首页> 外文期刊>Oncology Research >9-(3-(2-Nitro-1-imidazolyl)propylamino)-cyclopenteno(b)quinoline hydrochloride (NLCPQ-1). A novel DNA-affinic bioreductive agent as chemosensitizer: mechanistic studies. II.
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9-(3-(2-Nitro-1-imidazolyl)propylamino)-cyclopenteno(b)quinoline hydrochloride (NLCPQ-1). A novel DNA-affinic bioreductive agent as chemosensitizer: mechanistic studies. II.

机译:9-(3-(2-硝基-1-咪唑基)丙基氨基)-环戊烯(b)喹啉盐酸盐(NLCPQ-1)。一种新型的DNA亲和生物还原剂作为化学增敏剂:机理研究。二。

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摘要

NLCPQ-1 is a novel, weak, DNA-affinic bioreductive compound with enhanced chemosensitizing ability for commonly used chemotherapeutic agents, both in vitro and in vivo. In the present report we investigated possible mechanisms involved in the potentiation of cis-DDP and L-PAM in V79 cells. Potentiation was observed when cells were pretreated under hypoxic conditions with NLCPQ-1 prior to their aerobic exposure to each chemotherapeutic agent studied and in the presence of NLCPQ-1. The dominant mechanisms, under hypoxic pretreatment conditions, participating in the potentiation were: a) extensive DNA damage, as measured by the comet and alkaline elution assays, b) DNA, RNA, and protein synthesis inhibition, c) significant delay in the traverse through the S phase, as observed by flow cytometry, and possibly d) suppression of PLD repair. Apoptosis was also detected 36 h posttreatment in the chemotherapeutic drug-treated as well as the combination drug-treated cells. Glutathione depletion by NLCPQ-1 metabolites under hypoxic conditions was also involved in the potentiation process, but its contribution in potentiation was minimal.
机译:NLCPQ-1是一种新颖的,弱的,DNA亲和的生物还原性化合物,对体外和体内常用的化学治疗剂均具有增强的化学增敏能力。在本报告中,我们研究了V79细胞中顺式DDP和L-PAM增强的可能机制。当细胞在缺氧条件下用NLCPQ-1预处理,然后在有氧暴露于所研究的每种化学治疗剂之前和存在NLCPQ-1时,观察到增强作用。在缺氧预处理条件下,参与增强作用的主要机制是:a)广泛的DNA损伤,通过彗星和碱性洗脱测定法测量; b)DNA,RNA和蛋白质合成抑制; c)穿越的显着延迟通过流式细胞仪观察到的S期,以及d)抑制PLD修复。在化疗药物处理的以及联合药物处理的细胞中,在治疗后36小时也检测到凋亡。缺氧条件下NLCPQ-1代谢物对谷胱甘肽的消耗也参与了增强过程,但其对增强作用的贡献很小。

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