Evidence map›Paper›PMID 38401018›Full record

ArticleMolecular biology reports2024

The potential therapeutic effect of melatonin in oxaliplatin combination therapy against chemoresistant colorectal cancer cells.

Masoumeh Dehghanzad, Mohammad Mohammadi, Mohaddeseh Nejati, Farhad Pouremamali, Nazila Fathi Maroufi, Maryam Akbarzadeh, Naser Samadi, Mohammad Nouri

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.3field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 7 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

8 authors at 4 institutions in 3 countries.

Masoumeh DehghanzadDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohammad MohammadiDepartment of Medical Laboratory Science, Faculty of Medicine, Kermanshah Branch, Islamic Azad University, Kermanshah, Iran.
Mohaddeseh NejatiDepartment of Biology, Tonekabon Branch, Islamic Azad University, Tonekabon, Iran.
Farhad PouremamaliDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Nazila Fathi MaroufiDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Gholgasht Ave, Tabriz, Iran.
Maryam AkbarzadehDepartment of Biochemistry, Erasmus University Medical Center, Rotterdam, The Netherlands.
Naser SamadiDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Gholgasht Ave, Tabriz, Iran.
Mohammad NouriDepartment of Biochemistry, Faculty of Medicine, Tabriz University of Medical Sciences, Gholgasht Ave, Tabriz, Iran. nourimd@yahoo.com.ORCID http://orcid.org/0000-0002-5367-9956
Tabriz University of Medical Sciences · IRErasmus MC · NLIslamic Azad University of Kermanshah · IRIslamic Azad University Tonekabon · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOxaliplatin is one of the main therapeutics in colorectal cancer (CRC) chemotherapy. However, in light of multidrug resistance (MDR) phenotype development, the efficacy of oxaliplatin has decreased. This study aimed to assess the potential therapeutic effect of melatonin in oxaliplatin combination therapy for drug-resistant colorectal cancer cells. METHODS AND

resultsInitially, the oxaliplatin-resistant cell line was created of LS174T (LS174T/DR) by using the oxaliplatin IC50 concentration and resting cycles. MTT assays and flow cytometry were applied for assessing cell viability and apoptotic cells. The mRNA expression level of Bax, Bcl2, MT1, MT2, and ABCB1 as well as protein levels of ABCB1, Bcl2, BAX were measured by the qRT-PCR and western blot techniques respectively. P-gp activity was assessed by Rho123 staining. The IC50 concentration of oxaliplatin in resistant cells was increased from 500.7 ± 0.2 nM to 7119 ± 0.1 nM. Bcl2, MT1, MT2, and ABCB1 mRNA plus protein expression levels of Bcl2 and ABCB1 were significantly reduced in resistant cells, along with a marked increase in Bax mRNA and protein levels compared to parental cells. Rho 123 staining revealed a marked reduction in P-gp activities in the combination-treated group compared to the oxaliplatin-treated group.

conclusionsThe results of cytotoxicity assays, MTT, and flow cytometry revealed that the combination of melatonin and oxaliplatin exerts synergistic effects on induction of oxaliplatin's cytotoxicity in CRC. Our research suggests that combining the treatments of melatonin and oxaliplatin may be considered as a new approach to overcoming oxaliplatin resistance in CRC patients.

Indexed as

Colorectal NeoplasmsMelatoninApoptosisATP Binding Cassette Transporter, Subfamily B, Member 1bcl-2-Associated X ProteinCell Line, TumorDrug Resistance, NeoplasmHumansOxaliplatinRNA, MessengerATP Binding Cassette Transporter, Subfamily B, Member 1bcl-2-Associated X ProteinMelatoninOxaliplatinRNA, MessengerColorectal cancerDrug resistanceMelatoninOxaliplatin

Identifiers

PMID38401018
OpenAlexW4392131480

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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.