Evidence map›Paper›PMID 15247189›Full record

ArticleGut2004

Expression of somatostatin receptors in normal and cirrhotic human liver and in hepatocellular carcinoma.

H Reynaert, K Rombouts, A Vandermonde, D Urbain, U Kumar, P Bioulac-Sage, M Pinzani, J Rosenbaum, A Geerts

Open access · hybridAbstract read
In one paragraph

Article in Gut, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Somatostatin analogues in advanced hepatocellular carcinoma: an updated systematic review and meta-analysis of randomized controlled trials.Medical science monitor : international medical journal of experimental and clinical research · 2011
    Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Octreotide and hepatocellular carcinoma.British journal of cancer · 2007
    Trial
  6. Review
  7. Review
  8. Physiological bio-distribution ofAnnals of nuclear medicine · 2025
    Article
  9. Review
  10. Article
  11. Somatostatin and Somatostatin Receptors in Tumour Biology.International journal of molecular sciences · 2023
    Review
  12. Article
  13. Article
  14. QuantitativeJournal of nuclear medicine : official publication, Society of Nuclear Medicine · 2021
    Article
  15. Article
  16. Physiological Biodistribution ofMolecular imaging and radionuclide therapy · 2021
    Article
  17. Review
  18. Review
  19. Review
  20. Comparative evaluation ofEJNMMI research · 2020
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

H ReynaertLaboratory for Molecular Liver Cell Biology, Free University of Brussels (VUB), Belgium. Hendrik.Reynaert@az.vub.ac.be
K Rombouts
A Vandermonde
D Urbain
U Kumar
P Bioulac-Sage
M Pinzani
J Rosenbaum
A Geerts
Universitair Ziekenhuis Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSomatostatin analogues have been used with conflicting results to treat advanced hepatocellular carcinoma (HCC). The aim of this study was to investigate expression of somatostatin receptor (SSTR) subtypes in human liver, and to examine the effect of selective SSTR agonists on proliferation, apoptosis, and migration of hepatoma cells (HepG2, HuH7) and hepatic stellate cells (HSCs).

methodsExpression of SSTRs in cell lines, normal and cirrhotic liver, and HCC was examined by immunohistochemistry and reverse transcription-polymerase chain reaction. Effects of SSTR agonists on proliferation and apoptosis of tumour cells and HSCs were assessed by the 5-bromo-2' deoxyuridine and TUNEL methods, respectively. The influence of SSTR agonists on migration was investigated using Boyden chambers.

resultsIn normal liver, both hepatocytes and HSCs were negative for all five SSTRs. Cirrhotic liver and HCC as well as cultured hepatoma cells and HSCs expressed all five SSTRs, both at the protein and mRNA levels, except for HuH7 cells which did not immunoreact with SSTR3. None of the agonists influenced proliferation or apoptosis. However, compared with untreated cells, L-797,591, an SSTR1 agonist, reduced migration of HepG2, HuH7, and HSCs significantly to 88 (7)% (p<0.05), 83 (11)% (p<0.05), and 67 (13)% (p<0.01), respectively.

conclusionsCirrhotic liver and HCC express SSTRs. Although the somatostatin analogues used in this study did not affect proliferation and apoptosis, stimulation of SSTR1 may decrease invasiveness of HCC by reducing migration of hepatoma cells and/or HSCs. Clinical trials evaluating somatostatin analogues for the treatment of HCC should take these findings into account.

Indexed as

ApoptosisBase SequenceCarcinoma, HepatocellularCell DivisionCell Line, TumorHumansImmunohistochemistryLiver CirrhosisLiver NeoplasmsReceptors, SomatostatinReverse Transcriptase Polymerase Chain ReactionRNA, MessengerRNA, NeoplasmReceptors, SomatostatinRNA, MessengerRNA, Neoplasmsomatostatin receptor 2somatostatin receptor 3somatostatin receptor type 1

Identifiers

PMID15247189
PMCPMC1774160
OpenAlexW2088486874

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.