Evidence map›Paper›PMID 27458171›Full record

ArticleOncotarget2017

Capsazepine inhibits JAK/STAT3 signaling, tumor growth, and cell survival in prostate cancer.

Jong Hyun Lee, Chulwon Kim, Seung Ho Baek, Jeong-Hyeon Ko, Seok Geun Lee, Woong Mo Yang, Jae-Young Um, Gautam Sethi, Kwang Seok Ahn

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 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
6.3field-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

59 citing papers in PubMed, 124 citations in OpenAlex.

  1. Review
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  3. Article
  4. Review
  5. Anticancer Activity of Region B Capsaicin Analogs.Journal of medicinal chemistry · 2023
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  7. Article
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  11. Unraveling the Potential Role of NEDD4-like E3 Ligases in Cancer.International journal of molecular sciences · 2022
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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

9 authors at 2 institutions in 2 countries.

Jong Hyun LeeCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Chulwon KimCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Seung Ho BaekCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Jeong-Hyeon KoCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Seok Geun LeeCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Woong Mo YangCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Jae-Young UmCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Gautam SethiDepartment of Pharmacology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore 117597.
Kwang Seok AhnCollege of Korean Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Kyung Hee University · KRNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persistent STAT3 activation is seen in many tumor cells and promotes malignant transformation. Here, we investigated whether capsazepine (Capz), a synthetic analogue of capsaicin, exerts anticancer effects by inhibiting STAT3 activation in prostate cancer cells. Capz inhibited both constitutive and induced STAT3 activation in human prostate carcinoma cells. Capz also inhibited activation of the upstream kinases JAK1/2 and c-Src. The phosphatase inhibitor pervanadate reversed Capz-induced STAT3 inhibition, indicating that the effect of Capz depends on a protein tyrosine phosphatase. Capz treatment increased PTPε protein and mRNA levels. Moreover, siRNA-mediated knockdown of PTPε reversed the Capz-induced induction of PTPε and inhibition of STAT3 activation, indicating that PTPε is crucial for Capz-dependent STAT3 dephosphorylation. Capz also decreased levels of the protein products of various oncogenes, which in turn inhibited proliferation and invasion and induced apoptosis. Finally, intraperitoneal Capz administration decreased tumor growth in a xenograft mouse prostate cancer model and reduced p-STAT3 and Ki-67 expression. These data suggest that Capz is a novel pharmacological inhibitor of STAT3 activation with several anticancer effects in prostate cancer cells.

Indexed as

A549 CellsAnimalsAntineoplastic AgentsApoptosisCapsaicinCell Line, TumorCell ProliferationCell SurvivalEnzyme ActivationHumansJanus Kinase 1Ki-67 AntigenMaleMiceMice, Inbred BALB CMice, NudeAntineoplastic AgentsCapsaicincapsazepineJAK1 protein, humanJanus Kinase 1Ki-67 AntigenpervanadateProtein Tyrosine PhosphatasesPTPRE protein, humanReceptor-Like Protein Tyrosine Phosphatases, Class 4RNA, Small InterferingSTAT3 protein, humanSTAT3 Transcription FactorVanadatesapoptosiscapsazepineprostate cancerPTPeSTAT3

Identifiers

PMID27458171
PMCPMC5392279
OpenAlexW2504338811

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.