Evidence map›Paper›PMID 36063095›Full record

ArticleThe journal of international advanced otology2022

Comparison of Cytotoxic and Ototoxic Effects of Lipoplatin and Cisplatin in Neuroblastoma In Vivo Tumor Model.

Hande Evin Eskicioğlu, Yüksel Olgun, Tekincan Çağrı Aktaş, Safiye Aktas, Efsun Kolatan, Efe Serinan, Zekiye Altun, Günay Kırkım, Osman Yılmaz, Nur Olgun

Open access · diamondAbstract read
In one paragraph

Article in The journal of international advanced otology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
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

10 authors at 1 institution in 1 country.

Hande Evin EskicioğluDokuz Eylül University, Vocational School of Health Services,İzmir, Turkey; Department of Otorhinolaryngology Unit of Hearing Speech and Balance, Dokuz Eylül University Hospital, İzmir, Turkey; Department of Basic Oncology, Dokuz Eylül University, Institute of Oncology, İzmir, Turkey.
Yüksel OlgunDepartment of Otorhinolaryngology, Dokuz Eylül University Faculty of Medicine, İzmir, Turkey.
Tekincan Çağrı AktaşDepartment of Basic Oncology, Dokuz Eylül University, Institute of Oncology, İzmir, Turkey.
Safiye AktasDepartment of Basic Oncology, Dokuz Eylül University, Institute of Oncology, İzmir, Turkey.
Efsun KolatanDepartment of Laboratory Animals, Dokuz Eylül University, Institute of Health Sciences, İzmir, Turkey.
Efe SerinanDepartment of Basic Oncology, Dokuz Eylül University, Institute of Oncology, İzmir, Turkey.
Zekiye AltunDepartment of Basic Oncology, Dokuz Eylül University, Institute of Oncology, İzmir, Turkey.
Günay KırkımDokuz Eylül University, Vocational School of Health Services,İzmir, Turkey; Department of Otorhinolaryngology Unit of Hearing Speech and Balance, Dokuz Eylül University Hospital, İzmir, Turkey.
Osman YılmazDepartment of Laboratory Animals, Dokuz Eylül University, Institute of Health Sciences, İzmir, Turkey.
Nur OlgunDepartment of Pediatric Oncology, Dokuz Eylül University, Institute of Oncology, İzmir, Turkey.
Dokuz Eylül University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to compare the cytotoxic, cytostatic, and ototoxic effects of lipoplatin compared to cisplatin application in the subcutaneous xenograft nude mouse neuroblastoma tumor model.

methodsIn this study, C1300 neuroblastoma cells were administered subcutaneously to 21 male nude mice. When the tumor reached 150 mm3 diameter, mice were randomized into 3 groups. Saline, cisplatin, and lipoplatin were given intraperitoneally. The auditory function tests were performed before administration and 72 hours after administration. Mice were sacrificed and the tumor and cochlea were removed after 72 hours. Histopathologic evaluation of necrosis and apoptosis was determined by the TdT-mediated dUTP-biotin nick end labeling (TUNEL) method. Cyclooxygenase 2, superoxide dismutase 2, and inducible nitric oxide synthase levels were determined by immunohistochemistry in tissue samples.

resultsApoptosis and necrosis rates were higher in lipoplatin group than in cisplatin group (P=.035 and P=.010, respectively) in tumor tissue. In the spiral ganglion, apoptosis and necrosis were lower in the lipoplatin group than in cisplatin group (P=.002 and P=.002, respectively). Cyclooxygenase 2 pattern in the cochlea was positive in both control and lipoplatin group and negative in cisplatin group (P=.001). Superoxide dismutase 2 and inducible nitric oxide synthase 2 protein expressions showed no difference between groups. The auditory functions were similar to baseline values and had a better threshold value in lipoplatin group than cisplatin group.

conclusionFor the treatment of neuroblastoma, the use of lipoplatin seems to be beneficial in reducing side effects of cisplatin. We recommend that the mechanism of these properties of lipoplatin should be evaluated in further studies.

Indexed as

Antineoplastic AgentsNeuroblastomaOtotoxicityAnimalsCisplatinCyclooxygenase 2MaleMiceMice, NudeNecrosisNitric Oxide Synthase Type IIAntineoplastic AgentsCisplatinCyclooxygenase 2lipoplatinNitric Oxide Synthase Type II

Identifiers

PMID36063095
PMCPMC9524363
OpenAlexW4294168208

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.