Evidence map›Paper›PMID 33742125›Full record

ArticleOncogene2021

NSD2 promotes tumor angiogenesis through methylating and activating STAT3 protein.

Da Song, Jingqin Lan, Yaqi Chen, Anyi Liu, Qi Wu, Chongchong Zhao, Yongdong Feng, Jing Wang, Xuelai Luo, Zhixin Cao and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
5.4field-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

33 citing papers in PubMed, 74 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Many faces of mammalian NSD methyltransferases.Cellular & molecular biology letters · 2026
    Review
  5. Review
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. KDM5D histone demethylase mediates p38α inactivation via its enzymatic activity to inhibit cancer progression.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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  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

13 authors at 3 institutions in 1 country.

Da SongGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Jingqin LanGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Yaqi ChenGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Anyi LiuGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Qi WuGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Chongchong ZhaoProteinomics Facility at Technology Center for Protein Sciences, Tsinghua University, Beijing, China.
Yongdong FengGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Jing WangDepartment of Immunology, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Xuelai LuoGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Zhixin CaoGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Xiaonian CaoGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China.
Junbo HuGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China. jbhu@tjh.tjmu.edu.cn.ORCID http://orcid.org/0000-0002-3582-999X
Guihua WangGI Cancer Research Institute, Tongji Hospital, Huazhong University of Science and Technology, Wuhan, China. ghwang@tjh.tjmu.edu.cn.ORCID http://orcid.org/0000-0001-5423-9357
Tongji Hospital · CNHuazhong University of Science and Technology · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor angiogenesis plays vital roles in tumorigenesis and development; regulatory mechanism of angiogenesis is still not been fully elucidated. NSD2, a histone methyltransferase catalyzing di-methylation of histone H3 at lysine 36, has been proved a critical molecule in proliferation, metastasis, and tumorigenesis. But its role in tumor angiogenesis remains unknown. Here we demonstrated that NSD2 promoted tumor angiogenesis in vitro and in vivo. Furthermore, we confirmed that the angiogenic function of NSD2 was mediated by STAT3. Momentously, we found that NSD2 promoted the methylation and activation of STAT3. In addition, mass spectrometry and site-directed mutagenesis assays revealed that NSD2 methylated STAT3 at lysine 163 (K163). Meanwhile, K to R mutant at K163 of STAT3 attenuated the activation and angiogenic function of STAT3. Taken together, we conclude that methylation of STAT3 catalyzed by NSD2 promotes the activation of STAT3 pathway and enhances the ability of tumor angiogenesis. Our findings investigate a NSD2-dependent methylation-phosphorylation regulation pattern of STAT3 and reveal that NSD2/STAT3/VEGFA axis might be a potential target for tumor therapy.

Indexed as

AnimalsCarcinogenesisColonic NeoplasmsHeterograftsHistone-Lysine N-MethyltransferaseHumansHuman Umbilical Vein Endothelial CellsMaleMethylationMiceMice, NudeNeovascularization, PathologicRepressor ProteinsSTAT3 Transcription FactorHistone-Lysine N-MethyltransferaseNSD2 protein, humanRepressor ProteinsSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID33742125
OpenAlexW3196841143

What OpenQuestion holds

Textmetadata
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.