Evidence map›Paper›PMID 27203672›Full record

ArticleOncotarget2016

Drug conjugated nanoparticles activated by cancer cell specific mRNA.

Nathan P Gossai, Jordan A Naumann, Nan-Sheng Li, Edward A Zamora, David J Gordon, Joseph A Piccirilli, Peter M Gordon

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Nanoswimmers Based on Capped Janus Nanospheres.Materials (Basel, Switzerland) · 2022
    Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Nanoparticles-Emerging Potential for Managing Leukemia and Lymphoma.Frontiers in bioengineering and biotechnology · 2017
    Review
  8. 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

7 authors at 3 institutions in 1 country.

Nathan P GossaiDepartment of Pediatrics, Division of Pediatric Hematology and Oncology, University of Minnesota, Minneapolis, MN, USA.
Jordan A NaumannDepartment of Pediatrics, Division of Pediatric Hematology and Oncology, University of Minnesota, Minneapolis, MN, USA.
Nan-Sheng LiDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Edward A ZamoraDepartment of Pediatrics, Division of Pediatric Hematology and Oncology, University of Minnesota, Minneapolis, MN, USA.
David J GordonDepartment of Pediatrics, Division of Pediatric Hematology/Oncology, University of Iowa, Iowa City, IA, USA.
Joseph A PiccirilliDepartment of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL, USA.
Peter M GordonDepartment of Pediatrics, Division of Pediatric Hematology and Oncology, University of Minnesota, Minneapolis, MN, USA.
University of Minnesota · USUniversity of Chicago · USUniversity of Iowa · US

Funding

Women's CancerP30CA077598 · NCI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI Jeffrey S. Miller · 1998 to 2026
$100.4M
Autophagy and Apoptosis in the Response of c-KIT Cancers to Targeted TherapyK08CA154782 · NCI · UNIVERSITY OF MINNESOTA · PI GORDON, PETER M · 2011 to 2015
$717k
NCI NIH HHS K08 CA154782NCI NIH HHS P30 CA077598
6 · The paper itself

Abstract

We describe a customizable approach to cancer therapy in which a gold nanoparticle (Au-NP) delivers a drug that is selectively activated within the cancer cell by the presence of an mRNA unique to the cancer cell. Fundamental to this approach is the observation that the amount of drug released from the Au-NP is proportional to both the presence and abundance of the cancer cell specific mRNA in a cell. As proof-of-principle, we demonstrate both the efficient delivery and selective release of the multi-kinase inhibitor dasatinib from Au-NPs in leukemia cells with resulting efficacy in vitro and in vivo. Furthermore, these Au-NPs reduce toxicity against hematopoietic stem cells and T-cells. This approach has the potential to improve the therapeutic efficacy of a drug and minimize toxicity while being highly customizable with respect to both the cancer cell specific mRNAs targeted and drugs activated.

Indexed as

3T3 CellsAnimalsAntineoplastic AgentsCell Line, TumorDasatinibDrug CarriersGoldHEK293 CellsHumansK562 CellsMetal NanoparticlesMiceNeoplasmsRNA, MessengerXenograft Model Antitumor AssaysAntineoplastic AgentsDasatinibDrug CarriersGoldRNA, Messengeranti-sensedrug deliverygold nanoparticlesleukemiamolecularly targeted therapy

Identifiers

PMID27203672
PMCPMC5122386
OpenAlexW2409722041

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.