Evidence map›Paper›PMID 36082856›Full record

ReviewCurrent topics in medicinal chemistry2022

Anticancer Properties of Kaempferol on Cellular Signaling Pathways.

Bidisha Sengupta, Pragnya Biswas, Debarshi Roy, Justin Lovett, Laken Simington, Darrell R Fry, Kaelin Travis

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.4field-weighted citation impact, top 18% 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

8 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. [Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2025
    Article
  7. Article
  8. 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

7 authors at 3 institutions in 2 countries.

Bidisha SenguptaDepartment of Chemistry and Biochemistry, Stephen F. Austin State University, Nacogdoches, Texas, USA.
Pragnya BiswasSchool of Biotechnology, Presidency University, Kolkata, India.
Debarshi RoyDepartment of Biological Sciences, Alcorn State University, Lorman, Mississippi, USA.
Justin LovettDepartment of Chemistry and Biochemistry, Stephen F. Austin State University, Nacogdoches, Texas, USA.
Laken SimingtonDepartment of Chemistry and Biochemistry, Stephen F. Austin State University, Nacogdoches, Texas, USA.
Darrell R FryDepartment of Chemistry and Biochemistry, Stephen F. Austin State University, Nacogdoches, Texas, USA.
Kaelin TravisCenter of Biotechnology, Alcorn State University, Lorman, Mississippi, USA.
Stephen F. Austin State University · USAlcorn State University · USPresidency University · IN

Funding

Training and Mentoring Core P20GM103476 · NIGMS · UNIVERSITY OF SOUTHERN MISSISSIPPI · PI MICHAEL R GARRETT · 2012 to 2026
$60.2M
NIGMS NIH HHS P20 GM103476
6 · The paper itself

Abstract

Polyhydroxy compounds are secondary metabolites that are ubiquitous in plants of higher genera. They possess therapeutic properties against a wide spectrum of diseases, including cancers, neurodegenerative disorders, atherosclerosis, as well as cardiovascular disease. The phytochemical flavonol (a type of flavonoid) kaempferol (KMP) (3,5,7-trihydroxy-2-(4-hydroxyphenyl)- 4Hchromen-4-one) is abundant in cruciferous vegetables, including broccoli, kale, spinach, and watercress, as well as in herbs like dill, chives, and tarragon. KMP is predominantly hydrophobic in nature due to its diphenylpropane structure (a characteristic feature of flavonoids). Recent findings have indicated the promise of applying KMP in disease prevention due to its potential antioxidant, antimutagenic, antifungal, and antiviral activities. In the literature, there is evidence that KMP exerts its anticancer effects by modulating critical elements in cellular signal transduction pathways linked to apoptosis, inflammation, angiogenesis, and metastasis in cancer cells without affecting the viability of normal cells. It has been shown that KMP triggers cancer cell death by several mechanisms, including cell cycle arrest, caspase activation, metabolic alteration, and impacting human telomerase reverse-transcriptase gene expression. This review is aimed at providing critical insights into the influence of KMP on the intracellular cascades that regulate metabolism and signaling in breast, ovarian, and cervical cancer cells.

Indexed as

KaempferolsNeoplasmsAntioxidantsApoptosisHumansInflammationSignal TransductionAntioxidantsKaempferolsBreast cancerCancer therapyCervical cancerChemoresistance.Natural productOvarian cancer

Identifiers

PMID36082856
PMCPMC10754212
OpenAlexW4295082285

What OpenQuestion holds

Textmetadata
LicenceTDM
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.