Evidence map›Paper›PMID 42514188›Full record

ArticleLife (Basel, Switzerland)2026

Effects of ATP and Taxifolin on Atezolizumab-Induced Renal Injury: A Biochemical, Histopathological, and Immunofluorescence Evaluation.

Adil Furkan Kilic, Esra Tuba Sezgin, Gulbaniz Huseynova, Cengiz Sarigul, Mustafa Ozkaraca, Ali Gungor, Renad Mammadov, Halis Suleyman, Orhan Cimen

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Adil Furkan KilicDepartment of Internal Medicine, Faculty of Medicine, Atatürk University, 25240 Erzurum, Turkey.ORCID 0000-0003-2209-5437
Esra Tuba SezginAnesthesia Program, Vocational School of Health Services, Erzincan Binali Yıldırım University, 24002 Erzincan, Turkey.ORCID 0000-0003-3491-9798
Gulbaniz HuseynovaDepartment of Pharmacology, Azerbaijan Medical University, AZ1022 Baku, Azerbaijan.
Cengiz SarigulDepartment of Medical Biochemistry, Faculty of Medicine, Erzincan Binali Yıldırım University, 24100 Erzincan, Turkey.ORCID 0000-0001-8826-5502
Mustafa OzkaracaDepartment of Pathology, Faculty of Veterinary Medicine, Sivas Cumhuriyet University, 58140 Sivas, Turkey.ORCID 0000-0002-6359-6249
Ali GungorLaboratory and Veterinary Health Program, Vocational School of Health Services, Osmaniye Korkut Ata University, 80000 Osmaniye, Turkey.ORCID 0009-0008-7985-0986
Renad MammadovDepartment of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, 24100 Erzincan, Turkey.
Halis SuleymanDepartment of Pharmacology, Faculty of Medicine, Erzincan Binali Yıldırım University, 24100 Erzincan, Turkey.ORCID 0000-0002-9239-4099
Orhan CimenDepartment of General Surgery, Faculty of Medicine, Erzincan Binali Yıldırım University, 24100 Erzincan, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs), particularly programmed death-ligand 1 (PD-L1) inhibitors such as atezolizumab, have significantly improved outcomes in cancer therapy. However, these agents may cause immune-related adverse effects, including nephrotoxicity associated with oxidative stress and cellular stress responses. This study aimed to investigate and comparatively evaluate the protective effects of adenosine triphosphate (ATP) and taxifolin against atezolizumab-induced renal tissue injury in rats.

methodsAnimals were divided into four groups: healthy (HG), atezolizumab (ATZ), ATP + atezolizumab (ATAZ), and taxifolin + atezolizumab (TXAZ). ATP (4 mg/kg, i.p.) and taxifolin (50 mg/kg, oral) were administered for six days, while atezolizumab (10 mg/kg, i.p.) was given on days 1 and 4. On day 7, renal tissues were collected for biochemical, histopathological, and double immunofluorescence analyses.

resultsAtezolizumab significantly increased malondialdehyde (MDA) levels and decreased total glutathione (tGSH), superoxide dismutase (SOD), and catalase (CAT) levels, indicating enhanced oxidative stress and impaired antioxidant defense. These changes were accompanied by tubular degeneration and increased expression of apoptotic markers. Both ATP and taxifolin significantly ameliorated these alterations; however, ATP demonstrated a more pronounced protective effect.

conclusionsIn conclusion, ATP and taxifolin attenuated the biochemical, histopathological, and immunofluorescence alterations associated with atezolizumab administration. ATP exhibited a more pronounced protective effect than taxifolin under the conditions of this experimental model. Nevertheless, further experimental studies are required to elucidate the mechanisms underlying these effects.

Indexed as

antioxidant defenseapoptosisatezolizumabATPnephrotoxicityoxidative stresstaxifolin

Identifiers

PMID42514188
PMCPMC13413056

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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.