Evidence map›Paper›PMID 35955525›Full record

ReviewInternational journal of molecular sciences2022

Regulation of Cell Signaling Pathways and Non-Coding RNAs by Baicalein in Different Cancers.

Ammad Ahmad Farooqi, Gulnara Kapanova, Sundetgali Kalmakhanov, Gulnur Tanbayeva, Kairat S Zhakipbekov, Venera S Rakhmetova, Marat K Syzdykbayev

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.1field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Phytochemical Characterization ofFood science & nutrition · 2026
    Article
  2. Review
  3. 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

7 authors at 5 institutions in 2 countries.

Ammad Ahmad FarooqiDepartment of Molecular Oncology, Institute of Biomedical and Genetic Engineering (IBGE), Islamabad 44000, Pakistan.ORCID 0000-0003-2209-7483
Gulnara KapanovaScientific Center of Anti-Infectious Drugs, 75 al-Faraby Ave, Almaty 050040, Kazakhstan.
Sundetgali KalmakhanovAl-Farabi Kazakh National University, 71 al-Farabi Ave, Almaty 050040, Kazakhstan.
Gulnur TanbayevaAl-Farabi Kazakh National University, 71 al-Farabi Ave, Almaty 050040, Kazakhstan.
Kairat S ZhakipbekovDepartment of Organization and Management and Economics of Pharmacy and Clinical Pharmacy, Asfendiyarov Kazakh National Medical University KazNMU, Tole Bi St. 94, Almaty 050000, Kazakhstan.
Venera S RakhmetovaDepartment Internal Diseases, Astana Medical University, Nur-Sultan 010000, Kazakhstan.
Marat K SyzdykbayevDepartment of Anesthesiology, Reanimatology and Narcology, Semey Medical University, Semey 071400, Kazakhstan.
Al-Farabi Kazakh National University · KZAstana Medical University · KZInstitute of Biomedical and Genetic Engineering · PKKazakh National Medical University · KZSemey Medical University · KZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Landmark discoveries in molecular oncology have provided a wide-angle overview of the heterogenous and therapeutically challenging nature of cancer. The power of modern 'omics' technologies has enabled researchers to deeply and comprehensively characterize molecular mechanisms underlying cellular functions. Interestingly, high-throughput technologies have opened new horizons for the design and scientific fool-proof evaluation of the pharmacological properties of targeted chemical compounds to tactfully control the activities of the oncogenic protein networks. Groundbreaking discoveries have galvanized the expansion of the repertoire of available pharmacopoeia to therapeutically target a myriad of deregulated oncogenic pathways. Natural product research has undergone substantial broadening, and many of the drugs which constitute the backbone of modern pharmaceuticals have been derived from the natural cornucopia. Baicalein has gradually gained attention because of its unique ability to target different oncogenic signal transduction cascades in various cancers. We have partitioned this review into different sub-sections to provide a broader snapshot of the oncogenic pathways regulated by baicalein. In this review, we summarize baicalein-mediated targeting of WNT/β-catenin, AKT/mTOR, JAK/STAT, MAPK, and NOTCH pathways. We also critically analyze how baicalein regulates non-coding RNAs (microRNAs and long non-coding RNAs) in different cancers. Finally, we conceptually interpret baicalein-mediated inhibition of primary and secondary growths in xenografted mice.

Indexed as

FlavanonesMicroRNAsNeoplasmsAnimalsCarcinogenesisMiceSignal TransductionbaicaleinFlavanonesMicroRNAsbaicaleincancercell signalingmetastasisnatural products

Identifiers

PMID35955525
PMCPMC9368823
OpenAlexW4289134397

What OpenQuestion 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 OpenQuestion graph.