Evidence map›Paper›PMID 30006924›Full record

ArticleInternational journal of cancer2018

Triptolide inhibits Wnt signaling in NSCLC through upregulation of multiple Wnt inhibitory factors via epigenetic modifications to Histone H3.

Isaac Nardi, Theresa Reno, Xinwei Yun, Terra Sztain, Jami Wang, Huifang Dai, Li Zheng, Binghui Shen, Jae Kim, Dan Raz

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

22 citing papers in PubMed, 38 citations in OpenAlex.

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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

10 authors at 2 institutions in 2 countries.

Isaac NardiCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.ORCID 0000-0003-3604-9917
Theresa RenoCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.
Xinwei YunCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.
Terra SztainCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.
Jami WangCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.
Huifang DaiDepartment of Cancer Genetics and Epigenetics, Duarte, California.
Li ZhengDepartment of Cancer Genetics and Epigenetics, Duarte, California.
Binghui ShenDepartment of Cancer Genetics and Epigenetics, Duarte, California.
Jae KimCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.
Dan RazCity of Hope Medical Center, Division of Thoracic Surgery, Baum Family Thoracic Oncology laboratory; Beckman Research Institute.
City Of Hope National Medical Center · USCancer Genetics (United States) · US

Funding

Transgenic Mouse FacilityP30CA033572 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI STANLEY R. HAMILTON · 1985 to 2026
$86.3M
Oncology Research Career Development ProgramK12CA001727 · NCI · CITY OF HOPE NATIONAL MEDICAL CENTER · PI MORTIMER, JOANNE E. · 1992 to 2024
$14.6M
Function Analysis of FEN-1 Nuclease in Genome StabilityR01CA073764 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI BINGHUI SHEN · 2002 to 2026
$7.9M
Functional Analysis of Structure Specific Nucleases in Genome Stability and CancersR50CA211397 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ZHENG, LI · 2016 to 2025
$3.3M
Doris Duke Charitable Foundation 2016105NCI NIH HHS K12 CA001727NCI NIH HHS P30 CA033572NCI NIH HHS R01 CA073764NCI NIH HHS R50 CA211397
6 · The paper itself

Abstract

In the last decade, it has become clear that epigenetic changes act together with genetic mutations to promote virtually every stage of tumorigenesis and cancer progression. This knowledge has triggered searches for "epigenetic drugs" that can be developed into new cancer therapies. Here we report that triptolide reduced lung cancer incidence from 70% to 10% in a Fen1 E160D transgenic mouse model and effectively inhibited cancer growth and metastasis in A549 and H460 mouse xenografts. We found that triptolide induced lung cancer cell apoptosis that was associated with global epigenetic changes to histone 3 (H3). These global epigenetic changes in H3 are correlated with an increase in protein expression of five Wnt inhibitory factors that include WIF1, FRZB, SFRP1, ENY2, and DKK1. Triptolide had no effect on DNA methylation status at any of the CpG islands located in the promoter regions of all five Wnt inhibitory factors. Wnt expression is implicated in promoting the development and progression of many lung cancers. Because of this, the potential to target Wnt signaling with drugs that induce epigenetic modifications provides a new avenue for developing novel therapies for patients with these tumor types.

Indexed as

A549 CellsAnimalsAntineoplastic Agents, AlkylatingCarcinoma, Non-Small-Cell LungCell Line, TumorDiterpenesEpigenesis, GeneticEpoxy CompoundsHistonesHumansLung NeoplasmsMice, Inbred NODMice, SCIDPhenanthrenesUp-RegulationWnt Signaling PathwayAntineoplastic Agents, AlkylatingDiterpenesEpoxy CompoundsHistonesPhenanthrenestriptolidedemethylationhistone 3lung cancertriptolideWnt signaling

Identifiers

PMID30006924
PMCPMC6483070
OpenAlexW2884259565

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.