Evidence map›Paper›PMID 22911792›Full record

ArticlePloS one2012

Evidence of prognostic relevant expression profiles of heat-shock proteins and glucose-regulated proteins in oesophageal adenocarcinomas.

Julia Slotta-Huspenina, Daniela Berg, Karina Bauer, Claudia Wolff, Katharina Malinowsky, Lukas Bauer, Enken Drecoll, Marcus Bettstetter, Marcus Feith, Axel Walch and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Targeted Hsp70 fluorescence molecular endoscopy detects dysplasia in Barrett's esophagus.European journal of nuclear medicine and molecular imaging · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Hsp27 and Hsp70 Expression in Esophageal SquamousAsian Pacific journal of cancer prevention : APJCP · 2017
    Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Implications of Bit1 and AIF overexpressions in esophageal squamous cell carcinoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2014
    Article
  13. Article
  14. 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

13 authors at 4 institutions in 2 countries.

Julia Slotta-HuspeninaInstitute of Pathology, Technische Universität München, Munich, Germany. slotta.huspenina@lrz.tum.de
Daniela Berg
Karina Bauer
Claudia Wolff
Katharina Malinowsky
Lukas Bauer
Enken Drecoll
Marcus Bettstetter
Marcus Feith
Axel Walch
Heinz Höfler
Karl-Friedrich Becker
Rupert Langer
Technical University of Munich · DEInstitute of Bioinformatics and Systems Biology · DEPraxis für Humangenetik · DEUniversity of Bern · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A high percentage of oesophageal adenocarcinomas show an aggressive clinical behaviour with a significant resistance to chemotherapy. Heat-shock proteins (HSPs) and glucose-regulated proteins (GRPs) are molecular chaperones that play an important role in tumour biology. Recently, novel therapeutic approaches targeting HSP90/GRP94 have been introduced for treating cancer. We performed a comprehensive investigation of HSP and GRP expression including HSP27, phosphorylated (p)-HSP27((Ser15)), p-HSP27((Ser78)), p-HSP27((Ser82)), HSP60, HSP70, HSP90, GRP78 and GRP94 in 92 primary resected oesophageal adenocarcinomas by using reverse phase protein arrays (RPPA), immunohistochemistry (IHC) and real-time quantitative RT-PCR (qPCR). Results were correlated with pathologic features and survival. HSP/GRP protein and mRNA expression was detected in all tumours at various levels. Unsupervised hierarchical clustering showed two distinct groups of tumours with specific protein expression patterns: The hallmark of the first group was a high expression of p-HSP27((Ser15, Ser78, Ser82)) and low expression of GRP78, GRP94 and HSP60. The second group showed the inverse pattern with low p-HSP27 and high GRP78, GRP94 and HSP60 expression. The clinical outcome for patients from the first group was significantly improved compared to patients from the second group, both in univariate analysis (p = 0.015) and multivariate analysis (p = 0.029). Interestingly, these two groups could not be distinguished by immunohistochemistry or qPCR analysis. In summary, two distinct and prognostic relevant HSP/GRP protein expression patterns in adenocarcinomas of the oesophagus were detected by RPPA. Our approach may be helpful for identifying candidates for specific HSP/GRP-targeted therapies.

Indexed as

Gene Expression ProfilingGene Expression Regulation, NeoplasticAdenocarcinomaAdultAgedAged, 80 and overCluster AnalysisEndoplasmic Reticulum Chaperone BiPEsophageal NeoplasmsFemaleHeat-Shock ProteinsHSP70 Heat-Shock ProteinsHumansImmunohistochemistryMaleMembrane ProteinsEndoplasmic Reticulum Chaperone BiPglucose-regulated proteinsHeat-Shock ProteinsHSP70 Heat-Shock ProteinsHSPA5 protein, humanMembrane ProteinsNeoplasm ProteinsRNA, Messenger

Identifiers

PMID22911792
PMCPMC3404067
OpenAlexW2095457644

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.