Evidence map›Paper›PMID 28445124›Full record

ArticleOncotarget2017

A novel triazolonaphthalimide induces apoptosis and inhibits tumor growth by targeting DNA and DNA-associated processes.

Liyan Ji, Simin Yang, Shasha Li, Shan Liu, Shunan Tang, Zhongqiu Liu, Xiangbao Meng, Siwang Yu

Abstract read
In one paragraph

Article in Oncotarget, 2017. 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
–field-weighted citation impact
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.

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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

8 authors.

Liyan JiDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.
Simin YangDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.
Shasha LiDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.
Shan LiuDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.
Shunan TangDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.
Zhongqiu LiuInternational Institute for Translational Chinese Medicine, Guangzhou Traditional Chinese Medicine University, Guangzhou 510006, China.
Xiangbao MengDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.
Siwang YuDepartment of Chemical Biology, Peking University School of Pharmaceutical Sciences, Beijing 100191, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA and DNA-associated processes have been classes of the most important targets of chemotherapeutic drugs. As classic DNA intercalators and topoisomerase inhibitors, naphthalimides have been extensively investigated as potential anti-cancer drugs. We recently synthesized a novel series of triazolonaphthalimides with excellent anti-cancer activities. In the present study, one of the most potent triazolonaphthalimides, LSS-11, was investigated. LSS-11 bound to DNA in vitro and in cell mainly by minor groove binding and significantly increased the stability of DNA, which could be fundamental for the biological activities of LSS-11. In addition to inhibiting DNA topoisomerase II-catalyzed decatenation of knotted circulated DNA, LSS-11 dramatically inhibited DNA replication mediated by polymerase chain reaction and isothermal helicase-dependent amplification, as well as the expression of luciferase driven by a minimal TA promoter in cell. Furthermore, LSS-11 exhibited strong cytotoxicity in selected human colon cancer cell lines by inducing cell cycle arrest and apoptosis, which was accompanied by DNA damage response. Finally, LSS-11 potently inhibited the growth of S180 murine sarcoma and SW480 human colorectal cancer xenografts in vivo without significant major toxicities. These results suggest that LSS-11 deserves further research and development as a novel anti-cancer agent, and provided new understandings of mechanisms by which LSS-11 inhibited multiple DNA-associated processes and tumor growth.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCell CycleCell ProliferationColonic NeoplasmsDNADNA ReplicationDNA Topoisomerases, Type IIHCT116 CellsHumansMaleMiceMice, Inbred BALB CMice, NudeNaphthalimidesAntineoplastic AgentsDNADNA Topoisomerases, Type IILSS-11NaphthalimidesTriazolescell cycle arrestDNA bindingDNA replicationtopoisomerase 2triazolonaphthalimide

Identifiers

PMID28445124
PMCPMC5514917

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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.