Evidence map›Paper›PMID 37759583›Full record

ArticleBiology2023

Protective Effect of Daidzein against Diethylnitrosamine/Carbon Tetrachloride-Induced Hepatocellular Carcinoma in Male Rats.

Samir A E Bashandy, Hossam Ebaid, Jameel Al-Tamimi, Iftekhar Hassan, Enayat A Omara, Marawan A Elbaset, Ibrahim M Alhazza, Jamal A Siddique

Abstract read
In one paragraph

Article in Biology, 2023. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Current investigations for liver fibrosis treatment: between repurposing the FDA-approved drugs and the other emerging approaches.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2023
    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

8 authors.

Samir A E BashandyPharmacology Department, National Research Centre, 33 El-Bohouth St., Dokki, Cairo 12622, Egypt.
Hossam EbaidZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0003-3318-7820
Jameel Al-TamimiZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Iftekhar HassanZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.ORCID 0000-0001-6993-9954
Enayat A OmaraPathology Department, National Research Centre, 33 El-Bohouth St., Dokki, Cairo 12622, Egypt.
Marawan A ElbasetPharmacology Department, National Research Centre, 33 El-Bohouth St., Dokki, Cairo 12622, Egypt.
Ibrahim M AlhazzaZoology Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia.
Jamal A SiddiqueDepartment of Materials Engineering and Chemistry, Faculty of Civil Engineering, Czech Technical University (CVUT), Praha 6, 16629 Prague, Czech Republic.

Funding

Deanship of Scientific Research at King Saud University for funding the work through the research group Project no. RG-1436-004 Deanship of Scientific Research at King Saud University for funding the work through the research group Project no. RG-1436-004
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the second-largest cause of death among all cancer types. Many drugs have been used to treat the disease for a long time but have been mostly discontinued because of their side effects or the development of resistance in the patients with HCC. The administration of DZ orally is a great focus to address the clinical crisis. Daidzein (DZ) is a prominent isoflavone polyphenolic chemical found in soybeans and other leguminous plants. It has various pharmacological effects, including anti-inflammatory, antihemolytic, and antioxidant. This present study investigates the protective effect of DZ on chemically induced HCC in rat models. The DZ was administered orally four weeks before HCC induction and continued during treatment. Our study included four treatment groups: control (group 1, without any treatment), HCC-induced rats (group II), an HCC group treated with DZ at 20 mg/kg (group III), and an HCC group treated with DZ at 40 mg/kg (group IV). HCC rats showed elevation in all the HCC markers (AFP, GPC3, and VEGF), liver function markers (ALP, ALT, and AST), inflammatory markers (IL-6, TNF-α, and CRP), and lipid markers concomitant with a decrease in antioxidant enzymes and protein. However, groups III and IV demonstrated dose-dependent alleviation in the previous parameters resulting from HCC. In addition, the high dose of DZ reduces many hepatological changes in HCC rats. All study parameters improved with DZ administration. Due to its antioxidant and anti-inflammatory characteristics, DZ is a promising HCC treatment option for clinical use.

Indexed as

CCL4Daidzeinhepatocellular carcinomainflammatory markers

Identifiers

PMID37759583
PMCPMC10525464

What OpenQuestion holds

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Registered trials

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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.