Ylikorkala O, Kauppila A, Viinikka L
Obstet Gynecol. 1981 Oct;58(4):483-6.
Serial measurements of 6-keto-PGF1 alpha (a stable metabolite of prostacyclin), thromboxane B2 (TxB2, a stable metabolite of thromboxane A2), and 13,14-dihydro-15-keto-PGF2 alpha (M-PGF2 alpha, a stable metabolite of prostaglandin F2 alpha) were made from plasma of 9 women with metastatic ovarian or uterine malignancies before and after the combined administration of doxorubicin, cyclophosphamide, 5-fluorouracil, and cis-platinum. Elevated basal levels of TxB2 were detected in all patients, elevated levels of 6-keto-PGF1 alpha in 5 patients and elevated levels of M-PGF2 alpha in 3 patients. The use of chemotherapy was accompanied by a significant increase of 37% (P less than .01) in the M-PGF2 alpha level on the day after treatment and by significant decreases of 30 to 40% (P less than .05) in 6-keto-PGF1 alpha and TxB2 levels, which became apparent immediately after the treatment and persisted for 3 to 5 days. Thus, malignancies may be accompanied by increased production of prostacyclin and thromboxane A2, which can be lowered by cytostatics.
对9名患有转移性卵巢或子宫恶性肿瘤的女性患者,在联合使用阿霉素、环磷酰胺、5-氟尿嘧啶和顺铂前后,对其血浆中的6-酮-前列环素F1α(前列环素的稳定代谢产物)、血栓素B2(TXB2,血栓素A2的稳定代谢产物)以及13,14-二氢-15-酮-前列腺素F2α(M-PGF2α,前列腺素F2α的稳定代谢产物)进行了系列测定。所有患者均检测到TXB2基础水平升高,5名患者6-酮-前列环素F1α水平升高,3名患者M-PGF2α水平升高。化疗后,治疗后次日M-PGF2α水平显著升高37%(P<0.01),6-酮-前列环素F1α和TXB2水平显著降低30%至40%(P<0.05),治疗后立即出现并持续3至5天。因此,恶性肿瘤可能伴随着前列环素和血栓素A2生成增加,而细胞抑制剂可降低其水平。