Evidence map›Paper›PMID 34914014›Full record

ReviewJournal of mammary gland biology and neoplasia2021

Advances in Analyzing the Breast Cancer Lipidome and Its Relevance to Disease Progression and Treatment.

Ashley V Ward, Steven M Anderson, Carol A Sartorius

Open access · greenAbstract readReview
In one paragraph

Review in Journal of mammary gland biology and neoplasia, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

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  20. Omics-Based Investigations of Breast Cancer.Molecules (Basel, Switzerland) · 2023
    Review
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

3 authors at 2 institutions in 1 country.

Ashley V WardCancer Biology Graduate Program, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA.ORCID 0000-0002-8008-7497
Steven M AndersonDepartment of Pathology, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA.
Carol A SartoriusDepartment of Pathology, University of Colorado, Anschutz Medical Campus, Aurora, CO, USA. carol.sartorius@cuanschutz.edu.ORCID 0000-0002-9170-3988
University of Colorado Anschutz Medical Campus · USUniversity of Colorado Cancer Center · US

Funding

Progesterone Receptor (PR) Signaling Cross Talk Drives ER+ Breast CancerR01CA229697 · NCI · UNIVERSITY OF MINNESOTA · PI Carol A Lange, Douglas Yee · 2020 to 2026
$3.6M
Training Program in Cancer BiologyT32CA190216 · NCI · UNIVERSITY OF COLORADO DENVER · PI Craig T. Jordan · 2016 to 2026
$3.5M
NRSA Training CoreTL1TR002533 · NCATS · UNIVERSITY OF COLORADO DENVER · PI CICUTTO, LISA · 2018 to 2022
$3.0M
Hormones and Tumor Initiating Cells in Human Breast CancersR01CA140985 · NCI · UNIVERSITY OF COLORADO DENVER · PI SARTORIUS, CAROL ANN · 2011 to 2020
$3.0M
Altered Lipid Metabolism in Luminal Breast Cancer Stem Cells and Endocrine ResistanceF31CA261053 · NCI · UNIVERSITY OF COLORADO DENVER · PI WARD, ASHLEY VANESSA · 2021 to 2022
$70k
NCATS NIH HHS TL1 TR002533NCI NIH HHS F31 CA261053NCI NIH HHS R01 CA140985NCI NIH HHS R01 CA229697NCI NIH HHS T32 CA190216NIH HHS F31CA261053NIH HHS R01CA140985NIH HHS T32CA190216NIH HHS TL1TR002533
6 · The paper itself

Abstract

Abnormal lipid metabolism is common in breast cancer with the three main subtypes, hormone receptor (HR) positive, human epidermal growth factor 2 (HER2) positive, and triple negative, showing common and distinct lipid dependencies. A growing body of studies identify altered lipid metabolism as impacting breast cancer cell growth and survival, plasticity, drug resistance, and metastasis. Lipids are a class of nonpolar or polar (amphipathic) biomolecules that can be produced in cells via de novo synthesis or acquired from the microenvironment. The three main functions of cellular lipids are as essential components of membranes, signaling molecules, and nutrient storage. The use of mass spectrometry-based lipidomics to analyze the global cellular lipidome has become more prevalent in breast cancer research. In this review, we discuss current lipidomic methodologies, highlight recent breast cancer lipidomic studies and how these findings connect to disease progression and therapeutic development, and the potential use of lipidomics as a diagnostic tool in breast cancer. A better understanding of the breast cancer lipidome and how it changes during drug resistance and tumor progression will allow informed development of diagnostics and novel targeted therapies.

Indexed as

Breast NeoplasmsLipidomicsDisease ProgressionFemaleHumansLipid MetabolismLipidsTumor MicroenvironmentLipidsBreast cancerFatty acidLipidLipidomics

Identifiers

PMID34914014
PMCPMC8883833
OpenAlexW4200606003

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.