Table 4.
Principal oxidative and reductive steroidogenic reactions catalyzed by 17βHSD types 1–6
17βHSD type | Type 1 | Type 2 | Type 3 | Type 4 | Type 5 | Type 6 |
---|---|---|---|---|---|---|
Other names | AKR1C3 | RODH | ||||
Preferred direction | Reduction | Oxidation | Reduction | Oxidation | Reduction | Oxidation |
Favored cofactor in intact cells | NADPH | NAD+ | NADPH | NAD+ | NADPH | NAD+ |
Estrone → estradiol | Major | Minor | ||||
Estradiol → estrone | Major | Trace | ||||
16OH-estrone → estriol | Major | |||||
Estriol → 16OH-estrone | Major | Trace | ||||
DHEA → androstenediol | Modest | Modest | ||||
Androstenedione → testosterone | Trace | Major | Minor | |||
Testosterone → androstenedione | Major | Trace | ||||
DHT → 5α-androstane-3,20dione | Major | Trace | Modest | |||
5α-Androstane-3,20dione → DHT | Major | |||||
DHT → 5α-androstane-3α,17βdiol | Modest | |||||
5α-Androstane-3α,17βdiol → DHT | Modest | |||||
5α-Androstane-3α,17βdiol → androsterone | Modest | |||||
Androsterone → 5α-androstane 3,20dione | Modest |
These enzymes catalyze other reactions as well: 17βHSD6 (RODH) also acts as an isomerase with modest activity to convert 5α-androstane 3α,17βdiol to 5α-androstane 3β,17βdiol and androsterone to 3β-androsterone. © W. L. Miller and R. J. Auchus.