Evidence map›Paper›PMID 29415996›Full record

ArticleCell death & disease2018

Antitumor activity of EGFR-specific CAR T cells against non-small-cell lung cancer cells in vitro and in mice.

He Li, Yao Huang, Du-Qing Jiang, Lian-Zhen Cui, Zhou He, Chao Wang, Zhi-Wei Zhang, Hai-Li Zhu, Yong-Mei Ding, Lin-Fang Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
4.6field-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

71 citing papers in PubMed, 105 citations in OpenAlex.

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11 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

He LiDepartments of Respiratory and Critical Care Medicine, Changhai Hospital, The Second Military Medical University, 200438, Shanghai, China.
Yao HuangDepartment of Biliary Tract Surgery I, The Eastern Hepatobiliary Surgery Hospital, The Second Military Medical University, 200438, Shanghai, China.
Du-Qing JiangShanghai Cell Therapy Research Institute, 201805, Shanghai, China.
Lian-Zhen CuiShanghai Cell Therapy Research Institute, 201805, Shanghai, China.
Zhou HeShanghai Cell Therapy Research Institute, 201805, Shanghai, China.
Chao WangShanghai Cell Therapy Research Institute, 201805, Shanghai, China.
Zhi-Wei ZhangShanghai Cell Therapy Research Institute, 201805, Shanghai, China.
Hai-Li ZhuLaboratory of Gene and Viral Therapy, The Eastern Hepatobiliary Surgery Hospital, The Second Military Medical University, 200438, Shanghai, China.
Yong-Mei DingDepartment of Biotherapy, The Eastern Hepatobiliary Surgery Hospital, The Second Military Medical University, 200438, Shanghai, China.
Lin-Fang LiShanghai Cell Therapy Research Institute, 201805, Shanghai, China.
Qiang LiDepartments of Respiratory and Critical Care Medicine, Changhai Hospital, The Second Military Medical University, 200438, Shanghai, China. qiangli19621217@126.com.
Hua-Jun JinShanghai Cell Therapy Research Institute, 201805, Shanghai, China. hj-jin@hotmail.com.
Qi-Jun QianShanghai Cell Therapy Research Institute, 201805, Shanghai, China. qianqj@sino-gene.cn.
Shanghai Cell Therapy Research Institute · CNEastern Hepatobiliary Surgery Hospital · CNSecond Military Medical University · CNShanghai First People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Effective control of non-small-cell lung cancer (NSCLC) remains clinically challenging, especially during advanced stages of the disease. This study developed an adoptive T-cell treatment through expression of a chimeric antigen receptor (CAR) to target human epidermal growth factor receptor (EGFR) in NSCLC. We optimized the non-viral piggyBac transposon system to engineer human T cells for the expression of EGFR-CAR, consisting of EGFR scFv, transmembrane domain, and intracellular 4-1BB-CD3ζ signaling domains. The modified CAR T cells exhibited expansion capability and anticancer efficacy in a time- and antigen-dependent manner in vitro as well as regression of EGFR-positive human lung cancer xenografts in vivo. EGFR-CAR T therapy is a promising strategy to improve the efficacy and potency of the adoptive immunotherapy in NSCLC. Moreover, EGFR-CAR T therapy could become a clinical application for NSCLC patients in the future.

Indexed as

AnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorDisease Models, AnimalErbB ReceptorsFemaleHumansImmunotherapy, AdoptiveLung NeoplasmsMiceRandom AllocationReceptors, Antigen, T-CellT-LymphocytesXenograft Model Antitumor AssaysEGFR protein, mouseErbB ReceptorsReceptors, Antigen, T-Cell

Identifiers

PMID29415996
PMCPMC5833445
OpenAlexW2791850255

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.