Evidence map›Paper›PMID 20054000›Full record

ArticleThe Journal of biological chemistry2010

Akt Cys-310-targeted inhibition by hydroxylated benzene derivatives is tightly linked to their immunosuppressive effects.

Ji Yeon Lee, Yong Gyu Lee, Jaehwi Lee, Keum-Jin Yang, Ae Ra Kim, Joo Young Kim, Moo-Ho Won, Jongsun Park, Byong Chul Yoo, Sanghee Kim and 2 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

25 citing papers in PubMed, 58 citations in OpenAlex.

  1. Article
  2. Article
  3. Hydroquinone suppresses IFN-β expression by targeting AKT/IRF3 pathway.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  4. Beauvericin, a cyclic peptide, inhibits inflammatory responses in macrophages by inhibiting the NF-κB pathway.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  5. JS-III-49, a hydroquinone derivative, exerts anti-inflammatory activity by targeting Akt and p38.The Korean journal of physiology & pharmacology : official journal of the Korean Physiological Society and the Korean Society of Pharmacology · 2017
    Article
  6. Journal of ginseng research · 2017
    Article
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  18. Therapeutic Effect of the Tuber of Alisma orientale on Lipopolysaccharide-Induced Acute Lung Injury.Evidence-based complementary and alternative medicine : eCAM · 2013
    Article
  19. Article
  20. Article
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

12 authors at 8 institutions in 2 countries.

Ji Yeon LeeSchool of Bioscience and Biotechnology and Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 200-701.
Yong Gyu LeeSchool of Bioscience and Biotechnology and Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 200-701.
Jaehwi LeeCollege of Pharmacy, Chung-Ang University, Seoul 156-756.
Keum-Jin YangDepartment of Pharmacology, Daejeon Regional Cancer Center, Cancer Research Institute, College of Medicine, Chungnam National University, Daejeon 310-010.
Ae Ra KimSchool of Bioscience and Biotechnology and Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 200-701.
Joo Young KimSchool of Bioscience and Biotechnology and Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 200-701.
Moo-Ho WonDepartment of Anatomy and Neurobiology and Institute of Neurodegeneration and Neuroregeneration, College of Medicine, Hallym University, Chucheon 200-702.
Jongsun ParkDepartment of Pharmacology, Daejeon Regional Cancer Center, Cancer Research Institute, College of Medicine, Chungnam National University, Daejeon 310-010.
Byong Chul YooResearch Institute and Hospital, National Cancer Center, Goyang 410-769.
Sanghee KimCollege of Pharmacy, Seoul National University, Seoul 151-741.
Won-Jea ChoCollege of Pharmacy, Chonnam National University, Kwangju 500-757, Korea.
Jae Youl ChoSchool of Bioscience and Biotechnology and Institute of Bioscience and Biotechnology, Kangwon National University, Chuncheon 200-701. Electronic address: jaecho@kangwon.ac.kr.
Kangwon National University · KRChonnam National University · KRChung-Ang University · KRChungnam National University · KRHallym University · KRNational Cancer Center · USRegional Cancer Center · USSeoul National University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The hydroxylated benzene metabolite hydroquinone (HQ) is mainly generated from benzene, an important industrial chemical, and is also a common dietary component. Although numerous reports have addressed the tumorigenesis-inducing effects of HQ, few papers have explored its molecular regulatory mechanism in immunological responses. In this study we characterized Akt (protein kinase B)-targeted regulation by HQ and its derivatives, in suppressing inflammatory responses using cellular, molecular, biochemical, and immunopharmacological approaches. HQ down-regulated inflammatory responses such as NO production, surface levels of pattern recognition receptors, and cytokine gene expression with IC(50) values that ranged from 5 to 10 microm. HQ inhibition was mediated by blocking NF-kappaB activation via suppression of its translocation pathway, which is composed of Akt, I kappaB alpha kinase beta, and I kappaB alpha. Of the targets in this pathway, HQ directly targeted and bound to the sulfhydryl group of Cys-310 of Akt and sequentially interrupted the phosphorylation of both Thr-308 and Ser-473 by mediation of beta-mercaptoethanol, according to the liquid chromatography/mass spectroscopy analysis of the interaction of HQ with an Akt-derived peptide. Therefore, our data suggest that Akt and its target site Cys-310 can be considered as a prime molecular target of HQ-mediated immunosuppression and for novel anti-Akt-targeted immunosuppressive drugs.

Indexed as

AnimalsBenzeneChromatography, LiquidCysteineHydroquinonesImmunosuppressive AgentsInhibitory Concentration 50MaleMass SpectrometryMercaptoethanolMiceMice, Inbred C57BLMice, Inbred ICRMicroscopy, ConfocalProto-Oncogene Proteins c-aktBenzeneCysteinehydroquinoneHydroquinonesImmunosuppressive AgentsMercaptoethanolProto-Oncogene Proteins c-akt

Identifiers

PMID20054000
PMCPMC2843240
OpenAlexW2018137536

What OpenQuestion holds

Textmetadata
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.