Batra S, Iosif C S
Department of Obstetrics and Gynecology, University of Lund, Lund, Sweden.
Int J Oncol. 1998 Jun;12(6):1295-8. doi: 10.3892/ijo.12.6.1295.
Using PK 11195, a high affinity ligand for peripheral benzodiazepine receptor (PBZr) binding sites in isolated mitochondria (m-fraction) and microsomal fraction (p-fraction) from human ovaries and ovarian tumors were studied. Binding in both m and p-fractions from ovaries and tumors were saturable and of high affinity. The PBZr density in m- and p-fractions from ovaries was very similar whereas the binding in m-fraction in ovarian tumors was nearly 3-fold higher than p-fraction. There was no significant difference in the binding affinities (KD values) for PK 11195 in the various fractions. The selective increase in the density of PBZr in mitochondria of tumors suggests an association with energy demand and utilization. The role of a relatively high density of PBZr in microsomal fractions remains to be elucidated.
使用PK 11195,对来自人卵巢和卵巢肿瘤的分离线粒体(m组分)和微粒体组分(p组分)中的外周苯二氮䓬受体(PBZr)结合位点的高亲和力配体进行了研究。卵巢和肿瘤的m组分和p组分中的结合都是可饱和的且具有高亲和力。卵巢的m组分和p组分中的PBZr密度非常相似,而卵巢肿瘤的m组分中的结合比p组分高近3倍。不同组分中PK 11195的结合亲和力(KD值)没有显著差异。肿瘤线粒体中PBZr密度的选择性增加表明与能量需求和利用有关。微粒体组分中相对高密度的PBZr的作用仍有待阐明。