Publication: Tetraspanin CD63 independently predicts poor prognosis in colorectal cancer
Authors
Kaprio, Tuomas ; Hagström, Jaana ; Andersson, Leif C. ; Haglund, Caj
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Publisher
Universidad de Murcia, Departamento de Biologia Celular e Histiologia
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DOI
https://doi.org/10.14670/HH-18-209
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info:eu-repo/semantics/article
Description
Abstract
CD63, a member of the tetraspanin family, is
expressed in endosomes and enriched in exosomes.
Tetraspanins participate in a variety of physiological
processes, including cellular differentiation, cell-cell
fusion, and cell migration. CD63 reportedly carries both
protumorigenic and tumor suppressor properties, and
appears to be upregulated in breast cancer, astrocytoma,
and melanoma. Yet, the effect of CD63 on cancer
prognosis remains unclear, and no previous reports
examined it in colorectal cancer (CRC). Identifying
novel biomarkers will allow us to better differentiate
patients with an increased risk of recurrence and who
might benefit from adjuvant therapy. We applied
immunohistochemistry with antibodies to human CD63
on 620 consecutive CRC patients treated at the Helsinki
University Hospital. We evaluated the associations
between CD63 expression and clinicopathological
parameters and patient prognosis. We found that CD63
expression associated with an advanced stage, poor
differentiation, and mucinous histology. We found no
association between CD63 expression and age, sex or
tumor location. CD63 expression predicted an
unfavorable prognosis in CRC (p=0.00001, log-rank
test) and in a subgroup of patients with metastasized
CRC (p=0.011). Cox’s multivariate analysis identified
CD63 as an independent factor predicting an
unfavorable prognosis in CRC and in the subgroup with
metastasized disease.
We show for the first time that CD63 immunohisto-
chemistry expression represents an independent marker
of an unfavorable prognosis in CRC and associates with
unfavorable clinicopathological parameters. Our results
support the hypothesis that a higher tissue expression of
CD63 in CRC, indicating an epithelial-to-mesenchymal
transition (EMT)-associated secretory phenotype,
associated with an adverse outcome.
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Citation
Histology and Histopathology Vol. 35, nº8 (2020)
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