Evidence map›Paper›PMID 35220526›Full record

ReviewMolecular biology reports2022

The effects of Ginsenosides on PI3K/AKT signaling pathway.

Soudeh Ghafouri-Fard, Neda Balaei, Hamed Shoorei, Syed Muhammad Farid Hasan, Bashdar Mahmud Hussen, Seyedeh Fahimeh Talebi, Mohammad Taheri, Seyed Abdulmajid Ayatollahi

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular biology reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-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

18 citing papers in PubMed, 20 citations in OpenAlex.

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  15. Anti-leukemia effects of ginsenoside monomer: A narrative review of pharmacodynamics study.Current therapeutic research, clinical and experimental · 2024
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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

8 authors at 6 institutions in 4 countries.

Soudeh Ghafouri-FardDepartment of Medical Genetics, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Neda BalaeiDepartment of Pharmacology, Tabriz University of Medical Sciences, Tabriz, Iran.
Hamed ShooreiDepartment of Anatomical Sciences, Faculty of Medicine, Birjand University of Medical Sciences, Birjand, Iran.
Syed Muhammad Farid HasanDepartment of Pharmaceutics, Faculty of Pharmacy and Pharmaceutical Sciences, University of Karachi, Karachi, Pakistan.
Bashdar Mahmud HussenDepartment of Pharmacognosy, College of Pharmacy, Hawler Medical University, Kurdistan Region, Iraq.
Seyedeh Fahimeh TalebiDepartment of Pharmacology, College of Pharmacy, Birjand University of Medical Sciences, Birjand, Iran.
Mohammad TaheriInstitute of Human Genetics, Jena University Hospital, Jena, Germany. mohammad.taheri@uni-jena.de.
Seyed Abdulmajid AyatollahiPhytochemistry Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran. a_ayatollahi@sbmu.ac.ir.
Birjand University of Medical Sciences · IRShahid Beheshti University of Medical Sciences · IRHawler Medical University · IQJena University Hospital · DETabriz University of Medical Sciences · IRUniversity of Karachi · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ginsenosides belong to a group of steroid glycosides that are extracted from the plant genus Panax (ginseng). This plant has been used for a long time for the treatment of a variety of disorders in traditional medicine. Recent studies have assessed the biological impact of Ginsenosides in cell culture or animal models. Animal studies have shown their beneficial impacts in the remedy of pathological conditions in different tissues. The ameliorating effects of Ginsenosides in diverse pathogenic conditions can be attributed to their effects on the production of reactive oxygen species. These substances mainly affect the activity of AMPK/AKT and PI3K/AKT pathways. The beneficial effects of Ginsenosides have been appraised in diabetes-related complications, spinal cord injury, cerebral ischemia, myocardial ischemia, and other disorders which are associated with oxidative stress. Moreover, these substances have been shown to interfere with the pathologic conditions during carcinogenesis. In the current study, we explain these impacts in two distinct sections including non-neoplastic conditions and neoplastic conditions.

Indexed as

GinsenosidesPanaxAnimalsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktSignal TransductionGinsenosidesPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktGene expressionGinsenosideSignaling pathway

Identifiers

PMID35220526
PMCPMC9270311
OpenAlexW4214740208

What Socratic 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 Socratic graph.