Evidence map›Paper›PMID 34586726›Full record

ArticleClinical and translational medicine2021

Selenium sulfide disrupts the PLAGL2/C-MET/STAT3-induced resistance against mitochondrial apoptosis in hepatocellular carcinoma.

Tianfeng Yang, Jian Huo, Rui Xu, Qi Su, Wenjuan Tang, Dongdong Zhang, Man Zhu, Yingzhuan Zhan, Bingling Dai, Yanmin Zhang

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-weighted citation impact, top 19% 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

14 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. STAT3 axis in cancer and cancer stem cells: From oncogenesis to targeted therapies.Biochimica et biophysica acta. Reviews on cancer · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Review
  7. [Research progress on ferroptosis regulation in tumor immunity of hepatocellular carcinoma].Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2024
    Review
  8. Review
  9. Review
  10. 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

10 authors at 1 institution in 1 country.

Tianfeng YangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Jian HuoSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Rui XuSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Qi SuSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Wenjuan TangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Dongdong ZhangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Man ZhuSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Yingzhuan ZhanSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Bingling DaiSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.
Yanmin ZhangSchool of Pharmacy, Health Science Center, Xi'an Jiaotong University, Xi'an, P. R. China.ORCID 0000-0001-7307-9408
Shaanxi University of Science and Technology · CN

Funding

Fundamental Research Funds for the Central Universities xtr0118022National Natural Science Foundation of China 81773772
6 · The paper itself

Abstract

backgroundHepatocellular carcinoma (HCC) is the third leading cause of cancer-related deaths worldwide. Overexpression of pleomorphic adenoma gene like-2 (PLAGL2) is associated with tumorigenesis. However, its function in HCC is unclear, and there are currently no anti-HCC drugs that target PLAGL2. Drug repositioning may facilitate the development of PLAGL2-targeted drug candidates.

methodsThe expression of PLAGL2 in HCC clinical tissue samples and HCC cell lines was analyzed by western blotting. The constructed HCC cell models were used to confirm the underlying function of PLAGL2 as a therapeutic target. Multiple in vitro and in vivo assays were conducted to determine the anti-proliferative and apoptosis-inducing effects of selenium sulfide (SeS

resultsPLAGL2 expression was higher in HCC tumor tissues than in normal adjacent tissues. Its overexpression promoted the resistance of HCC cells of mitochondrial apoptosis through the regulation of the downstream C-MET/STAT3 signaling axis. SeS

conclusionsOur data reveal an important role of PLAGL2 in apoptosis resistance in HCC and highlight the potential of using SeS

Indexed as

AnimalsApoptosisCarcinoma, HepatocellularCell Line, TumorDNA-Binding ProteinsHumansLiverLiver NeoplasmsMaleMiceMice, NudeMitochondriaProto-Oncogene Proteins c-metRNA-Binding ProteinsSelenium CompoundsSignal TransductionDNA-Binding ProteinsPLAGL2 protein, humanProto-Oncogene Proteins c-metRNA-Binding ProteinsSelenium Compoundsselenium disulfideSTAT3 protein, humanSTAT3 Transcription FactorTranscription FactorsC-MET/STAT3HCCPLAGL2selenium sulfide

Identifiers

PMID34586726
PMCPMC8441139
OpenAlexW3200084846

What OpenQuestion holds

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LicenceCC BY
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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.