Evidence map›Paper›PMID 32823513›Full record

ArticleCancers2020

RETRACTED: HSP70-eIF4G Interaction Promotes Protein Synthesis and Cell Proliferation in Hepatocellular Carcinoma.

Meng Wang, Kai Wei, Baifeng Qian, Svenja Feiler, Anastasia Lemekhova, Markus W Büchler, Katrin Hoffmann

RetractedErratum issuedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

10 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. The Emerging Role of Stress Granules in Hepatocellular Carcinoma.International journal of molecular sciences · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Meng WangDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.ORCID 0000-0003-0963-0175
Kai WeiDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.ORCID 0000-0002-0488-6537
Baifeng QianDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.
Svenja FeilerDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.
Anastasia LemekhovaDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.
Markus W BüchlerDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.
Katrin HoffmannDepartment of General, Visceral, and Transplantation Surgery; Ruprecht Karls University, Im Neuenheimer Feld 110, 69120 Heidelberg, Germany.
Heidelberg University · DE

Funding

Stiftung Chirurgie Heidelberg we will provide it later
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the third leading cause of cancer-related death worldwide and features various tumor escape mechanisms from treatment-induced stress. HSP70 plays a critical role in cell protection under stress. eIF4G physiologically regulates the formation of the protein-ribosomal complex and maintains cellular protein synthesis. However, the precise cooperation of both in HCC remains poorly understood. In this study, we demonstrate that HSP70 expression is positively correlated with eIF4G in tumor specimens from 25 HCC patients, in contrast to the adjacent non-tumorous tissues, and that both influence the survival of HCC patients. Mechanistically, this study indicates that HSP70 and eIF4G interact with each other in vitro. We further show that the HSP70-eIF4G interaction contributes to promoting cellular protein synthesis, enhancing cell proliferation, and inhibiting cell apoptosis. Collectively, this study reveals the pivotal role of HSP70-eIF4G interaction as an escape mechanism in HCC. Therefore, modulation of the HSP70-eIF4G interaction might be a potential novel therapeutic target of HCC treatment.

Indexed as

eIF4Ghepatocellular carcinomaHSP70interactionprotein synthesis

Identifiers

PMID32823513
PMCPMC7464799
OpenAlexW3048661912

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.