Evidence map›Paper›PMID 33127962›Full record

SynthesisScientific reports2020

Signal transduction pathway mutations in gastrointestinal (GI) cancers: a systematic review and meta-analysis.

Alireza Tabibzadeh, Fahimeh Safarnezhad Tameshkel, Yousef Moradi, Saber Soltani, Maziar Moradi-Lakeh, G Hossein Ashrafi, Nima Motamed, Farhad Zamani, Seyed Abbas Motevalian, Mahshid Panahi and 4 more

Open access · goldAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in Scientific reports, 2020. 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
2.3field-weighted citation impact, top 11% 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, 26 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Expanding Therapeutic Opportunities for Extrapulmonary Neuroendocrine Carcinoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2022
    Review
  10. Article
  11. Review
  12. Article
  13. The emerging role of miR-10 family in gastric cancer.Cell cycle (Georgetown, Tex.) · 2021
    Review
  14. 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

14 authors at 6 institutions in 2 countries.

Alireza TabibzadehDepartment of Virology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Fahimeh Safarnezhad TameshkelStudent Research Committee, Iran University of Medical Sciences, Tehran, Iran.
Yousef MoradiSocial Determinants of Health Research Center, Research Institute for Health Development, Kurdistan University of Medical Sciences, Sanandaj, Iran.
Saber SoltaniDepartment of Virology, Tehran University of Medical Sciences, Tehran, Iran.
Maziar Moradi-LakehGastrointestinal and Liver Disease Research Center, Iran University of Medical Sciences, Tehran, Iran.
G Hossein AshrafiCancer Theme SEC Faculty, Kingston University, Penrhyn Road, London, KT1 2EE, UK.
Nima MotamedDepartment of Social Medicine, Zanjan University of Medical Sciences, Zanjan, Iran.
Farhad ZamaniGastrointestinal and Liver Disease Research Center, Iran University of Medical Sciences, Tehran, Iran.
Seyed Abbas MotevalianDepartment of Epidemiology, School of Public Health, Iran University of Medical Sciences, Tehran, Iran.
Mahshid PanahiGastrointestinal and Liver Disease Research Center, Iran University of Medical Sciences, Tehran, Iran.
Maryam EsghaeiDepartment of Virology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Hossein AjdarkoshGastrointestinal and Liver Disease Research Center, Iran University of Medical Sciences, Tehran, Iran.
Alireza Mousavi-JarrahiSchool of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mohammad Hadi Karbalaie NiyaGastrointestinal and Liver Disease Research Center, Iran University of Medical Sciences, Tehran, Iran. karbalai.mh@iums.ac.ir.
Iran University of Medical Sciences · IRKingston University · GBKurdistan University of Medical Sciences · IRShahid Beheshti University of Medical Sciences · IRTehran University of Medical Sciences · IRZanjan University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The present study was conducted to evaluate the prevalence of the signaling pathways mutation rate in the Gastrointestinal (GI) tract cancers in a systematic review and meta-analysis study. The study was performed based on the PRISMA criteria. Random models by confidence interval (CI: 95%) were used to calculate the pooled estimate of prevalence via Metaprop command. The pooled prevalence indices of signal transduction pathway mutations in gastric cancer, liver cancer, colorectal cancer, and pancreatic cancer were 5% (95% CI: 3-8%), 12% (95% CI: 8-18%), 17% (95% CI: 14-20%), and 20% (95% CI: 5-41%), respectively. Also, the mutation rates for Wnt pathway and MAPK pathway were calculated to be 23% (95% CI, 14-33%) and 20% (95% CI, 17-24%), respectively. Moreover, the most popular genes were APC (in Wnt pathway), KRAS (in MAPK pathway) and PIK3CA (in PI3K pathway) in the colorectal cancer, pancreatic cancer, and gastric cancer while they were beta-catenin and CTNNB1 in liver cancer. The most altered pathway was Wnt pathway followed by the MAPK pathway. In addition, pancreatic cancer was found to be higher under the pressure of mutation compared with others based on pooled prevalence analysis. Finally, APC mutations in colorectal cancer, KRAS in gastric cancer, and pancreatic cancer were mostly associated gene alterations.

Indexed as

MutationSignal TransductionAdenomatous Polyposis Coli ProteinClass I Phosphatidylinositol 3-KinasesDNA Mutational AnalysisGastrointestinal NeoplasmsHumansMAP Kinase Signaling SystemPrevalenceProto-Oncogene Proteins p21(ras)Wnt Signaling PathwayAdenomatous Polyposis Coli ProteinAPC protein, humanClass I Phosphatidylinositol 3-KinasesKRAS protein, humanPIK3CA protein, humanProto-Oncogene Proteins p21(ras)

Identifiers

PMID33127962
PMCPMC7599243
OpenAlexW3096158121

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.