Evidence map›Paper›PMID 29936454›Full record

ArticleIn vivo (Athens, Greece)

Partial Protection of Paclitaxel-induced Neurotoxicity by Antioxidants.

Yaeko Hara, Hiroshi Sakagami, Haixia Shi, Tomoyuki Abe, Nobuaki Tamura, Hiroshi Takeshima, Norio Horie, Takahiro Kaneko, Hiroshi Shiratsuchi, Tadayoshi Kaneko

Open access · diamondAbstract read
In one paragraph

Article in In vivo (Athens, Greece). The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Yaeko HaraDepartment of Oral Maxillofacial Surgery, Nihon University School of Dentistry, Tokyo, Japan.
Hiroshi SakagamiMeikai University Research Institute of Odontology, Meikai University School of Dentistry, Saitama, Japan sakagami@dent.meikai.ac.jp.
Haixia ShiMeikai University Research Institute of Odontology, Meikai University School of Dentistry, Saitama, Japan.
Tomoyuki AbeDivision of Geriatric Dentistry, Meikai University School of Dentistry, Saitama, Japan.
Nobuaki TamuraDivision of Geriatric Dentistry, Meikai University School of Dentistry, Saitama, Japan.
Hiroshi TakeshimaDivision of Geriatric Dentistry, Meikai University School of Dentistry, Saitama, Japan.
Norio HorieDepartment of Oral and Maxillofacial Surgery, Saitama Medical Center, Saitama Medical University, Saitama, Japan.
Takahiro KanekoDepartment of Oral and Maxillofacial Surgery, Saitama Medical Center, Saitama Medical University, Saitama, Japan.
Hiroshi ShiratsuchiDepartment of Oral Maxillofacial Surgery, Nihon University School of Dentistry, Tokyo, Japan.
Tadayoshi KanekoDepartment of Oral Maxillofacial Surgery, Nihon University School of Dentistry, Tokyo, Japan.
Meikai University · JPSaitama Medical University · JPSocial Insurance Saitama Chuo Hospital · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

aimIn order to search for substances that reduce the neurotoxicity of paclitaxel, the sensitivity of differentiated rat neuronal PC12 cells to paclitaxel was compared to that of malignant and non-malignant cells, and the extent to which four antioxidants can alleviate paclitaxel-induced neurotoxicity was investigated. MATERIALS AND

methodsViability of cells was determined by the MTT method. Cytotoxicity was evaluated as the concentration that reduced cell viability by 50% (CC

resultsPaclitaxel was three-fold more cytotoxic towards human oral squamous cell carcinoma cell lines (Ca9-22, HSC-2, HSC-3. HSC-4) than human normal epithelial and mesenchymal (human gingival fibroblast, human periodontal ligament fibroblast, human pulp cell) normal cells, confirming its antitumor potential. However, paclitaxel at as low a concentration as 5 ng/ml significantly reduced neurite formation in nerve growth factor-induced differentiated PC12 cells, although complete killing of cells was not achieved even at 2,000-fold higher concentration (10 μM). Paclitaxel-induced neurotoxicity was enhanced with the prolongation of incubation time and reduction of inoculation cell density. Four antioxidants, namely docosahexaenoic acid, acetyl-L-carnitine hydrochloride, N-acetyl-L-cysteine and sodium ascorbate, only partially protected PC12 cells from paclitaxel-induced toxicity.

conclusionThe present study suggests the involvement of both oxidative and other mechanisms in paclitaxel-induced neurotoxicity.

Indexed as

AnimalsAntioxidantsAscorbic AcidCarcinoma, Squamous CellCell DifferentiationCell SurvivalCisplatinHL-60 CellsHumansMouth NeoplasmsNerve Growth FactorNeuritesNeurotoxicity SyndromesPaclitaxelPC12 CellsRatsAntioxidantsAscorbic AcidCisplatinNerve Growth FactorNGF protein, humanPaclitaxelanticancer drugdifferentiation stageNeurotoxicityNGFPC12

Identifiers

PMID29936454
PMCPMC6117766
OpenAlexW2810136776

What OpenQuestion holds

Textmetadata
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.