Evidence map›Paper›PMID 30773944›Full record

ArticleFree radical research2019

Celastrol suppresses nitric oxide synthases and the angiogenesis pathway in colorectal cancer.

Yanfeng Gao, Shuang Zhou, Lizhi Pang, Juechen Yang, Han John Li, Xiongwei Huo, Steven Y Qian

Open access · greenAbstract read
In one paragraph

Article in Free radical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
9.3field-weighted citation impact, top 2% 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

29 citing papers in PubMed, 54 citations in OpenAlex.

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  7. Recent Trends in anti-tumor mechanisms and molecular targets of celastrol.International journal of biological sciences · 2024
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  20. S-Nitrosylation in Tumor Microenvironment.International journal of molecular sciences · 2021
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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

7 authors at 4 institutions in 2 countries.

Yanfeng Gaoa Department of Anesthesiology , the First Affiliated Hospital of Xi'an Jiaotong University , Xi'an, China.
Shuang Zhoub Department of Neurosurgery , Neuroscience Institute, Baylor Scott and White Health , Temple , USA.
Lizhi Pangc Department of Pharmaceutical Sciences , North Dakota State University , Fargo , USA.
Juechen Yangd Department of Computer Science , North Dakota State University , Fargo , USA.
Han John Lie Department of Pharmacy , Medical Center Hospital , Odessa , USA.
Xiongwei Huof Department of General Surgery , the First Affiliated Hospital of Xi'an Jiaotong University , Xi'an, China.
Steven Y Qianc Department of Pharmaceutical Sciences , North Dakota State University , Fargo , USA.
North Dakota State University · USFirst Affiliated Hospital of Xi'an Jiaotong University · CNBaylor Scott & White Health · USMedical Center Hospital · 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

The thunder god vine (Tripterygium wilfordii Hook. F) is traditionally used for inflammation-related diseases in traditional Chinese medicine. In recent years, celastrol (a natural compound from the root of the thunder god vine) has attracted great interest for its potential anticancer activities. The free radical nitric oxide (NO) is known to play a critical role in colorectal cancer growth by promoting tumour angiogenesis. However, how celastrol influences the NO pathway and its mechanism against colorectal cancer is largely unknown. In this study, we investigated the effects and mechanism of celastrol on nitric oxide synthase (NOS) and the angiogenesis pathway in colorectal cancer. Our data show that celastrol inhibited HT-29 and HCT116 cell proliferation, migration, and NOS activity in the cytoplasm. The antiproliferation activity of celastrol was associated with the inhibition of iNOS and eNOS in colorectal cancer cells. Treatment with celastrol inhibited colorectal cancer cell growth and migration, and was associated with suppression of the expression of key genes (TYMP, CDH5, THBS2, LEP, MMP9, and TNF) and proteins (IL-1b, MMP-9, PDGF, Serpin E1, and TIMP-4) involved in the angiogenesis pathway. In addition, combinational use of celastrol with 5-fluorouracil, salinomycin, 1400 W, and L-NIO showed enhanced inhibition of colorectal cancer cell proliferation and migration. In sum, our study suggests that celastrol could suppress colorectal cancer cell growth and migration, likely through suppressing NOS activity and inhibiting the angiogenesis pathway.

Indexed as

Cell ProliferationColorectal NeoplasmsHumansNitric Oxide SynthasePentacyclic TriterpenesSignal TransductionTripterygiumTriterpenescelastrolNitric Oxide SynthasePentacyclic TriterpenesTriterpenesAngiogenesiscelastrolcolorectal cancernitric oxide synthase inhibitors

Identifiers

PMID30773944
PMCPMC6715291
OpenAlexW2915279648

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.