p53 and canine tissue
Jeffrey Smoot
jsmoot at cas.org
Tue Sep 2 09:07:41 EST 1997
De Groote Dominic wrote:
>
> Hello,
>
> Does anybody know an antibody directed against p53 which crossreacts
> with canine tissue.
>
> Thanks,
>
> De Groote Dominic
Suggest you correspond with these folks.
--
Jeffrey Smoot (jsmoot at cas.org)
614-447-3600 X3198
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TI p53 Tumor suppressor protein overexpression in osteogenic tumors of
dogs
AU Sagartz, J. E.; Bodley, W. L.; Gamblin, R. M.; Couto, C. G.; Tierney,
L. A.; Capen, C. C.
CS College Veterinary Medicine, Ohio State University, Columbus, OH, USA
SO Vet. Pathol. (1996), 33(2), 213-21
AB Alterations in the p53 tumor suppressor gene have been implicated in
the genesis and/or progression of the majority of human cancers,
including osteosarcoma. Stabilization of the protein by mutation or
interaction with other proteins prolongs its half-life, rendering it
detectable by immunohistochem. Osteosarcoma is the most common
primary canine bone tumor and is characterized by frequent early
metastases. Multilobular tumors of bone involve primarily flat bones
of the head and are low-grade malignancies with lower metastatic
potential. The objectives here were to det. the prevalence of p53
protein overexpression in 106 osteogenic tumors of dogs using an
indirect immunohistochem. method and to compare p53 overexpression
between tumors with different clin. behavior. A polyclonal p53
antibody (CM-1) served as the primary antibody. Tumors were scored
based upon an est. of the percentage of tumor cells stained.
Differences in the prevalence of overexpression were obsd. between
osteosarcomas (72%) and multilobular tumors of bone (20%).
Osteosarcomas of the appendicular skeleton had a higher prevalence of
p53 overexpression (84%) than did osteosarcomas of the axial skeleton
(56%). Apparently, the p53 tumor suppressor protein is overexpressed
in the majority of canine osteosarcomas. The higher prevalence of
overexpression in osteosarcomas vs. multilobular tumors of bone and
in osteosarcomas of the appendicular skeleton vs. those of the axial
skeleton suggests that alterations in p53 expression correlate with
highly aggressive tumor behavior.
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