Ringborg U, Hansson J, Jungnelius U, Lewensohn R, Skog S
Radiumhemmet, Karolinska Hospital, Stockholm, Sweden.
Anticancer Res. 1990 Mar-Apr;10(2A):297-301.
Melphalan inhibits the incorporation of 3H-thymidine and 3H-uridine significantly more in phytohaemagglutinin (PHA)-stimulated human lymphocytes than in a human melanoma cell line (RPMI 8322). Melphalan - induced total DNA cross-linking was 1.7 times higher and DNA interstrand cross-linking was 1.8 times higher in the PHA-stimulated lymphocytes than in the melanoma cells. A higher level of DNA cross-linking was required in melanoma cells than in PHA-stimulated lymphocytes to obtain similar levels of inhibition of incorporation of 3H-thymidine and 3H-uridine. The outflow of cells from G1 to S phase was significantly more inhibited by melphalan in the lymphocytes than in the melanoma cells. Thus the melanoma cells can replicate and transcribe DNA in the presence of levels of DNA damage, which in PHA-stimulated lymphocytes strongly inhibit DNA and RNA synthesis.
美法仑对植物血凝素(PHA)刺激的人淋巴细胞中3H-胸腺嘧啶核苷和3H-尿苷掺入的抑制作用,明显强于对人黑色素瘤细胞系(RPMI 8322)的抑制作用。在PHA刺激的淋巴细胞中,美法仑诱导的总DNA交联比黑色素瘤细胞高1.7倍,DNA链间交联比黑色素瘤细胞高1.8倍。为了获得相似水平的3H-胸腺嘧啶核苷和3H-尿苷掺入抑制,黑色素瘤细胞比PHA刺激的淋巴细胞需要更高水平的DNA交联。与黑色素瘤细胞相比,美法仑对淋巴细胞中从G1期到S期的细胞流出抑制作用明显更强。因此,黑色素瘤细胞能够在存在一定水平DNA损伤的情况下进行DNA复制和转录,而这种程度的DNA损伤在PHA刺激的淋巴细胞中会强烈抑制DNA和RNA合成。