Evidence map›Paper›PMID 30693272›Full record

ArticleFrontiers in oncology2018

Aspirin Inhibits Natural Killer/T-Cell Lymphoma by Modulation of VEGF Expression and Mitochondrial Function.

Hongyu Zhang, Jianping Lu, Yun Jiao, Qi Chen, Min Li, Zichen Wang, Zhendong Yu, Xiaodong Huang, Athena Yao, Qiong Gao and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Aspirin Combined with Antifungal Drugs SuppressesJournal of microbiology and biotechnology · 2025
    Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
  9. Acetylsalicylic Acid-Primus Inter Pares in Pharmacology.Molecules (Basel, Switzerland) · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Aspirin Induces Mitochondrial CaInternational journal of molecular sciences · 2020
    Article
  15. Review
  16. 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

13 authors at 7 institutions in 1 country.

Hongyu ZhangDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Jianping LuDepartment of Child Psychiatry, Kangning Hospital of Shenzhen, Shenzhen, China.
Yun JiaoDepartment of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, China.
Qi ChenDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Min LiInstitute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, China.
Zichen WangDepartment of Child Psychiatry, Kangning Hospital of Shenzhen, Shenzhen, China.
Zhendong YuDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Xiaodong HuangInstitute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, China.
Athena YaoInstitute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, China.
Qiong GaoDepartment of Gynecology, The Eighth Affiliated Hospital, Sun Yat-sen University, Shenzhen, China.
Weiguo XieInstitute of Rehabilitation Center, Tongren Hospital of Wuhan University, Wuhan, China.
Ling LiDepartment of Pediatrics, Hainan Maternal and Child Health Hospital, Haikou, China.
Paul YaoDepartment of Hematology, Peking University Shenzhen Hospital, Shenzhen, China.
Peking University Shenzhen Hospital · CNWuhan Third Hospital · CNHainan Maternal and Child Health Hospital · CNJinzhou Kangning Hospital · CNEighth Affiliated Hospital of Sun Yat-sen UniversityShenzhen KangNing Hospital · CNTongren Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extranodal nasal-type natural killer/T-cell lymphoma (NKTCL) is an Epstein-Barr virus (EBV)-associated lymphoma with a strong tendency relapse or be refractory in response to chemotherapy. Development of a new strategy for NKTCL treatment is still quite necessary. In this study, we found that aspirin treatment suppresses VEGF expression in NKTCL SNK-6 cells. Further investigation showed that aspirin treatment increases histone methylation in the range of -100~0 that is proximal to the transcription start site on the VEGF promoter, subsequently decreasing the binding ability of Sp1 to the VEGF promoter with VEGF suppression. Furthermore, aspirin treatment modulates mitochondrial function with increased ROS formation and apoptosis in NKTCL cells. Aspirin treatment alone slightly inhibits NKTCL SNK-6 tumor growth and EBV replication; while in the presence of histone deacetylase inhibitor (HDACi) chidamide (CDM), aspirin significantly suppresses the VEGF signaling pathway with increased ROS overgeneration and EBV inhibition. We also showed that with the addition of chidamide, aspirin significantly suppresses NKTCL tumor growth in both

Indexed as

aspirinepstein-barr virusmitochondriaNKTCLreactive oxygen species

Identifiers

PMID30693272
PMCPMC6339948
OpenAlexW2908748587

What Socratic 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 Socratic graph.