Allen Lee F, Sebolt-Leopold Judith, Meyer Mark B
Department of Cancer Molecular Sciences, Ann Arbor, MI, USA.
Semin Oncol. 2003 Oct;30(5 Suppl 16):105-16. doi: 10.1053/j.seminoncol.2003.08.012.
Several key growth factors, cytokines, and proto-oncogenes transduce their growth- and differentiation-promoting signals through the mitogen-activated protein kinase or extracellular signal-regulated protein kinase (ERK) cascade. Overexpression or constitutive activation of this pathway has been shown to play an important role in the pathogenesis and progression of breast and other cancers, making the components of this signaling cascade potentially important as therapeutic targets. CI-1040 (PD184352) is an orally active, highly specific, small-molecule inhibitor of one of the key components of this pathway (MEK1/MEK2), and thereby effectively blocks the phosphorylation of ERK and continued signal transduction through this pathway. Antitumor activity has been seen in preclinical models with this compound, particularly for pancreas, colon, and breast cancers, which has been shown to correlate with its inhibition of pERK. Clinically, CI-1040 has been shown to be well tolerated in phase I studies, with safety and pharmacokinetic profiles that permit continuous daily dosing. Biomarker studies have shown target inhibition in patients, and antitumor activity has also been observed with a partial response in one patient with pancreatic cancer and stable disease in approximately 25% of phase I patients. Given the central role of the ERK/mitogen-activated protein kinase pathway in mediating growth-promoting signals for a diverse group of upstream stimuli, inhibitors of MEK, as a key central mediator, could have significant clinical benefit in the treatment of breast and other cancers.
几种关键的生长因子、细胞因子和原癌基因通过丝裂原活化蛋白激酶或细胞外信号调节蛋白激酶(ERK)级联传导其促进生长和分化的信号。该信号通路的过表达或组成型激活已被证明在乳腺癌和其他癌症的发病机制及进展中起重要作用,使得该信号级联的组成成分作为治疗靶点具有潜在的重要性。CI-1040(PD184352)是一种口服活性、高度特异性的小分子抑制剂,作用于该信号通路的关键成分之一(MEK1/MEK2),从而有效阻断ERK的磷酸化以及通过该信号通路的持续信号转导。在临床前模型中已观察到该化合物具有抗肿瘤活性,特别是对胰腺癌、结肠癌和乳腺癌,其抗肿瘤活性已被证明与其对pERK的抑制作用相关。在临床上,CI-1040在I期研究中已显示出良好的耐受性,其安全性和药代动力学特征允许每日持续给药。生物标志物研究表明该药物在患者体内具有靶点抑制作用,并且在一名胰腺癌患者中观察到部分缓解,在约25%的I期患者中观察到疾病稳定,显示出抗肿瘤活性。鉴于ERK/丝裂原活化蛋白激酶信号通路在介导多种上游刺激的生长促进信号中起核心作用,MEK作为关键的中央介质,其抑制剂在乳腺癌和其他癌症的治疗中可能具有显著的临床益处。