Evidence map›Paper›PMID 27021743›Full record

ArticleHuman gene therapy2016

Rescue Effects and Underlying Mechanisms of Intragland Shh Gene Delivery on Irradiation-Induced Hyposalivation.

Bo Hai, Qingguo Zhao, Lizheng Qin, Dharanipathy Rangaraj, Veera R Gutti, Fei Liu

Open access · greenAbstract read
In one paragraph

Article in Human gene therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Identifying Fibrogenic Cells Following Salivary Gland Obstructive Injury.bioRxiv : the preprint server for biology · 2023
    Article
  4. Identifying fibrogenic cells following salivary gland obstructive injury.Frontiers in cell and developmental biology · 2023
    Article
  5. Gene Therapeutic Delivery to the Salivary Glands.Advances in experimental medicine and biology · 2023
    Article
  6. Article
  7. Article
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  10. Review
  11. Review
  12. Article
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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

6 authors at 1 institution in 1 country.

Bo Hai1 Institute for Regenerative Medicine, College of Medicine, Texas A&M Health Science Center , Temple, Texas.
Qingguo Zhao1 Institute for Regenerative Medicine, College of Medicine, Texas A&M Health Science Center , Temple, Texas.
Lizheng Qin1 Institute for Regenerative Medicine, College of Medicine, Texas A&M Health Science Center , Temple, Texas.
Dharanipathy Rangaraj3 Department of Radiation Oncology, Baylor Scott & White Hospital , Temple, Texas.
Veera R Gutti3 Department of Radiation Oncology, Baylor Scott & White Hospital , Temple, Texas.
Fei Liu1 Institute for Regenerative Medicine, College of Medicine, Texas A&M Health Science Center , Temple, Texas.
Capital Medical University · CN

Funding

Mechanisms of Hedgehog Mediated Rescue of Radiation-induced HyposalivationR01DE022975 · NIDCR · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI LIU, FEI · 2012 to 2015
$1.4M
NIDCR NIH HHS 1R01DE022975-01NIDCR NIH HHS R01 DE022975
6 · The paper itself

Abstract

Irreversible hypofunction of salivary glands is common in head and neck cancer survivors treated with radiotherapy and can only be temporarily relieved with current treatments. We found in an inducible sonic hedgehog (Shh) transgenic mouse model that transient activation of the Hedgehog pathway after irradiation rescued salivary gland function in males by preserving salivary stem/progenitor cells and parasympathetic innervation. To translate these findings into feasible clinical application, we evaluated the effects of Shh gene transfer to salivary glands of wild-type mice on irradiation-induced hyposalivation. Shh or control GFP gene was delivered by noninvasive retrograde ductal instillation of corresponding adenoviral vectors. In both male and female mice, Shh gene delivery efficiently activated Hedgehog/Gli signaling, and significantly improved stimulated saliva secretion and preserved saliva-producing acinar cells after irradiation. In addition to preserving parasympathetic innervation through induction of neurotrophic factors, Shh gene delivery also alleviated the irradiation damage of the microvasculature, likely via inducing angiogenic factors, but did not expand the progeny of cells responsive to Hedgehog/Gli signaling. These data indicate that transient activation of the Hedgehog pathway by gene delivery is promising to rescue salivary function after irradiation in both sexes, and the Hedgehog/Gli pathway may function mainly in cell nonautonomous manners to achieve the rescue effect.

Indexed as

Genetic TherapyGene Transfer TechniquesAdenoviridaeAnimalsDisease Models, AnimalFemaleGenetic VectorsHedgehog ProteinsMaleMiceMice, TransgenicMicrovesselsRadiationRegenerationSignal TransductionSubmandibular GlandHedgehog ProteinsShh protein, mouse

Identifiers

PMID27021743
PMCPMC4841000
OpenAlexW2313117848

What OpenQuestion holds

Textmetadata
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.