Evidence map›Paper›PMID 30837996›Full record

ArticleFrontiers in immunology2019

Genome-Wide CRISPR Screening Identifies JAK1 Deficiency as a Mechanism of T-Cell Resistance.

Ping Han, Qiang Dai, Lilv Fan, Hao Lin, Xiaoqing Zhang, Fanlin Li, Xuanming Yang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2019. 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
1.0field-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

19 citing papers in PubMed, 26 citations in OpenAlex.

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  13. The Immunogenetics of Melanoma.Advances in experimental medicine and biology · 2022
    Article
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  16. USP22 deficiency in melanoma mediates resistance to T cells through IFNγ-JAK1-STAT1 signal axis.Molecular therapy : the journal of the American Society of Gene Therapy · 2021
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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

7 authors at 1 institution in 1 country.

Ping HanSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Qiang DaiSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Lilv FanSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Hao LinSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Xiaoqing ZhangSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Fanlin LiSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Xuanming YangSchool of Life Sciences and Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Shanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Somatic gene mutations play a critical role in immune evasion by tumors. However, there is limited information on genes that confer immunotherapy resistance in melanoma. To answer this question, we established a whole-genome knockout B16/ovalbumin cell line by clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated protein-9 nuclease technology, and determined by

Indexed as

Adoptive TransferAnimalsAntigen PresentationCell Line, TumorClustered Regularly Interspaced Short Palindromic RepeatsCRISPR-Cas SystemsGene EditingGenomeGenome-Wide Association StudyJanus Kinase 1MelanomaMelanoma, ExperimentalMiceMice, Inbred C57BLT-LymphocytesJak1 protein, mouseJanus Kinase 1CRISPR/Cas9immunotherapyJAK1 deficiencymelanomaT-cell resistance

Identifiers

PMID30837996
PMCPMC6389627
OpenAlexW2912334303

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.