Evidence map›Paper›PMID 28672785›Full record

ArticleMarine drugs2017

Comprehensive Expression Profiling and Functional Network Analysis of Porphyra-334, One Mycosporine-Like Amino Acid (MAA), in Human Keratinocyte Exposed with UV-radiation.

Sung-Suk Suh, Sung Gu Lee, Ui Joung Youn, Se Jong Han, Il-Chan Kim, Sanghee Kim

Abstract read
In one paragraph

Article in Marine drugs, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 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

6 authors.

Sung-Suk SuhDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. sung-suk.suh@kopri.re.kr.
Sung Gu LeeDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. holynine@kopri.re.kr.
Ui Joung YounDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. ujyoun@kopri.re.kr.
Se Jong HanDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. hansj@kopri.re.kr.
Il-Chan KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. ickim@kopri.re.kr.
Sanghee KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. sangheekim@kopri.re.kr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mycosporine-like amino acids (MAAs) have been highlighted as pharmacologically active secondary compounds to protect cells from harmful UV-radiation by absorbing its energy. Previous studies have mostly focused on characterizing their physiological properties such as antioxidant activity and osmotic regulation. However, molecular mechanisms underlying their UV-protective capability have not yet been revealed. In the present study, we investigated the expression profiling of porphyra-334-modulated genes or microRNA (miRNAs) in response to UV-exposure and their functional networks, using cDNA and miRNAs microarray. Based on our data, we showed that porphyra-334-regulated genes play essential roles in UV-affected biological processes such as Wnt (Wingless/integrase-1) and Notch pathways which exhibit antagonistic relationship in various biological processes; the UV-repressed genes were in the Wnt signaling pathway, while the activated genes were in the Notch signaling. In addition, porphyra-334-regulated miRNAs can target many genes related with UV-mediated biological processes such as apoptosis, cell proliferation and translational elongation. Notably, we observed that functional roles of the target genes for up-regulated miRNAs are inversely correlated with those for down-regulated miRNAs; the former genes promote apoptosis and translational elongation, whereas the latter function as inhibitors in these processes. Taken together, these data suggest that porphyra-334 protects cells from harmful UV radiation through the comprehensive modulation of expression patterns of genes involved in UV-mediated biological processes, and that provide a new insight to understand its functional molecular networks.

Indexed as

CyclohexanonesTranscriptomeUltraviolet RaysBase CompositionCell LineGene Expression RegulationGlycineHumansKeratinocytesMicroRNAsOligonucleotide Array Sequence AnalysisCyclohexanonesGlycineMicroRNAsporphyra-334microRNAsMycosporine-like amino acids (MAAs)Notch pathwayporphyra-334UV-radiationWnt pathway

Identifiers

PMID28672785
PMCPMC5532638

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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.