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[培美曲塞:从临床前到临床]

[Pemetrexed: from preclinic to clinic].

作者信息

Lansiaux Amélie, Lokiec François

机构信息

Laboratoire de Pharmacologie, Centre Oscar Lambret, 3 rue Frédéric Combemale, BP 307, 59020 Lille Cedex.

出版信息

Bull Cancer. 2007;94 Spec No Actualites:S134-8.

Abstract

The pemetrexed (Alimta) is a new generation antifolate prescribed in the treatment of mesothelioma in association with cisplatin and in the 2nd line treatment of locally advanced or metastatic non-small lung cancer. Pemetrexed is an original molecule, different from the other antifolates. On the opposite methotrexate, pemetrexed inhibits several enzymes involved in the synthesis of purines and pyrimidines, in particular thymidylate synthase, dihydrofolate reductase, glycinamide ribonucleotide formyltransferase and 5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase. Pemetrexed is transported in cells by three receptors, which make easier its cellular penetration. On the other hand, the polyglutamation of the product by the folylpolyglutamate synthetase increases considerably its activity notably towards the thymidylate synthase. Finally, unlike methotrexate, pemetrexed presents an atypical effect on cellular synchronisation. The wide spectre of activity of pemetrexed confers it a therapeutic advantage with regard to the other antifolates specific of one or other one enzymes. The clinical results show an anti-tumoral activity against non-small lung cancer and in mesothelioma and recently towards other solid tumours, in particular in head an neck, colon and mammary cancers.

摘要

培美曲塞(力比泰)是一种新一代抗叶酸药物,用于与顺铂联合治疗间皮瘤以及用于局部晚期或转移性非小细胞肺癌的二线治疗。培美曲塞是一种原创分子,与其他抗叶酸药物不同。与甲氨蝶呤相反,培美曲塞抑制参与嘌呤和嘧啶合成的多种酶,特别是胸苷酸合成酶、二氢叶酸还原酶、甘氨酰胺核糖核苷酸甲酰基转移酶和5-氨基咪唑-4-甲酰胺核糖核苷酸甲酰基转移酶。培美曲塞通过三种受体在细胞内转运,这使其更容易穿透细胞。另一方面,该产物经叶酰聚谷氨酸合成酶进行多聚谷氨酸化后,其活性显著增加,尤其是对胸苷酸合成酶的活性。最后,与甲氨蝶呤不同,培美曲塞对细胞同步化呈现非典型作用。培美曲塞广泛的活性谱使其相对于其他针对一种或另一种酶的特异性抗叶酸药物具有治疗优势。临床结果显示其对非小细胞肺癌、间皮瘤具有抗肿瘤活性,最近对其他实体瘤也有活性,特别是对头颈部癌、结肠癌和乳腺癌。

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