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Welcome to the web
supplement to the
paper published in the
"The
American Journal of
Pathology, Volume 165,
pages 107-113":
The novel
marker, DOG1, is
expressed ubiquitously
in GI Stromal Tumors
irrespective of KIT or
PDGFA mutation
status.
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Abstract:
Accurate diagnosis of gastrointestinal stromal tumors (GISTs) has
gained increasing importance since
imatinib mesylate, an inhibitor of the
KIT tyrosine kinase, was found to
reduce tumor growth. Currently, the
diagnosis of GISTs relies heavily on
KIT (CD117) immunoreactivity.
However, KIT- negative GISTs have been
reported and some of these tumors have
been shown to harbor a mutation in the
PDGFRA gene. We recently
characterized gene expression patterns
in GISTs using cDNA microarrays, and
found that the gene FLJ10261, encoding
a hypothetical protein, was highly
expressed in GISTs, compared to other
mesenchymal tumors. Synthetic
peptides based on the gene sequence,
which we call DOG1, were used to
generate a rabbit antiserum. The
immunoreactivity of this antiserum was
assessed on two soft tissue tumor
microarrays (TMAs). The first TMA
included duplicate cores of 460 soft
tissue tumors, including 22
KIT-immunoreactive GISTs. The second
TMA included 127 GIST cases for which
the KIT and PDGFRA mutation status was
known. 136 of 139 (97.8%) of scorable
GISTs on these two arrays demonstrated
immunoreactivity with DOG1 antisera.
The immunohistochemistry results were
confirmed by in situ hybridization for
DOG1, KIT and PDGFRA. Other neoplasms
in the differential diagnosis of GIST,
including desmoid fibromatosis (0/17)
and Schwannoma (0/3), were
immunonegative for DOG1. Only four
non-GIST cases, including two from the
abdomen, were immunoreactive for DOG1,
with one of these also reacting for
KIT. All 7 GIST cases with a PDGFRA
mutation were DOG1 positive, while
most of these failed to react for KIT.
In addition, 4 of 5 scorable PDGFRA
mutants were also positive by PDGFRA
in situ hybridization. Two
DOG1-positive, KIT-negative GISTs on
the first TMA were observed to be
PDGFRA positive by in situ
hybridization and subsequently found
to harbor mutations in exon 18 of
PDGFRA. Digital images of over 4,000
immunostains and in situ
hybridizations are available at the
accompanying website. DOG1, a
protein of unknown function, is
expressed strongly on the cell surface
of GISTs and is rarely expressed in
other soft tissue tumors. Use of
antisera against DOG1 may aid in the
diagnosis of GISTs, including those
that fail to express KIT
antigen.
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