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Molecular mechanism implicated in Pemetrexed-induced apoptosis in human melanoma cells

机译:培美曲塞诱导人黑素瘤细胞凋亡的分子机制

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摘要

BackgroundMetastatic melanoma is a lethal skin cancer and its incidence is rising every year. It represents a challenge for oncologist, as the current treatment options are non-curative in the majority of cases; therefore, the effort to find and/or develop novel compounds is mandatory. Pemetrexed (Alimta®, MTA) is a multitarget antifolate that inhibits folate-dependent enzymes: thymidylate synthase, dihydrofolate reductase and glycinamide ribonucleotide formyltransferase, required for de novo synthesis of nucleotides for DNA replication. It is currently used in the treatment of mesothelioma and non-small cell lung cancer (NSCLC), and has shown clinical activity in other tumors such as breast, colorectal, bladder, cervical, gastric and pancreatic cancer. However, its effect in human melanoma has not been studied yet.
机译:背景转移性黑色素瘤是一种致命的皮肤癌,其发病率每年都在上升。这对肿瘤科医生来说是一个挑战,因为在大多数情况下,当前的治疗方法无法治愈。因此,寻找和/或开发新化合物的努力是强制性的。 Pemetrexed(MTA,MTA)是一种多靶点抗叶酸药物,可抑制叶酸依赖性酶:胸腺嘧啶合酶,二氢叶酸还原酶和甘氨酰胺核糖核苷酸甲酰基转移酶,这是从头合成DNA复制核苷酸所必需的。它目前用于治疗间皮瘤和非小细胞肺癌(NSCLC),并已在其他肿瘤(如乳腺癌,结肠直肠癌,膀胱癌,宫颈癌,胃癌和胰腺癌)中显示出临床活性。但是,尚未研究其在人黑素瘤中的作用。

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