Hormones and Cancer Research Unit, 45 Boulevard Brune, 75014 Paris, France.
Maturitas. 2009 Dec;65 Suppl 1:S17-21. doi: 10.1016/j.maturitas.2009.11.006. Epub 2009 Dec 3.
It is well documented that breast tissue, both normal and cancerous, contains all the enzymatic systems necessary for the bioformation and metabolic transformation of estrogens, androgens and progesterone. These include sulfatases, aromatase, hydroxysteroid-dehydrogenases, sulfotransferases, hydroxylases and glucuronidases. The control of these enzymes plays an important role in the development and pathogenesis of hormone-dependent breast cancer. As discussed in this review, various progestogens including dydrogesterone and its 20alpha-dihydro-derivative, medrogestone, promegestone, nomegestrol acetate and norelgestromin can reduce intratissular levels of estradiol in breast cancer by blocking sulfatase and 17beta-hydroxysteroid-dehydrogenase type 1 activities. A possible correlation has been postulated between breast cell proliferation and estrogen sulfotransferase activity. Progesterone is largely transformed in the breast; normal breast produces mainly 4-ene derivatives, whereas 5alpha-derivatives are most common in breast cancer tissue. It has been suggested that this specific conversion of progesterone may be involved in breast carcinogenesis. In conclusion, treatment with anti-aromatases combined with anti-sulfatase or 17beta-hydroxysteroid-dehydrogenase type 1 could provide new therapeutic possibilities in the treatment of patients with hormone-dependent breast cancer.
有大量文献记载,乳腺组织,无论是正常组织还是癌变组织,都包含有生物合成和代谢转化雌激素、雄激素和孕激素所必需的所有酶系统。这些酶包括硫酸酯酶、芳香酶、羟甾类脱氢酶、磺基转移酶、羟化酶和葡萄糖醛酸酶。这些酶的调控在激素依赖性乳腺癌的发生和发展中起着重要作用。正如本综述所讨论的,各种孕激素,包括地屈孕酮及其 20α-二氢衍生物、美屈孕酮、普美孕酮、醋酸诺美孕酮和屈螺酮,通过阻断硫酸酯酶和 17β-羟甾类脱氢酶 1 型的活性,可降低乳腺癌组织内的雌二醇水平。有人假设乳腺癌细胞增殖与雌激素硫酸转移酶活性之间可能存在相关性。孕激素在乳腺中大量转化;正常乳腺主要产生 4-烯衍生物,而 5α-衍生物在乳腺癌组织中最常见。有人提出,这种孕激素的特异性转化可能与乳腺癌的发生有关。总之,用芳香酶抑制剂联合硫酸酯酶或 17β-羟甾类脱氢酶 1 抑制剂治疗可能为激素依赖性乳腺癌患者的治疗提供新的治疗可能性。