Evidence map›Paper›PMID 30717276›Full record

ArticleCancers2019

Cordycepin Suppresses Endothelial Cell Proliferation, Migration, Angiogenesis, and Tumor Growth by Regulating Focal Adhesion Kinase and p53.

Yi-Ting Lin, Shu-Man Liang, Ya-Ju Wu, Yi-Ju Wu, Yi-Jhu Lu, Yee-Jee Jan, Bor-Sheng Ko, Yung-Jen Chuang, Song-Kun Shyue, Cheng-Chin Kuo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. The role and mechanisms of cordycepin in inhibiting cancer cells.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica · 2024
    Review
  6. Review
  7. Article
  8. Article
  9. FAK in Cancer: From Mechanisms to Therapeutic Strategies.International journal of molecular sciences · 2022
    Review
  10. Review
  11. Article
  12. Observational
  13. 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

11 authors at 5 institutions in 1 country.

Yi-Ting LinInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan 350, Taiwan. 014260@nhri.org.tw.
Shu-Man LiangInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan 350, Taiwan. shu-man@nhri.org.tw.
Ya-Ju WuDepartment of Pathology, Taichung Veterans General Hospital, Chiayi Branch, Chiayi City 600, Taiwan. werepast@gmail.com.
Yi-Ju WuInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan 350, Taiwan. kathy614@livemail.tw.
Yi-Jhu LuInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan 350, Taiwan. yijhu@nhri.org.tw.
Yee-Jee JanDepartment of Pathology and Laboratory Medicine, Taichung Veterans General Hospital, Taichung 407, Taiwan. yejan@vghtc.gov.tw.
Bor-Sheng KoDepartment of Internal Medicine, National Taiwan University Hospital, Taipei 100, Taiwan. kevinkomd@gmail.com.
Yung-Jen ChuangInstitute of Bioinformatics and Structure Biology, National Tsing Hua University, Hsinchu 300, Taiwan. yjchuang@life.nthu.edu.tw.
Song-Kun ShyueInstitute of Biomedical Sciences, Academia Sinica, Taipei 115, Taiwan. skshyue@ibms.sinica.edu.tw. skshyue@ibms.sinica.edu.tw.
Cheng-Chin KuoInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan 350, Taiwan. kuocc@nhri.org.tw.
Jun-Yang LiouInstitute of Cellular and System Medicine, National Health Research Institutes, Zhunan 350, Taiwan. jliou@nhri.org.tw.
National Health Research Institutes · TWInstitute of Biomedical Sciences, Academia Sinica · TWNational Taiwan University Hospital · TWNational Tsing Hua University · TWTaichung Veterans General Hospital · TW

Funding

Ministry of Science and Technology, Taiwan 105-2320-B-400-021 and 106-2320-B-400-023National Health Research Institutes 06A1-CSPP07-014
6 · The paper itself

Abstract

Focal adhesion kinase (FAK) plays an important role in vascular development, including the regulation of endothelial cell (EC) adhesion, migration, proliferation, and survival. 3'-deoxyadenosine (cordycepin) is known to suppress FAK expression, cell migration, and the epithelial⁻mesenchymal transition in hepatocellular carcinoma (HCC). However, whether cordycepin affects FAK expression and cellular functions in ECs and the specific molecular mechanism remain unclear. In this study, we found that cordycepin suppressed FAK expression and the phosphorylation of FAK (p-FAK) at Tyr397 in ECs. Cordycepin inhibited the proliferation, wound healing, transwell migration, and tube formation of ECs. Confocal microscopy revealed that cordycepin significantly reduced FAK expression and decreased focal adhesion number of ECs. The suppressed expression of FAK was accompanied by induced p53 and p21 expression in ECs. Finally, we demonstrated that cordycepin suppressed angiogenesis in an in vivo angiogenesis assay and reduced HCC tumor growth in a xenograft nude mice model. Our study indicated that cordycepin could attenuate cell proliferation and migration and may result in the impairment of the angiogenesis process and tumor growth via downregulation of FAK and induction of p53 and p21 in ECs. Therefore, cordycepin may be used as a potential adjuvant for cancer therapy.

Indexed as

angiogenesiscordycepinendothelial cellsFAKp53

Identifiers

PMID30717276
PMCPMC6406613
OpenAlexW2914650899

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.