Evidence map›Paper›PMID 35370290›Full record

ArticleSignal transduction and targeted therapy2022

Identification of NOXA as a pivotal regulator of resistance to CAR T-cell therapy in B-cell malignancies.

Xin Yan, Deyun Chen, Yao Wang, Yelei Guo, Chuan Tong, Jianshu Wei, Yajing Zhang, Zhiqiang Wu, Weidong Han

Open access · goldAbstract read
In one paragraph

Article in Signal transduction and targeted therapy, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
4.9field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 52 citations in OpenAlex.

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  14. Ubiquitin-conjugating Enzymes in Cancer.International journal of biological sciences · 2026
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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

9 authors at 2 institutions in 1 country.

Xin Yan *School of Medicine, Nankai University, Tianjin, China.
Deyun Chen *Department of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Yao WangDepartment of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Yelei GuoDepartment of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Chuan TongDepartment of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Jianshu WeiDepartment of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Yajing ZhangDepartment of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China.
Zhiqiang WuDepartment of Bio-therapeutic, the First Medical Center, Chinese PLA General Hospital, Beijing, China. wuzhiqiang1006@163.com.
Weidong HanSchool of Medicine, Nankai University, Tianjin, China. hanwdrsw@163.com.ORCID 0000-0003-3207-3899
Chinese PLA General Hospital · CNNankai University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the remarkable success of chimeric antigen receptor (CAR) T-cell therapy for treating hematologic malignancies, resistance and recurrence still occur, while the markers or mechanisms underlying this resistance remain poorly understood. Here, via an unbiased genome-wide CRISPR/Cas9 screening, we identified loss of NOXA, a B-cell lymphoma 2 (BCL2) family protein in B-cell malignancies, as a pivotal regulator of resistance to CAR T-cell therapy by impairing apoptosis of tumor cells both in vitro and in vivo. Notably, low NOXA expression in tumor samples was correlated with worse survival in a tandem CD19/20 CAR T clinical trial in relapsed/refractory B-cell lymphoma. In contrast, pharmacological augmentation of NOXA expression by histone deacetylase (HDAC) inhibitors dramatically sensitized cancer cells to CAR T cell-mediated clearance in vitro and in vivo. Our work revealed the essentiality of NOXA in resistance to CAR T-cell therapy and suggested NOXA as a predictive marker for response and survival in patients receiving CAR T-cell transfusions. Pharmacological targeting of NOXA might provide an innovative therapeutic strategy to enhance CAR T-cell therapy.

Indexed as

NeoplasmsReceptors, Chimeric AntigenAntigens, CD19B-LymphocytesHumansImmunotherapy, AdoptiveAntigens, CD19Receptors, Chimeric Antigen

Identifiers

PMID35370290
PMCPMC8977349
OpenAlexW4224254421

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.