Evidence map›Paper›PMID 31371177›Full record

ArticleSurgery2019

Mimetic sHDL nanoparticles: A novel drug-delivery strategy to target triple-negative breast cancer.

Ton Wang, Chitra Subramanian, Minzhi Yu, Peter T White, Rui Kuai, Jaquelyn Sanchez, James J Moon, Barbara N Timmermann, Anna Schwendeman, Mark S Cohen

Open access · greenAbstract read
In one paragraph

Article in Surgery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Biomimetic nanoparticles for tumor immunotherapy.Frontiers in bioengineering and biotechnology · 2022
    Review
  4. Article
  5. 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

10 authors at 3 institutions in 1 country.

Ton WangUniversity of Michigan, Department of Surgery, Ann Arbor, MI.
Chitra SubramanianUniversity of Michigan, Department of Surgery, Ann Arbor, MI.
Minzhi YuUniversity of Michigan, College of Pharmacy, Ann Arbor, MI.
Peter T WhiteUniversity of Michigan, Department of Surgery, Ann Arbor, MI.
Rui KuaiBrigham and Women's Hospital, Department of Medicine, Boston, MA.
Jaquelyn SanchezUniversity of Michigan, Department of Pharmacology, Ann Arbor, MI.
James J MoonUniversity of Michigan, College of Pharmacy, Ann Arbor, MI; University of Michigan, Department of Biomedical Engineering, Ann Arbor, MI.
Barbara N TimmermannUniversity of Kansas, Department of Medicinal Chemistry, Lawrence, KS.
Anna SchwendemanUniversity of Michigan, College of Pharmacy, Ann Arbor, MI.
Mark S CohenUniversity of Michigan, Department of Surgery, Ann Arbor, MI; University of Michigan, Department of Pharmacology, Ann Arbor, MI. Electronic address: cohenmar@med.umich.edu.
University of Michigan · USBrigham and Women's Hospital · USUniversity of Kansas · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alexey I Nesvizhskii · 1988 to 2026
$178.2M
PREDOCTORAL TRAINING IN GENETICST32GM007544 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MORAN, JOHN V. · 1985 to 2022
$11.3M
University of Michigan Surgical Oncology Research Training ProgramT32CA009672 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JACQUELINE SARA JERUSS, WEIPING ZOU · 1991 to 2026
$6.0M
Synthetic HDL_a potential sepsis therapyR01GM113832 · NIGMS · UNIVERSITY OF KENTUCKY · PI LI, XIANG-AN, SCHWENDEMAN, ANNA · 2015 to 2019
$3.0M
Development and Evaluation of Purine and Coumarin Based Hsp90 Inhibitors`U01CA120458 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI BLAGG, BRIAN S J · 2007 to 2014
$2.6M
Nanomaterials for eliciting anti-tumor T-cells-Diversity SupplementR01CA210273 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MOON, JAMES J. · 2017 to 2021
$2.2M
Biomaterials for treatment of head and neck cancerR01CA173292 · NCI · UNIVERSITY OF KANSAS LAWRENCE · PI FORREST, MARCUS LAIRD · 2013 to 2017
$1.4M
Optimization and Investigation of Cruentaren A analogsR01CA216919 · NCI · UNIVERSITY OF NOTRE DAME · PI BLAGG, BRIAN S J, COHEN, MARK STEVEN · 2017 to 2021
$1.4M
Optimization of synthetic HDL nanoparticles for treatment Niemann-Pick Type CR21NS111191 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHWENDEMAN, ANNA · 2019 to 2019
$429k
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA173292NCI NIH HHS R01 CA210273NCI NIH HHS R01 CA216919NCI NIH HHS T32 CA009672NCI NIH HHS U01 CA120458NIGMS NIH HHS R01 GM113832NIGMS NIH HHS T32 GM007544NINDS NIH HHS R21 NS111191
6 · The paper itself

Abstract

backgroundWithanolides are naturally derived heat shock protein 90 inhibitors that are potent in preclinical models of triple negative breast cancers. Conjugation to synthetic high-density lipoprotein nanoparticles improves solubility and targets delivery to the scavenger receptor B1. Triple negative breast cancers highly overexpress the scavenger receptor B1, and we hypothesize that encapsulation of the novel withalongolide A 4,19,27-triacetate by synthetic high-density lipoprotein will have enhanced efficacy against triple negative breast cancers in vivo.

methodsValidated human triple negative breast cancer cell lines were evaluated for the scavenger receptor B1 expression by quantitative polymerase chain reaction and Western blot. Withalongolide A 4,19,27-triacetate inhibitory concentration

resultsTriple negative breast cancer cell lines had greater scavenger receptor B1 expression by quantitative polymerase chain reaction and Western blot versus controls. Fluorescent-labeled synthetic high-density lipoprotein uptake was scavenger receptor B1-mediated in vitro, and in vivo tumor uptake using IVIS imaging demonstrated significantly increased tumor radiant efficiency versus control. Inhibitory concentration

conclusionThe synthetic high-density lipoprotein withalongolide A 4,19,27-triacetate nanoconjugates are potent against triple negative breast cancers and show improved scavenger receptor B1-mediated targeting. Treatment with synthetic high-density lipoprotein-encapsulated withalongolide A 4,19,27-triacetate is able to significantly decrease the growth of tumor in mice compared with the control and has better efficacy than the current standard of care, warranting further evaluation as a novel therapeutic agent.

Indexed as

Lipoproteins, HDLNanoparticlesAnimalsAntineoplastic AgentsCell Line, TumorDrug Delivery SystemsFemaleHumansInhibitory Concentration 50Mice, NudeScavenger Receptors, Class BTriple Negative Breast NeoplasmsWithanolidesXenograft Model Antitumor AssaysAntineoplastic AgentsLipoproteins, HDLSCARB1 protein, humanScarb1 protein, mouseScavenger Receptors, Class Bwithalongolide A 4,19,27-triacetateWithanolides

Identifiers

PMID31371177
PMCPMC6861672
OpenAlexW2966028363

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.