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Antitumor efficacy of a monoclonal antibody that inhibits the activity of cancer-associated carbonic anhydrase XII

机译:抑制与癌症相关的碳酸酐酶XII活性的单克隆抗体的抗肿瘤功效

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摘要

Carbonic anhydrase XII (CA XII) is a membrane-tethered cell surface enzyme that is highly expressed on many human tumor cells. Carbonic anhydrase members in this class of exofacial molecules facilitate tumor metabolism by facilitating CO2 venting and intracellular pH regulation. Accordingly, inhibition of exofacial CAs has been proposed as a general therapeutic strategy to target cancer. The recent characterization of 6A10, the first CA XII-specific inhibitory monoclonal antibody, offered an opportunity to evaluate this strategy with regard to CA XII-mediated catalysis. Using functional assays, we showed that 6A10 inhibited exofacial CA activity in CA XIIexpressing cancer cells. 6A10 reduced spheroid growth in vitro under culture conditions where CA XII was active (i.e., alkaline pH) and where its catalytic activity was likely rate-limiting (i.e., restricted extracellular HCO3- supply). These in vitro results argued that the antibody exerted its growth-retarding effect by acting on the catalytic process, rather than on antigen binding per se. Notably, when administered in a mouse xenograft model of human cancer, 6A10 exerted a significant delay on tumor outgrowth. These results corroborate the notion that exofacial CA is critical for cancer cell physiology and they establish the immunotherapeutic efficacy of targeting CA XII using an inhibitory antibody.
机译:碳酸酐酶XII(CA XII)是一种在许多人类肿瘤细胞上高度表达的膜拴细胞表面酶。此类exacial分子中的碳酸酐酶成员通过促进CO2排放和细胞内pH调节来促进肿瘤代谢。因此,已经提出了抑制面外CAs作为靶向癌症的一般治疗策略。第一个CA XII特异性抑制性单克隆抗体6A10的最新特性为评估CA XII介导的催化这一策略提供了机会。使用功能分析,我们表明6A10抑制了表达CA XII的癌细胞中的面颊CA活性。 6A10在CA XII活跃(即碱性pH)且其催化活性可能会限制速率(即限制细胞外HCO3-供应)的培养条件下,降低了球体的生长。这些体外结果表明,该抗体通过作用于催化过程而不是自身的抗原结合而发挥其生长延缓作用。值得注意的是,当在人类癌症的小鼠异种移植模型中给药时,6A10显着延迟了肿瘤的生长。这些结果证实了面部外CA对癌细胞生理至关重要的观点,并且它们建立了使用抑制性抗体靶向CA XII的免疫治疗功效。

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