Evidence map›Paper›PMID 31218103›Full record

ArticleAmerican journal of cancer research2019

Antitumor activity of NKG2D CAR-T cells against human colorectal cancer cells in vitro and in vivo.

Xinna Deng, Fei Gao, Nan Li, Qingxia Li, Ye Zhou, Tao Yang, Ziqi Cai, Pingping Du, Fan Chen, Jianhui Cai

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

59 citing papers in PubMed, 74 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

10 authors at 3 institutions in 1 country.

Xinna DengDepartment of Surgery, Hebei Medical University Shijiazhuang, Hebei, China.
Fei GaoDepartment of Oncology and Immunotherapy, Hebei General Hospital Shijiazhuang, Hebei, China.
Nan LiDepartment of Gynecology, Second Hospital of Hebei Medical University Shijiazhuang, Hebei, China.
Qingxia LiDepartment of Oncology and Immunotherapy, Hebei General Hospital Shijiazhuang, Hebei, China.
Ye ZhouDepartment of Oncology and Immunotherapy, Hebei General Hospital Shijiazhuang, Hebei, China.
Tao YangDepartment of Urinary Surgery, Hebei General Hospital Shijiazhuang, Hebei, China.
Ziqi CaiHebei Engineering Technology Research Center for Cell Therapy, Hebei HOFOY Biotech Corporation Ltd. Shijiazhuang, Hebei, China.
Pingping DuHebei Engineering Technology Research Center for Cell Therapy, Hebei HOFOY Biotech Corporation Ltd. Shijiazhuang, Hebei, China.
Fan ChenHebei Engineering Technology Research Center for Cell Therapy, Hebei HOFOY Biotech Corporation Ltd. Shijiazhuang, Hebei, China.
Jianhui CaiDepartment of Surgery, Hebei Medical University Shijiazhuang, Hebei, China.
Hebei General Hospital · CNHebei Medical University · CNHebei Science and Technology Department · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer is one of the most common malignancies worldwide, as it is often diagnosed at an advanced stage. Chimeric antigen receptor (CAR) T cell therapy has demonstrated remarkable success and emerged as one of the most promising therapeutic strategies in multiple malignancies. The purpose of this study was to investigate the anti-tumor activity of NKG2D CAR-T cells against human colorectal cancer cells. A non-viral third-generation NKG2D CAR was constructed, and subsequently transduced into T cells to obtain the NKG2D CAR-T cells. In vitro, NKG2D CAR-T cells showed cytotoxicity against human colorectal cancer cells in a dose-dependent manner compared with untransduced T cells. In addition, IL-2 and IFN-γ secreted by these cells were significantly higher than those by untransduced T cells. In vivo, NKG2D CAR-T cells significantly suppressed tumor growth, reduced tumor sizes and extended overall survival of mice in a xenograft model of HCT-116 cells. Furthermore, human NKG2D-positive lymphocytes infiltration could be found in the tumor sections of NKG2D CAR-T cells-treated mice. There were no severe pathological changes found in vital organs in any of the treatment groups. NKG2D CAR-T cells showed excellent killing effect and represented a promising immunotherapeutic strategy against human colorectal cancer.

Indexed as

Chimeric antigen receptorcolorectal cancerminicircle DNANKG2D

Identifiers

PMID31218103
PMCPMC6556598
OpenAlexW2985952836

What OpenQuestion holds

Textmetadata
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.