z-logo
Premium
Somatostatin receptors in resected hepatocellular carcinoma: status and correlation with markers of poor prognosis
Author(s) -
Lequoy Marie,
DesboisMouthon Christèle,
Wendum Dominique,
Gupta Vandana,
Blachon JeanLuc,
Scatton Olivier,
Dumont Sylvie,
Bonnemaire Mireille,
Schmidlin Fabien,
Rosmorduc Olivier,
Fartoux Laetitia
Publication year - 2017
Publication title -
histopathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.626
H-Index - 124
eISSN - 1365-2559
pISSN - 0309-0167
DOI - 10.1111/his.13034
Subject(s) - hepatocellular carcinoma , immunohistochemistry , pathology , somatostatin receptor , cytokeratin , medicine , staining , receptor
Aims To investigate the status of somatostatin receptors ( SSTR s) in resected hepatocellular carcinoma ( HCC ). Methods and results Transcript and protein levels of SSTR 2, SSTR 3 and SSTR 5 were investigated, with real‐time polymerase chain reaction ( PCR ) and manual and automated immunohistochemistry ( IHC ), in 53 resected HCC s and paired non‐tumour tissues. SSTR 1, SSTR 4, SSTR 5 TMD 4 and SSTR 5 TMD 5 were analysed with real‐time PCR . SSTR 3 and SSTR 5 transcripts were expressed in ~25% of HCC s, but not in adjacent non‐tumour tissues. SSTR 1 and SSTR 2 transcripts were overexpressed in 42% and 32% of HCC s, respectively. SSTR 4, SSTR 5 TMD 4 and SSTR 5 TMD 5 were not detected. Membrane staining for SSTR 2 was detected in 38% of HCC s, whereas SSTR 5 protein was detectable in only 11% of HCC s. SSTR 3 protein was detected in the majority of HCC s and adjacent non‐tumour liver tissues, but membrane staining was <20% of that in HCC s. The results obtained with the two IHC methods were highly correlated ( P < 0.0001). Statistical analyses also showed a positive correlation between SSTR 2 membrane staining and cytokeratin 19 expression ( P = 0.04), serum α‐fetoprotein level ( P = 0.002), and poor differentiation ( P = 0.05). Conclusions Membrane SSTR 2 is detected reliably in HCC s by IHC , and is a potential therapeutic target, as it is coexpressed with markers of poor prognosis.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom