Publication: Elevated expression of G protein-coupled receptor 30 (GPR30) is associated with poor prognosis in patients with uterine cervical adenocarcinoma
Authors
Tagami, Yohei ; Ino, Yoshihiko ; Akimoto, Taishi ; Takasawa, Akira ; Takasawa, Kumi ; Aoyama, Tomoyuki ; Ueda, Asako ; Ota, Misaki ; Magara, Kazufumi ; Murata, Masaki ; Hasegawa, Tadashi ; Saito, Tsuyoshi ; Sawada, Norimasa ; Osanai, Makoto
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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-18-157
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info:eu-repo/semantics/article
Description
Abstract
Uterine cervical adenocarcinoma has a worse
prognosis than that of squamous cell carcinoma and
useful diagnostic and prognostic markers are needed.
Estrogen is one of the key regulators of several cancers,
however, the estrogen signaling has not been focused on
in cervical adenocarcinoma. Here, we shows expression
profile of classical estrogen receptor (ER) and a novel
membrane type estrogen receptor, G protein-coupled
receptor 30 (GPR30), in surgical specimens (n=53).
GPR30 was strongly expressed on the cell membrane
and in the cytoplasm in adenocarcinoma in situ (AIS)
and adenocarcinoma, and its expression was especially
strong at the invasion front in most of the cases of
GPR30-positive adenocarcinoma. Nuclear staining of
ER was strong in non-neoplastic glands, whereas it was
almost absent in most of the AIS and adenocarcinoma
cases. There was a weak but statistically significant
negative correlation between immunoreactivity of
GPR30 and that of ER in cervical AIS and
adenocarcinoma lesions (Spearman’s correlation, r=-
0.324, p=0.017). ROC curve analysis revealed that
immunoreactivity of GPR30 successfully distinguished
neoplasms from non-neoplastic glands with high
specificity (100%) and sensitivity (75.5%). GPR30
positivity was significantly correlated with histological
type (p=0.009), tumor diameter (p=0.003), tumor size
(p<0.001), lymphovascular infiltration (p=0.005) and
UICC stage (p<0.001). ER expression was correlated
only with tumor factor (p=0.047). GPR30-high patients
had poor prognosis with a significantly shorter overall
survival (OS) period (p=0.0309). GPR30 expression is a
potential diagnostic and prognostic marker.
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Citation
Histology and Histopathology Vol. 35, nÂş4 (2020)
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