Cancer cell metastasis is induced by actin-dependent cell migration and is affected by
cytoskeletal remodelling proteins. FMNL2 is one such protein which promotes colorectal
cancer (CRC) cell metastasis and amoeboid style invasion of melanoma cells. FMNL2
mRNA is subject to alternative splicing and studies suggest that the resulting encoded
proteins are likely to differ in their regulation, subcellular localization and activity. We
identified four FMNL2 isoforms (ITM, YHY, PMR and TQS) expressed in non-invasive
(SW480) and invasive (SW620) CRC cells, as well as in highly invasive A375 amoeboid
melanoma cells. qPCR data suggests that an “invasive” isoform (TQS) may be
preferentially expressed in highly invasive and amoeboid cell lines. Boyden chamber
invasion assay results show that FMNL2 knockdown inhibits amoeboid style invasion in
two melanoma cell lines and that TQS is the most efficient isoform at rescuing the
invasive phenotype. This study provides a further understanding of FMNL2’s role in
invasion and metastasis and identifies specific targets for the development of future
antimetastatic therapies.
| Identifer | oai:union.ndltd.org:uottawa.ca/oai:ruor.uottawa.ca:10393/24396 |
| Date | January 2013 |
| Creators | Péladeau, Christine |
| Contributors | Copeland, John |
| Publisher | Université d'Ottawa / University of Ottawa |
| Source Sets | Université d’Ottawa |
| Language | English |
| Detected Language | English |
| Type | Thesis |
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