Evidence map›Paper›PMID 31122284›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

Inhibition of RNA polymerase III transcription by Triptolide attenuates colorectal tumorigenesis.

Xia Liang, Renxiang Xie, Jinfeng Su, Bingqi Ye, Saisai Wei, Zhibing Liang, Rongpan Bai, Zhanghui Chen, Zhongxiang Li, Xiangwei Gao

Open access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
5.8field-weighted citation impact, top 4% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

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  16. Application Progress of Organoids in Colorectal Cancer.Frontiers in cell and developmental biology · 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

10 authors at 3 institutions in 1 country.

Xia LiangMedical Research Institute, & Guangdong Women and Children's Disease Precision Diagnosis and Treatment Engineering Technology Research Center, Baoan Maternal and Child Health Hospital, Jinan University, Shenzhen, 518102, China.
Renxiang XieDepartment of Public Health, Zhejiang University School of Medicine, Hangzhou, 310058, China.
Jinfeng SuMedical Research Institute, & Guangdong Women and Children's Disease Precision Diagnosis and Treatment Engineering Technology Research Center, Baoan Maternal and Child Health Hospital, Jinan University, Shenzhen, 518102, China.
Bingqi YeDepartment of Public Health, Zhejiang University School of Medicine, Hangzhou, 310058, China.
Saisai WeiSir Run-Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, 310058, China.
Zhibing LiangMedical Research Institute, & Guangdong Women and Children's Disease Precision Diagnosis and Treatment Engineering Technology Research Center, Baoan Maternal and Child Health Hospital, Jinan University, Shenzhen, 518102, China.
Rongpan BaiDepartment of Public Health, Zhejiang University School of Medicine, Hangzhou, 310058, China.
Zhanghui ChenAffiliated Central People's Hospital of Zhanjiang, Guangdong Medical University, Zhanjiang, 524045, China.
Zhongxiang LiMedical Research Institute, & Guangdong Women and Children's Disease Precision Diagnosis and Treatment Engineering Technology Research Center, Baoan Maternal and Child Health Hospital, Jinan University, Shenzhen, 518102, China. zhongxiangli@gmail.com.
Xiangwei GaoDepartment of Public Health, Zhejiang University School of Medicine, Hangzhou, 310058, China. xiangweigao@zju.edu.cn.
Zhejiang University · CNJinan University · CNGuangdong Medical College · CN

Funding

National Natural Science Foundation of China 81672847Natural Science Foundation of Zhejiang Province LQ19C050004Natural Science Foundation of Zhejiang Province LY16H040008
6 · The paper itself

Abstract

backgroundUpregulation of RNA polymerase (Pol) III products, including tRNAs and 5S rRNA, in tumor cells leads to enhanced protein synthesis and tumor formation, making it a potential target for cancer treatment. In this study, we evaluated the inhibition of Pol III transcription by triptolide and the anti-cancer effect of this drug in colorectal tumorigenesis.

methodsThe effect of triptolide on colorectal cancer development was assessed in colorectal cancer mouse models, 3D organoids, and cultured cells. Colorectal cancer cells were treated with triptolide. Pol III transcription was measured by real-time quantitative polymerase chain reaction (PCR). The formation of TFIIIB, a multi-subunit transcription factor for Pol III, was determined by chromatin immunoprecipitation (ChIP), co-immunoprecipitation (Co-IP), and fluorescence resonance energy transfer (FRET).

resultsTriptolide reduced both tumor number and tumor size in adenomatous polyposis coli (Apc) mutated (Apc

conclusionsTogether, our data suggest that inhibition of Pol III transcription with existing drugs such as triptolide provides a new avenue for developing novel therapies for colorectal cancer.

Indexed as

AnimalsCell Line, TumorCell ProliferationCell SurvivalColorectal NeoplasmsDiterpenesEpoxy CompoundsFemaleGene Expression Regulation, NeoplasticHCT116 CellsHumansMicePhenanthrenesPromoter Regions, GeneticRNA, Ribosomal, 5SRNA, TransferDiterpenesEpoxy CompoundsPhenanthrenesRNA, Ribosomal, 5SRNA, TransferTranscription Factor TFIIIBtriptolideColorectal cancerRNA polymerase IIITFIIIBTriptolide

Identifiers

PMID31122284
PMCPMC6533717
OpenAlexW2947704899

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.