Nelson J A, Falk R E
Institute of Medical Sciences, University of Toronto, Ontario, Canada.
Anticancer Res. 1993 Nov-Dec;13(6A):2287-92.
This study utilized phloridzin (P1) and its aglucone phloretin (P2), two known inhibitors of glucose transmembrane transport, to inhibit tumor cell growth in vivo. The efficacy of hydrazine sulfate as an anticachexic agent was also evaluated. Utilizing the rat mammary adenocarcinoma and Fischer bladder cell carcinoma cell lines, it has been shown that the i.p. administration of P1 and P2 can produce significant differences in mean tumor diameters as compared to the untreated controls.
本研究使用根皮苷(P1)及其苷元根皮素(P2)这两种已知的葡萄糖跨膜转运抑制剂,在体内抑制肿瘤细胞生长。还评估了硫酸肼作为抗恶病质药物的疗效。利用大鼠乳腺腺癌和Fischer膀胱癌细胞系,结果表明,与未治疗的对照组相比,腹腔注射P1和P2可使平均肿瘤直径产生显著差异。