Evidence map›Paper›PMID 27845768›Full record

ArticleMolecular therapy. Nucleic acids2016

Selection of a Novel Aptamer Against Vitronectin Using Capillary Electrophoresis and Next Generation Sequencing.

Christopher H Stuart, Kathryn R Riley, Olcay Boyacioglu, Denise M Herpai, Waldemar Debinski, Shadi Qasem, Frank C Marini, Christa L Colyer, William H Gmeiner

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Aptamer-based approaches forResearch in pharmaceutical sciences · 2020
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
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

9 authors at 2 institutions in 2 countries.

Christopher H StuartDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Kathryn R RileyDepartment of Chemistry, Wake Forest University, Winston-Salem, North Carolina, USA.
Olcay BoyaciogluDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Denise M HerpaiBrain Tumor Center of Excellence, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Waldemar DebinskiBrain Tumor Center of Excellence, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Shadi QasemDepartment of Pathology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Frank C MariniWake Forest Institute of Regenerative Medicine, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Christa L ColyerDepartment of Chemistry, Wake Forest University, Winston-Salem, North Carolina, USA.
William H GmeinerDepartment of Cancer Biology, Wake Forest School of Medicine, Winston-Salem, North Carolina, USA.
Wake Forest University · USForest Institute · US

Funding

Role of TEMs in brain tumor dispersalR01NS069964 · NINDS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI GOMEZ-MANZANO, CANDELARIA, MARINI, FRANK C. · 2010 to 2014
$1.7M
Regeneration, Repair and Remodeling of the Lower Urinary Tract P20DK097806 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI MARINI, FRANK C. · 2012 to 2015
$1.5M
NIDDK NIH HHS P20 DK097806NINDS NIH HHS R01 NS069964
6 · The paper itself

Abstract

Breast cancer (BC) results in ~40,000 deaths each year in the United States and even among survivors treatment of the disease may have devastating consequences, including increased risk for heart disease and cognitive impairment resulting from the toxic effects of chemotherapy. Aptamer-mediated drug delivery can contribute to improved treatment outcomes through the selective delivery of chemotherapy to BC cells, provided suitable cancer-specific antigens can be identified. We report here the use of capillary electrophoresis in conjunction with next generation sequencing to develop the first vitronectin (VN) binding aptamer (VBA-01; Kd 405 nmol/l, the first aptamer to vitronectin (VN; K

Identifiers

PMID27845768
PMCPMC5155323
OpenAlexW2549339690

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.