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Increased Expression of S100A6 (Calcyclin), a Calcium-binding Protein of the S100 Family, in Human Colorectal Adenocarcinomas
The expression of S100A6 (also known as Calcyclin/2A9/5B10/PRA) in surgically resected human colorectal adenocarcinomas was examined to investigate whether S100A6 plays a role in the malignancy of human tumor cells. Western blot analysis using the lysates from colorectal adenocarcinomas and adjacent...
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Published in: | Clinical cancer research 2000-01, Vol.6 (1), p.172-177 |
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Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | The
expression of S100A6 (also known as Calcyclin/2A9/5B10/PRA) in
surgically resected human colorectal adenocarcinomas was examined to
investigate whether S100A6 plays a role in the malignancy of human
tumor cells. Western blot analysis using the lysates from colorectal
adenocarcinomas and adjacent normal mucosa from 10 patients revealed
that the average S100A6 level of adenocarcinomas was significantly
higher (about 2.4-fold) than that of normal mucosa. Immunohistochemical
analysis using formalin-fixed paraffin-embedded surgical specimens and
monoclonal anti-S100A6 antibody (mAbA6) demonstrated that 2 (5%) of 42
normal mucosa and 6 (46%) of 13 adenoma specimens were mAbA6-positive
and showed granular staining localized at the supranuclear regions of
epithelial cells, whereas 23 (55%) of 42 adenocarcinomas and 13
(100%) of 13 carcinoma cells that metastasized to the liver were
mAbA6-positive and showed diffuse cytoplasmic staining. A significant
correlation between S100A6 expression and Dukes’ tumor stage or
lymphatic permeation but not with other clinicopathological factors was
shown. S100A6 was stained more intensely in peripheral portions than in
central portions of adenocarcinomas, whereas Ki-67 (a growth marker)
was stained equally in these two portions. These results suggest that
S100A6 may be involved in the progression and invasive process of human
colorectal adenocarcinomas. |
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ISSN: | 1078-0432 1557-3265 |