Evidence map›Paper›PMID 30796510›Full record

ArticleJournal of cancer research and clinical oncology2019

CIK cell-based delivery of recombinant adenovirus KGHV500 carrying the anti-p21Ras scFv gene enhances the anti-tumor effect and safety in lung cancer.

Xin-Rui Lin, Xin-Liang Zhou, Qiang Feng, Xin-Yan Pan, Shu-Ling Song, Hong Fang, Jin Lei, Ju-Lun Yang

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 17 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

8 authors at 2 institutions in 1 country.

Xin-Rui LinGraduate School, Kunming Medical University, Chenggong District, Kunming, People's Republic of China.
Xin-Liang ZhouDepartment of Pathology, Medical Faculty, Kunming University of Science and Technology, Kunming, People's Republic of China.
Qiang FengDepartment of Pathology, 920th Hospital of the Joint Logistics Support Force of PLA, 212 Daguan Road, Kunming, 650032, Yunnan, People's Republic of China.
Xin-Yan PanDepartment of Pathology, 920th Hospital of the Joint Logistics Support Force of PLA, 212 Daguan Road, Kunming, 650032, Yunnan, People's Republic of China.
Shu-Ling SongDepartment of Pathology, 920th Hospital of the Joint Logistics Support Force of PLA, 212 Daguan Road, Kunming, 650032, Yunnan, People's Republic of China.
Hong FangDepartment of Pathology, 920th Hospital of the Joint Logistics Support Force of PLA, 212 Daguan Road, Kunming, 650032, Yunnan, People's Republic of China.
Jin LeiDepartment of Pathology, 920th Hospital of the Joint Logistics Support Force of PLA, 212 Daguan Road, Kunming, 650032, Yunnan, People's Republic of China.
Ju-Lun YangGraduate School, Kunming Medical University, Chenggong District, Kunming, People's Republic of China. yangjulun@sina.com.ORCID http://orcid.org/0000-0002-0934-5238
Kunming University of Science and Technology · CNKunming Medical University · CN

Funding

Applied Basic Research Foundation of Yunnan Province (CN) 2013FA059National Natural Science Foundation of China 81460464The Applied Basic Research Project Youth Foundation of Yunnan Province 2017FD248
6 · The paper itself

Abstract

purposeAdenovirus (Ads) is one of the most popular vectors used in gene therapy for the treatment of cancer. However, systemic therapy is limited by circulating antiviral antibodies and poor viral delivery in vivo. In this study, we used cytokine-induced killer (CIK) cells as delivery vehicles of Ads KGHV500 carrying the anti-p21Ras scFv gene to treat Ras gene-related lung cancer and investigate the anti-tumor effect in vitro and in vivo.

methodsThe human lung cancer cell line A549 was employed to investigate the anti-tumor activity of recombinant Ads KGHV500 harboring the anti-p21Ras scFv gene using MTT, wound healing, transwell invasion, and apoptosis assays in vitro. Next, CIK cells were used as delivery vehicles to deliver KGHV500 carrying the anti-p21Ras scFv gene to treat A549-transplanted tumors in nude mice, and viral replication, p21Ras scFv expression, and the therapeutic efficacy were assessed.

resultsIn vitro studies showed that KGHV500 had potent anti-tumor activity. In addition, in vivo, this combination therapy significantly inhibited the growth of lung cancer xenografts compared with mice treated with KGHV500 alone. KGHV500 and anti-p21Ras scFv were observed in tumor tissue, but were nearly undetectable in normal tissues.

conclusionsThe co-delivery of anti-p21Ras scFv by CIK cells and KGHV500 could increase the anti-tumor effect and safety, and possess considerable advantages for the treatment of Ras-related cancer.

Indexed as

AdenoviridaeAnimalsApoptosisCell Line, TumorCytokine-Induced Killer CellsCytotoxicity Tests, ImmunologicDisease Models, AnimalFemaleGene ExpressionGenetic TherapyGenetic VectorsHumansImmunohistochemistryImmunotherapy, AdoptiveLung NeoplasmsMiceProto-Oncogene Proteins p21(ras)Single-Chain AntibodiesAdenovirusAnti-p21Ras scFvCarrierCIK cellsLung cancerTherapy

Identifiers

PMID30796510
PMCPMC11810408
OpenAlexW2916182802

What OpenQuestion holds

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Registered trials

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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.