Evidence map›Paper›PMID 28438053›Full record

ArticleIntegrative cancer therapies2018

Scorpion Venom Causes Upregulation of p53 and Downregulation of Bcl-x

Abdulrahman Khazim Al-Asmari, Anvarbatcha Riyasdeen, Mozaffarul Islam

Open access · goldAbstract read
In one paragraph

Article in Integrative cancer therapies, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

17 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Role of STAT3 signaling pathway in breast cancer.Cell communication and signaling : CCS · 2020
    Pooled it
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  8. Article
  9. The journal of venomous animals and toxins including tropical diseases · 2025
    Article
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  12. Article
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  15. Article
  16. Review
  17. Pleiotropic Anticancer Properties of Scorpion Venom Peptides:Drug design, development and therapy · 2020
    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

3 authors at 1 institution in 1 country.

Abdulrahman Khazim Al-Asmari1 Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.
Anvarbatcha Riyasdeen1 Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.
Mozaffarul Islam1 Prince Sultan Military Medical City, Riyadh, Kingdom of Saudi Arabia.
Riyadh Armed Forces Hospital · SA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Scorpion venoms efficiently block the normal neurotransmitter signaling pathway by prejudicing the ion channel operating mechanism in the body system. Besides its negative effect, venoms also possess some beneficial qualities for humans. They have also been shown to exhibit anticancer properties in various cancer types. This unique property of the venom as an anticancer agent is mainly a result of its role in initiating apoptosis and inhibiting several signaling cascade mechanisms that promote cancer cell proliferation and growth. In this study, we examine the effect of venom on phenotypic changes as well as changes at the molecular levels in colorectal and breast cancer cell lines. A dramatic decrease in cell invasion was observed in both cancer cell lines on venom treatment. Additionally, there was decrease in IL-6, RhoC, Erk

Indexed as

AgedApoptosisbcl-X ProteinBH3 Interacting Domain Death Agonist ProteinBreast NeoplasmsCell Line, TumorCell ProliferationCell SurvivalColorectal NeoplasmsDNA DamageDown-RegulationFemaleHumansMAP Kinase Signaling SystemScorpion VenomsSignal TransductionBCL2L1 protein, humanbcl-X ProteinBH3 Interacting Domain Death Agonist ProteinBID protein, humanScorpion VenomsSTAT3 protein, humanSTAT3 Transcription FactorTP53 protein, humanTumor Suppressor Protein p53Bcl-XLBIDIL-6P53scorpion venomSTAT3

Identifiers

PMID28438053
PMCPMC6041906
OpenAlexW2609187513

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.