Evidence map›Paper›PMID 35493211›Full record

ArticleRSC advances2021

Design and synthesis of water-soluble grifolin prodrugs for DNA methyltransferase 1 (DNMT1) down-regulation.

Liguo Wang, Yue Wu, Zhenzhen Li, Tianlong Lan, Xu Zhao, Wenxing Lv, Feng Shi, Xiangjian Luo, Yu Rao, Ya Cao

Open access · goldAbstract read
In one paragraph

Article in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Review
  2. Epigenetics-targeted drugs: current paradigms and future challenges.Signal transduction and targeted therapy · 2024
    Review
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 1 country.

Liguo WangKey Laboratory of Protein Sciences, School of Pharmaceutical Sciences, Tsinghua University Beijing 100084 China yrao@tsinghua.edu.cn.ORCID https://orcid.org/0000-0003-0437-8222
Yue WuKey Laboratory of Protein Sciences, School of Pharmaceutical Sciences, Tsinghua University Beijing 100084 China yrao@tsinghua.edu.cn.
Zhenzhen LiKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Central South University Changsha 410078 China ycao98@vip.sina.com.
Tianlong LanKey Laboratory of Protein Sciences, School of Pharmaceutical Sciences, Tsinghua University Beijing 100084 China yrao@tsinghua.edu.cn.ORCID https://orcid.org/0000-0002-9435-9959
Xu ZhaoKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Central South University Changsha 410078 China ycao98@vip.sina.com.
Wenxing LvKey Laboratory of Protein Sciences, School of Pharmaceutical Sciences, Tsinghua University Beijing 100084 China yrao@tsinghua.edu.cn.
Feng ShiKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Central South University Changsha 410078 China ycao98@vip.sina.com.
Xiangjian LuoKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Central South University Changsha 410078 China ycao98@vip.sina.com.
Yu RaoKey Laboratory of Protein Sciences, School of Pharmaceutical Sciences, Tsinghua University Beijing 100084 China yrao@tsinghua.edu.cn.ORCID https://orcid.org/0000-0002-4356-8531
Ya CaoKey Laboratory of Carcinogenesis and Invasion, Chinese Ministry of Education, Central South University Changsha 410078 China ycao98@vip.sina.com.
Ministry of Education of the People's Republic of China · CNTsinghua University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation and gene silencing play indispensable roles in the epigenetic landscape and gene expression. DNA methyltransferase 1 (DNMT1), a member of the DNMT family, which catalyzes the addition of methyl groups on DNA has been identified to have a close relationship with tumorigenesis. But DNMT1 inhibitors are rare except for the highly toxic nucleoside derivates. Grifolin is a unique natural product which down-regulates DNMT1 and has low toxicity. However, the poor solubility and stability of grifolin limit its application. Herein, we synthesized PEG5-Grifolin as a water-miscible prodrug of grifolin. The half-life of PEG5-Grifolin at 25 °C was considerably extended, revealing excellent stability. Meanwhile, PEG5-Grifolin suppressed tumor growth of by downregulating DNMT1 and reactivating the expression of several tumor suppressor genes

Identifiers

PMID35493211
PMCPMC9044205
OpenAlexW4205298657

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.