Evidence map›Paper›PMID 30719606›Full record

ArticleMolecular biology reports2019

Antiproliferative and apoptotic effects of caffeic acid on SK-Mel-28 human melanoma cancer cells.

Luana Paula Pelinson, Charles Elias Assmann, Taís Vidal Palma, Ivana Beatrice Mânica da Cruz, Micheli Mainardi Pillat, Aline Mânica, Naiara Stefanello, Grazielle Castagna Cezimbra Weis, Audrei de Oliveira Alves, Cinthia Melazzo de Andrade and 4 more

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Article in Molecular biology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

53 citing papers in PubMed, 107 citations in OpenAlex.

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  17. Adjuvant Properties of Caffeic Acid in Cancer Treatment.International journal of molecular sciences · 2024
    Review
  18. Phytotherapeutic potential ofIn silico pharmacology · 2024
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  19. Review
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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

14 authors at 3 institutions in 1 country.

Luana Paula PelinsonPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Charles Elias AssmannPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Taís Vidal PalmaLaboratory of Oxidative Biochemistry, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Ivana Beatrice Mânica da CruzLaboratory of Biogenomics, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Micheli Mainardi PillatDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP, Brazil.
Aline MânicaPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Naiara StefanelloPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Grazielle Castagna Cezimbra WeisLaboratory of Biogenomics, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Audrei de Oliveira AlvesLaboratory of Biogenomics, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Cinthia Melazzo de AndradeLaboratory of Oxidative Biochemistry, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Henning UlrichDepartment of Biochemistry, Institute of Chemistry, University of São Paulo, São Paulo, SP, Brazil.
Vera Maria Melchiors MorschPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Maria Rosa Chitolina SchetingerPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil.
Margarete Dulce BagatiniPPGBtox, CCNE, Federal University of Santa Maria, Santa Maria, RS, Brazil. margaretebagatini@yahoo.com.br.ORCID http://orcid.org/0000-0001-9263-4980
Universidade Federal de Santa Maria · BRUniversidade de São Paulo · BRUniversidade Federal da Fronteira Sul · BR

Funding

CAPES CAPES/PROEX ? Process numbers: 23038.005848/2018-31 and 88882.182142/2018-01National Council for Scientific and Technological Development 449485/2014-5
6 · The paper itself

Abstract

Cutaneous melanoma (CM) is an extremely aggressive cancer presenting low survival and high mortality. The vast majority of patients affected by this disease does not respond or show resistance to the chemotherapeutic drugs, which makes the treatment ineffective. In this sense, the necessity for the development of new agents to assist in CM therapy is extremely important. One of the sources of great interest in this search are compounds of natural origin. Among these compounds, caffeic acid has demonstrated a broad spectrum of pharmacological activities as well as antitumor effects in some types of cancer. Therefore, the objective of this work was to investigate the possible antitumor effect of caffeic acid on the SK-Mel-28 cell line, human CM cells. Cells were cultured in flasks with culture medium containing fetal bovine serum, antibiotic, and antifungal, and maintained in ideal conditions. Cells were treated with 25 µM, 50 µM, 100 µM, 150 µM and 200 µM of caffeic acid and dacarbazine at 1 mg/mL. We verified the effect on cell viability and cell death, apoptosis, cell cycle, colony formation and gene expression of caspases. Results showed a decrease in cell viability, cell death induction by apoptosis, inhibition of colony formation, modulation of cell cycle and alterations in gene expression of caspases after caffeic acid treatment. These results suggest an antitumor effect of the compound on SK-Mel-28 cells. This study provides original information on mechanisms by which caffeic acid may play a key role in preventing tumor progression in human melanoma cells.

Indexed as

AdultAntineoplastic AgentsApoptosisCaffeic AcidsCaspasesCell CycleCell Cycle ProteinsCell DivisionCell Line, TumorCell ProliferationCell SurvivalCutaneous Malignant MelanomaDacarbazineFemaleHealthy VolunteersHumansAntineoplastic Agentscaffeic acidCaffeic AcidsCaspasesCell Cycle ProteinsDacarbazineApoptosisCell cycleCytotoxicityGene expressionMelanomaNatural compounds

Identifiers

PMID30719606
OpenAlexW2912429260

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.