Macdonald Joanna, Henri Justin, Roy Kislay, Hays Emma, Bauer Michelle, Veedu Rakesh Naduvile, Pouliot Normand, Shigdar Sarah
School of Medicine, Deakin University, Geelong, VIC 3128, Australia.
Centre for Comparative Genomics, Murdoch University, Perth, WA 6150, Australia.
Cancers (Basel). 2018 Jan 12;10(1):19. doi: 10.3390/cancers10010019.
The epithelial cell adhesion molecule (EpCAM), or CD326, was one of the first cancer associated biomarkers to be discovered. In the last forty years, this biomarker has been investigated for use in personalized cancer therapy, with the first monoclonal antibody, edrecolomab, being trialled in humans more than thirty years ago. Since then, several other monoclonal antibodies have been raised to EpCAM and tested in clinical trials. However, while monoclonal antibody therapy has been investigated against EpCAM for almost 40 years as primary or adjuvant therapy, it has not shown as much promise as initially heralded. In this review, we look at the reasons why and consider alternative targeting options, such as aptamers, to turn this almost ubiquitously expressed epithelial cancer biomarker into a viable target for future personalized therapy.
上皮细胞粘附分子(EpCAM),即CD326,是最早被发现的癌症相关生物标志物之一。在过去的四十年里,人们一直在研究这种生物标志物用于个性化癌症治疗,三十多年前就对首个单克隆抗体爱必妥单抗进行了人体试验。从那时起,又研发了其他几种针对EpCAM的单克隆抗体并在临床试验中进行了测试。然而,尽管针对EpCAM的单克隆抗体疗法作为主要或辅助疗法已被研究了近40年,但它并未展现出最初所宣称的那么大的前景。在这篇综述中,我们探讨其中的原因,并考虑替代靶向选择,如适配体,以便将这种几乎普遍表达的上皮癌生物标志物转化为未来个性化治疗的可行靶点。