Evidence map›Paper›PMID 35123522›Full record

ReviewJournal of hematology & oncology2022

Designing strategies of small-molecule compounds for modulating non-coding RNAs in cancer therapy.

Rongyan Zhao, Jiahui Fu, Lingjuan Zhu, Yi Chen, Bo Liu

Open access · goldAbstract readReview
In one paragraph

Review in Journal of hematology & oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
10.4field-weighted citation impact, top 1% 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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 111 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

5 authors at 2 institutions in 1 country.

Rongyan Zhao *State Key Laboratory of Biotherapy and Cancer Center, and Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Jiahui Fu *State Key Laboratory of Biotherapy and Cancer Center, and Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Lingjuan Zhu *State Key Laboratory of Biotherapy and Cancer Center, and Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yi ChenState Key Laboratory of Biotherapy and Cancer Center, and Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China. toddychan@163.com.
Bo LiuState Key Laboratory of Biotherapy and Cancer Center, and Department of Gastrointestinal Surgery, West China Hospital, Sichuan University, Chengdu, 610041, China. liubo2400@163.com.
Sichuan University · CNState Key Laboratory of Biotherapy

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Non-coding RNAs (ncRNAs) have been defined as a class of RNA molecules transcribed from the genome but not encoding proteins, such as microRNAs, long non-coding RNAs, Circular RNAs, and Piwi-interacting RNAs. Accumulating evidence has recently been revealing that ncRNAs become potential druggable targets for regulation of several small-molecule compounds, based on their complex spatial structures and biological functions in cancer therapy. Thus, in this review, we focus on summarizing some new emerging designing strategies, such as high-throughput screening approach, small-molecule microarray approach, structure-based designing approach, phenotypic screening approach, fragment-based designing approach, and pharmacological validation approach. Based on the above-mentioned approaches, a series of representative small-molecule compounds, including Bisphenol-A, Mitoxantrone and Enoxacin have been demonstrated to modulate or selectively target ncRNAs in different types of human cancers. Collectively, these inspiring findings would provide a clue on developing more novel avenues for pharmacological modulations of ncRNAs with small-molecule drugs for future cancer therapeutics.

Indexed as

Drug DiscoveryAnimalsAntineoplastic AgentsDrug DesignGene Expression Regulation, NeoplasticHumansNeoplasmsRNA, UntranslatedSmall Molecule LibrariesAntineoplastic AgentsRNA, UntranslatedSmall Molecule LibrariesCancer therapyDesigning strategyDrug discoveryNon-coding RNA (ncRNA)Small-molecule compound

Identifiers

PMID35123522
PMCPMC8817562
OpenAlexW4210277123

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.