Evidence map›Paper›PMID 31984217›Full record

ArticleOncoscience2019

SOCS1: phosphorylation, dimerization and tumor suppression.

Frédéric Lessard, Emmanuelle Saint-Germain, Lian Mignacca, Gerardo Ferbeyre

Open access · diamondAbstract read
In one paragraph

Article in Oncoscience, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

8 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. A novel inhibitor ofActa pharmaceutica Sinica. B · 2022
    Article
  7. Emerging roles of ferroptosis in glioma.Frontiers in oncology · 2022
    Review
  8. 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

4 authors at 1 institution in 1 country.

Frédéric LessardDépartement de Biochimie et Médecine Moléculaire, Université de Montréal, Montréal, Québec, Canada.
Emmanuelle Saint-GermainDépartement de Biochimie et Médecine Moléculaire, Université de Montréal, Montréal, Québec, Canada.
Lian MignaccaDépartement de Biochimie et Médecine Moléculaire, Université de Montréal, Montréal, Québec, Canada.
Gerardo FerbeyreDépartement de Biochimie et Médecine Moléculaire, Université de Montréal, Montréal, Québec, Canada.
Université de Montréal · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Suppressor of cytokine signaling (SOCS) family members are upregulated following JAK-STAT pathway activation by cytokines. SOCS proteins are recognized inhibitors of cytokine signaling playing roles in cell growth and differentiation. Moreover, SOCS1 and SOCS3 have been shown to be involved in tumor suppression through their ability to interact with p53 leading to the activation of its transcriptional program and showing the implication of SOCS family members in the regulation of apoptosis, ferroptosis and senescence. More recently, we demonstrated that the SRC family of non-receptor tyrosine kinases (SFK) can phosphorylate SOCS1 leading to its homodimerization and inhibiting its interaction with p53. Then, we reactivated the SOCS1-p53 tumor suppressor axis with the SFK inhibitor dasatinib in combination with the p53 activating compound PRIMA. This work suggests new avenues for cancer treatment and leaves open several new questions that deserve to be addressed.

Indexed as

cytokine singlingP53SH2 domainsSRC kinases

Identifiers

PMID31984217
PMCPMC6959930
OpenAlexW3011531441

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.