Evidence map›Paper›PMID 28489574›Full record

ArticleOncotarget2017

Targeting neurokinin-3 receptor: a novel anti-angiogenesis strategy for cancer treatment.

Ting Wang, Siwei Chen, Shihui Wang, Liang Shi, Chenggong Wang, Jingxin Zhang, Yanfeng Gao, Guodong Li, Yuanming Qi, Xiuli An and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.3field-weighted citation impact, top 41% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Noval insights and therapeutic strategies for tumor-induced kidney pathologies.Journal of experimental & clinical cancer research : CR · 2024
    Article
  6. Synergistic Antitumor Effect ofMolecules (Basel, Switzerland) · 2023
    Article
  7. Review
  8. Review
  9. Article
  10. 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 1 institution in 1 country.

Ting WangSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Siwei ChenSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Shihui WangSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Liang ShiSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Chenggong WangSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Jingxin ZhangSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Yanfeng GaoSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Guodong LiSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Yuanming QiSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Xiuli AnSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Lixiang ChenSchool of Life Science, Zhengzhou University, Zhengzhou, 450001, P.R. China.
Zhengzhou University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Angiogenesis is essential for tumor growth and metastasis, controlling angiogenesis is a promising strategy in cancer treatment. However, thus farther severe side effects of anti-angiogenic drugs have been rather demonstrated, stimulating interest in seeking novel targets of anti-angiogenesis. Neurokinin receptors, also known as tachykinin receptors, are usually considered as drug targets due to diverse physiological functions and their tractability. Although Neurokinin B, the selective natural agonist of neurokinin-3 receptor, have been shown to exhibit anti-angiogenesis activity, the effect and mechanism of neurokinin-3 receptor-mediated angiogenesis still remains unclear. In the present study, we demonstrated that [Mephe7]NKB, an analogue of NKB, possess significant anti-angiogenic effect on CAM. Furthermore, by introducing the tumor angiogenesis homing sequence (NGR), we designed and synthesized two novel agonist analogues of NK3R, NK3R-A1 and NK3R-A2. Both of the two analogues exhibit more efficient anti-migration effect on HUVECs by activating NK3R in vitro, and showed potent antitumor activities with no significant side effects in vivo. Taken together, our results illuminated that NK3R might be a potential novel target for the anti-angiogenesis therapy. Notably, NK3R-A1 might be used as a template for the development of the anti-tumor drugs on the basis of the anti-angiogenesis strategy.

Indexed as

Angiogenesis InhibitorsAnimalsCell Line, TumorCell MovementCells, CulturedChick EmbryoChorioallantoic MembraneFemaleHumansHuman Umbilical Vein Endothelial CellsMice, Inbred BALB CNeurokinin BReceptors, Neurokinin-3Sarcoma, ExperimentalTumor BurdenAngiogenesis InhibitorsNeurokinin BReceptors, Neurokinin-3anti-angiogenesisantitumor therapyneurokinin 3 receptorneurokinin B

Identifiers

PMID28489574
PMCPMC5522309
OpenAlexW2607051027

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.