Evidence map›Paper›PMID 37000908›Full record

ArticleChemical research in toxicology2023

Anticancer Drug Doxorubicin Spontaneously Reacts with GTP and dGTP.

German Mejia, Linjia Su, Popular Pandey, Kevin Jeanne Dit Fouque, Anthony J McGoron, Francisco Fernandez-Lima, Jin He, Alexander M Mebel, Fenfei Leng

Open access · greenAbstract read
In one paragraph

Article in Chemical research in toxicology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 4 citations in OpenAlex.

No citing paper in PubMed yet.

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 1 institution in 1 country.

German MejiaBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.
Linjia SuBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0001-5227-6605
Popular PandeyBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0002-1899-3480
Kevin Jeanne Dit FouqueBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.
Anthony J McGoronBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0003-3714-4676
Francisco Fernandez-LimaBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0002-1283-4390
Jin HeBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0002-2633-9809
Alexander M MebelDepartment of Chemistry and Biochemistry, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0002-7233-3133
Fenfei LengBiomolecular Sciences Institute, Florida International University, Miami, Florida 33199, United States.ORCID 0000-0002-9024-1216
Florida International University · US

Funding

Development of Multidimensional, Linear and Differential Ion Mobility MS Separations for Middle-Down ProteoformsR01GM134247 · NIGMS · FLORIDA INTERNATIONAL UNIVERSITY · PI FERNANDEZ-LIMA, FRANCISCO · 2019 to 2022
$1.7M
Targeting transcription-coupled DNA supercoiling for discovering antibiotics against bacterial DNA gyraseR21AI125973 · NIAID · FLORIDA INTERNATIONAL UNIVERSITY · PI LENG, FENFEI · 2017 to 2018
$478k
Novel gyrase inhibitors targeting Mycobacterium tuberculosisR21AI178134 · NIAID · FLORIDA INTERNATIONAL UNIVERSITY · PI LENG, FENFEI, NEFZI, ADEL · 2023 to 2024
$422k
NIAID NIH HHS R21 AI125973NIGMS NIH HHS R01 GM134247
6 · The paper itself

Abstract

Here, we reported a spontaneous reaction between anticancer drug doxorubicin and GTP or dGTP. Incubation of doxorubicin with GTP or dGTP at 37 °C or above yields a covalent product: the doxorubicin-GTP or -dGTP conjugate where a covalent bond is formed between the C14 position of doxorubicin and the 2-amino group of guanine. Density functional theory calculations show the feasibility of this spontaneous reaction. Fluorescence imaging studies demonstrate that the doxorubicin-GTP and -dGTP conjugates cannot enter nuclei although they rapidly accumulate in human SK-OV-3 and NCI/ADR-RES cells. Consequently, the doxorubicin-GTP and -dGTP conjugates are less cytotoxic than doxorubicin. We also demonstrate that doxorubicin binds to ATP, GTP, and other nucleotides with a dissociation constant (

Indexed as

Antineoplastic AgentsAdenosine TriphosphateDeoxyguanine NucleotidesDoxorubicinGuanosine TriphosphateHumansAdenosine TriphosphateAntineoplastic AgentsDeoxyguanine Nucleotidesdeoxyguanosine triphosphateDoxorubicinGuanosine Triphosphate

Identifiers

PMID37000908
PMCPMC11822961
OpenAlexW4362458463

What OpenQuestion holds

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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.