[No authors listed]
Carbohydrate antigen 19â9 (CA19â9) is the most important biomarker for pancreatic cancer. Approximately 5â10% of individuals are Lewis antigen negative with scarce secretion of CA19â9 and fucosylation deficiency. However, the characteristics of Lewisânegative pancreatic cancer are unidentified. Clinicopathological characteristics of 853 patients with pancreatic cancer were examined. Pancreatic cancer cell lines were sequenced for Lewis status. Morphological and molecular features of pancreatic cancer cells were compared. Orthotopic animal modes were established. Lewisânegative patients had poorer outcome (P<0.001), higher metastatic rate (P=0.004), lower CA19â9 expression (P<0.001) and higher MUC16 expression (P<0.001) than Lewisâpositive patients. Lewisânegative cells (CaPanâ1, MiaPaCaâ2 and Pancâ1) showed a shuttle shape with scarce pseudopods. Overall, Lewisânegative cells had higher proliferation rate, higher migration ability, lower fucosylation, lower CA19â9 expression and higher MUC16 expression than Lewisâpositive cells (BxPCâ3, SU8686, SW1990). Lewisânegative cell line MiaPaCaâ2 corresponded to larger orthotopic tumor than Lewisâpositive cells SU8686. Potential proteoglycans were identified in Lewisâpositive cancer, including EGFR, HSPG2, ADAM17, GPC1, ITGA2, CD40, IL6ST and GGT1. Therefore, Lewisânegative pancreatic cancer is an aggressive subgroup with special clinical and molecular features.
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