Evidence map›Paper›PMID 29783729›Full record

ArticleInternational journal of molecular sciences2018

RETRACTED: Chlorogenic Acid Improves the Regorafenib Effects in Human Hepatocellular Carcinoma Cells.

Maria Grazia Refolo, Catia Lippolis, Nicola Carella, Aldo Cavallini, Caterina Messa, Rosalba D'Alessandro

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in International journal of molecular sciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 58 citations in OpenAlex.

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  13. Evaluation of cytotoxic and apoptotic effects of the extracts and phenolic compounds ofSaudi pharmaceutical journal : SPJ : the official publication of the Saudi Pharmaceutical Society · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Maria Grazia RefoloLaboratory of Cellular and Molecular Biology, Department of Clinical Pathology, National Institute for Digestive Diseases, IRCCS "Saverio de Bellis", Via Turi 27, 70013 Castellana Grotte, BA, Italy. maria.refolo@irccsdebellis.it.
Catia LippolisLaboratory of Cellular and Molecular Biology, Department of Clinical Pathology, National Institute for Digestive Diseases, IRCCS "Saverio de Bellis", Via Turi 27, 70013 Castellana Grotte, BA, Italy. catiuscia85@hotmail.it.
Nicola CarellaLaboratory of Cellular and Molecular Biology, Department of Clinical Pathology, National Institute for Digestive Diseases, IRCCS "Saverio de Bellis", Via Turi 27, 70013 Castellana Grotte, BA, Italy. nicola.carella@irccsdebellis.it.
Aldo CavalliniLaboratory of Cellular and Molecular Biology, Department of Clinical Pathology, National Institute for Digestive Diseases, IRCCS "Saverio de Bellis", Via Turi 27, 70013 Castellana Grotte, BA, Italy. cavaldo@libero.it.
Caterina MessaLaboratory of Cellular and Molecular Biology, Department of Clinical Pathology, National Institute for Digestive Diseases, IRCCS "Saverio de Bellis", Via Turi 27, 70013 Castellana Grotte, BA, Italy. caterina.messa@irccsdebellis.it.
Rosalba D'AlessandroLaboratory of Cellular and Molecular Biology, Department of Clinical Pathology, National Institute for Digestive Diseases, IRCCS "Saverio de Bellis", Via Turi 27, 70013 Castellana Grotte, BA, Italy. rosalba.dalessandro@irccsdebellis.it.
Gastroenterology Hospital "Saverio de Bellis" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chlorogenic acid (CGA) is a polyphenol present in many human dietary foods. Several studies indicated a beneficial role of CGA in the prevention of cancer and an enhancement of chemotherapy when combined with CGA in the treatment of human hepatocarcinoma (HCC). Drug toxicity, resistance and subsequent disease progression represent a problem in HCC management, although treatment with the multikinase inhibitor Regorafenib improved overall survival. This study focused on the evaluation of the effects of combined treatment using both low Regorafenib concentrations and CGA as natural compound in HCC cells. The analysis of cell proliferation by Ki67 staining and cell cycle progression showed that CGA enhanced Regorafenib-mediated cell growth inhibition. Moreover, CGA potentiated the apoptotic effect of Regorafenib by the activation of the pro-apoptotic Annexin V, Bax and Caspase 3/7 and the inhibition of anti-apoptotic Bcl2 and Bcl-xL. Combined treatments were also effective in inhibiting cell motility. The mechanisms underlying the positive effects of combining CGA and Regorafenib were also addressed and an increased inhibition of MAPK (mitogen-activated protein kinase)and PI3K/Akt/mTORC (phosphatidylinositol-3-kinase (PI3K)/Akt and the mammalian target of rapamycin (mTOR) signaling was observed. Overall, these data demonstrated that co-treatment with Regorafenib and CGA enhanced Regorafenib action, reducing its cytotoxicity in HCC cells. In conclusion, this drug combination could be considered as a safe and more effective approach in HCC therapy.

Indexed as

Drug SynergismAntineoplastic AgentsApoptosisCell CycleCell MovementChlorogenic AcidHep G2 CellsHumansMAP Kinase Signaling SystemMechanistic Target of Rapamycin Complex 1Phenylurea CompoundsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPyridinesAntineoplastic AgentsChlorogenic AcidMechanistic Target of Rapamycin Complex 1Phenylurea CompoundsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktPyridinesregorafenibChlorogenic acidcombined treatmentsHCC cells

Identifiers

PMID29783729
PMCPMC5983789
OpenAlexW2804160141

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.