Evidence map›Paper›PMID 37662968›Full record

ArticleMolecular therapy. Nucleic acids2023

Leverage of nuclease-deficient CasX for preventing pathological angiogenesis.

Haote Han, Yanhui Yang, Yunjuan Jiao, Hui Qi, Zhuo Han, Luping Wang, Lijun Dong, Jingkui Tian, Bart Vanhaesebroeck, Xiaopeng Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 25% 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

5 citing papers in PubMed, 6 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

13 authors at 6 institutions in 2 countries.

Haote HanInstitute of Basic Medicine and Cancer, Chinese Academy of Sciences, Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou 310000, People's Republic of China.
Yanhui YangNingxia Key Laboratory of Prevention and Control of Common Infectious Diseases, the School of Basic Medical Sciences, Ningxia Medical University, Yinchuan 750004, People's Republic of China.
Yunjuan JiaoDepartment of Histology and Embryology, Xiangya School of Medicine, Central South University, Changsha 410013, People's Republic of China.
Hui QiShenzhen Eye Hospital, Jinan University, Shenzhen Eye Institute, Shenzhen 518000, People's Republic of China.
Zhuo HanInstitute of Basic Medicine and Cancer, Chinese Academy of Sciences, Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou 310000, People's Republic of China.
Luping WangInstitute of Basic Medicine and Cancer, Chinese Academy of Sciences, Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou 310000, People's Republic of China.
Lijun DongShenzhen Eye Hospital, Jinan University, Shenzhen Eye Institute, Shenzhen 518000, People's Republic of China.
Jingkui TianInstitute of Basic Medicine and Cancer, Chinese Academy of Sciences, Cancer Hospital of the University of Chinese Academy of Sciences, Zhejiang Cancer Hospital, Hangzhou 310000, People's Republic of China.
Bart VanhaesebroeckCancer Institute, University College London, London NW1 2BU, UK.
Xiaopeng LiThe Third Affiliated Hospital of Xinxiang Medical University, Xinxiang 453003, China.
Junwen LiuDepartment of Histology and Embryology, Xiangya School of Medicine, Central South University, Changsha 410013, People's Republic of China.
Gaoen MaThe Third Affiliated Hospital of Xinxiang Medical University, Xinxiang 453003, China.
Hetian LeiThe Third Affiliated Hospital of Xinxiang Medical University, Xinxiang 453003, China.
Zhejiang Cancer Hospital · CNJinan University · CNCentral South University · CNXinxiang Medical University · CNNingxia Medical University · CNUniversity College London · GB

Funding

Cancer Research UK 25722
6 · The paper itself

Abstract

Gene editing with a CRISPR/Cas system is a novel potential strategy for treating human diseases. Pharmacological inhibition of phosphoinositide 3-kinase (PI3K) δ suppresses retinal angiogenesis in a mouse model of oxygen-induced retinopathy. Here we show that an innovative system of adeno-associated virus (AAV)-mediated CRISPR/nuclease-deficient (d)CasX fused with the Krueppel-associated box (KRAB) domain is leveraged to block (81.2% ± 6.5%)

Indexed as

angiogenesisCRISPR/dCasX-KRABMT: RNA/DNA editingoxygen-induced retinopathyPI3KδPik3cdrAAV1

Identifiers

PMID37662968
PMCPMC10469388
OpenAlexW4385613128

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.