Went Philip Th, Lugli Alessandro, Meier Sandra, Bundi Marcel, Mirlacher Martina, Sauter Guido, Dirnhofer Stephan
Institute for Pathology, University of Basel, Basel, Switzerland.
Hum Pathol. 2004 Jan;35(1):122-8. doi: 10.1016/j.humpath.2003.08.026.
Expression of the transmembrane glycoprotein EpCam (epithelial cellular adhesion molecule) occurs in normal epithelium of different organs and was described in carcinomas of various sites. Specific anti-EpCam therapies are now being used in clinical trials. Thus, it is of interest to know which tumor types express or overexpress this protein, and in what frequency. We therefore analyzed EpCam expression by immunohistochemistry on a tissue microarray containing 3900 tissue samples of 134 different histological tumor types and subtypes. EpCam expression was detected in 98 of 131 tumor categories. At least a weak EpCam expression in >10% of tumors was observed in 87 of 131 different tumor categories. Adenocarcinomas of the colon (81%) and pancreas (78%), as well as hormone-refractory adenocarcinomas of the prostate (71%), were identified as particularly promising therapy targets with a high fraction of strongly positive tumors. Most soft-tissue tumors and all lymphomas were EpCam negative. It is concluded that anti-EpCam therapies, if proven to be successful, will have broad applications in a wide variety of carcinomas.
跨膜糖蛋白EpCam(上皮细胞黏附分子)在不同器官的正常上皮组织中表达,并在各种部位的癌组织中也有描述。目前,特异性抗EpCam疗法正在临床试验中使用。因此,了解哪些肿瘤类型表达或过度表达这种蛋白以及其表达频率具有重要意义。为此,我们通过免疫组织化学方法对包含134种不同组织学肿瘤类型和亚型的3900个组织样本的组织芯片进行了EpCam表达分析。在131种肿瘤类别中,有98种检测到EpCam表达。在131种不同肿瘤类别中,有87种在超过10%的肿瘤中观察到至少微弱的EpCam表达。结肠腺癌(81%)、胰腺腺癌(78%)以及前列腺激素难治性腺癌(71%)被确定为特别有前景的治疗靶点,其中大部分肿瘤为强阳性。大多数软组织肿瘤和所有淋巴瘤的EpCam呈阴性。得出的结论是,如果抗EpCam疗法被证明是成功的,它将在多种癌组织中得到广泛应用。