Evidence map›Paper›PMID 28191273›Full record

ArticleOxidative medicine and cellular longevity2017

Oxidative Stress Triggered by Apigenin Induces Apoptosis in a Comprehensive Panel of Human Cervical Cancer-Derived Cell Lines.

Raquel P Souza, Patrícia de S Bonfim-Mendonça, Fabrícia Gimenes, Bianca A Ratti, Vanessa Kaplum, Marcos L Bruschi, Celso V Nakamura, Sueli O Silva, Silvya S Maria-Engler, Marcia E L Consolaro

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

46 citing papers in PubMed, 92 citations in OpenAlex.

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  17. Antitumor Effects of MicroencapsulatedMaterials (Basel, Switzerland) · 2023
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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 2 institutions in 1 country.

Raquel P SouzaPostgraduate Program in Bioscience and Physiopathology, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil; Clinical Cytology and STD Laboratory, Department of Clinical Analysis and Biomedicine, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.
Patrícia de S Bonfim-MendonçaClinical Cytology and STD Laboratory, Department of Clinical Analysis and Biomedicine, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.ORCID 0000-0002-0116-2189
Fabrícia GimenesPostgraduate Program in Bioscience and Physiopathology, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil; Clinical Cytology and STD Laboratory, Department of Clinical Analysis and Biomedicine, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.
Bianca A RattiPostgraduate Program in Bioscience and Physiopathology, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.
Vanessa KaplumPostgraduate Program in Pharmaceutical Sciences, Laboratory of Research and Development of Drug Delivery Systems, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.
Marcos L BruschiPostgraduate Program in Pharmaceutical Sciences, Laboratory of Research and Development of Drug Delivery Systems, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.
Celso V NakamuraPostgraduate Program in Pharmaceutical Sciences, Laboratory of Research and Development of Drug Delivery Systems, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.
Sueli O SilvaPostgraduate Program in Bioscience and Physiopathology, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil; Postgraduate Program in Pharmaceutical Sciences, Laboratory of Research and Development of Drug Delivery Systems, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil.ORCID 0000-0001-9303-0804
Silvya S Maria-EnglerPostgraduate Program in Pharmaceutical Science-Clinical Analysis Area, Universidade de São Paulo (USP), Av. Lineu Prestes 580, 05508-900 São Paulo, SP, Brazil.
Marcia E L ConsolaroPostgraduate Program in Bioscience and Physiopathology, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil; Clinical Cytology and STD Laboratory, Department of Clinical Analysis and Biomedicine, Universidade Estadual de Maringá (UEM), Av. Colombo 5790, 87025-210 Maringá, PR, Brazil; Postgraduate Program in Pharmaceutical Science-Clinical Analysis Area, Universidade de São Paulo (USP), Av. Lineu Prestes 580, 05508-900 São Paulo, SP, Brazil.ORCID 0000-0001-9102-4865
Universidade Estadual de Maringá · BRUniversidade de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recently, the cytotoxic effects of apigenin (4',5,7-trihydroxyflavone), particularly its marked inhibition of cancer cell viability both in vitro and in vivo, have attracted the attention of the anticancer drug discovery field. Despite this, there are few studies of apigenin in cervical cancer, and these studies have mostly been conducted using HeLa cells. To evaluate the possibility of apigenin as a new therapeutic candidate for cervical cancer, we evaluated its cytotoxic effects in a comprehensive panel of human cervical cancer-derived cell lines including HeLa (human papillomavirus/HPV 18-positive), SiHa (HPV 16-positive), CaSki (HPV 16 and HPV 18-positive), and C33A (HPV-negative) cells in comparison to a nontumorigenic spontaneously immortalized human epithelial cell line (HaCaT). Our results demonstrated that apigenin had a selective cytotoxic effect and could induce apoptosis in all cervical cancer cell lines which were positively marked with Annexin V, but not in HaCaT (control cells). Additionally, apigenin was able to induce mitochondrial redox impairment, once it increased ROS levels and H

Indexed as

Uterine Cervical NeoplasmsAntineoplastic AgentsApigeninApoptosisCell Line, TumorFemaleHumansOxidative StressAntineoplastic AgentsApigenin

Identifiers

PMID28191273
PMCPMC5278229
OpenAlexW2573774431

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.