Evidence map›Paper›PMID 36176604›Full record

ArticleBioengineering & translational medicine2022

Carboxymethyl chitosan prolongs adenovirus-mediated expression of IL-10 and ameliorates hepatic fibrosis in a mouse model.

Yannian Gou, Yaguang Weng, Qian Chen, Jinghong Wu, Hao Wang, Jiamin Zhong, Yang Bi, Daigui Cao, Piao Zhao, Xiangyu Dong and 11 more

Open access · goldAbstract read
In one paragraph

Article in Bioengineering & translational medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

14 citing papers in PubMed, 22 citations in OpenAlex.

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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

21 authors at 3 institutions in 3 countries.

Yannian GouMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Yaguang WengMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Qian ChenHealth Management Center, Deyang People's Hospital Deyang China.
Jinghong WuMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Hao WangMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Jiamin ZhongMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Yang BiMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Daigui CaoMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Piao ZhaoMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Xiangyu DongMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
Meichun GuoMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.
William WagstaffMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Bryce Hendren-SantiagoMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Connie ChenMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Andrew YoussefMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Rex C HaydonMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Hue H LuuMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Russell R ReidMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Le ShenMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.
Tong-Chuan HeMolecular Oncology Laboratory, Department of Orthopaedic Surgery and Rehabilitation Medicine The University of Chicago Medical Center Chicago Illinois USA.ORCID https://orcid.org/0000-0001-7721-3934
Jiaming FanMinistry of Education Key Laboratory of Diagnostic Medicine, and Department of Clinical Biochemistry, School of Laboratory Medicine Chongqing Medical University Chongqing China.ORCID https://orcid.org/0000-0001-8523-4188
University of Chicago Medical Center · USMinistry of Education · THDeyang Stomatological Hospital · CN

Funding

VIRAL ONCOLOGY CORE FACILITYP30CA014599 · NCI · UNIVERSITY OF CHICAGO · PI KUNLE ODUNSI · 1985 to 2026
$122.1M
MEDICAL SCIENTIST TRAININGT32GM007281 · NIGMS · UNIVERSITY OF CHICAGO · PI CLARK, MARCUS RAMSAY · 1985 to 2022
$32.1M
Re-Engineering Translational Research at the University of ChicagoUL1TR000430 · NCATS · UNIVERSITY OF CHICAGO · PI SOLWAY, JULIAN · 2012 to 2016
$20.2M
NCATS NIH HHS UL1 TR000430NCI NIH HHS P30 CA014599NIGMS NIH HHS T32 GM007281
6 · The paper itself

Abstract

Effective and safe liver-directed gene therapy has great promise in treating a broad range of liver diseases. While adenoviral (Ad) vectors have been widely used for efficacious in vivo gene delivery, their translational utilities are severely limited due to the short duration of transgene expression and solicitation of host immune response. Used as a promising polymeric vehicle for drug release and nucleic acid delivery, carboxymethyl chitosan (CMC) is biocompatible, biodegradable, anti-microbial, inexpensive, and easy accessible. Here, by exploiting its biocompatibility, controlled release capability and anti-inflammatory activity, we investigated whether CMC can overcome the shortcomings of Ad-mediated gene delivery, hence improving the prospect of Ad applications in gene therapy. We demonstrated that in the presence of optimal concentrations of CMC, Ad-mediated transgene expression lasted up to 50 days after subcutaneous injection, and at least 7 days after intrahepatic injection. Histologic evaluation and immunohistochemical analysis revealed that CMC effectively alleviated Ad-induced host immune response. In our proof-of-principle experiment using the CCl

Indexed as

adenovirus vectorcarboxymethyl chitosan (CMC)chitosangene deliverygene therapyhepatic fibrosishost immune response

Identifiers

PMID36176604
PMCPMC9472002
OpenAlexW4214947531

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.