Activated leukocyte cell adhesion molecule (CD166)--its prognostic power for colorectal cancer patients.

Abstract Background The activated leukocyte cell adhesion molecule (ALCAM, CD166) has been reported to be involved in tumorigenesis of colorectal cancer (CRC) and to function as a cancer stem cell marker. Controversial data exist regarding the prognostic power of ALCAM expression in CRC. Here, we evaluate the expression of ALCAM in a cohort of CRC patients and its usage as a prognostic marker for survival. Materials and methods Tissue specimens from 299 patients with CRC treated between 1993 and 2006 were analyzed via ALCAM immunohistochemistry (clone MOG/07) using a tissue microarray. Results were correlated with clinical, histopathological, and patient survival data (Chi-square test, Kaplan–Meier analysis, and log-rank test, respectively). Multivariate analysis also was performed (Cox regression). Results ALCAM is expressed in most primary (76%) and secondary (62%) CRC lesions ( P  = 0.014). Immunohistochemistry revealed an inverse association with tumor grading ( P  = 0.002) but not with any other clinical or histopathological data. Kaplan–Meier survival analysis revealed a significant overall survival benefit in the group of ALCAM-positive patients ( P = 0.019). Multivariate analysis showed that ALCAM is an independent positive prognostic marker for overall survival ( P = 0.023). Conclusions ALCAM expression is a positive prognostic marker for overall survival of CRC patients, and its detection might help to optimize the existing prognostic staging system. Elevated expression in higher differentiated tumors might indicate a potential role in the early steps of tumorigenesis, and its loss might be associated with reduced cellular adhesion, resulting in a higher metastatic potential of the tumor. Further studies must be conducted investigating these hypotheses.