Evidence map›Paper›PMID 25225353›Full record

ArticleMolecular & cellular proteomics : MCP2014

Integrative quantitative proteomics unveils proteostasis imbalance in human hepatocellular carcinoma developed on nonfibrotic livers.

Luc Negroni, Said Taouji, Daniela Arma, Nestor Pallares-Lupon, Kristen Leong, Lee Anne Beausang, Martin Latterich, Roger Bossé, Charles Balabaud, Jean-Marie Schmitter and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular & cellular proteomics : MCP, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 31% 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

13 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. CNDP2: An Enzyme Linking Metabolism and Cardiovascular Diseases?Journal of cardiovascular translational research · 2025
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. [Research advances in application of isobaric tags for relative and absolute quantitation in proteomics of hepatocellular carcinoma].Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2016
    Review
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

14 authors at 5 institutions in 2 countries.

Luc NegroniFrom the ‡UMR 5248 CNRS-Université Bordeaux-IPB, Bordeaux, France; §Université de Bordeaux, Bordeaux, France;
Said Taouji§Université de Bordeaux, Bordeaux, France; ¶INSERM, UMR-U1053, Team ≪ Endoplasmic Reticulum Stress and Cancer ≫, Bordeaux, France. ‖BMYscreen, Bordeaux, France;
Daniela ArmaFrom the ‡UMR 5248 CNRS-Université Bordeaux-IPB, Bordeaux, France; ¶INSERM, UMR-U1053, Team ≪ Endoplasmic Reticulum Stress and Cancer ≫, Bordeaux, France. **INSERM, UMR-U1053, ≪ Repteam ≫, Bordeaux, France;
Nestor Pallares-Lupon§Université de Bordeaux, Bordeaux, France; ¶INSERM, UMR-U1053, Team ≪ Endoplasmic Reticulum Stress and Cancer ≫, Bordeaux, France.
Kristen Leong‡‡BioScale, Inc., 4 Maguire Rd, Lexington, MA 02421, USA;
Lee Anne Beausang‡‡BioScale, Inc., 4 Maguire Rd, Lexington, MA 02421, USA;
Martin Latterich‡‡BioScale, Inc., 4 Maguire Rd, Lexington, MA 02421, USA; §§Proteogenomics Research Institute for Systems Medicine, San Diego, California 92121;
Roger Bossé¶¶PerkinElmer, Waltham, Massachusetts 02451;
Charles Balabaud§Université de Bordeaux, Bordeaux, France; **INSERM, UMR-U1053, ≪ Repteam ≫, Bordeaux, France;
Jean-Marie SchmitterFrom the ‡UMR 5248 CNRS-Université Bordeaux-IPB, Bordeaux, France; §Université de Bordeaux, Bordeaux, France;
Paulette Bioulac-Sage§Université de Bordeaux, Bordeaux, France; **INSERM, UMR-U1053, ≪ Repteam ≫, Bordeaux, France;
Jessica Zucman-Rossi‖‖Inserm, UMR-1162, Génomique fonctionnelle des Tumeurs solides, IUH, Paris, F-75010 France; Université Paris Descartes, Labex Immuno-Oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France; Université Paris 13, Sorbonne Paris Cité, UFR SMBH, F-93000 Bobigny, France; Université Paris Diderot, F-75013 Paris;
Jean Rosenbaum§Université de Bordeaux, Bordeaux, France; **INSERM, UMR-U1053, ≪ Repteam ≫, Bordeaux, France;
Eric Chevet§Université de Bordeaux, Bordeaux, France; ¶INSERM, UMR-U1053, Team ≪ Endoplasmic Reticulum Stress and Cancer ≫, Bordeaux, France. ‖BMYscreen, Bordeaux, France; Centre Régional de Lutte Contre le Cancer Eugène Marquis, 35000 Rennes, France eric.chevet@inserm.fr.
Université de Bordeaux · FRCentre National de la Recherche Scientifique · FRProterixBio (United States) · USDélégation Paris 5 · FRPerkinElmer (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proteomics-based clinical studies represent promising resources for the discovery of novel biomarkers or for unraveling molecular mechanisms underlying particular diseases. Here, we present a discovery study of hepatocellular carcinoma developed on nonfibrotic liver (nfHCC) that combines complementary quantitative iTRAQ-based proteomics and phosphoproteomics approaches. Using both approaches, we compared a set of 24 samples (18 nfHCC versus six nontumor liver tissue). We identified 43 proteins (67 peptides) differentially expressed and 32 peptides differentially phosphorylated between the experimental groups. The functional analysis of the two data sets pointed toward the deregulation of a protein homeostasis (proteostasis) network including the up-regulation of the Endoplasmic Reticulum (ER) resident HSPA5, HSP90B1, PDIA6, and P4HB and of the cytosolic HSPA1B, HSP90AA1, HSPA9, UBC, CNDP2, TXN, and VCP as well as the increased phosphorylation of the ER resident calnexin at Ser583. Antibody-based validation approaches (immunohistochemistry, immunoblot, Alphascreen(®), and AMMP(®)) on independent nfHCC tumor sets (up to 77 samples) confirmed these observations, thereby indicating a common mechanism occurring in nfHCC tumors. Based on these results we propose that adaptation to proteostasis imbalance in nfHCC tumors might confer selective advantages to those tumors. As such, this model could provide an additional therapeutic opportunity for those tumors arising on normal liver by targeting the tumor proteostasis network. Data are available via ProteomeXchange with identifier PXD001253.

Indexed as

Gene Expression Regulation, NeoplasticAdenosine TriphosphatasesAgedAged, 80 and overAntigens, NeoplasmCalnexinCarcinoma, HepatocellularCell Cycle ProteinsDipeptidasesEndoplasmic Reticulum Chaperone BiPFemaleGene Expression ProfilingHeat-Shock ProteinsHumansLiverLiver CirrhosisAdenosine TriphosphatasesAntigens, NeoplasmCalnexinCell Cycle ProteinsCNDP2 protein, humanDipeptidasesEndoplasmic Reticulum Chaperone BiPHeat-Shock ProteinsHSPA5 protein, humanNeoplasm ProteinsP4HB protein, humanPDIA6 protein, humanPhosphoproteinsProcollagen-Proline DioxygenaseProtein Disulfide-IsomerasesThioredoxinsTXN protein, humanUBC antigenValosin Containing ProteinVCP protein, human

Identifiers

PMID25225353
PMCPMC4256498
OpenAlexW2079492794

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.