Evidence map›Paper›PMID 37569364›Full record

ArticleInternational journal of molecular sciences2023

Phospho-DIGE Identified Phosphoproteins Involved in Pathways Related to Tumour Growth in Endometrial Cancer.

Valeria Capaci, Giorgio Arrigoni, Lorenzo Monasta, Michelangelo Aloisio, Giulia Rocca, Giovanni Di Lorenzo, Danilo Licastro, Federico Romano, Giuseppe Ricci, Blendi Ura

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Article
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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

10 authors.

Valeria CapaciInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0002-0110-5942
Giorgio ArrigoniDepartment of Biomedical Sciences, University of Padova, 35131 Padova, Italy.ORCID 0000-0002-4103-2733
Lorenzo MonastaInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0001-7774-548X
Michelangelo AloisioInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.
Giulia RoccaDepartment of Biomedical Sciences, University of Padova, 35131 Padova, Italy.
Giovanni Di LorenzoInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0002-8845-1206
Danilo LicastroAREA Science Park, Basovizza, 34149 Trieste, Italy.
Federico RomanoInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0003-2157-8330
Giuseppe RicciInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.ORCID 0000-0002-8031-1102
Blendi UraInstitute for Maternal and Child Health, IRCCS Burlo Garofolo, 34137 Trieste, Italy.

Funding

Italian Ministry of Health 5x1000 SD 18\19.
6 · The paper itself

Abstract

Endometrial cancer (EC) is the most common gynecologic malignancy of the endometrium. This study focuses on EC and normal endometrium phosphoproteome to identify differentially phosphorylated proteins involved in tumorigenic signalling pathways which induce cancer growth. We obtained tissue samples from 8 types I EC at tumour stage 1 and 8 normal endometria. We analyzed the phosphoproteome by two-dimensional differential gel electrophoresis (2D-DIGE), combined with immobilized metal affinity chromatography (IMAC) and mass spectrometry for protein and phosphopeptide identification. Quantities of 34 phosphoproteins enriched by the IMAC approach were significantly different in the EC compared to the endometrium. Validation using Western blotting analysis on 13 patients with type I EC at tumour stage 1 and 13 endometria samples confirmed the altered abundance of HBB, CKB, LDHB, and HSPB1. Three EC samples were used for in-depth identification of phosphoproteins by LC-MS/MS analysis. Bioinformatic analysis revealed several tumorigenic signalling pathways. Our study highlights the involvement of the phosphoproteome in EC tumour growth. Further studies are needed to understand the role of phosphorylation in EC. Our data shed light on mechanisms that still need to be ascertained but could open the path to a new class of drugs that could hinder EC growth.

Indexed as

Endometrial NeoplasmsPhosphoproteinsChromatography, AffinityChromatography, LiquidFemaleHumansProteomeTandem Mass SpectrometryPhosphoproteinsProteome2D-DIGEendometrial cancermass spectrometryphosphoproteins

Identifiers

PMID37569364
PMCPMC10419128

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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.