Nath Kavindra, Nelson David S, Heitjan Daniel F, Zhou Rong, Leeper Dennis B, Glickson Jerry D
Department of Radiology, University of Pennsylvania, Philadelphia, PA, USA.
NMR Biomed. 2015 Mar;28(3):395-403. doi: 10.1002/nbm.3260.
We seek to exploit the natural tendency of melanomas and other tumors to convert glucose to lactate as a method for the selective intracellular acidification of cancer cells and for the potentiation of the activity of nitrogen-mustard antineoplastic agents. We performed this study to evaluate whether the induction of hyperglycemia (26 mM) could enhance the effects of lonidamine (LND, 100 mg/kg; intraperitoneally) on the induction of intracellular acidification, bioenergetic decline and potentiation of the activity of melphalan (LPAM) against DB-1 melanoma xenografts in mice. Intracellular pH (pHi ), extracellular pH (pHe ) and bioenergetics (β-nucleoside triphosphate to inorganic phosphate ratio, β-NTP/Pi) were reduced by 0.7 units (p < 0.001), 0.3 units (p > 0.05) and 51.4% (p < 0.05), respectively. The therapeutic response to LPAM (7.5 mg/kg; intravenously) + LND (100 mg/kg; intraperitoneally) was reduced by about a factor of three under hyperglycemic conditions relative to normoglycemia, producing a growth delay of 7.76 days (tumor doubling time, 5.31 days; cell kill, 64%) compared with LND alone of 1.70 days and LPAM alone of 0.29 days. Under normoglycemic conditions, LND plus LPAM produced a growth delay of 17.75 days, corresponding to a cell kill of 90% at the same dose for each of these agents. The decrease in tumor cell kill under hyperglycemic conditions correlates with an increase in tumor ATP levels resulting from increased glycolytic activity. However, hyperglycemia substantially increases lactic acid production in tumors by a factor of approximately six (p < 0.05), but hyperglycemia did not increase the effects of LND on acidification of the tumor, most probably because of the strong buffering action of carbon dioxide (the pKa of carbonic acid is 6.4). Therefore, this study demonstrates that the addition of glucose during treatment with LND diminishes the activity of this agent.
我们试图利用黑色素瘤和其他肿瘤将葡萄糖转化为乳酸的自然倾向,作为一种使癌细胞选择性细胞内酸化并增强氮芥类抗肿瘤药物活性的方法。我们开展这项研究,以评估高血糖(26 mM)的诱导是否能增强氯尼达明(LND,100 mg/kg;腹腔注射)对细胞内酸化诱导、生物能量下降以及美法仑(LPAM)对小鼠DB-1黑色素瘤异种移植瘤活性增强的影响。细胞内pH(pHi)、细胞外pH(pHe)和生物能量学(β-核苷三磷酸与无机磷酸的比率,β-NTP/Pi)分别降低了0.7个单位(p < 0.001)、0.3个单位(p > 0.05)和51.4%(p < 0.05)。相对于正常血糖情况,在高血糖条件下,对LPAM(7.5 mg/kg;静脉注射)+ LND(100 mg/kg;腹腔注射)的治疗反应降低了约三倍,与单独使用LND时的1.70天和单独使用LPAM时的0.29天相比,产生了7.76天的生长延迟(肿瘤倍增时间为5.31天;细胞杀伤率为64%)。在正常血糖条件下,LND加LPAM产生了17.75天的生长延迟,对应于相同剂量下每种药物90%的细胞杀伤率。高血糖条件下肿瘤细胞杀伤率的降低与糖酵解活性增加导致的肿瘤ATP水平升高相关。然而,高血糖使肿瘤中乳酸生成量大幅增加了约六倍(p < 0.05),但高血糖并未增强LND对肿瘤酸化的作用,很可能是由于二氧化碳的强大缓冲作用(碳酸的pKa为6.4)。因此,本研究表明,在使用LND治疗期间添加葡萄糖会降低该药物的活性。