Bellone Stefania, Frera Gianluca, Landolfi Gianpiero, Romani Chiara, Bandiera Elisabetta, Tognon Germana, Roman Juan J, Burnett Alexander F, Pecorelli Sergio, Santin Alessandro D
Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, University of Arkansas for Medical Sciences, Little Rock, AR 72205-7199, USA.
Gynecol Oncol. 2007 Sep;106(3):513-20. doi: 10.1016/j.ygyno.2007.04.028. Epub 2007 May 31.
To evaluate and compare epidermal growth factor type-1 receptor (EGF-R1) expression in short term and established cervical cancer cell lines generated from primary and metastatic/recurrent sites of disease. To evaluate the sensitivity of cervical cancer cell lines to treatment with a chimeric MAb against EGFR-1 (Cetuximab).
EGFR-1 expression was evaluated by flow cytometry on 22 cervical cancer cell lines including 14 primary cervical cancer cell lines obtained from cervical biopsies (11 patients) and recurrent sites of disease (three patients) as well as eight established cell lines. Tumor cell lines were tested for sensitivity to Cetuximab-mediated complement-dependent cytotoxicity (CDC) and antibody-dependent cellular cytotoxicity (ADCC) in 51Cr release assays. Finally, Cetuximab-mediated inhibition of cell proliferation was also tested.
Fourteen out of fourteen (100%) primary tumors and seven out of eight (87.5%) established cervical cancer cell lines expressed EGFR-1 by flow cytometry. Cell lines from recurrent/metastatic sites of disease expressed higher levels of EGFR-1 when compared to those obtained from primary sites (p>0.05). Minimal CDC was detected in the majority of cervical cancer cell lines exposed to complement+/-Cetuximab in the absence of peripheral blood lymphocytes (PBL). In contrast, cervical tumor cell lines were found highly sensitive to Cetuximab-mediated ADCC when challenged with PBL from either healthy donors or cervical cancer patients. Importantly, ADCC was further increased in the presence of complement. Finally, tumor proliferation was significantly inhibited by Cetuximab in all cervical tumors tested.
EGFR-1 is highly expressed in primary and recurrent cervical tumors. Cetuximab might be a novel and attractive therapeutic strategy in patients harboring chemotherapy-resistant, recurrent, or metastatic cervical cancer.
评估并比较从疾病的原发部位和转移/复发部位产生的短期和已建立的宫颈癌细胞系中表皮生长因子1型受体(EGF-R1)的表达。评估宫颈癌细胞系对一种针对EGFR-1的嵌合单克隆抗体(西妥昔单抗)治疗的敏感性。
通过流式细胞术评估22个宫颈癌细胞系中的EGFR-1表达,其中包括14个从宫颈活检(11例患者)和疾病复发部位(3例患者)获得的原发性宫颈癌细胞系以及8个已建立的细胞系。在51Cr释放试验中测试肿瘤细胞系对西妥昔单抗介导的补体依赖性细胞毒性(CDC)和抗体依赖性细胞毒性(ADCC)的敏感性。最后,还测试了西妥昔单抗介导的细胞增殖抑制作用。
通过流式细胞术,14个原发性肿瘤中的14个(100%)和8个已建立的宫颈癌细胞系中的7个(87.5%)表达EGFR-1。与从原发部位获得的细胞系相比,来自疾病复发/转移部位的细胞系表达更高水平的EGFR-1(p>0.05)。在没有外周血淋巴细胞(PBL)的情况下,在大多数暴露于补体+/-西妥昔单抗的宫颈癌细胞系中检测到最小的CDC。相反,当用来自健康供体或宫颈癌患者的PBL进行攻击时,发现宫颈肿瘤细胞系对西妥昔单抗介导的ADCC高度敏感。重要的是,在补体存在的情况下ADCC进一步增加。最后,在所有测试的宫颈肿瘤中,西妥昔单抗显著抑制肿瘤增殖。
EGFR-1在原发性和复发性宫颈肿瘤中高表达。西妥昔单抗可能是对化疗耐药、复发或转移性宫颈癌患者的一种新颖且有吸引力的治疗策略。