Evidence map›Paper›PMID 33536189›Full record

ArticleMolecular cancer therapeutics2021

Lipidome-based Targeting of STAT3-driven Breast Cancer Cells Using Poly-l-glutamic Acid-coated Layer-by-Layer Nanoparticles.

Isidora Tošić, Lisa N Heppler, Susana P Egusquiaguirre, Natalie Boehnke, Santiago Correa, Daniel F Costa, Elizabeth A Grossman Moore, Sharmistha Pal, Douglas S Richardson, Alexander R Ivanov and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer therapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

  1. 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

14 authors at 7 institutions in 3 countries.

Isidora TošićDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.ORCID https://orcid.org/0000-0001-8489-7668
Lisa N HepplerDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Susana P EgusquiaguirreDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Natalie BoehnkeKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts.ORCID https://orcid.org/0000-0002-3468-2033
Santiago CorreaKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts.ORCID https://orcid.org/0000-0001-8230-4945
Daniel F CostaKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts.ORCID https://orcid.org/0000-0002-0992-1637
Elizabeth A Grossman MooreDepartment of Chemistry, Molecular and Cell Biology, University of California at Berkeley, Berkeley, Massachusetts.
Sharmistha PalDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Douglas S RichardsonHarvard Center for Biological Imaging, Harvard University, Cambridge, Massachusetts.ORCID https://orcid.org/0000-0002-3189-2190
Alexander R IvanovDepartment of Chemistry and Chemical Biology, Barnett Institute of Chemical and Biological Analysis, Northeastern University, Boston, Massachusetts.ORCID https://orcid.org/0000-0002-4691-8488
Daphne A Haas-KoganDepartment of Radiation Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts.
Daniel K NomuraDepartment of Chemistry, Molecular and Cell Biology, University of California at Berkeley, Berkeley, Massachusetts.
Paula T HammondKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, Massachusetts.
David A FrankDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts. david_frank@dfci.harvard.edu.
Dana-Farber Cancer Institute · USHarvard University · USMassachusetts Institute of Technology · USUniversity of California, Berkeley · USHarvard University Press · USInstitute for Soldier Nanotechnologies · USNortheastern University · US

Funding

Effect of methodological and biological variability on molecular profiling of extracellular vesicles in cancer detectionR01CA218500 · NCI · NORTHEASTERN UNIVERSITY · PI DEL MONTE, FEDERICA, GHIRAN, IONITA CALIN · 2018 to 2022
$4.0M
Dual STAT3/NF-kB Inhibitors for Targeted Cancer TherapyR01CA160979 · NCI · DANA-FARBER CANCER INST · PI FRANK, DAVID A. · 2012 to 2016
$1.8M
Deep Proteomic Profiling of Rare CellsR01GM120272 · NIGMS · NORTHEASTERN UNIVERSITY · PI IVANOV, ALEXANDER R. · 2016 to 2019
$1.5M
NCI NIH HHS R01 CA160979NCI NIH HHS R01 CA218500NIGMS NIH HHS R01 GM120272
6 · The paper itself

Abstract

The oncogenic transcription factor STAT3 is aberrantly activated in 70% of breast cancers, including nearly all triple-negative breast cancers (TNBCs). Because STAT3 is difficult to target directly, we considered whether metabolic changes driven by activated STAT3 could provide a therapeutic opportunity. We found that STAT3 prominently modulated several lipid classes, with most profound effects on N-acyl taurine and arachidonic acid, both of which are involved in plasma membrane remodeling. To exploit these metabolic changes therapeutically, we screened a library of layer-by-layer (LbL) nanoparticles (NPs) differing in the surface layer that modulates interactivity with the cell membrane. We found that poly-l-glutamic acid (PLE)-coated NPs bind to STAT3-transformed breast cancer cells with 50% greater efficiency than to nontransformed cells, and the heightened PLE-NP binding to TNBC cells was attenuated by STAT3 inhibition. This effect was also observed in densely packed three-dimensional breast cancer organoids. As STAT3-transformed cells show greater resistance to cytotoxic agents, we evaluated whether enhanced targeted delivery via PLE-NPs would provide a therapeutic advantage. We found that cisplatin-loaded PLE-NPs induced apoptosis of STAT3-driven cells at lower doses compared with both unencapsulated cisplatin and cisplatin-loaded nontargeted NPs. In addition, because radiation is commonly used in breast cancer treatment, and may alter cellular lipid distribution, we analyzed its effect on PLE-NP-cell binding. Irradiation of cells enhanced the STAT3-targeting properties of PLE-NPs in a dose-dependent manner, suggesting potential synergies between these therapeutic modalities. These findings suggest that cellular lipid changes driven by activated STAT3 may be exploited therapeutically using unique LbL NPs.

Indexed as

Drug Delivery SystemsGlutamic AcidHumansLipidomicsNanoparticlesSTAT3 Transcription FactorTriple Negative Breast NeoplasmsGlutamic AcidSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID33536189
PMCPMC8026705
OpenAlexW3128397573

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.