Somatostatin receptors in resected hepatocellular carcinoma: status and correlation with markers of poor prognosis

被引:13
作者
Lequoy, Marie [1 ,2 ]
Desbois-Mouthon, Christele [2 ]
Wendum, Dominique [2 ,3 ]
Gupta, Vandana [4 ]
Blachon, Jean-Luc [5 ]
Scatton, Olivier [2 ,6 ]
Dumont, Sylvie [2 ,3 ]
Bonnemaire, Mireille [5 ]
Schmidlin, Fabien [5 ]
Rosmorduc, Olivier [2 ,7 ]
Fartoux, Laetitia [2 ,7 ]
机构
[1] St Antoine Hosp, AP HP, Dept Hepatol, Paris, France
[2] UPMC Univ Paris 06, Sorbonne Univ, St Antoine Res Ctr, Paris, France
[3] St Antoine Hosp, AP HP, Dept Pathol, Paris, France
[4] Ipsen Biosci Inc, Oncol & Biomarkers, Cambridge, MA USA
[5] Ipsen Innovat R& D, Les Ulis, France
[6] Hop La Pitie Salpetriere, AP HP, Dept Hepatobiliary Surg, Paris, France
[7] Hop La Pitie Salpetriere, AP HP, Dept Hepatol, Paris, France
关键词
hepatocellular carcinoma; immunohistochemistry; liver resection; prognosis; somatostatin receptors; SSTR2; INTRAHEPATIC RECURRENCE; NEUROENDOCRINE DIFFERENTIATION; LIVER; EXPRESSION; OCTREOTIDE; ANALOGS; HEPATOCARCINOMA; MANAGEMENT; SUBTYPES; SURGERY;
D O I
10.1111/his.13034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aims: To investigate the status of somatostatin receptors (SSTRs) in resected hepatocellular carcinoma (HCC). Methods and results: Transcript and protein levels of SSTR2, SSTR3 and SSTR5 were investigated, with real-time polymerase chain reaction (PCR) and manual and automated immunohistochemistry (IHC), in 53 resected HCCs and paired non-tumour tissues. SSTR1, SSTR4, SSTR5TMD4 and SSTR5TMD5 were analysed with real-time PCR. SSTR3 and SSTR5 transcripts were expressed in similar to 25% of HCCs, but not in adjacent non-tumour tissues. SSTR1 and SSTR2 transcripts were overexpressed in 42% and 32% of HCCs, respectively. SSTR4, SSTR5TMD4 and SSTR5TMD5 were not detected. Membrane staining for SSTR2 was detected in 38% of HCCs, whereas SSTR5 protein was detectable in only 11% of HCCs. SSTR3 protein was detected in the majority of HCCs and adjacent non-tumour liver tissues, but membrane staining was <20% of that in HCCs. The results obtained with the two IHC methods were highly correlated (P < 0.0001). Statistical analyses also showed a positive correlation between SSTR2 membrane staining and cytokeratin 19 expression (P = 0.04), serum a-fetoprotein level (P = 0.002), and poor differentiation (P = 0.05). Conclusions: Membrane SSTR2 is detected reliably in HCCs by IHC, and is a potential therapeutic target, as it is coexpressed with markers of poor prognosis.
引用
收藏
页码:492 / 498
页数:7
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