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ALCAM regulates motility, invasiveness, and adherens junction formation in uveal melanoma cells
Journal article   Open access   Peer reviewed

ALCAM regulates motility, invasiveness, and adherens junction formation in uveal melanoma cells

Karry M Jannie, Christopher S Stipp and Joshua A Weiner
PloS one, Vol.7(6), pp.e39330-e39330
2012
DOI: 10.1371/journal.pone.0039330
PMCID: PMC3383762
PMID: 22745734
url
https://doi.org/10.1371/journal.pone.0039330View
Published (Version of record) Open Access

Abstract

ALCAM, a member of the immunoglobulin superfamily, has been implicated in numerous developmental events and has been repeatedly identified as a marker for cancer metastasis. Previous studies addressing ALCAM's role in cancer have, however, yielded conflicting results. Depending on the tumor cell type, ALCAM expression has been reported to be both positively and negatively correlated with cancer progression and metastasis in the literature. To better understand how ALCAM might regulate cancer cell behavior, we utilized a panel of defined uveal melanoma cell lines with high or low ALCAM levels, and directly tested the effects of manipulating these levels on cell motility, invasiveness, and adhesion using multiple assays. ALCAM expression was stably silenced by shRNA knockdown in a high-ALCAM cell line (MUM-2B); the resulting cells displayed reduced motility in gap-closure assays and a reduction in invasiveness as measured by a transwell migration assay. Immunostaining revealed that the silenced cells were defective in the formation of adherens junctions, at which ALCAM colocalizes with N-cadherin and ß-catenin in native cells. Additionally, we stably overexpressed ALCAM in a low-ALCAM cell line (MUM-2C); intriguingly, these cells did not exhibit any increase in motility or invasiveness, indicating that ALCAM is necessary but not sufficient to promote metastasis-associated cell behaviors. In these ALCAM-overexpressing cells, however, recruitment of ß-catenin and N-cadherin to adherens junctions was enhanced. These data confirm a previously suggested role for ALCAM in the regulation of adherens junctions, and also suggest a mechanism by which ALCAM might differentially enhance or decrease invasiveness, depending on the type of cadherin adhesion complexes present in tissues surrounding the primary tumor, and on the cadherin status of the tumor cells themselves.
Adherens Junctions - genetics Immunohistochemistry Melanoma - metabolism Uveal Neoplasms - genetics Cell Adhesion - genetics Humans Reverse Transcriptase Polymerase Chain Reaction Adherens Junctions - metabolism Blotting, Western Cell Movement - genetics Cell Movement - physiology Activated-Leukocyte Cell Adhesion Molecule - metabolism Flow Cytometry Cell Adhesion - physiology Melanoma - genetics Cell Line, Tumor Uveal Neoplasms - metabolism Activated-Leukocyte Cell Adhesion Molecule - genetics

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