Andreoni A, Colasanti A, Colasanti P, Mastrocinque M, Riccio P, Roberti G
Centro di Endocrinologia ed Oncologia Sperimentale-C.N.R., Napoli, Italy.
Photochem Photobiol. 1994 May;59(5):529-33. doi: 10.1111/j.1751-1097.1994.tb02978.x.
Administering a light dose of 90 J/cm2 at 599 nm during incubation with hypericin to a highly differentiated normal epithelial cell line (FRTL-5), derived from Fisher rat thyroid, and to a neoplastic cell line (MPTK-6), derived from the lung metastases of a thyroid carcinoma induced in Fisher rats, produces cell kill at drug doses 1000 times lower than those necessary to cause the same mortality in the dark. The photocytocidal activity of this polycyclic quinone drug on neoplastic cells is superior to that of antitumor anthraquinone drugs, such as daunomycin and mitoxanthrone, and to the photosensitized antiviral activity previously reported for hypericin.
在用金丝桃素孵育期间,对源自Fisher大鼠甲状腺的高分化正常上皮细胞系(FRTL - 5)以及源自Fisher大鼠诱导的甲状腺癌肺转移灶的肿瘤细胞系(MPTK - 6),以599 nm波长给予90 J/cm²的低剂量光照,产生细胞杀伤所需的药物剂量比在黑暗中导致相同死亡率所需剂量低1000倍。这种多环醌类药物对肿瘤细胞的光细胞杀伤活性优于抗肿瘤蒽醌类药物,如柔红霉素和米托蒽醌,也优于先前报道的金丝桃素的光敏抗病毒活性。