Evidence map›Paper›PMID 30809100›Full record

ArticleCancer management and research2019

Activated Wnt signaling promotes growth and progression of AFP-producing gastric cancer in preclinical models.

Dongshao Chen, Xiaoting Lin, Cheng Zhang, Guo An, Zhongwu Li, Bin Dong, Lin Shen, Jing Gao, Xiaotian Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.5field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
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.

Dongshao ChenDepartment of Gastrointestinal Oncology, zhangxiaotianmed@163.com; gaojing_pumc@163.com.
Xiaoting LinDepartment of Gastrointestinal Oncology, zhangxiaotianmed@163.com; gaojing_pumc@163.com.
Cheng ZhangDepartment of Gastrointestinal Oncology, zhangxiaotianmed@163.com; gaojing_pumc@163.com.
Guo AnDepartment of Laboratory Animal.
Zhongwu LiDepartment of Pathology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing 100142, China.
Bin DongDepartment of Pathology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education, Beijing), Peking University Cancer Hospital and Institute, Beijing 100142, China.
Lin ShenDepartment of Gastrointestinal Oncology, zhangxiaotianmed@163.com; gaojing_pumc@163.com.
Jing GaoDepartment of Gastrointestinal Oncology, zhangxiaotianmed@163.com; gaojing_pumc@163.com.
Xiaotian ZhangDepartment of Gastrointestinal Oncology, zhangxiaotianmed@163.com; gaojing_pumc@163.com.
Zhaotong University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCharacterized by elevated AFP levels in serum, AFP-producing gastric cancer (APGC) is a very special type of gastric cancer (GC) that is difficult to treat and has poor prognosis. However, little is known about the role of AFP in GC, which was investigated in this study with in vitro and in vivo experiments.

methodsAPGC cells were established with lentivirus infection and validated by PCR assay and ELISA in HCG27 and AGS cells. Cell growth, migration, and invasion were determined by CCK8, transwell assays, and animal experiments. RNA sequencing, Western blot, dual-luciferase-reporter assays, and RNA interference were employed to understand mechanisms underlying AFP activity, followed by therapeutic investigations for APGC.

resultsAPGC cells featured significantly increased AFP levels in cellular supernatants. AFP potentiated growth and aggression in GC cell lines and their derived xenografts. Wnt-signaling activation was responsible for AFP function, indicated by decreased Axin 1 and pGSK3β, followed by cascade activation of β-catenin, downstream transcription factors TCF1/TCF7, and the target gene -

conclusionAFP played a critical role in APGC through activating Wnt signaling, and targeting Wnt pathways might be a promising strategy against APGC.

Indexed as

AFPAFP-producing gastric canceralpha-fetoproteinAPGCAxin 1Wnt signalingWnt-signaling inhibitor

Identifiers

PMID30809100
PMCPMC6376882
OpenAlexW2911633213

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.