Evidence map›Paper›PMID 28927053›Full record

ArticleOncology letters2017

Synthesis, biological evaluation and mechanism studies of matrine derivatives as anticancer agents.

Lihe Jiang, Lichuan Wu, Fangfang Yang, Nadin Almosnid, Xu Liu, Jun Jiang, Elliot Altman, Lisheng Wang, Ying Gao

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.6field-weighted citation impact, top 34% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Anti-Tumor Activities of Bioactive Phytochemicals inCancer management and research · 2020
    Review
  7. 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

9 authors at 2 institutions in 2 countries.

Lihe JiangThe Center for Drug Screening and Research, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P.R. China.
Lichuan WuThe Center for Drug Screening and Research, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P.R. China.
Fangfang YangThe Center for Drug Screening and Research, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P.R. China.
Nadin AlmosnidDepartment of Biology, Tennessee Center for Botanical Medicine Research, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Xu LiuThe Center for Drug Screening and Research, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P.R. China.
Jun JiangThe Center for Drug Screening and Research, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P.R. China.
Elliot AltmanDepartment of Biology, Tennessee Center for Botanical Medicine Research, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Lisheng WangThe Center for Drug Screening and Research, School of Chemistry and Chemical Engineering, Guangxi University, Nanning, Guangxi 530004, P.R. China.
Ying GaoDepartment of Biology, Tennessee Center for Botanical Medicine Research, Middle Tennessee State University, Murfreesboro, TN 37132, USA.
Guangxi University · CNMiddle Tennessee State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A total of five matrine derivatives were synthesized and evaluated for their anti-proliferation activity using a panel of four human cancer cell lines, including A549 lung, BT20 breast, MCF-7 breast and U2OS osteosarcoma cells. The YF3-5, YF3-7 and YF3-9, three novel compounds, demonstrated increased anti-proliferation activity compared with matrine, of which YF3-5 revealed the strongest anti-proliferation activity with a half-maximal inhibitory concentration value of 15.49-16.67 µM against the four human cancer cell lines. The anti-proliferation mechanism underlying YF3-5 was investigated in the A549 human lung cancer cell line and the results demonstrated that YF3-5 exerted its anti-proliferation activity through the induction of apoptosis and oxidative stress, in addition to arresting the cell cycle at the G

Indexed as

anti-proliferationapoptosiscell cyclematrine derivativesoxidative stress

Identifiers

PMID28927053
PMCPMC5588119
OpenAlexW2669797491

What OpenQuestion holds

Textmetadata
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.