Evidence map›Paper›PMID 24553120›Full record

ArticleCell cycle (Georgetown, Tex.)2014

Successful β cells islet regeneration in streptozotocin-induced diabetic baboons using ultrasound-targeted microbubble gene therapy with cyclinD2/CDK4/GLP1.

Shuyuan Chen, Raul A Bastarrachea, Brad J Roberts, V Saroja Voruganti, Patrice A Frost, Edna J Nava-Gonzalez, Hector E Arriaga-Cazares, Jiaxi Chen, Pintong Huang, Ralph A DeFronzo and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
5.9field-weighted citation impact, top 4% 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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  12. GLP-1 nanomedicine alleviates gut inflammation.Nanomedicine : nanotechnology, biology, and medicine · 2017
    Article
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  15. Review
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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

12 authors at 6 institutions in 3 countries.

Shuyuan ChenBaylor Research Institute; Dallas, TX USA.
Raul A BastarracheaTexas Biomedical Research Institute; San Antonio, TX USA; Southwest National Primate Research Center; San Antonio, TX USA.
Brad J RobertsBaylor Research Institute; Dallas, TX USA; Department of Internal Medicine; Division of Cardiology; Baylor Heart and Vascular Institute; Baylor University Medical Center; Dallas, TX USA.
V Saroja VorugantiTexas Biomedical Research Institute; San Antonio, TX USA.
Patrice A FrostTexas Biomedical Research Institute; San Antonio, TX USA; Southwest National Primate Research Center; San Antonio, TX USA.
Edna J Nava-GonzalezTexas Biomedical Research Institute; San Antonio, TX USA; University of Nuevo Leon School of Nutrition and Public Health; Monterrey, Mexico.
Hector E Arriaga-CazaresTexas Biomedical Research Institute; San Antonio, TX USA; Hospital Infantil de Tamaulipas; Ciudad Victoria, Mexico.
Jiaxi ChenBaylor Research Institute; Dallas, TX USA.
Pintong HuangDepartment of Ultrasonography; The 2nd Affiliated Hospital of Zhejiang University College of Medicine; Hangzhou, Zhejiang Province, PR China.
Ralph A DeFronzoDiabetes Division; Department of Medicine; The University of Texas Health Science Center at San Antonio; San Antonio, TX USA.
Anthony G ComuzzieTexas Biomedical Research Institute; San Antonio, TX USA; Southwest National Primate Research Center; San Antonio, TX USA.
Paul A GrayburnDepartment of Internal Medicine; Division of Cardiology; Baylor Heart and Vascular Institute; Baylor University Medical Center; Dallas, TX USA.
Texas Biomedical Research Institute · USBaylor University Medical Center · USBaylor Institute for Rehabilitation · USBaylor University · USDiabetes Australia · AUSecond Affiliated Hospital of Zhejiang University · CN

Funding

The Southwest National Primate Research Center Supplement- Infrastructure improvements of ABSL2 holding areasP51OD011133 · OD · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI Larry S. Schlesinger · 2012 to 2026
$129.7M
WNV REPLIVAX VACCINE IN NON-HUMAN PRIMATESP51RR013986 · NCRR · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI GAUDUIN, MARIE-CLAIRE ELISABETH · 1999 to 2011
$79.1M
VETERINARY SERVICES--COREP01HL028972 · NHLBI · TEXAS BIOMEDICAL RESEARCH INSTITUTE · PI RICE, KAREN S · 1985 to 2012
$42.0M
EXTRAMULAR RESEARCH FACILITIES CONSTRUCTIONC06RR017515 · NCRR · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI SHADE, ROBERT E · 2003 to 2003
$3.1M
EXTRAMURAL RES FACILITIES CONSTRC06RR015456 · NCRR · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI VANDEBERG, JOHN L · 2001 to 2001
$1.1M
MOLECULAR AND BIOCHEMICAL GENETICS LABORATORY RENOVATIONC06RR013556 · NCRR · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI SHADE, ROBERT E · 1998 to 1998
–
BABOON F-CAGE FACILITY FOR PRIMATE RESEARCH CENTERC06RR014578 · NCRR · SOUTHWEST FOUNDATION FOR BIOMEDICAL RES · PI VANDEBERG, JOHN L · 1999 to 1999
–
NCRR NIH HHS C06 RR013556NCRR NIH HHS C06 RR014578NCRR NIH HHS C06 RR015456NCRR NIH HHS C06 RR017515NCRR NIH HHS P51 RR013986NHLBI NIH HHS P01 HL028972NIH HHS P51 OD011133
6 · The paper itself

Abstract

Both major forms of diabetes mellitus (DM) involve β-cell destruction and dysfunction. New treatment strategies have focused on replenishing the deficiency of β-cell mass common to both major forms of diabetes by islet transplantation or β-cell regeneration. The pancreas, not the liver, is the ideal organ for islet regeneration, because it is the natural milieu for islets. Since islet mass is known to increase during obesity and pregnancy, the concept of stimulating pancreatic islet regeneration in vivo is both rational and physiologic. This paper proposes a novel approach in which non-viral gene therapy is targeted to pancreatic islets using ultrasound targeted microbubble destruction (UTMD) in a non-human primate model (NHP), the baboon. Treated baboons received a gene cocktail comprised of cyclinD2, CDK, and GLP1, which in rats results in robust and durable islet regeneration with normalization of blood glucose, insulin, and C-peptide levels. We were able to generate important preliminary data indicating that gene therapy by UTMD can achieve in vivo normalization of the intravenous (IV) glucose tolerance test (IVGTT) curves in STZ hyperglycemic-induced conscious tethered baboons. Immunohistochemistry clearly demonstrated evidence of islet regeneration and restoration of β-cell mass.

Indexed as

Genetic TherapyAnimalsCyclin D2Cyclin-Dependent Kinase 4Diabetes Mellitus, ExperimentalGlucagon-Like Peptide-1 ReceptorInsulin-Secreting CellsIslets of LangerhansPapioPilot ProjectsRegenerationStreptozocinUltrasonic WavesCyclin D2Cyclin-Dependent Kinase 4Glucagon-Like Peptide-1 ReceptorStreptozocinbaboonsCDK4cell cycle regulationCyclinD2diabetesdifferentiationgene therapyGLP-1insulin gene promoterislets regenerationnonhuman primatesproliferation

Identifiers

PMID24553120
PMCPMC4013164
OpenAlexW1982756407

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.