Evidence map›Paper›PMID 36768427›Full record

ReviewInternational journal of molecular sciences2023

The Critical Impact of Sphingolipid Metabolism in Breast Cancer Progression and Drug Response.

Paola Antonia Corsetto, Stefania Zava, Angela Maria Rizzo, Irma Colombo

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. 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
–field-weighted citation impact
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.

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  19. Bee Venom Toxic Effect on MDA-MB-231 Breast Cancer Cells andAnti-cancer agents in medicinal chemistry · 2024
    Article
  20. 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

4 authors.

Paola Antonia CorsettoDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via D. Trentacoste 2, 20134 Milano, Italy.ORCID 0000-0003-3849-8548
Stefania ZavaDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via D. Trentacoste 2, 20134 Milano, Italy.
Angela Maria RizzoDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via D. Trentacoste 2, 20134 Milano, Italy.ORCID 0000-0002-8582-0432
Irma ColomboDepartment of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Via D. Trentacoste 2, 20134 Milano, Italy.ORCID 0000-0002-9021-3119

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is the second leading cause of cancer-related death in women in the world, and its management includes a combination of surgery, radiation therapy, chemotherapy, and immunotherapy, whose effectiveness depends largely, but not exclusively, on the molecular subtype (Luminal A, Luminal B, HER2+ and Triple Negative). All breast cancer subtypes are accompanied by peculiar and substantial changes in sphingolipid metabolism. Alterations in sphingolipid metabolite levels, such as ceramides, dihydroceramide, sphingosine, sphingosine-1-phosphate, and sphingomyelin, as well as in their biosynthetic and catabolic enzymatic pathways, have emerged as molecular mechanisms by which breast cancer cells grow, respond to or escape therapeutic interventions and could take on diagnostic and prognostic value. In this review, we summarize the current landscape around two main themes: 1. sphingolipid metabolites, enzymes and transport proteins that have been found dysregulated in human breast cancer cells and/or tissues; 2. sphingolipid-driven mechanisms that allow breast cancer cells to respond to or evade therapies. Having a complete picture of the impact of the sphingolipid metabolism in the development and progression of breast cancer may provide an effective means to improve and personalize treatments and reduce associated drug resistance.

Indexed as

Breast NeoplasmsCeramidesFemaleHumansLipid MetabolismSphingolipidsSphingomyelinsCeramidesSphingolipidsSphingomyelinsbiomarkersbreast cancerceramidedrug resistancedrug sensitivitylipidsmetabolismsphingolipidssphingomyelin

Identifiers

PMID36768427
PMCPMC9916652

What OpenQuestion holds

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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.