Abstract
E-cadherin expressed highly in 95C and lowly in 95D lung cancer cells which were from the same patient, but core-fucosylated E-cadherin highly expressed in 95D cells. Therefore, Fut8 and Fut8-RNAi constructs were transfected into 95C and 95D cells, respectively. In Fut8-transfectants, reduction of nuclear β-catenin was noted when E-cadherin was core-fucosylated, while accumulation of nuclear β-catenin was observed in Fut8-RNAi transfectants. In E-cadherin-negative MDA-MB-231 cells either Fut8 or Fut8-RNAi transfection couldn't affect nuclear β-catenin. However, cotransfection of E-cadherin with Fut8 caused nuclear β-catenin reduction. Furthermore, enhanced binding of E-cadheirn with β-catenin as well as α-catenin were observed in Fut8-transfectants, and reduction of tyrosine 654 phosphorylation on β-catenin and its transcriptional activity were also noted at the same time. Overall, the current results suggested that core-fucosylated E-cadherin regulated nuclear β-catenin accumulation in lung cancer cells.
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Abbreviations
- LCA:
-
lens culinaris agglutinin
- Fut8:
-
α1,6-fucosyltransferase
- siFut8:
-
Fut RNAi
- IP:
-
Immunoprecipitation
- TCF:
-
T-cell factor
- 95D cells:
-
giant cell carcinoma of lung with highly metastatic potential
- 95C cells:
-
giant cell carcinoma of lung with low metastatic potential
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Acknowledgement
This work was supported by Natural Science Foundation of China (30070183, 30570414), Shanghai Leading Academic Discipline Project (B110), and Wenzhou Scientific and Technological Bureau (H2006023).
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Hu, P., Shi, B., Geng, F. et al. E-cadherin core fucosylation regulates nuclear β-catenin accumulation in lung cancer cells. Glycoconj J 25, 843–850 (2008). https://doi.org/10.1007/s10719-008-9144-6
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DOI: https://doi.org/10.1007/s10719-008-9144-6