Evidence map›Paper›PMID 25966677›Full record

ReviewWiley interdisciplinary reviews. Nanomedicine and nanobiotechnology

Targeted nanoparticles for image-guided treatment of triple-negative breast cancer: clinical significance and technological advances.

Jasmine M Miller-Kleinhenz, Erica N Bozeman, Lily Yang

Abstract readReview
In one paragraph

Review in Wiley interdisciplinary reviews. Nanomedicine and nanobiotechnology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

34 citing papers in PubMed, 73 citations in OpenAlex.

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  20. Stem Cell Mimicking Nanoencapsulation for Targeting Arthritis.International journal of nanomedicine · 2021
    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 1 institution in 1 country.

Jasmine M Miller-KleinhenzWinship Cancer Institute, Department of Surgery, Emory University School of Medicine, Atlanta, GA, USA.
Erica N BozemanWinship Cancer Institute, Department of Surgery, Emory University School of Medicine, Atlanta, GA, USA.
Lily YangWinship Cancer Institute, Department of Surgery, Emory University School of Medicine, Atlanta, GA, USA.
Emory University · US

Funding

Theranostic Nano particles for Targeted Treatment of Pancreatic CancerU01CA151810 · NCI · EMORY UNIVERSITY · PI MAO, HUI, YANG, LILY · 2010 to 2014
$2.2M
Targeted Therapy of Triple Negative Breast Cancer Using Theranostic NanoparticlesR01CA154129 · NCI · EMORY UNIVERSITY · PI YANG, LILY · 2011 to 2015
$1.7M
NCI NIH HHS R01 CA154129NCI NIH HHS R01 CA154129A03S1NCI NIH HHS U01 CA151810
6 · The paper itself

Abstract

Effective treatment of triple-negative breast cancer (TNBC) with its aggressive tumor biology, highly heterogeneous tumor cells, and poor prognosis requires an integrated therapeutic approach that addresses critical issues in cancer therapy. Multifunctional nanoparticles with the abilities of targeted drug delivery and noninvasive imaging for monitoring drug delivery and responses to therapy, such as theranostic nanoparticles, hold great promise toward the development of novel therapeutic approaches for the treatment of TNBC using a single therapeutic platform. The biological and pathological characteristics of TNBC provide insight into several potential molecular targets for current and future nanoparticle-based therapeutics. Extensive tumor stroma, highly proliferative cells, and a high rate of drug resistance are all barriers that must be appropriately addressed in order for these nanotherapeutic platforms to be effective. Utilization of the enhanced permeability and retention effect coupled with active targeting of cell surface receptors expressed by TNBC cells, and tumor-associated endothelial cells, stromal fibroblasts, and macrophages is likely to overcome such barriers to facilitate more effective drug delivery. An in-depth summary of current studies investigating targeted nanoparticles in preclinical TNBC mouse and human xenograft models is presented. This review aims to outline the current status of nanotherapeutic options for TNBC patients, identification of promising molecular targets, challenges associated with the development of targeted nanotherapeutics, the research done by our group as well as by others, and future perspectives on the nanomedicine field and ways to translate current preclinical studies into the clinic.

Indexed as

Drug Delivery SystemsAnimalsBreast NeoplasmsDrug CarriersErbB ReceptorsFemaleFolate Receptor 1HumansHyaluronan ReceptorsLiposomesMagnetic Resonance ImagingMiceMucin-1NanomedicineNanoparticlesNanotubes, CarbonCD44 protein, humanCXCR4 protein, humanDrug CarriersEGFR protein, humanErbB ReceptorsFolate Receptor 1Hyaluronan ReceptorsLiposomesMUC1 protein, humanMucin-1Nanotubes, CarbonReceptor, IGF Type 1Receptors, CXCR4Receptors, Urokinase Plasminogen ActivatorWnt Proteins

Identifiers

PMID25966677
PMCPMC4604004
OpenAlexW2137621491

What OpenQuestion 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 OpenQuestion graph.