Evidence map›Paper›PMID 22451657›Full record

ArticleThe Journal of biological chemistry2012

Engulfment protein GULP is regulator of transforming growth factor-β response in ovarian cells.

Cheng-I J Ma, Cyril Martin, Zhong Ma, Anouar Hafiane, Meiou Dai, Jean-Jacques Lebrun, Robert S Kiss

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.3field-weighted citation impact, top 44% 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, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Transcription-translation error:Informatics in medicine unlocked · 2021
    Article
  8. Article
  9. Article
  10. Article
  11. Efferocytosis Signaling in the Regulation of Macrophage Inflammatory Responses.Journal of immunology (Baltimore, Md. : 1950) · 2017
    Review
  12. Article
  13. Article
  14. 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

7 authors at 2 institutions in 2 countries.

Cheng-I J MaDepartment of Medicine, McGill University, Montreal, Quebec H3A 1A1, Canada.
Cyril Martin
Zhong Ma
Anouar Hafiane
Meiou Dai
Jean-Jacques Lebrun
Robert S Kiss
McGill University · CACarter Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transforming growth factor β (TGF-β) is a key regulatory molecule with pleiotropic effects on cell growth, migration, and invasion. As a result, impairment of proper TGF-β signaling is central to tumorigenesis and metastasis. The TGF-β receptor V (TGFBRV or LRP1) has been shown to be responsible for TGF-β-mediated cell growth inhibition in Chinese hamster ovary (CHO) cells. The LRP1 adapter protein GULP mediates internalization of the various LRP1-specific ligands, and we hypothesize that GULP acts as a novel regulator of TGF-β signaling in ovarian cells. CHO cells that overexpress exogenous GULP (FL) demonstrate enhancement in growth inhibition, migration, and invasion from TGF-β treatment, whereas cells that lack GULP (AS) show impairment of growth inhibition and decreased migration and invasion. The enhanced TGF-β response in FL cells was confirmed by a prolonged TGF-β-induced SMAD3 phosphorylation, whereas a shortening of the phosphorylation event is observed in AS cells. Mechanistically, the presence of GULP retains the TGF-β in a signaling-competent early endosome for enhanced signaling. To address this mechanism in a physiological setting, TGF-β insensitive ovarian adenocarcinoma cells (HEY) have a very low GULP expression level, similar to the observation made in a wide selection of human ovarian adenocarcinomas. Transfection of GULP into the HEY cells restored the TGF-β responsiveness, as measured by SMAD3 phosphorylation and impairment of cell growth. Because GULP expression positively regulates TGF-β signaling leading to growth inhibition, this may represent an attractive target to achieve TGF-β responsiveness in ovarian cells.

Indexed as

Cell MovementAdaptor Proteins, Signal TransducingAdenocarcinomaAnimalsCHO CellsCricetinaeCricetulusEndosomesFemaleGene Expression Regulation, NeoplasticHumansMiceNeoplasm InvasivenessNeoplasm ProteinsOvarian NeoplasmsSmad3 ProteinAdaptor Proteins, Signal TransducingGULP1 protein, humanNeoplasm ProteinsSmad3 ProteinSMAD3 protein, humanTransforming Growth Factor beta

Identifiers

PMID22451657
PMCPMC3370247
OpenAlexW1894641575

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.