Evidence map›Paper›PMID 30974882›Full record

ArticleMolecules (Basel, Switzerland)2019

The Comprehensive Roles of ATRANORIN, A Secondary Metabolite from the Antarctic Lichen

Young-Jun Jeon, Sanghee Kim, Ji Hee Kim, Ui Joung Youn, Sung-Suk Suh

Open access · goldAbstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.0field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 31 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

5 authors at 3 institutions in 2 countries.

Young-Jun JeonComprehensive Cancer Center, The Ohio State University, Columbus, OH 43210, USA. jeon.81@osu.edu.
Sanghee KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. sangheekim@kopri.re.kr.ORCID 0000-0001-8367-573X
Ji Hee KimDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. jhalgae@kopri.re.kr.
Ui Joung YounDivision of Polar Life Sciences, Korea Polar Research Institute, Incheon 21990, Korea. ujyoun@kopri.re.kr.
Sung-Suk SuhDepartment of Bioscience, Mokpo National University, Muan 58554, Korea. sungsuksuh@mokpo.ac.kr.
Korea Polar Research Institute · KRMokpo National University · KRThe Ohio State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most deadly genetic diseases, but surprisingly chemotherapeutic approaches against HCC are only limited to a few targets. In particular, considering the difficulty of a chemotherapeutic drug development in terms of cost and time enforces searching for surrogates to minimize effort and maximize efficiency in anti-cancer therapy. In spite of the report that approximately one thousand lichen-derived metabolites have been isolated, the knowledge about their functions and consequences in cancer development is relatively limited. Moreover, one of the major second metabolites from lichens, Atranorin has never been studied in HCC. Regarding this, we comprehensively analyze the effect of Atranorin by employing representative HCC cell lines and experimental approaches. Cell proliferation and cell cycle analysis using the compound consistently show the inhibitory effects of Atranorin. Moreover, cell death determination using Annexin-V and (Propidium Iodide) PI staining suggests that it induces cell death through necrosis. Lastly, the metastatic potential of HCC cell lines is significantly inhibited by the drug. Taken these together, we claim a novel functional finding that Atranorin comprehensively suppresses HCC tumorigenesis and metastatic potential, which could provide an important basis for anti-cancer therapeutics.

Indexed as

Carcinoma, HepatocellularCell Transformation, NeoplasticHydroxybenzoatesLiver NeoplasmsCell Line, TumorCell ProliferationHumansLichensatranorinHydroxybenzoatesatranorincell cyclecell deathhepatocellular carcinoma (HCC), lichen

Identifiers

PMID30974882
PMCPMC6480312
OpenAlexW2935882101

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.