Evidence map›Paper›PMID 32509768›Full record

ReviewFrontiers in cell and developmental biology2020

Horizontal Gene Transfer: From Evolutionary Flexibility to Disease Progression.

Melissa Emamalipour, Khaled Seidi, Sepideh Zununi Vahed, Ali Jahanban-Esfahlan, Mehdi Jaymand, Hasan Majdi, Zohreh Amoozgar, L T Chitkushev, Tahereh Javaheri, Rana Jahanban-Esfahlan and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed
6.9field-weighted citation impact, top 2% 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

95 citing papers in PubMed, 187 citations in OpenAlex.

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  15. Frontiers in cellular neuroscience · 2026
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35 more citing papers are in PubMed but not listed here.

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 6 institutions in 3 countries.

Melissa EmamalipourDrug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Khaled SeidiBiotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Sepideh Zununi VahedKidney Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Ali Jahanban-EsfahlanStem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Mehdi JaymandNano Drug Delivery Research Center, Health Technology Institute, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Hasan MajdiDepartment of Medical Nanotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Zohreh AmoozgarEdwin L. Steele Laboratories, Department of Radiation Oncology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
L T ChitkushevDepartment of Computer Science, Metropolitan College, Boston University, Boston, MA, United States.
Tahereh JavaheriHealth Informatics Lab, Metropolitan College, Boston University, Boston, MA, United States.
Rana Jahanban-EsfahlanDepartment of Medical Biotechnology, School of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.
Peyman ZareFaculty of Medicine, Cardinal Stefan Wyszyński University in Warsaw, Warsaw, Poland.
Tabriz University of Medical Sciences · IRBoston University · USBiotechnology Research Center · IRCardinal Stefan Wyszyński University in Warsaw · PLKermanshah University of Medical Sciences · IRMassachusetts General Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Flexibility in the exchange of genetic material takes place between different organisms of the same or different species. This phenomenon is known to play a key role in the genetic, physiological, and ecological performance of the host. Exchange of genetic materials can cause both beneficial and/or adverse biological consequences. Horizontal gene transfer (HGT) or lateral gene transfer (LGT) as a general mechanism leads to biodiversity and biological innovations in nature. HGT mediators are one of the genetic engineering tools used for selective introduction of desired changes in the genome for gene/cell therapy purposes. HGT, however, is crucial in development, emergence, and recurrence of various human-related diseases, such as cancer, genetic-, metabolic-, and neurodegenerative disorders and can negatively affect the therapeutic outcome by promoting resistant forms or disrupting the performance of genome editing toolkits. Because of the importance of HGT and its vital physio- and pathological roles, here the variety of HGT mechanisms are reviewed, ranging from extracellular vesicles (EVs) and nanotubes in prokaryotes to cell-free DNA and apoptotic bodies in eukaryotes. Next, we argue that HGT plays a role both in the development of useful features and in pathological states associated with emerging and recurrent forms of the disease. A better understanding of the different HGT mediators and their genome-altering effects/potentials may pave the way for the development of more effective therapeutic and diagnostic regimes.

Indexed as

antibiotic resistanceapoptotic bodiescancercell-free DNAevolutionexosomeshorizontal gene transfertransposable elements

Identifiers

PMID32509768
PMCPMC7248198
OpenAlexW3025727691

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.