Evidence map›Paper›PMID 32106543›Full record

ArticleCancers2020

The Role of p53-Mediated Signaling in the Therapeutic Response of Colorectal Cancer to 9F, a Spermine-Modified Naphthalene Diimide Derivative.

Lei Gao, Chaochao Ge, Senzhen Wang, Xiaojuan Xu, Yongli Feng, Xinna Li, Chaojie Wang, Yuxia Wang, Fujun Dai, Songqiang Xie

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 15 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 1 institution in 1 country.

Lei GaoKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Chaochao GeKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Senzhen WangKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Xiaojuan XuPharmaceutical College, Henan University, Kaifeng 475004, Henan, China.
Yongli FengKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Xinna LiKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Chaojie WangKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Yuxia WangCollege of Chemistry and Chemical Engineering, Henan University, Kaifeng 475004, Henan, China.
Fujun DaiKey Laboratory of Natural Medicine and Immuno-Engineering, Henan University, Kaifeng 475004, Henan, China.
Songqiang XiePharmaceutical College, Henan University, Kaifeng 475004, Henan, China.
Henan University · CN

Funding

China Postdoctoral Science Foundation Funded Project 2019M652527Innovative Research Team (in Science and Technology) in University of Henan Province 19IRTSTHN004National Natural Science Foundation of China 81703004, U1904151, 81772832 and 81573465Postgraduate Education Reform Project of Henan Province 2019SJGLX081YYoung Talents Research and Cultivation Program of Henan Medical School 2019011
6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most prevalent cancers due to its frequency and high rate of mortality. Polyamine-vectorized anticancer drugs possess multiple biological properties. Of these drugs, 9F has been shown to inhibit tumor growth and the metastasis of hepatocellular carcinoma. This current study aims to investigate the effects of 9F on CRC and determine its molecular mechanisms of action. Our findings demonstrate that 9F inhibits CRC cell growth by inducing apoptosis and cell cycle arrest, and suppresses migration, invasion and angiogenesis in vitro, resulting in the inhibition of tumor growth and metastasis in vivo. Based on RNA-seq data, further bioinformatic analyses suggest that 9F exerts its anticancer activities through p53 signaling, which is responsible for the altered expression of key regulators of the cell cycle, apoptosis, the epithelial-to-mesenchymal transition (EMT), and angiogenesis. In addition, 9F is more effective than amonafide against CRC. These results show that 9F can be considered as a potential strategy for CRC treatment.

Indexed as

colorectal cancernaphthalimidep53polyamine

Identifiers

PMID32106543
PMCPMC7139676
OpenAlexW3009013144

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.