Evidence map›Paper›PMID 31673018›Full record

ArticleScientific reports2019

A novel nucleoside rescue metabolic pathway may be responsible for therapeutic effect of orally administered cordycepin.

Jong Bong Lee, Masar Radhi, Elena Cipolla, Raj D Gandhi, Sarir Sarmad, Atheer Zgair, Tae Hwan Kim, Wanshan Feng, Chaolong Qin, Cecilia Adrower and 6 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
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  17. Observational
  18. Article
  19. The Novel Nucleoside Analogue ProTide NUC-7738 Overcomes Cancer Resistance MechanismsClinical cancer research : an official journal of the American Association for Cancer Research · 2021
    Article
  20. RSC advances · 2021
    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

16 authors at 4 institutions in 5 countries.

Jong Bong LeeSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Masar RadhiSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Elena CipollaSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Raj D GandhiSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Sarir SarmadSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Atheer ZgairSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Tae Hwan KimCollege of Pharmacy, Catholic University of Daegu, Gyeongsan, 38430, Republic of Korea.
Wanshan FengSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Chaolong QinSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Cecilia AdrowerSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
Catherine A OrtoriSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.
David A BarrettSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.ORCID http://orcid.org/0000-0001-6900-9474
Leonid KaganDepartment of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ, 08854, USA.
Peter M FischerSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.ORCID http://orcid.org/0000-0002-5866-9271
Cornelia H de MoorSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK.ORCID http://orcid.org/0000-0001-8776-0085
Pavel GershkovichSchool of Pharmacy, University of Nottingham, Nottingham, NG7 2RD, UK. pavel.gershkovich@nottingham.ac.uk.ORCID http://orcid.org/0000-0003-3136-0933
University of Nottingham · GBRutgers, The State University of New Jersey · USUniversity of Rome Tor Vergata · ITDaegu Catholic University · KR

Funding

Arthritis Research UK 20795Biotechnology and Biological Sciences Research Council BB/J014508/1Versus Arthritis 20795
6 · The paper itself

Abstract

Although adenosine and its analogues have been assessed in the past as potential drug candidates due to the important role of adenosine in physiology, only little is known about their absorption following oral administration. In this work, we have studied the oral absorption and disposition pathways of cordycepin, an adenosine analogue. In vitro biopharmaceutical properties and in vivo oral absorption and disposition of cordycepin were assessed in rats. Despite the fact that numerous studies showed efficacy following oral dosing of cordycepin, we found that intact cordycepin was not absorbed following oral administration to rats. However, 3'-deoxyinosine, a metabolite of cordycepin previously considered to be inactive, was absorbed into the systemic blood circulation. Further investigation was performed to study the conversion of 3'-deoxyinosine to cordycepin 5'-triphosphate in vitro using macrophage-like RAW264.7 cells. It demonstrated that cordycepin 5'-triphosphate, the active metabolite of cordycepin, can be formed not only from cordycepin, but also from 3'-deoxyinosine. The novel nucleoside rescue metabolic pathway proposed in this study could be responsible for therapeutic effects of adenosine and other analogues of adenosine following oral administration. These findings may have importance in understanding the physiology and pathophysiology associated with adenosine, as well as drug discovery and development utilising adenosine analogues.

Indexed as

DeoxyadenosinesAdministration, OralAnimalsCaco-2 CellsHumansMaleMetabolic Networks and PathwaysMiceRatsRats, Sprague-DawleyRAW 264.7 CellscordycepinDeoxyadenosines

Identifiers

PMID31673018
PMCPMC6823370
OpenAlexW2982467793

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.