Evidence map›Paper›PMID 27351915›Full record

ArticleNature communications2016

A peptide for targeted, systemic delivery of imaging and therapeutic compounds into acute brain injuries.

Aman P Mann, Pablo Scodeller, Sazid Hussain, Jinmyoung Joo, Ester Kwon, Gary B Braun, Tarmo Mölder, Zhi-Gang She, Venkata Ramana Kotamraju, Barbara Ranscht and 5 more

Open access · goldAbstract readEvaluation Study
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 95 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
95citing papers in PubMed, 1 pooled it
10.8field-weighted citation impact, top 1% 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

95 citing papers in PubMed, 1 synthesis or guideline pooled it, 176 citations in OpenAlex.

  1. Systematic Review of Peptide CAQK: Properties, Applications, and Outcomes.International journal of molecular sciences · 2024
    Pooled it
  2. Review
  3. Article
  4. Review
  5. Peptide-functionalized nanoparticles for brain-targeted therapeutics.Drug delivery and translational research · 2026
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Review
  19. Porous silicon and silica carriers for delivery of peptide therapeutics.Drug delivery and translational research · 2024
    Review
  20. Article

35 more citing papers are in PubMed but not listed here.

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

15 authors at 5 institutions in 2 countries.

Aman P MannCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Pablo ScodellerCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Sazid HussainCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Jinmyoung JooDepartment of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, USA.ORCID http://orcid.org/0000-0003-1574-9842
Ester KwonBroad Institute of Harvard and MIT, Cambridge, Massachusetts 02142, USA.
Gary B BraunCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Tarmo MölderLaboratory of Cancer Biology, Institute of Biomedicine and Translational Medicine, University of Tartu, 50411 Tartu, Estonia.
Zhi-Gang SheCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Venkata Ramana KotamrajuCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Barbara RanschtCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Stan KrajewskiCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Tambet TeesaluLaboratory of Cancer Biology, Institute of Biomedicine and Translational Medicine, University of Tartu, 50411 Tartu, Estonia.
Sangeeta BhatiaBroad Institute of Harvard and MIT, Cambridge, Massachusetts 02142, USA.
Michael J SailorDepartment of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, USA.ORCID http://orcid.org/0000-0002-4809-9826
Erkki RuoslahtiCancer Research Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, California 92037, USA.
Sanford Burnham Prebys Medical Discovery Institute · USBroad Institute · USUniversity of California San Diego · USUniversity of Tartu · EEUniversity of California, Santa Barbara · US

Funding

Tumor Microenvironment and Cancer ImmunologyP30CA030199 · NCI · SANFORD BURNHAM PREBYS MEDICAL DISCOVERY INSTITUTE · PI ELENA B PASQUALE · 1985 to 2026
$107.2M
VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Paula T Hammond · 1985 to 2026
$93.9M
U of Calif, San Diego Neuroscience Microscopy ImagingP30NS047101 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI GLEESON, JOSEPH G, ZHENG, BINHAI · 2003 to 2022
$9.0M
NCI NIH HHS P30 CA014051NCI NIH HHS P30 CA030199NINDS NIH HHS P30 NS047101Wellcome Trust
6 · The paper itself

Abstract

Traumatic brain injury (TBI) is a major health and socio-economic problem, but no pharmacological agent is currently approved for the treatment of acute TBI. Thus, there is a great need for advances in this field. Here, we describe a short peptide (sequence CAQK) identified by in vivo phage display screening in mice with acute brain injury. The CAQK peptide selectively binds to injured mouse and human brain, and systemically injected CAQK specifically homes to sites of brain injury in mouse models. The CAQK target is a proteoglycan complex upregulated in brain injuries. Coupling to CAQK increased injury site accumulation of systemically administered molecules ranging from a drug-sized molecule to nanoparticles. CAQK-coated nanoparticles containing silencing oligonucleotides provided the first evidence of gene silencing in injured brain parenchyma by systemically administered siRNA. These findings present an effective targeting strategy for the delivery of therapeutics in clinical management of acute brain injuries.

Indexed as

Drug Delivery SystemsPeptidesAgedAnimalsBrain Injuries, TraumaticExtracellular MatrixHumansMaleMiceMiddle AgedPeptides

Identifiers

PMID27351915
PMCPMC4931241
OpenAlexW2473132821

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.