthors
Whitcomb JM,Schwartz AGdoi
10.1093/carcin/6.3.333subject
Has Abstractpub_date
1985-03-01 00:00:00pages
333-5issue
3eissn
0143-3334issn
1460-2180journal_volume
6pub_type
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