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KMID : 0338420190340030618
Korean Journal of Internal Medicine
2019 Volume.34 No. 3 p.618 ~ p.625
¥â-Catenin expression is associated with cell invasiveness in pancreatic cancer
Nan Jin Niang

Kim Ok-Ran
Lee Myung-Ah
Abstract
Background/Aims: This study was tried to determine the role of ¥â-catenin in invasion in pancreatic cancer.

Methods: We analyzed cancer invasiveness according to ¥â-catenin expression in pancreatic cancer cell line. We also investigated the change in cancer invasiveness when ¥â-catenin expression was changed. To enhance ¥â-catenin activity, we treated low ¥â-catenin cancer cell line, PANC1, with Wnt-3a conditioned media and transected ¥â-catenin. We also treated high ¥â-catenin expressing cell line, BxPC3, with XAV939, ¥â-catenin inhibitor and siRNA for ¥â-catenin to inhibit ¥â-catenin expression.

Results: The high ¥â-catenin expressing cancer cell line, BxPC3 showed higher invasiveness, and low ¥â-catenin expressing cell lines, PANC1and MIA-PaCa-2, were less invasive. By adding the Wnt-3a conditioned media or performing transfection with ¥â-catenin in PANC1, cell invasiveness was increased (p < 0.05 and p < 0.01, respectively). On inhibition of ¥â-catenin by XAV939 and siRNA in BxPC3 cell line, invasiveness was significantly decreased (p < 0.01). It was not correlated with the expression of cluster of differentiation 44 (CD44) or CD44 variant 6 (CD44v6), the invasion related protein. On analysis of association with metastasis in human tissue, Wnt-3a expression was statistically correlated with the development of metastasis (p = 0.029).

Conclusions: Based on our data, ¥â-catenin may be involved in cancer invasion in pancreatic cancer, and it is not associated with CD44, the invasion related protein.
KEYWORD
Pancreatic neoplasms, Beta-catenin, Invasiveness
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