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Applicability of Combination with Tirapazamine in Boron Neutron Capture Therapy

机译:替拉帕明联合应用在硼中子俘获治疗中的适用性

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摘要

SCC VII tumor‐bearing mice were continuously given 5‐bromo‐2′‐deoxyuridine (BrdU) to label all proliferating cells. After injection of tirapazamine (TPZ), a bioreductive agent, combined with sodium borocaptate‐10B (BSH) or dl‐p‐boronophenylalanine‐10B (BPA) administration, the tumors were irradiated with thermal neutrons, and then isolated and incubated with cytochalasin‐B (a cytokinesis blocker). The micronucleus (MN) frequency in cells without BrdU labeling (quiescent (Q) cells) was determined by means of immunofluorescence staining for BrdU, and that for total cells was obtained from tumors not pretreated with BrdU. Even when no 10B‐compound was administered, TPZ increased the MN frequency of tumor cells including Q cells, resulting in reduction of the difference in MN frequency between total and Q cells, mainly by increasing the MN frequency of Q cells. TPZ increased the MN frequency of Q cells when combined with BPA administration, but TPZ showed no apparent effect on each cell population when combined with BSH. Namely, TPZ reduced the difference in MN frequency between total and Q cells caused by 10B‐compound administration, especially when BPA was administered. From the viewpoint of the overall cell killing effect in boron neutron capture therapy (BNCT), combination with TPZ appeared to be useful in BPA‐BNCT, but not in BSH‐BNCT.
机译:连续给SCC VII荷瘤小鼠5-溴2'-脱氧尿苷(BrdU)标记所有增殖细胞。注射了生物还原剂替拉帕明(TPZ)后,与硼captate- 10 B(BSH)或dl-p-boronophenylalanine- 10 B(BPA)联合给药,用热中子照射肿瘤,然后分离并与细胞松弛素-B(细胞分裂阻滞剂)一起孵育。通过对BrdU进行免疫荧光染色来确定未标记BrdU的细胞(静止(Q)细胞)中的微核(MN)频率,而总细胞的频率是从未经BrdU预处理的肿瘤中获得的。即使不使用 10 B-化合物,TPZ也会增加包括Q细胞在内的肿瘤细胞的MN频率,导致总细胞和Q细胞之间MN频率差异的减少,主要是通过增加MN频率Q细胞。与BPA联合使用时,TPZ增加了Q细胞的MN频率,但与BSH联合使用时,TPZ对每个细胞群均无明显影响。即,TPZ减少了由 10 B-化合物给药引起的总细胞和Q细胞之间的MN频率差异,尤其是在给予BPA时。从硼中子捕获疗法(BNCT)的整体细胞杀伤作用的观点来看,与TPZ结合在BPA-BNCT中似乎有用,但在BSH-BNCT中却没有。

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