Evidence map›Paper›PMID 30464401›Full record

ArticleDrug design, development and therapy2018

Arminin 1a-C, a novel antimicrobial peptide from ancient metazoan

Xiaolei Liang, Ruirui Wang, Wenshan Dou, Li Zhao, Lanxia Zhou, Junfang Zhu, Kairong Wang, Jiexi Yan

Abstract read
In one paragraph

Article in Drug design, development and therapy, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

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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.

Xiaolei LiangThe Reproductive Medicine Special Hospital of the First Hospital of Lanzhou University, Key Laboratory for Reproductive Medicine and Embryo, Lanzhou, China.
Ruirui WangThe First Clinical Medical College, Lanzhou University, Lanzhou, China.
Wenshan DouThe Second Clinical Medical College, Lanzhou University, Lanzhou, China.
Li ZhaoThe Key Laboratory, The First Hospital of Lanzhou University, Lanzhou, China, yanjx_1121@163.com.
Lanxia ZhouThe Key Laboratory, The First Hospital of Lanzhou University, Lanzhou, China, yanjx_1121@163.com.
Junfang ZhuThe Key Laboratory, The First Hospital of Lanzhou University, Lanzhou, China, yanjx_1121@163.com.
Kairong WangSchool of Basic Medical Sciences, Institute of Biochemistry and Molecular Biology, Lanzhou University, Lanzhou, China.
Jiexi YanThe Key Laboratory, The First Hospital of Lanzhou University, Lanzhou, China, yanjx_1121@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeDue to the emergence of multidrug resistance (MDR), traditional antileukemia drugs no longer meet the treatment needs. Therefore, new antileukemia drugs with different action mechanisms are urgently needed to cope with this situation. MATERIALS AND

methodsArminin 1a-C is an antimicrobial peptide (AMP) developed from the ancient metazoan marine

resultsOur results showed that Arminin 1a-C formed an α-helical structure and efficaciously suppressed the viability of leukemia cell lines whether or not they were multidrug resistant or sensitive, and there were no obvious differences between these cell lines. Arminin 1a-C exhibited distinct selectivity between noncancerous and cancerous cell lines. Arminin 1a-C interfered with K562/adriamycin (ADM) cell (a kind of multidrug-resistant leukemia cell line) proliferation in a very rapid manner and formed pores in its cell membrane, making it difficult to develop resistance against Arminin 1a-C.

conclusionOur data show that Arminin 1a-C possesses great potential as a therapeutic candidate for the treatment of multidrug-resistant leukemia.

Indexed as

AnimalsAntimicrobial Cationic PeptidesAntineoplastic AgentsCell ProliferationCells, CulturedCell SurvivalDose-Response Relationship, DrugDrug Resistance, MultipleDrug Resistance, NeoplasmDrug Screening Assays, AntitumorHumansHydraProtein ConformationStructure-Activity RelationshipAntimicrobial Cationic PeptidesAntineoplastic AgentsArminin 1aantileukemiaantimicrobial peptideArminin 1a-Cmultidrug resistance

Identifiers

PMID30464401
PMCPMC6217004

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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.