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. 2015 Jun;19(6):283-7.
doi: 10.1089/gtmb.2015.0014. Epub 2015 Apr 15.

Downregulation of VANGL1 inhibits cellular invasion rather than cell motility in hepatocellular carcinoma cells without stimulation

Affiliations

Downregulation of VANGL1 inhibits cellular invasion rather than cell motility in hepatocellular carcinoma cells without stimulation

Gokhan Ozan Cetin et al. Genet Test Mol Biomarkers. 2015 Jun.

Abstract

Aims: The Wnt planar cell polarity (PCP) pathway is one of the Wnt pathways which plays a critical role in cell proliferation and fate. The VANGL1 protein is one of Wnt-PCP pathway components. It is known that Wnt-PCP pathway has major roles in cell motility but its role in hepatocellular carcinoma (HCC) progression through invasion and metastasis needs to be clarified.

Methods: We silenced VANGL1 gene expression in the HepG2 HCC cell line by stable transfection with a vector containing siRNA template for VANGL1 and investigated the change in cell invasion and motility.

Results: Transfected cells with the siRNA template showed significantly suppressed invasive capacity when compared to controls although cellular motility was only slightly affected.

Conclusion: Our study showed a basal role for VANGL1 with respect to the invasive capacity of HCC cells. This suggests that the Wnt-PCP pathway may play a role in progression of HCC through cellular invasion but further studies are needed to clarify its role in cell motility.

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Figures

<b>FIG. 1.</b>
FIG. 1.
Relative quantification of VANGL1 expression with real-time polymerase chain reaction (PCR) in hepatocellular cancer cell lines.
<b>FIG. 2.</b>
FIG. 2.
(a) VANGL1 expression of HEP-G2 cells transfected with pSilencer plasmid. pSIL-VANGL1 cells carry the shRNA template for VANGL1 and pSIL where the control cells transfected with the control pSilencer vector. Relative quantification of VANGL1 expression with real-time PCR in transfected cells showing the degree of gene silencing (p=0.0009). *Indicates the significance. (b) Western blot analysis of VANGL1 expression in the cells transfected with siRNA.
<b>FIG. 3.</b>
FIG. 3.
The change in the number of (a) invasive (p=0.03) and (b) motile HEP-G2 cells after transfection with VANGL1 siRNA. *Indicates the significance. pSIL-VANGL1 cells carry the shRNA template for VANGL1 and pSIL where the control cells transfected with the control pSilencer vector.

References

    1. Albini A, Iwamoto Y, Kleinman HK, et al. (1987) A rapid in vitro assay for quantitating the invasive potential of tumor cells. Cancer Res 47:3239–3245 - PubMed
    1. An SM, Ding QP, Li LS. (2013) Stem cell signaling as a target for novel drug discovery: recent progress in the WNT and Hedgehog pathways. Acta Pharmacol Sin 34:777–783 - PMC - PubMed
    1. Anastas JN, Biechele TL, Robitaille M, et al. (2012) A protein complex of SCRIB, NOS1AP and VANGL1 regulates cell polarity and migration, and is associated with breast cancer progression. Oncogene 31:3696–3708 - PMC - PubMed
    1. Brinckerhoff CE, Rutter JL, Benbow U. (2000) Interstitial collagenases as markers of tumor progression. Clin Cancer Res 6:4823–4830 - PubMed
    1. Cho SB, Park YL, Park SJ, et al. (2011) KITENIN is associated with activation of AP-1 target genes via MAPK cascades signaling in human hepatocellular carcinoma progression. Oncol Res 19:115–123 - PubMed

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