Evidence map›Paper›PMID 30311444›Full record

ArticleCancer medicine2018

Sestrin 2 confers primary resistance to sorafenib by simultaneously activating AKT and AMPK in hepatocellular carcinoma.

Jimin Dai, Qichao Huang, Kunwei Niu, Bo Wang, Yijie Li, Chen Dai, Zhinan Chen, Kaishan Tao, Jingyao Dai

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  5. Sestrin2 serves as a scaffold protein to maintain cardiac energy and metabolic homeostasis during pathological stress.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Review
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  7. Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Sestrins in Physiological Stress Responses.Annual review of physiology · 2021
    Review
  18. Sestrin2-Mediated Autophagy Contributes to Drug ResistanceFrontiers in cell and developmental biology · 2021
    Article
  19. Review
  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

9 authors at 2 institutions in 1 country.

Jimin DaiDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.
Qichao HuangState Key Laboratory of Cancer Biology and Experimental Teaching Center of Basic Medicine, Air Force Medical University, Xi'an, China.ORCID 0000-0002-1071-1696
Kunwei NiuDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.
Bo WangDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.
Yijie LiDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.
Chen DaiDepartment of Orthopedics, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.
Zhinan ChenDepartment of Cell Biology, National Translational Science Center for Molecular Medicine, Air Force Medical University, Xi'an, China.
Kaishan TaoDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.ORCID 0000-0002-8573-0445
Jingyao DaiDepartment of Hepatobiliary Surgery, The First Affiliated Hospital of Air Force Medical University, Xi'an, China.ORCID 0000-0001-8510-3647
Air Force Engineering University · CNXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the malignancy derived from normal hepatocytes with increasing incidence and extremely poor prognosis worldwide. The only approved first-line systematic treatment agent for HCC, sorafenib, is capable to effectively improve advanced HCC patients' survival. However, it is gradually recognized that the therapeutic response to sorafenib could be drastically diminished after short-term treatment, defined as primary resistance. The present study is aimed to explore the role of stress-inducible protein Sestrin2 (SESN2), one of the most important sestrins family members, in sorafenib primary resistance. Herein, we initially found that SESN2 expression was significantly up-regulated in both HCC cell lines and tissues compared to normal human hepatocytes and corresponding adjacent liver tissues, respectively. In addition, SESN2 expression was highly correlated with sorafenib IC

Indexed as

Drug Resistance, NeoplasmAMP-Activated Protein KinasesApoptosisCarcinoma, HepatocellularCell Line, TumorCell ProliferationGene Expression Regulation, NeoplasticHumansLiver NeoplasmsNuclear ProteinsPhosphorylationProto-Oncogene Proteins c-aktSestrinsSignal TransductionSorafenibUp-RegulationAMP-Activated Protein KinasesNuclear ProteinsProto-Oncogene Proteins c-aktSESN2 protein, humanSestrinsSorafenibAKTAMPKhepatocellular carcinomaprimary resistanceSestrin2sorafenib

Identifiers

PMID30311444
PMCPMC6247041
OpenAlexW2896036304

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.