Evidence map›Paper›PMID 34070567›Full record

ReviewJournal of personalized medicine2021

Conjugation of Natural Triterpenic Acids with Delocalized Lipophilic Cations: Selective Targeting Cancer Cell Mitochondria.

Anna Yu Spivak, Darya A Nedopekina, Rinat R Gubaidullin, Mikhail V Dubinin, Konstantin N Belosludtsev

Open access · goldAbstract readReview
In one paragraph

Review in Journal of personalized medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.4field-weighted citation impact, top 10% 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, 36 citations in OpenAlex.

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  15. Targeting Energy Metabolism in Cancer Treatment.International journal of molecular sciences · 2022
    Review
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  18. Review
  19. Article
  20. NovelInternational journal of molecular sciences · 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

5 authors at 2 institutions in 1 country.

Anna Yu SpivakOrganic Synthesis Laboratory, Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 450075 Ufa, Russia.ORCID 0000-0001-8752-2853
Darya A NedopekinaOrganic Synthesis Laboratory, Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 450075 Ufa, Russia.ORCID 0000-0002-3845-9541
Rinat R GubaidullinOrganic Synthesis Laboratory, Institute of Petrochemistry and Catalysis, Russian Academy of Sciences, 450075 Ufa, Russia.
Mikhail V DubininDepartment of Biochemistry, Cell Biology and Microbiology, Mari State University, 424001 Yoshkar-Ola, Russia.ORCID 0000-0002-7453-3390
Konstantin N BelosludtsevDepartment of Biochemistry, Cell Biology and Microbiology, Mari State University, 424001 Yoshkar-Ola, Russia.ORCID 0000-0001-5392-7035
Institute of Catalysis and Petrochemistry · RUMari State University · RU

Funding

Russian Science Foundation 19-73-00155
6 · The paper itself

Abstract

Currently, a new line of research on mitochondria-targeted anticancer drugs is actively developing in the field of biomedicine and medicinal chemistry. The distinguishing features of this universal target for anticancer agents include presence of mitochondria in the overwhelming majority, if not all types of transformed cells, crucial importance of these cytoplasmic organelles in energy production, regulation of cell death pathways, as well as generation of reactive oxygen species and maintenance of calcium homeostasis. Hence, mitochondriotropic anticancer mitocan agents, acting through mitochondrial destabilization, have good prospects in cancer therapy. Available natural pentacyclic triterpenoids are considered promising scaffolds for development of new mitochondria-targeted anticancer agents. These secondary metabolites affect the mitochondria of tumor cells and initiate formation of reactive oxygen species. The present paper focuses on the latest research outcomes of synthesis and study of cytotoxic activity of conjugates of pentacyclic triterpenoids with some mitochondria-targeted cationic lipophilic molecules and highlights the advantages of applying them as novel mitocan agents compared to their prototype natural triterpenic acids.

Indexed as

anti-cancer agentsdelocalized lipophilic cationsmitocansmitochondriamitochondrial targetingtriterpenic acids

Identifiers

PMID34070567
PMCPMC8226687
OpenAlexW3165521089

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.