Martyn P, Smith D L, Adams J B
School of Biochemistry, University of New South Wales, Sydney, Australia.
J Steroid Biochem. 1987 Oct;28(4):393-8. doi: 10.1016/0022-4731(87)91056-9.
The properties of fatty acyl coenzyme A: estradiol-17 beta acyl transferase in microsomes derived from pooled human mammary cancer tissue have been examined. A pH optimum of 5.5 was found and addition of long-chained fatty acyl CoAs increased estradiol-17 beta (E2) 17-monoacyl ester synthesis; the apparent Km for E2 being 8 microM when oleoyl CoA, linolenoyl CoA or palmitoyl CoA were employed. Testosterone, dehydroepiandrosterone, and 5-androsterone-3 beta, 17 beta-diol acted as competitive inhibitors with Ki values of 36, 36 and 46 microM, respectively. The composition of E2 fatty acyl esters (E2-L) formed by incubation of [3H]E2 with human mammary cancer tissue and human mammary cancer cell lines has been determined by HPLC. Although the composition of E2-L in estrogen receptor negative cell lines (MDA-MB-231 and MDA-MB-330) was generally similar to that found for MCF-7 cells (estrogen receptor positive) and pooled human mammary cancer tissue, the former cell lines contained a 3-fold higher relative concentration of E2-17 beta stearate. MCF-7 cells were exposed to 30 nM [3H]E2 and the composition of the isolated [3H]E2-L fraction studied at various time intervals. At 0.5 h, the intracellular concentration of E2-L was 1.8 +/- 0.4 (SEM) pmol/mg DNA which increased to values of 3.6 +/- 0.6 and 4.3 +/- 0.5 at 4 h and 16 h, respectively. In the subsequent 3 h following transfer to medium lacking [3H]E2, the concentration of E2-L declined to 3.7 +/- 0.3 pmol/mg DNA. The subfraction of E2-L composed of E2-17 beta arachidonate, linolenate and docosahexaenoate, was seen to decline in relative abundance after 0.5 h and to reach significantly lower relative levels at 16 h, and again in the 3 h period following estrogen withdrawal. The data suggests that these components, derived from essential fatty acids, are more metabolically active. This may then provide a new lead to link these novel estrogen derivatives with the established relationship between unsaturated fatty acids and an increased mammary cancer incidence.
已对源自汇集的人乳腺癌组织的微粒体中脂肪酰基辅酶A:雌二醇-17β酰基转移酶的特性进行了研究。发现最适pH为5.5,添加长链脂肪酰基辅酶A可增加雌二醇-17β(E2)17-单酰酯的合成;当使用油酰辅酶A、亚麻酸酰辅酶A或棕榈酰辅酶A时,E2的表观Km为8μM。睾酮、脱氢表雄酮和5-雄甾酮-3β,17β-二醇作为竞争性抑制剂,Ki值分别为36、36和46μM。通过高效液相色谱法测定了[3H]E2与人乳腺癌组织和人乳腺癌细胞系孵育形成的E2脂肪酰酯(E2-L)的组成。虽然雌激素受体阴性细胞系(MDA-MB-231和MDA-MB-330)中E2-L的组成通常与MCF-7细胞(雌激素受体阳性)和汇集的人乳腺癌组织中发现的组成相似,但前一种细胞系中E2-17β硬脂酸酯的相对浓度高3倍。将MCF-7细胞暴露于30 nM [3H]E2,并在不同时间间隔研究分离的[3H]E2-L组分的组成。在0.5小时时,E2-L的细胞内浓度为1.8±0.4(SEM)pmol/mg DNA,在4小时和16小时时分别增加到3.6±0.6和4.3±0.5的值。在转移到缺乏[3H]E2的培养基后的随后3小时内,E2-L的浓度降至3.7±0.3 pmol/mg DNA。由E2-17β花生四烯酸酯、亚麻酸酯和二十二碳六烯酸酯组成的E2-L亚组分在0.5小时后相对丰度下降,并在16小时时达到显著较低的相对水平,在雌激素撤药后的3小时期间再次下降。数据表明,这些源自必需脂肪酸的组分代谢活性更高。这可能进而为将这些新型雌激素衍生物与不饱和脂肪酸与乳腺癌发病率增加之间已确立的关系联系起来提供新的线索。