Abstract
Formins are cytoskeleton regulating proteins
characterized by a common FH2 structural domain. As key
players in the assembly of actin filaments, formins
direct dynamic cytoskeletal processes that influence cell
shape, movement and adhesion. The large number of formin
genes, fifteen in the human, suggests distinct tasks and
expression patterns for individual family members, in
addition to overlapping functions. Several formins have
been associated with invasive cell properties in
experimental models, linking them to cancer biology. One
example is FMNL1, which is considered to be a leukocyte
formin and is known to be overexpressed in lymphomas.
Studies on FMNL1 and many other formins have been
hampered by a lack of research tools, especially
antibodies suitable for staining paraffin-embedded
formalin-fixed tissues. Here we characterize, using
bioinformatics tools and a validated antibody, the
expression pattern of FMNL1 in human tissues and study
its subcellular distribution. Our results indicate that
FMNL1 expression is not restricted to hematopoietic
tissues and that neoexpression of FMNL1 can be seen in
epithelial cancer.
Original language | English |
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Pages (from-to) | 460-470 |
Journal | Journal of Histochemistry and Cytochemistry |
Volume | 62 |
Issue number | 6 |
DOIs | |
Publication status | Published - 2014 |
MoE publication type | A1 Journal article-refereed |
Keywords
- actin cytoskeleton
- immunohistochemistry
- formins
- FMNL1
- FRL1