Ectopic expression of vascular cell adhesion molecule-1 as a new mechanism for tumor immune evasion.
Ontology highlight
ABSTRACT: Immune escape is an important reason why the immune system cannot control tumor growth, but how escape variants emerge during immunotherapy remains poorly understood. Here, we identify a new mechanism of tumor immune escape using an in vivo selection strategy. We generated a highly immune-resistant cancer cell line (P3) by subjecting a susceptible cancer cell line (P0/TC-1) to multiple rounds of in vivo immune selection. Microarray analysis of P0 and P3 revealed that vascular cell adhesion molecule-1 (VCAM-1) is up-regulated in the P3-resistant variant. Retroviral transfer of VCAM-1 into P0 significantly increased its resistance against a vaccine-induced immune response. Analysis of tumors showed a dramatic decrease in the number of tumor-infiltrating cluster of differentiation 8(+) (CD8(+
SUBMITTER: Lin KY
PROVIDER: S-EPMC3172051 | biostudies-literature | 2007 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA