Kikuchi Y, Kita T, Miyauchi M, Hirata J, Sasa H, Nagata I, Fukushima M
Department of Obstetrics and Gynecology, National Defense Medical College, Saitama, Japan.
J Cancer Res Clin Oncol. 1992;118(6):453-7. doi: 10.1007/BF01629429.
Effects of antineoplastic prostaglandins (PG) on human ovarian cancer cell growth were examined by using HR cells derived from ascites of a patient with serous cystadenocarcinoma of the ovary. With regard to inhibition of cancer cell proliferation in vitro, the effects of delta 7-PGA1 was most marked, followed by that of delta 12-PGJ2, PGJ2 and PGD2. When antineoplastic prostaglandins were administered to nude mice bearing HR cells, tumor growth in groups treated with PGJ2 and delta 12-PGJ2 alone was significantly inhibited 63 days after tumor inoculation, compared to that in an untreated group. Consequently, a significant prolongation of median survival was obtained with delta 12-PGJ2, compared to that in untreated groups and in groups with cisplatin alone. In addition, when prostaglandins were administered together with cisplatin, adjuvant inhibitory effects on the tumor growth were obtained 35, 56 and 63 days after tumor inoculation. Subsequently a significant prolongation of median survival was observed when cisplatin was combined with PGD2 or delta 7-PGA1, compared to the results in groups treated with PGD2 alone, delta 7-PGA1 alone or cisplatin alone. Combination of PGJ2 or delta 12-PGJ2 and cisplatin resulted in a significant decrease of hematocrit and body weight 63 days after tumor inoculation, suggesting a deterioration of the median survival. These results suggest that combination of PGD2 or delta 7-PGA1 with cisplatin may be of clinical use for ovarian cancer resistant to cisplatin.
利用源自一名卵巢浆液性囊腺癌患者腹水的HR细胞,研究了抗肿瘤前列腺素(PG)对人卵巢癌细胞生长的影响。关于体外对癌细胞增殖的抑制作用,δ7 - PGA1的作用最为显著,其次是δ12 - PGJ2、PGJ2和PGD2。当将抗肿瘤前列腺素给予荷HR细胞的裸鼠时,与未治疗组相比,单独用PGJ2和δ12 - PGJ2治疗的组在接种肿瘤63天后肿瘤生长受到显著抑制。因此,与未治疗组和单独使用顺铂的组相比,δ12 - PGJ2使中位生存期显著延长。此外,当前列腺素与顺铂联合给药时,在接种肿瘤35、56和63天后对肿瘤生长有辅助抑制作用。随后,与单独用PGD2、单独用δ7 - PGA1或单独用顺铂治疗的组相比,当顺铂与PGD2或δ7 - PGA1联合使用时,观察到中位生存期显著延长。PGJ2或δ12 - PGJ2与顺铂联合使用导致接种肿瘤63天后血细胞比容和体重显著下降,提示中位生存期恶化。这些结果表明,PGD2或δ7 - PGA1与顺铂联合使用可能对顺铂耐药的卵巢癌具有临床应用价值。