Evidence map›Paper›PMID 25787158›Full record

ArticleScientific reports2015

Indole diketopiperazines from endophytic Chaetomium sp 88194 induce breast cancer cell apoptotic death.

Fu-qian Wang, Qing-yi Tong, Hao-ran Ma, Hong-feng Xu, Song Hu, Wei Ma, Yong-bo Xue, Jun-jun Liu, Jian-ping Wang, Hong-ping Song and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.1field-weighted citation impact, top 5% 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

16 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  12. Endophytic Fungus Isolated FromFrontiers in oncology · 2018
    Article
  13. Review
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  15. Inhibition of biofilm in Bacillus amyloliquefaciens Q-426 by diketopiperazines.World journal of microbiology & biotechnology · 2016
    Article
  16. Article
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

13 authors at 3 institutions in 1 country.

Fu-qian WangDepartment of Pharmacy, Wuhan First Hospital, Wuhan 430022, Hubei, People's Republic of China.
Qing-yi TongHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Hao-ran MaDepartment of Pharmacy, Wuhan First Hospital, Wuhan 430022, Hubei, People's Republic of China.
Hong-feng XuDepartment of Pharmacy, Wuhan First Hospital, Wuhan 430022, Hubei, People's Republic of China.
Song HuDepartment of Pharmacy, Wuhan First Hospital, Wuhan 430022, Hubei, People's Republic of China.
Wei MaDepartment of Pharmacy, Wuhan First Hospital, Wuhan 430022, Hubei, People's Republic of China.
Yong-bo XueHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Jun-jun LiuHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Jian-ping WangHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Hong-ping SongPuai Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Jin-wen ZhangTongji Hospital Affiliated to Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Geng ZhangDepartment of Pharmacy, Wuhan First Hospital, Wuhan 430022, Hubei, People's Republic of China.
Yong-hui ZhangHubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, People's Republic of China.
Wuhan Third Hospital · CNHuazhong University of Science and Technology · CNTongji Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diketopiperazines are important secondary metabolites of the fungi with variety bioactivities. Several species belonging to genus Chaetomium produce compounds of this class, such as chetomin. To identify new antitumor agents, secondary metabolites of fungus Chaetomium sp 88194 were investigated and three new indole diketopiperazines, Chaetocochins G (1), Oidioperazines E (2) and Chetoseminudin E (3), along with two known compounds Chetoseminudins C (4) and N-acetyl-β-oxotryptamine (5), were obtained. Chaetocochins G and Chetoseminudin E were recrystallized in CHCl3 containing a small amount of MeOH, and their structures with absolute configuration were established by spectroscopic data interpretation and single-crystal X-ray diffraction analysis. The absolute configuration of Oidioperazines E was defined by comparing of experimental and calculated electronic circular dichroism spectra. These isolates were also evaluated the anticancer activity, and Chaetocochins G displayed more potent cytotoxicity in MCF-7 cells than the common chemotherapeutic agent (5-fluorouracil) associated with G2/M cell cycle arrest. More importantly, Chaetocochins G induced cell apoptotic death via caspase-3 induction and proteolytic cleavage of poly (ADP-ribose) polymerase, concomitantly with increased Bax and decreased Bcl-2 expression. Our findings suggested that indole diketopiperazines from endophytic Chaetomium sp 88194 may be potential resource for developing anti-cancer reagents.

Indexed as

Antineoplastic AgentsApoptosisApoptosis Regulatory ProteinsCell Cycle CheckpointsCell Line, TumorCell ProliferationChaetomiumDiketopiperazinesGene ExpressionHumansIndolesMCF-7 CellsMolecular StructureNuclear Magnetic Resonance, BiomolecularAntineoplastic AgentsApoptosis Regulatory ProteinsDiketopiperazinesindoleIndoles

Identifiers

PMID25787158
PMCPMC4365412
OpenAlexW1989778305

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Registered trials

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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.