Evidence map›Paper›PMID 28388537›Full record

ArticleOncotarget2017

NDV-D90 suppresses growth of gastric cancer and cancer-related vascularization.

Hong Sui, Kaibing Wang, Rui Xie, Xi Li, Kunpeng Li, Yuxian Bai, Xishan Wang, Bin Bai, Dan Chen, Jiazhuang Li and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-weighted citation impact, top 16% 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

12 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  8. Syncytia Formation in Oncolytic Virotherapy.Molecular therapy oncolytics · 2019
    Review
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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

11 authors at 4 institutions in 1 country.

Hong SuiDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Kaibing WangDepartment of Intervention, The Second Hospital Affiliated Harbin Medical University, Harbin 150086, China.
Rui XieDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Xi LiDivision of Swine Disease, National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Medicine, Harbin 150069, China.
Kunpeng LiDivision of Swine Disease, National Key Laboratory of Veterinary Biotechnology, Harbin Veterinary Medicine, Harbin 150069, China.
Yuxian BaiDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Xishan WangDepartment of Abdominal Surgery, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100021, China.
Bin BaiDepartment of Intervention, The Second Hospital Affiliated Harbin Medical University, Harbin 150086, China.
Dan ChenDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Jiazhuang LiDepartment of Medical Oncology, Harbin Medical University Cancer Hospital, Harbin 150040, China.
Baozhong ShenDepartment of Radiology, The Fourth Hospital of Harbin Medical University, Harbin 150001, China.
Harbin Medical University · CNHarbin Veterinary Research Institute · CNThird Affiliated Hospital of Harbin Medical University · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent reports suggest promises on using oncolytic Newcastle disease viruses (NDV) to treat different cancers, while the effects of a NDV-D90 strain on gastric cancer remain unknown. Here we showed that NDV-D90 induced gastric cancer cell apoptosis in a dose-dependent manner in 3 gastric cancer cell lines BGC-823, SGC-7901 and MKN-28. Pronounced reduction in cell invasion was detected in NDV-D90-treated BGC-823 and SGC-7901 cells, but not in MKN-28 cells. The increases in cell apoptosis and reduction in cell growth in NDV-D90-treated gastric cancer cells seemingly resulted from augmentation of p38 signaling and suppression of ERK1/2 and Akt signaling. In vivo, orthotopic injection of NDV-D90 impaired tumor growth and induced intratumoral necrosis. Tumor cells that had been pre-treated with NDV-D90 showed defect in development of implanted tumor. Moreover, NDV-D90 appeared to reduce gastric tumor vascularization, possibly through suppression of vascular endothelial growth factor A and Matrix Metallopeptidase 2. Together, our data suggest that NDV-D90 may have potential anti-cancer effects on gastric cancer.

Indexed as

AnimalsCell Line, TumorCell ProliferationCell SurvivalHumansMAP Kinase Signaling SystemMiceNeoplasm InvasivenessNeovascularization, PathologicNewcastle disease virusOncolytic VirotherapyStomach NeoplasmsXenograft Model Antitumor Assaysapoptosisgastric cancermatrix metallopeptidase 2 (MMP-2)newcastle disease viruses (NDV)vascular endothelial growth factor A (VEGF-A)

Identifiers

PMID28388537
PMCPMC5470987
OpenAlexW2599080367

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.