Evidence map›Paper›PMID 28271058›Full record

ReviewFrontiers in chemistry2017

Peptides with Dual Antimicrobial and Anticancer Activities.

Mário R Felício, Osmar N Silva, Sônia Gonçalves, Nuno C Santos, Octávio L Franco

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in chemistry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 182 papers.

0numbers the graph read from it
0cells of the map it votes in
182citing papers in PubMed
25.4field-weighted citation impact, top 1% 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

182 citing papers in PubMed, 386 citations in OpenAlex.

  1. Effects of Antimicrobial Peptides on Bacterial Cells.Methods in molecular biology (Clifton, N.J.) · 2027
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  3. Enhanced anticancer efficacy ofMaterials today. Bio · 2026
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122 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

5 authors at 3 institutions in 2 countries.

Mário R FelícioInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa Lisbon, Portugal.
Osmar N SilvaS-Inova Biotech, Pós-graduação em Biotecnologia, Universidade Católica Dom Bosco Campo Grande, Brazil.
Sônia GonçalvesInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa Lisbon, Portugal.
Nuno C SantosInstituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa Lisbon, Portugal.
Octávio L FrancoS-Inova Biotech, Pós-graduação em Biotecnologia, Universidade Católica Dom BoscoCampo Grande, Brazil; Programa de Pós-Graduação em Patologia Molecular, Universidade de BrasíliaBrasília, Brazil.
University of Lisbon · PTUniversidade Católica Dom Bosco · BRUniversidade de Brasília · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, the number of people suffering from cancer and multi-resistant infections has increased, such that both diseases are already seen as current and future major causes of death. Moreover, chronic infections are one of the main causes of cancer, due to the instability in the immune system that allows cancer cells to proliferate. Likewise, the physical debility associated with cancer or with anticancer therapy itself often paves the way for opportunistic infections. It is urgent to develop new therapeutic methods, with higher efficiency and lower side effects. Antimicrobial peptides (AMPs) are found in the innate immune system of a wide range of organisms. Identified as the most promising alternative to conventional molecules used nowadays against infections, some of them have been shown to have dual activity, both as antimicrobial and anticancer peptides (ACPs). Highly cationic and amphipathic, they have demonstrated efficacy against both conditions, with the number of nature-driven or synthetically designed peptides increasing year by year. With similar properties, AMPs that can also act as ACPs are viewed as future chemotherapeutic drugs, with the advantage of low propensity to resistance, which started this paradigm in the pharmaceutical market. These peptides have already been described as molecules presenting killing mechanisms at the membrane level, but also acting toward intracellular targets, which increases their success compartively to one-target specific drugs. This review will approach the desirable characteristics of small peptides that demonstrated dual activity against microbial infections and cancer, as well as the peptides engaged in clinical trials.

Indexed as

anticancer peptides (ACPs)antimicrobial peptides (AMPs)bacteriacancermulti-resistant infections

Identifiers

PMID28271058
PMCPMC5318463
OpenAlexW2591017015

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.