Evidence map›Paper›PMID 35707368›Full record

ArticleFrontiers in oncology2022

Evaluation of Galanin Expression in Colorectal Cancer: An Immunohistochemical and Transcriptomic Study.

Iman M Talaat, Nada M Yakout, Ahmed S A Soliman, Thenmozhi Venkatachalam, Arya Vinod, Leen Eldohaji, Vidhya Nair, Amal Hareedy, Alaa Kandil, Wael M Abdel-Rahman and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 19 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. 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

12 authors at 4 institutions in 3 countries.

Iman M TalaatDepartment of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Nada M YakoutPathology Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Ahmed S A SolimanPathology Department, National Research Center, Cairo, Egypt.
Thenmozhi VenkatachalamSharjah Institute for Medical Research, University of Sharjah, Sharjah, United Arab Emirates.
Arya VinodSharjah Institute for Medical Research, University of Sharjah, Sharjah, United Arab Emirates.
Leen EldohajiSharjah Institute for Medical Research, University of Sharjah, Sharjah, United Arab Emirates.
Vidhya NairSharjah Institute for Medical Research, University of Sharjah, Sharjah, United Arab Emirates.
Amal HareedyPathology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Alaa KandilClinical Oncology and Nuclear Medicine Department, Faculty of Medicine, Alexandria University, Cairo, Egypt.
Wael M Abdel-RahmanSharjah Institute for Medical Research, University of Sharjah, Sharjah, United Arab Emirates.
Rifat HamoudiDepartment of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Maha Saber-AyadDepartment of Clinical Sciences, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
University of Sharjah · AEAlexandria University · EGCairo University · EGNational Water Research Center · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) represents around 10% of all cancers, with an increasing incidence in the younger age group. The gut is considered a unique organ with its distinctive neuronal supply. The neuropeptide, human galanin, is widely distributed in the colon and expressed in many cancers, including the CRC. The current study aimed to explore the role of galanin at different stages of CRC. Eighty-one CRC cases (TNM stages I - IV) were recruited, and formalin-fixed paraffin-embedded samples were analyzed for the expression of galanin and galanin receptor 1 (GALR1) by immunohistochemistry (IHC). Galanin intensity was significantly lower in stage IV (n= 6) in comparison to other stages (p= 0.037 using the Mann-Whitney U test). Whole transcriptomics analysis using NGS was performed for selected samples based on the galanin expression by IHC [early (n=5) with high galanin expression and late (n=6) with low galanin expression]. Five differentially regulated pathways (using Absolute GSEA) were identified as drivers for tumor progression and associated with higher galanin expression, namely, cell cycle, cell division, autophagy, transcriptional regulation of TP53, and immune system process. The top shared genes among the upregulated pathways are

Indexed as

bioinformaticscolorectal cancergalaninGALR1immunohistochemistryTIMER 2transcriptomic analysis

Identifiers

PMID35707368
PMCPMC9190230
OpenAlexW4281754259

What Socratic 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 Socratic graph.