Evidence map›Paper›PMID 34181134›Full record

ReviewBiochemical genetics2022

Potential Therapeutic Effects of Melatonin Mediate via miRNAs in Cancer.

Pirouz Pourmohammad, Nazila Fathi Maroufi, Mohsen Rashidi, Vahid Vahedian, Farhad Pouremamali, Yousef Faridvand, Mahsa Ghaffari-Novin, Alireza Isazadeh, Saba Hajazimian, Hamid Reza Nejabati and 1 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Biochemical genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 26 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

11 authors at 5 institutions in 1 country.

Pirouz Pourmohammad *Department of Clinical Biochemistry, School of Medicine, Ardabil University of Medical Science, Ardabil, Islamic Republic of Iran.
Nazila Fathi Maroufi *Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Mohsen Rashidi *Department of Pharmacology, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran.
Vahid VahedianResearchers Club of Tums Preclinical Core Facility (TPCF), Tehran University of Medical Science (TUMS), Tehran, Iran.
Farhad PouremamaliDepartment of Medical Biotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Yousef FaridvandStudent Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Mahsa Ghaffari-NovinFaculty of Veterinary Medicine, Karaj Branch, Islamic Azad University, Karaj, Iran.
Alireza IsazadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Saba HajazimianImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Hamid Reza NejabatiDepartment of Biochemistry and Clinical Laboratories, Faculty of Medicine Stem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran. nejabati_hr@yahoo.com.
Mohammad NouriDepartment of Biochemistry and Clinical Laboratories, Faculty of Medicine Stem Cell and Regenerative Medicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran. nourimd@yahoo.com.ORCID http://orcid.org/0000-0002-5367-9956
Tabriz University of Medical Sciences · IRArdabil University of Medical Sciences · IRIslamic Azad University, Karaj · IRMazandaran University of Medical Sciences · IRUniversity of Tehran · IR

Funding

tabriz university of medical sciences 59577
6 · The paper itself

Abstract

miRNAs are evolutionarily conserved non-coding ribonucleic acids with a length of between 19 and 25 nucleotides. Because of their ability to regulate gene expression, miRNAs have an important function in the controlling of various biological processes, such as cell cycle, differentiation, proliferation, and apoptosis. Owing to the long-standing regulative potential of miRNAs in tumor-suppressive pathways, scholars have recently paid closer attention to the expression profile of miRNAs in various types of cancer. Melatonin, an indolic compound secreted from pineal gland and some peripheral tissues, has been considered as an effective anti-tumor hormone in a wide spectrum of cancers. Furthermore, it induces apoptosis, inhibits tumor metastasis and invasion, and also angiogenesis. A growing body of evidence indicates the effects of melatonin on miRNAs expression in broad spectrum of diseases, including cancer. Due to the long-term effects of the regulation of miRNAs expression, melatonin could be a promising therapeutic factor in the treatment of cancers via the regulation of miRNAs. Therefore, in this review, we will discuss the effects of melatonin on miRNAs expression in various types of cancers.

Indexed as

MelatoninMicroRNAsNeoplasmsApoptosisHumansMelatoninMicroRNAsAnti-tumorCancerMelatoninmiRNAs

Identifiers

PMID34181134
OpenAlexW3177265049

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.