Evidence map›Paper›PMID 29844359›Full record

ArticleCell death & disease2018

Various stress stimuli rewire the profile of liver secretome in a p53-dependent manner.

Meital Charni-Natan, Hilla Solomon, Alina Molchadsky, Adi Jacob-Berger, Naomi Goldfinger, Varda Rotter

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 29% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Environmental Stress Responses ofFrontiers in genetics · 2018
    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

6 authors at 1 institution in 1 country.

Meital Charni-NatanDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Hilla SolomonDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Alina MolchadskyDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Adi Jacob-BergerDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Naomi GoldfingerDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Varda RotterDepartment of Molecular Cell Biology, Weizmann Institute of Science, Rehovot, Israel. varda.rotter@weizmann.ac.il.
Weizmann Institute of Science · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Liver is an important secretory organ that consistently manages various insults in order to retain whole-body homeostasis. Importantly, it was suggested that the tumor-suppressor p53 plays a role in a variety of liver physiological processes and thus it is being regarded as a systemic homeostasis regulator. Using high-throughput mass spectrometric analysis, we identified various p53-dependent liver secretome profiles. This allowed a global view on the role of p53 in maintaining the harmony of liver and whole-body homeostasis. We found that p53 altered the liver secretome differently under various conditions. Under physiological conditions, p53 controls factors that are related mainly to lipid metabolism and injury response. Upon exposure to various types of cancer therapy agents, the hepatic p53 is activated and induces the secretion of proteins related to additional pathways, such as hemostasis, immune response, and cell adhesion. Interestingly, we identified a possible relationship between p53-dependent liver functions and lung tumors. The latter modify differently liver secretome profile toward the secretion of proteins mainly related to cell migration and immune response. The notion that p53 may rewire the liver secretome profile suggests a new non-cell autonomous role of p53 that affect different liver functions and whole organism homeostasis.

Indexed as

Stress, PhysiologicalAnimalsAntineoplastic AgentsCell Line, TumorGene Expression Regulation, NeoplasticHumansLiverLung NeoplasmsMice, Inbred C57BLMice, KnockoutTumor Suppressor Protein p53Antineoplastic AgentsTumor Suppressor Protein p53

Identifiers

PMID29844359
PMCPMC5974134
OpenAlexW2806606242

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.