Evidence map›Paper›PMID 22565023›Full record

ReviewNeuroscience letters2012

Targeted drug delivery to the peripheral nervous system using gene therapy.

Darren Wolfe, Marina Mata, David J Fink

Abstract readReview
In one paragraph

Review in Neuroscience letters, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.0field-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

23 citing papers in PubMed, 45 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. TET1 Overexpression Mitigates Neuropathic Pain Through Rescuing the Expression of μ-Opioid Receptor and Kv1.2 in the Primary Sensory Neurons.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2019
    Article
  8. Long noncoding RNA (lncRNA): a target in neuropathic pain.Expert opinion on therapeutic targets · 2019
    Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Augmenting glial cell-line derived neurotrophic factor signaling to treat painful neuropathies.Proceedings of the National Academy of Sciences of the United States of America · 2014
    Article
  20. 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.

Darren WolfeDiamyd Inc., Pittsburgh, PA, USA.
Marina Mata
David J Fink
VA Ann Arbor Healthcare System · US

Funding

PRE-CLINICAL VECTOR PRODUCTIONP01DK044935 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI GOINS, WILLIAM F. · 1993 to 2010
$11.8M
GENE TRANSFER FOR PREVENTION OF DIABETIC NEUROPATHYR01NS038850 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINK, DAVID J. · 1999 to 2012
$3.3M
Preclinical Development of an NT3-expressing HSV VectorU01NS069378 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI FINK, DAVID J. · 2011 to 2013
$3.1M
Gene Therapy for PainR01NS044507 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FINK, DAVID J. · 2002 to 2005
$1.8M
NIDDK NIH HHS P01 DK044935NINDS NIH HHS R01 NS038850NINDS NIH HHS R01 NS044507NINDS NIH HHS U01 NS069378
6 · The paper itself

Abstract

Gene transfer to target delivery of neurotrophic factors to the primary sensory afferent for treatment of polyneuropathy, or of inhibitory neurotransmitters for relief of chronic pain, offers the possibility of a highly selective targeted release of bioactive molecules within the nervous system. Preclinical studies with non-replicating herpes simplex virus (HSV)-based vectors injected into the skin to transduce neurons in the dorsal root ganglion have demonstrated efficacy in reducing-pain related behaviors in animal models of inflammatory pain, neuropathic pain, and pain caused by cancer, and in preventing progression of sensory neuropathy caused by toxins, chemotherapeutic drugs or resulting from diabetes. Successful completion of the first phase 1 clinical trial of HSV-mediated gene transfer in patients with intractable pain from cancer has set the stage for further clinical trials of this approach.

Indexed as

Genetic TherapyAnimalsChronic PainClinical Trials as TopicDiabetic NeuropathiesEnkephalinsGenetic VectorsHerpesviridaeHumansIntractable PainNeoplasmsNerve Growth FactorsNeurotransmitter AgentsPeripheral Nervous SystemPolyneuropathiesProtein PrecursorsEnkephalinsNerve Growth FactorsNeurotransmitter AgentsproenkephalinProtein Precursors

Identifiers

PMID22565023
PMCPMC3458184
OpenAlexW1981242932

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.