Evidence map›Paper›PMID 41612765›Full record

ReviewBiotechnology and applied biochemistry2026

Therapeutic Potential of Ginger Rhizomes (Zingiber officinale) on Leukemia.

Abdolhossein Hajizadeh, Parmida Nafei, Kimiya Seraj, Faranak Zargari, Nassim Rastgar, Farshad Zare, Obid Khamidov, Ghadeer Mohammed Ali Basha, Mustafa Sattar, Mehdi Amirhooshangi and 2 more

Abstract readReview
In one paragraph

Review in Biotechnology and applied biochemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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

12 authors.

Abdolhossein HajizadehShiraz University of Medical Sciences, Shiraz, Iran.
Parmida NafeiFaculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.
Kimiya SerajFaculty of Pharmacy, Hamedan University of Medical Science, Hamedan, Iran.ORCID https://orcid.org/0009-0006-6508-8615
Faranak ZargariFaculty of Pharmacy, Urmia University of Medical Sciences, Urmia, West Azerbaijan, Iran.
Nassim RastgarDepartment of Pharmacology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Farshad ZareStudent Research Committee, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Obid KhamidovDepartment of Medical Radiology, Samarkand State Medical University, Samarkand, Uzbekistan.
Ghadeer Mohammed Ali BashaCollege of Medicine, University of Baghdad, Baghdad, Iraq.
Mustafa SattarFaculty of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Mehdi AmirhooshangiNeurosciences Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Nima GhavamikiaCardiovascular Research Institute, Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.
Payam Ali-KhiaviStudent Research Committee, School of Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID https://orcid.org/0009-0001-9514-2209

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Leukemia continues to provide a significant therapeutic challenge due to relapse, medication resistance, and treatment-associated toxicity, which frequently hinder sustained disease management. Rhizomes of ginger (Zingiber officinale) possess bioactive phenolics, notably 6-gingerol and 6-shogaol derivatives, which have demonstrated antileukemia efficacy in preclinical models. This study rigorously assesses the evidence regarding ginger-derived preparations and isolated compounds in both acute and chronic leukemia models, focusing on recurring mechanisms and translational viability. In leukemia cell line investigations and sparse resistant-model data, ginger-related interventions are consistently linked to diminished viability and the induction of mitochondrial apoptosis, typically indicated by alterations in Bax/Bcl-2 ratios, PARP breakage, and caspase-related measurements. Numerous studies indicate redox modulation, often characterized by elevated intracellular reactive oxygen species in leukemic cells, coupled with diminished pro-survival signaling, such as PI3K/Akt, as indicated by decreased pAkt and survivin levels. The suggested immunomodulatory and anti-inflammatory effects, encompassing alterations in NK-cell activity and cytokines like TNF-α and IL-6, are inadequately substantiated within leukemia-specific immunological contexts. Interpretation is limited by the variability in extract composition and chemical characterisation, inconsistent dose and exposure circumstances, dependence on endpoint markers without causative manipulation, and a lack of leukemia-specific clinical data. Ginger-derived compounds exhibit multi-target biological activity that necessitates further exploration through standardized and chemically defined preparations, pharmacokinetic and pharmacodynamic characterization, clinically relevant exposure benchmarks, and meticulously designed leukemia-focused translational and early-phase clinical studies to elucidate safety, efficacy, and compatibility with current therapies.

Indexed as

Antineoplastic Agents, PhytogenicLeukemiaRhizomeZingiber officinaleAnimalsApoptosisCatecholsHumansAntineoplastic Agents, PhytogenicCatecholscancerginger rhizomesleukemiamolecular mechanisms

Identifiers

PMID41612765
PMCPMC13446437

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.