Evidence map›Paper›PMID 34065551›Full record

ReviewPharmaceutics2021

Targeting Mitochondrial Oncometabolites: A New Approach to Overcome Drug Resistance in Cancer.

Martina Godel, Giacomo Ortone, Dario Pasquale Anobile, Martina Pasino, Giulio Randazzo, Chiara Riganti, Joanna Kopecka

Open access · goldAbstract readReview
In one paragraph

Review in Pharmaceutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
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  7. The bioenergetic landscape of cancer.Molecular metabolism · 2024
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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

7 authors at 1 institution in 1 country.

Martina GodelDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.
Giacomo OrtoneDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.
Dario Pasquale AnobileDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.
Martina PasinoDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.
Giulio RandazzoDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.
Chiara RigantiDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.ORCID 0000-0001-9787-4836
Joanna KopeckaDepartment of Oncology, University of Torino, via Santena 5/bis, 10126 Torino, Italy.ORCID 0000-0003-3612-3953
University of Turin · IT

Funding

Associazione Italiana per la Ricerca sul Cancro IG21408
6 · The paper itself

Abstract

Drug resistance is the main obstacle for a successful cancer therapy. There are many mechanisms by which cancers avoid drug-mediated death, including alterations in cellular metabolism and apoptotic programs. Mitochondria represent the cell's powerhouse and the connection between carbohydrate, lipid and proteins metabolism, as well as crucial controllers of apoptosis, playing an important role not only in tumor growth and progression, but also in drug response. Alterations in tricarboxylic acid cycle (TCA) caused by mutations in three TCA enzymes-isocitrate dehydrogenase, succinate dehydrogenase and fumarate hydratase-lead to the accumulation of 2-hydroxyglutarate, succinate and fumarate respectively, collectively known as oncometabolites. Oncometabolites have pleiotropic effects on cancer biology. For instance, they generate a pseudohypoxic phenotype and induce epigenetic changes, two factors that may promote cancer drug resistance leading to disease progression and poor therapy outcome. This review sums up the most recent findings about the role of TCA-derived oncometabolites in cancer aggressiveness and drug resistance, highlighting possible pharmacological strategies targeting oncometabolites production in order to improve the efficacy of cancer treatment.

Indexed as

cancer drug resistancecancer metabolismmitochondrial oncometabolites

Identifiers

PMID34065551
PMCPMC8161136
OpenAlexW3160076767

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.