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首页> 外文期刊>Critical reviews in oncology/hematology >The biological properties of cetuximab.
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The biological properties of cetuximab.

机译:西妥昔单抗的生物学特性。

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Cetuximab is a recombinant chimeric human murine immunoglobulin G1 antibody that binds to the extra-cellular domain of epidermal growth factor receptor with a higher affinity than either endogenous ligand. This binding inhibits receptor phosphorylation and activation and it leads to receptor internalization and degradation. Several studies have shown that cetuximab is able to inhibit growth of epidermal growth factor receptor (EGFR)-expressing tumour cells in vitro. Moreover, treatment with cetuximab results in a marked inhibition of tumour growth in nude mice bearing xenografts of human cancer cell lines. These results are linked to cetuximab biological effects as inhibition of cell cycle, tumour progression, neo-angiogenesis, invasion and metastatization, as well as increase and activation of pro-apoptotic molecules. Additionally, cetuximab potentiates, in combination, the effects of chemotherapy and radiation therapy in eradicating well-established tumours in nude mice and it may even reverse the resistance to some cytotoxic agents in these xenografts. Moreover, numerous clinical trials demonstrated cetuximab efficacy in different tumour types. It has been approved by Food and Drugs Administration in the treatment of metastatic colorectal cancer as single agent or in combination with chemotherapy, in locally and regionally advanced head and neck squamous cell carcinoma in combination with radiation, and as monotherapy for recurrent and metastatic head and neck squamous cell carcinoma after failing platinum-based chemotherapy. This paper will overview all the experimental and pre-clinical data on the biological properties of cetuximab.
机译:西妥昔单抗是一种重组的嵌合人类鼠类免疫球蛋白G1抗体,它以比任一内源配体更高的亲和力与表皮生长因子受体的胞外域结合。这种结合抑制受体的磷酸化和激活,并导致受体内在化和降解。几项研究表明,西妥昔单抗能够在体外抑制表达表皮生长因子受体(EGFR)的肿瘤细胞的生长。此外,用西妥昔单抗治疗可显着抑制携带人癌细胞系异种移植物的裸鼠的肿瘤生长。这些结果与西妥昔单抗的生物学效应有关,如细胞周期的抑制,肿瘤进展,新血管生成,侵袭和转移以及促凋亡分子的增加和激活。此外,西妥昔单抗联合增强了化学疗法和放射疗法在根除裸鼠中已确立的肿瘤方面的作用,甚至可能逆转了这些异种移植物中对某些细胞毒剂的耐药性。此外,许多临床试验证明西妥昔单抗在不同肿瘤类型中的疗效。它已被美国食品药品监督管理局(FDA)批准用于治疗转移性结直肠癌,作为单一药物或与化学疗法联合使用,可在局部和区域晚期头颈部鳞状细胞癌与放射治疗以及作为复发性和转移性头颅癌的单一疗法中使用。铂类化学疗法失败后的颈部鳞状细胞癌。本文将概述西妥昔单抗生物学特性的所有实验数据和临床前数据。

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