Evidence map›Paper›PMID 29673423›Full record

ArticleOncology research2019

Experimental and In Silico Analysis of Cordycepin and its Derivatives as Endometrial Cancer Treatment.

Pedro Fong, Cheng N Ao, Kai I Tou, Ka M Huang, Chi C Cheong, Li R Meng

Open access · hybridAbstract read
In one paragraph

Article in Oncology research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.5field-weighted citation impact, top 19% 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, 1 synthesis or guideline pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. 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

6 authors at 1 institution in 1 country.

Pedro FongSchool of Health Sciences, Macao Polytechnic Institute, Macao, P.R. China.
Cheng N AoSchool of Health Sciences, Macao Polytechnic Institute, Macao, P.R. China.
Kai I TouSchool of Health Sciences, Macao Polytechnic Institute, Macao, P.R. China.
Ka M HuangSchool of Health Sciences, Macao Polytechnic Institute, Macao, P.R. China.
Chi C CheongSchool of Health Sciences, Macao Polytechnic Institute, Macao, P.R. China.
Li R MengSchool of Health Sciences, Macao Polytechnic Institute, Macao, P.R. China.
Macao Polytechnic University · MO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aim of this study was to investigate the inhibition effects of cordycepin and its derivatives on endometrial cancer cell growth. Cytotoxicity MTT assays, clonogenic assays, and flow cytometry were used to observe the effects on apoptosis and regulation of the cell cycle of Ishikawa cells under various concentrations of cordycepin, cisplatin, and combinations of the two. Validated in silico docking simulations were performed on 31 cordycepin derivatives against adenosine deaminase (ADA) to predict their binding affinities and hence their potential tendency to be metabolized by ADA. Cordycepin has a significant dose-dependent inhibitory effect on cell proliferation. The combination of cordycepin and cisplatin produced greater inhibition effects than did cordycepin alone. Apoptosis investigations confirmed the ability of cordycepin to induce the apoptosis of Ishikawa cells. The in silico results indicate that compound MRS5698 is least metabolized by ADA and has acceptable drug likeness and safety profiles. This is the first study to confirm the cytotoxic effects of cordycepin on endometrial cancer cells. This study also identified cordycepin derivatives with promising pharmacological and pharmacokinetic properties for further investigation in the development of new treatments for endometrial cancer.

Indexed as

AdenosineAdenosine DeaminaseApoptosisCell CycleCell Line, TumorCisplatinDeoxyadenosinesEndometrial NeoplasmsFemaleHumansMolecular Docking SimulationAdenosineAdenosine DeaminaseCisplatincordycepinDeoxyadenosinesMRS5698

Identifiers

PMID29673423
PMCPMC7848235
OpenAlexW2800882342

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.