Evidence mapPaperPMID 32843130Full record

ArticleBMB reports2021

Hemistepsin A inhibits T0901317-induced lipogenesis in the liver.

Jae Kwang Kim, Il Je Cho, Eun Ok Kim, Dae Geon Lee, Dae Hwa Jung, Sung Hwan Ki, Sae Kwang Ku, Sang Chan Kim

Open access · goldAbstract readNews
In one paragraph

Article in BMB reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Hemistepsin A induces apoptosis by modulating the reactive oxygen species-dependent PI3K/Akt signaling pathway in human lung carcinoma A549 cells.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2025
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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 at 3 institutions in 1 country.

Jae Kwang KimCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610; Korean Medicine-Application Center, Korea Institute of Oriental Medicine, Daegu 41062, Korea.
Il Je ChoCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610, Korea.
Eun Ok KimCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610, Korea.
Dae Geon LeeCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610, Korea.
Dae Hwa JungCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610; Hani Bio Co., Ltd, Daegu 41059, Korea.
Sung Hwan KiCollege of Pharmacy, Chosun University, Gwangju 61452, Korea.
Sae Kwang KuCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610, Korea.
Sang Chan KimCollege of Korean Medicine, Daegu Haany University, Gyeongsan 38610, Korea.
Daegu Haany University · KRChosun University · KRKorea Institute of Oriental Medicine · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hemistepsin A (HsA) is a guaianolide sesquiterpene lactone that inhibits hepatitis and liver fibrosis. We evaluated the effects of HsA on liver X receptor (LXR)-mediated hepatic lipogenesis in vitro and in vivo. Up to 10 μM, HsA did not affect the viability of HepG2 and Huh7 cells. Pretreatment with 5-10 μM HsA significantly decreased the luciferase activity of the LXR response element, which was transactivated by T0901317, GW 3965, and LXRα/retinoid X receptor α overexpression. In addition, it significantly inhibited the mRNA expression of LXRα in HepG2 and Huh7 cells. It also suppressed the expression of sterol regulatory element-binding protein-1c and lipogenic genes and reduced the triglyceride accumulation triggered by T0901317. Intraperitoneal injection of HsA (5 and 10 mg/kg) in mice significantly alleviated the T0901317-mediated increases in hepatocyte diameter and the percentage of regions in hepatic parenchyma occupied by lipid droplets. Furthermore, HsA significantly attenuated hepatic triglyceride accumulation by restoring the impaired expression of LXRα-dependent lipogenic genes caused by T0901317. Therefore, based on its inhibition of the LXRα-dependent signaling pathway, HsA has prophylactic potential for steatosis. [BMB Reports 2021; 54(2): 106-111].

Indexed as

BenzenesulfonamidesCells, CulturedFluorocarbonsHumansHydrocarbons, FluorinatedLactonesLipogenesisLiverLiver X ReceptorsSesquiterpenesSulfonamidesBenzenesulfonamidesFluorocarbonshemistepsinHydrocarbons, FluorinatedLactonesLiver X ReceptorsSesquiterpenesSulfonamidesT0901317

Identifiers

PMID32843130
PMCPMC7907741
OpenAlexW3080704773

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.