Evidence map›Paper›PMID 29495357›Full record

ReviewInternational journal of molecular sciences2018

Regulation of Cell Signaling Pathways and miRNAs by Resveratrol in Different Cancers.

Ammad Ahmad Farooqi, Sumbul Khalid, Aamir Ahmad

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

37 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Review
  3. Challenges and Perspectives in ncRNA Research.Experientia supplementum (2012) · 2026
    Review
  4. Human miRNAs in Cancer: Statistical Trends and Cross Kingdom Approach.International journal of molecular sciences · 2025
    Article
  5. Review
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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

3 authors at 3 institutions in 2 countries.

Ammad Ahmad FarooqiInstitute of Biomedical and Genetic Engineering (IBGE), Islamabad 44000, Pakistan. ammadfarooqi@rlmclahore.com.
Sumbul KhalidDepartment of Bioinformatics and Biotechnology, International Islamic University, Islamabad 44000, Pakistan. sumbul.khalid@iiu.edu.pk.
Aamir AhmadDepartment of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama, Mobile, AL 36604, USA. aahmad@health.southalabama.edu.ORCID 0000-0003-1784-5723
Institute of Biomedical and Genetic Engineering · PKInternational Islamic University, Islamabad · PKUSA Mitchell Cancer Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genomic and proteomic studies have helped improve our understanding of the underlying mechanism(s) of cancer development and progression. Mutations, overexpressed oncogenes, inactivated/downregulated tumor suppressors, loss of apoptosis, and dysregulated signal transduction cascades are some of the well-studied areas of research. Resveratrol has gained considerable attention in the last two decades because of its pleiotropic anticancer activities. In this review, we have summarized the regulation of WNT, SHH (sonic hedgehog)/GLI (glioma-associated oncogene homolog), TGFβ1 (transforming growth factor beta 1)/SMAD, NOTCH, TRAIL (tumor necrosis factor-related apoptosis-inducing ligand), STAT (signal transducer and activator of transcription), and microRNAs by resveratrol in different cancers. The importance of these signaling pathways in cancer progression, along with their modulation by resveratrol, is discussed. Further, we also evaluate the mechanisms and implications of the downregulation of oncogenic miRNAs and the upregulation of tumor suppressor miRNAs by resveratrol, both of which also define its ability to inhibit tumor growth and metastasis. It is envisioned that designing effective clinical trials will be helpful for the identification of resveratrol responders and non-responders and the elucidation of how this phytochemical can be combined with current therapeutic options to improve their clinical efficacy and reduce off-target effects.

Indexed as

AnimalsAntineoplastic Agents, PhytogenicClinical Trials as TopicGene Expression Regulation, NeoplasticHedgehog ProteinsHumansMicroRNAsNeoplasmsReceptors, NotchResveratrolSignal TransductionSmad ProteinsSTAT Transcription FactorsStilbenesTNF-Related Apoptosis-Inducing LigandTransforming Growth Factor beta1Antineoplastic Agents, PhytogenicHedgehog ProteinsMicroRNAsReceptors, NotchResveratrolSmad ProteinsSTAT Transcription FactorsStilbenesTNF-Related Apoptosis-Inducing LigandTransforming Growth Factor beta1Zinc Finger Protein GLI1cell signalingmiRNAsresveratrol

Identifiers

PMID29495357
PMCPMC5877513
OpenAlexW2793324269

What OpenQuestion holds

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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.