Evidence map›Paper›PMID 30590117›Full record

ArticleNitric oxide : biology and chemistry2019

Nitric oxide synthase inhibitors 1400W and L-NIO inhibit angiogenesis pathway of colorectal cancer.

Yanfeng Gao, Shuang Zhou, Yi Xu, Sen Sheng, Steven Y Qian, Xiongwei Huo

Open access · greenAbstract read
In one paragraph

Article in Nitric oxide : biology and chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 43 citations in OpenAlex.

  1. Pooled it
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  5. Review
  6. Article
  7. Article
  8. Article
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  10. The Triple Crown: NO, CO, and HPharmacology & therapeutics · 2023
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  14. Review
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  17. Review
  18. S-Nitrosylation in Tumor Microenvironment.International journal of molecular sciences · 2021
    Review
  19. Revealing the Role of High-Density Lipoprotein in Colorectal Cancer.International journal of molecular sciences · 2021
    Review
  20. 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

6 authors at 4 institutions in 2 countries.

Yanfeng GaoDepartment of Anesthesiology, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Shuang ZhouDepartment of Neurosurgery, Neuroscience Institute, Baylor Scott and White Health, Temple, TX, 76502, USA.
Yi XuDepartment of Pharmaceutical Sciences, North Dakota State University, North Dakota, 58108, USA.
Sen ShengDepartment of Neurosurgery, Neuroscience Institute, Baylor Scott and White Health, Temple, TX, 76502, USA.
Steven Y QianDepartment of Pharmaceutical Sciences, North Dakota State University, North Dakota, 58108, USA. Electronic address: steven.qian@ndsu.edu.
Xiongwei HuoDepartment of General Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China. Electronic address: doctorhuoxw@163.com.
Baylor Scott & White Health · USFirst Affiliated Hospital of Xi'an Jiaotong University · CNDakota State University · USNorth Dakota State University · US

Funding

New Paradigm of Targeting COX-Catalyzed Free Radical Peroxidation in Colon CancerR15CA195499 · NCI · NORTH DAKOTA STATE UNIVERSITY · PI GUO, ANG · 2016 to 2016
$435k
NCI NIH HHS R15 CA195499
6 · The paper itself

Abstract

backgroundIt has been widely accepted that angiogenesis plays fundamental roles in colorectal cancer development, and therapeutic targeting of this pathway has achieved promising outcome. Recent reports have highlighted the involvement of nitric oxide synthases (NOS) in the development of angiogenesis in cancer; however, the mechanism and therapeutic value of NOS inhibitors in colon cancer are largely unknown.

objectiveIn this study, we investigated the effects and mechanism of the NOS inhibitors 1400W and L-NIO on the angiogenesis pathway in colorectal cancer cells.

methodsTwo colorectal cancer cell lines, HT 29 and HCT 116, were used for in vitro study. The expression of iNOS and eNOS in cells was knocked down via shRNA transfection. MTS assays and wound healing assays were performed to assess cell proliferation and migration after shRNA transfection or treatment with 1400W, L-NIO, and 5-fluorouracil. Human angiogenesis PCR arrays and proteome profiler human angiogenesis arrays were used to detect changes in key genes/proteins involved in modulating angiogenesis after 1400W and L-NIO treatment.

resultsKnockdown of iNOS and eNOS significantly inhibited colorectal cancer cell growth. Treatment with NOS inhibitors inhibited colorectal cancer cell growth and migration, and was associated with suppression of the expression of key genes/proteins involved in the angiogenesis pathway. In addition, the combined use of NOS inhibitors with 5-fluorouracil showed enhanced inhibition of cell proliferation and migration.

conclusionNOS inhibitors could suppress colorectal cancer cell growth and migration, likely via suppressing the angiogenesis pathway.

Indexed as

AmidinesAntineoplastic AgentsBenzylaminesCell ProliferationCell SurvivalColorectal NeoplasmsDose-Response Relationship, DrugDrug Screening Assays, AntitumorEnzyme InhibitorsHCT116 CellsHT29 CellsHumansNeovascularization, PathologicNitric Oxide SynthaseOrnithineStructure-Activity RelationshipAmidinesAntineoplastic AgentsBenzylaminesEnzyme InhibitorsN-(3-(aminomethyl)benzyl)acetamidineN(G)-iminoethylornithineNitric Oxide SynthaseOrnithine1400WAngiogenesisColorectal cancerL-NIONitric oxide synthase inhibitors

Identifiers

PMID30590117
PMCPMC6677402
OpenAlexW2905637957

What OpenQuestion holds

Textmetadata
LicenceTDM
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.