Evidence map›Paper›PMID 29325230›Full record

ArticleCancer science2018

Protocadherin-8 promotes invasion and metastasis via laminin subunit γ2 in gastric cancer.

Ying Lin, Xiaoxiao Ge, Xiaofei Zhang, Zheng Wu, Kaiyi Liu, Fengjuan Lin, Congqi Dai, Weijian Guo, Jin Li

Open access · goldAbstract read
In one paragraph

Article in Cancer science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Journal of Cancer · 2021
    Article
  19. Article
  20. 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 3 institutions in 1 country.

Ying LinDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0002-4321-0695
Xiaoxiao GeDepartment of Oncology, East Hospital, Tongji University School of Medicine, Shanghai, China.
Xiaofei ZhangDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, China.
Zheng WuDepartment of Medical Oncology, Ruijin Hospital, School of Medicine, Shanghai Jiaotong University, Shanghai, China.
Kaiyi LiuDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Fengjuan LinDepartment of Oncology, East Hospital, Tongji University School of Medicine, Shanghai, China.
Congqi DaiDepartment of Oncology, East Hospital, Tongji University School of Medicine, Shanghai, China.
Weijian GuoDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Jin LiDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID http://orcid.org/0000-0001-5523-0055
Shanghai Medical College of Fudan University · CNShanghai East Hospital · CNRuijin Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Growing evidence suggests that protocadherins (PCDH) play crucial roles in pathogenesis and progression of cancers, including gastric cancer (GC). Protocadherin-8 (PCDH8) was previously reported to be involved in metastasis of GC, but functional studies yielded inconsistent results and the molecular mechanism remained unknown. The present study aimed to explore the clinical relevance, function and molecular mechanism of PCDH8 in GC. Data from the GEPIA and Kaplan-Meier plotter databases showed that high expression of PCDH8 was significantly correlated with poorer prognosis in GC. Ectopic expression of PCDH8 in GC cells promoted invasion and migration in vitro and metastasis in vivo, and knockdown of PCDH8 inhibited invasion and migration in vitro. RNA sequencing followed by gene set enrichment analysis found a remarkable enrichment in the extracellular matrix receptor interaction pathway, with the expression of laminin subunit γ2 (LAMC2) being significantly increased in the PCDH8-overexpressing group. High expression of LAMC2 was significantly correlated to poor prognosis in GC in GEPIA database. Upregulation of LAMC2 following PCDH8 overexpression was further confirmed by immunohistochemistry in liver metastatic lesions of nude mice. To our knowledge, this is the first report of the metastasis-enhancing property and molecular mechanism through upregulation of LAMC2 of PCDH8 in cancer. High expression of PCDH8 could be used as a biomarker for poor prognosis in clinical practice.

Indexed as

AnimalsCadherinsCell Line, TumorCell MovementFemaleGene Expression Regulation, NeoplasticHumansLamininMaleMiceMice, NudeNeoplasm InvasivenessNeoplasm TransplantationPrognosisProtocadherinsStomach NeoplasmsCadherinsLAMC2 protein, humanLamininPCDH8 protein, humanProtocadherinsgastric cancerinvasionlaminin subunit γ2metastasisprotocadherin-8

Identifiers

PMID29325230
PMCPMC5834795
OpenAlexW2783179653

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.