Evidence map›Paper›PMID 34769312›Full record

ArticleInternational journal of molecular sciences2021

Adipose Tissue-Breast Cancer Crosstalk Leads to Increased Tumor Lipogenesis Associated with Enhanced Tumor Growth.

Peter Micallef, Yanling Wu, Marco Bauzá-Thorbrügge, Belén Chanclón, Milica Vujičić, Eduard Peris, C Joakim Ek, Ingrid Wernstedt Asterholm

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

14 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
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  6. Review
  7. The Power and Promise of Patient-Derived Xenografts of Human Breast Cancer.Cold Spring Harbor perspectives in medicine · 2024
    Review
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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

8 authors at 1 institution in 1 country.

Peter MicallefDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.
Yanling WuDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.
Marco Bauzá-ThorbrüggeDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.ORCID 0000-0002-2147-9386
Belén ChanclónDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.
Milica VujičićDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.ORCID 0000-0001-6582-6901
Eduard PerisDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.ORCID 0000-0002-9237-3263
C Joakim EkDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.
Ingrid Wernstedt AsterholmDepartment of Physiology, Institute of Neuroscience and Physiology, The Sahlgrenska Academy at University of Gothenburg, Box 432, SE-405 30 Göteborg, Sweden.ORCID 0000-0002-0755-5784
University of Gothenburg · SE

Funding

IngaBritt och Arne Lundbergs Forskningsstiftelse 2016-0045Novo Nordisk Foundation NNF19OC0056601Swedish Research Council 2013-07107, 2017-00792 and 2020-01463The Swedish Diabetes Foundation DIA2016-127
6 · The paper itself

Abstract

We sought to identify therapeutic targets for breast cancer by investigating the metabolic symbiosis between breast cancer and adipose tissue. To this end, we compared orthotopic E0771 breast cancer tumors that were in direct contact with adipose tissue with ectopic E0771 tumors in mice. Orthotopic tumors grew faster and displayed increased de novo lipogenesis compared to ectopic tumors. Adipocytes release large amounts of lactate, and we found that both lactate pretreatment and adipose tissue co-culture augmented de novo lipogenesis in E0771 cells. Continuous treatment with the selective FASN inhibitor Fasnall dose-dependently decreased the E0771 viability in vitro. However, daily Fasnall injections were effective only in 50% of the tumors, while the other 50% displayed accelerated growth. These opposing effects of Fasnall in vivo was recapitulated in vitro; intermittent Fasnall treatment increased the E0771 viability at lower concentrations and suppressed the viability at higher concentrations. In conclusion, our data suggest that adipose tissue enhances tumor growth by stimulating lipogenesis. However, targeting lipogenesis alone can be deleterious. To circumvent the tumor's ability to adapt to treatment, we therefore believe that it is necessary to apply an aggressive treatment, preferably targeting several metabolic pathways simultaneously, together with conventional therapy.

Indexed as

LipogenesisLipolysisOxygen ConsumptionAdipose TissueAnimalsBreast NeoplasmsFemaleGlycolysisHumansMiceMice, Inbred C57BLadipocytesadipose tissuebreast cancerE0771lipogenesislipolysisluminal Bmouse

Identifiers

PMID34769312
PMCPMC8585035
OpenAlexW3208279442

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.