Evidence map›Paper›PMID 29190976›Full record

ArticleOncotarget2017

Celastrol induces apoptosis in hepatocellular carcinoma cells via targeting ER-stress/UPR.

Bo Ren, Hui Liu, Hang Gao, Shutong Liu, Zehui Zhang, Andrew M Fribley, Michael U Callaghan, Zhixiang Xu, Qinghua Zeng, Yulin Li

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
7.1field-weighted citation impact, top 3% 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

20 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Recent Trends in anti-tumor mechanisms and molecular targets of celastrol.International journal of biological sciences · 2024
    Review
  7. Withaferin A and Celastrol Overwhelm Proteostasis.International journal of molecular sciences · 2023
    Review
  8. Autophagy in the pharmacological activities of celastrol (Review).Experimental and therapeutic medicine · 2023
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Celastrol Enhances the Anti-Liver Cancer Activity of Sorafenib.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  18. Review
  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

10 authors at 4 institutions in 2 countries.

Bo RenThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Hui LiuPathology, The Second Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou 310009, China.
Hang GaoThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Shutong LiuThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Zehui ZhangThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Andrew M FribleyCarman and Ann Adams Department of Pediatrics, Division of Hematology/Oncology, Wayne State University, Detroit, MI 48201, USA.
Michael U CallaghanCarman and Ann Adams Department of Pediatrics, Division of Hematology/Oncology, Wayne State University, Detroit, MI 48201, USA.
Zhixiang XuThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Qinghua ZengThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Yulin LiThe Key Laboratory of Pathobiology, Ministry of Education, Jilin University, Changchun 130021, China.
Jilin University · CNWayne State University · USSecond Affiliated Hospital of Zhejiang University · CNUniversity of Alabama at Birmingham · US

Funding

TGF-beta pathway polymorphisms and colon cancer riskR01CA108741 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PASCHE, BORIS · 2006 to 2008
$804k
Genomic screening to identify novel stress-inducing chemotherapies for carcinomaR00DE019678 · NIDCR · WAYNE STATE UNIVERSITY · PI FRIBLEY, ANDREW MICHAEL · 2011 to 2013
$726k
NCI NIH HHS R01 CA108741NIDCR NIH HHS R00 DE019678
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is one of the most serious and deadly diseases worldwide with limited options for effective treatment. Biomarker-based active compound targeting therapy may shed some light on novel drugs for HCC. The endoplasmic reticulum (ER) stress and unfolded protein response (UPR) play important roles in the regulation of cell fate and have become novel signaling targets for the development of anticancer drugs. Celastrol, a triterpene from traditional Chinese medicine, has been reported to possess anti-tumor effects on various cancers. We, along with several other research groups, have recently reported that UPR was induced by celastrol in several different cancers, including hepatocellular carcinoma. However, UPR status in HCC still remains unclear. The role of ER stress and autophagy in response to celastrol also has yet to be elucidated. Our results demonstrated that celastrol could cause G2/M phase rest and inhibit proliferation in HepG2 and Bel7402. Exposure to celastrol resulted in the activation of the intrinsic apoptotic pathway, via ER stress and the UPR. In murine syngeneic model studies celastrol inhibited H22 tumor growth via the induction of ER stress and apoptosis. Our study suggests that celastrol is a potential drug for HCC therapy via targeting ER-stress/UPR.

Indexed as

apoptosisautophagycelastrolER stresshepatocellular carcinoma

Identifiers

PMID29190976
PMCPMC5696242
OpenAlexW2763851830

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.