Evidence map›Paper›PMID 32002586›Full record

ArticleInflammation research : official journal of the European Histamine Research Society ... [et al.]2020

Igalan from Inula helenium (L.) suppresses the atopic dermatitis-like response in stimulated HaCaT keratinocytes via JAK/STAT3 signaling.

Thien T P Dao, Kwangho Song, Jee Young Kim, Yeong Shik Kim

Abstract read
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In one paragraph

Article in Inflammation research : official journal of the European Histamine Research Society ... [et al.], 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.0field-weighted citation impact, top 12% 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

13 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
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  5. Fatty Acid-Rich Fraction ofPlants (Basel, Switzerland) · 2025
    Article
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  7. Article
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  10. Unveiling the Ability of Witch Hazel (International journal of molecular sciences · 2022
    Article
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  12. Article
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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

4 authors at 1 institution in 1 country.

Thien T P DaoCollege of Pharmacy and Natural Product Research Institute, Seoul National University, 1 Gwanak-ro 1, Gwanak-gu, Seoul, 08826, South Korea.
Kwangho SongCollege of Pharmacy and Natural Product Research Institute, Seoul National University, 1 Gwanak-ro 1, Gwanak-gu, Seoul, 08826, South Korea.
Jee Young KimCollege of Pharmacy and Natural Product Research Institute, Seoul National University, 1 Gwanak-ro 1, Gwanak-gu, Seoul, 08826, South Korea.
Yeong Shik KimCollege of Pharmacy and Natural Product Research Institute, Seoul National University, 1 Gwanak-ro 1, Gwanak-gu, Seoul, 08826, South Korea. kims@snu.ac.kr.ORCID http://orcid.org/0000-0003-1353-3925
Seoul National University · KR

Funding

Korea Institute of Science and Technology KIST370C-20190043National Research Foundation of Korea NRF-2017R1A2B4009301
6 · The paper itself

Abstract

objectiveThis study aimed to evaluate the protective effect of igalan, a sesquiterpene lactone isolated from Inula helenium (L.), on inhibiting inflammation, regulating the epidermal differentiation gene expression, and reactive oxygen species scavenging in atopic dermatitis (AD)-like inflammatory keratinocytes.

methodsHaCaT human keratinocytes were treated with igalan at indicated concentrations before being activated by a combination of TNF-α and IFN-γ or IL-4 representative for T-helper 1 and T-helper 2 cell cytokines, which are associated with AD pathogenesis.

resultsBy inhibiting the NF-κB pathway as well as the STAT activation, igalan could downregulate several marker inflammatory genes in AD, such as TARC/CCL17, MDC/CCL22, and RANTES/CCL5. In contrast, igalan, acting as JAK inhibitor, could promote the mRNA expression levels of the genes FLG, LOR, KRT10, and DSC1, which encode for essential proteins responsible for keratinocyte differentiation, by inhibiting STAT3 signaling. Furthermore, igalan exerts its antioxidant effect through activating the Nrf2 pathway, triggering the expression of some enzymes that contribute to preventing intracellular ROS generation during inflammation.

conclusionThese findings indicate that igalan, via suppressing JAK/STAT3 signaling, could impair the production of pro-inflammatory chemokines and enhance expression levels of several genes involved in keratinocyte differentiation in AD-like stimulated keratinocytes.

Indexed as

Cell DifferentiationCytokinesDermatitis, AtopicEpidermisFilaggrin ProteinsHaCaT CellsHumansInflammationInterferon-gammaInterleukin-4InulaJanus Kinase 1KeratinocytesLactonesNF-kappa B p50 SubunitPlant ExtractsCytokinesFilaggrin ProteinsFLG protein, humanIFNG protein, humanIL4 protein, humanInterferon-gammaInterleukin-4JAK1 protein, humanJanus Kinase 1LactonesNF-kappa B p50 SubunitNFKB1 protein, humanPlant ExtractsReactive Oxygen SpeciesSesquiterpenesSTAT3 protein, humanSTAT3 Transcription FactorTumor Necrosis Factor-alphaAntioxidantAtopic dermatitisJAK/STAT3 signalingNf-κb pathwayNrf2 activationSesquiterpene lactones

Identifiers

PMID32002586
OpenAlexW3003187899

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.