Evidence map›Paper›PMID 32509141›Full record

ArticleOxidative medicine and cellular longevity2020

Apatinib, a Novel Tyrosine Kinase Inhibitor, Promotes ROS-Dependent Apoptosis and Autophagy via the Nrf2/HO-1 Pathway in Ovarian Cancer Cells.

Xiaodan Sun, Ji Li, Yizhuo Li, Shouhan Wang, Qingchang Li

Open access · hybridAbstract read
In one paragraph

Article in Oxidative medicine and cellular longevity, 2020. 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
2.2field-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

25 citing papers in PubMed, 43 citations in OpenAlex.

  1. Trial
  2. Article
  3. Autophagy in Ovarian Cancer, an Opportunity or an Additional Threat?International journal of molecular sciences · 2026
    Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Role of autophagy and its regulation by noncoding RNAs in ovarian cancer.Experimental biology and medicine (Maywood, N.J.) · 2023
    Review
  14. Article
  15. Article
  16. p53 mApoptosis : an international journal on programmed cell death · 2022
    Article
  17. Article
  18. Article
  19. Development of targeted therapy of NRF2Cellular signalling · 2021
    Review
  20. Review
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

5 authors at 2 institutions in 1 country.

Xiaodan SunDepartment of Pathology, College of Basic Medical Sciences, China Medical University, Shenyang 110122, China.ORCID https://orcid.org/0000-0002-5119-383X
Ji LiDepartment of Pathology, College of Basic Medical Sciences, China Medical University, Shenyang 110122, China.ORCID https://orcid.org/0000-0001-7928-4824
Yizhuo LiDepartment of Pathology, College of Basic Medical Sciences, China Medical University, Shenyang 110122, China.ORCID https://orcid.org/0000-0003-4214-8305
Shouhan WangDepartment of Hepatopancreatobiliary Surgery, Jilin Cancer Hospital, Changchun 130012, China.ORCID https://orcid.org/0000-0002-6014-196X
Qingchang LiDepartment of Pathology, College of Basic Medical Sciences, China Medical University, Shenyang 110122, China.ORCID https://orcid.org/0000-0002-6317-7386
China Medical University · CNJilin Province Tumor Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Apatinib, a new-generation oral tyrosine kinase inhibitor targeting the vascular endothelial growth factor receptor 2 (VEGFR2) signaling pathway, shows favorable therapeutic effects in various malignant tumors. However, its effect on ovarian cancer has not yet been characterized. Here, we demonstrated that apatinib inhibited ovarian cancer cell growth and migration in a concentration-dependent manner. Further, we found that apatinib could directly act on tumor cells and promote ROS-dependent apoptosis and autophagy. Mechanistically, we showed that apatinib suppressed glutathione to generate ROS via the downregulation of the nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase 1 (HO-1) pathway and maintained an antitumor effect at a low level of VEGFR2 in ovarian cancer, suggesting that combination of apatinib with Nrf2 inhibitor may be a promising therapy strategy for patients with ovarian cancer.

Indexed as

Antineoplastic AgentsApoptosisAutophagyCell Line, TumorFemaleHeme Oxygenase-1HumansNeovascularization, PathologicNF-E2-Related Factor 2Ovarian NeoplasmsProtein Kinase InhibitorsPyridinesReactive Oxygen SpeciesSignal TransductionVascular Endothelial Growth Factor Receptor-2Antineoplastic AgentsapatinibHeme Oxygenase-1HMOX1 protein, humanNFE2L2 protein, humanNF-E2-Related Factor 2Protein Kinase InhibitorsPyridinesReactive Oxygen SpeciesVascular Endothelial Growth Factor Receptor-2

Identifiers

PMID32509141
PMCPMC7244982
OpenAlexW3025053953

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.