Evidence map›Paper›PMID 26872378›Full record

ArticleOncotarget2016

The expression of presenilin 1 enhances carcinogenesis and metastasis in gastric cancer.

Ping Li, Xi Lin, Jun-Rong Zhang, Yun Li, Jun Lu, Fei-Chao Huang, Chao-Hui Zheng, Jian-Wei Xie, Jia-Bin Wang, Chang-Ming Huang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.7field-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

26 citing papers in PubMed, 40 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Role of Presenilin-1 in Aggressive Human Melanoma.International journal of molecular sciences · 2022
    Article
  10. Article
  11. Article
  12. Tumor reversion: a dream or a reality.Biomarker research · 2021
    Review
  13. Article
  14. Combined Scutellarin and CFrontiers in oncology · 2021
    Article
  15. Article
  16. Article
  17. Article
  18. 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

10 authors at 2 institutions in 1 country.

Ping LiDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Xi LinDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Jun-Rong ZhangDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Yun LiKey Laboratory of The Ministry of Education for Gastrointestinal Cancer, School of Basic Medical Sciences, Fujian Medical University, Fuzhou, People's Republic of China.
Jun LuDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Fei-Chao HuangDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Chao-Hui ZhengDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Jian-Wei XieDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Jia-Bin WangDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Chang-Ming HuangDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, People's Republic of China.
Union Hospital · CNFujian Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Presenilin 1 (PS-1, encoded by PSEN1) is a part of the gamma- (γ-) secretase complex. Mutations in PSEN1 cause the majority of cases of familial Alzheimer's disease (FAD). Although in recent years PS-1 has been implicated as a tumor enhancer in various cancers, nothing is known regarding its role in gastric cancer (GC). In the present study, we investigate the role and clinical significance of PS-1 in GC. We observed that PS-1 was significantly upregulated and amplified in GC tissues and cell lines, and its aberrant expression was positively correlated with lymph node metastasis and with poor overall survival. Furthermore, PS-1 promoted tumor invasion and metastasis of GC both in vitro and vivo without affecting the proliferation of GC cells (MGC-803 and MKN-45). The results of treatment with the γ-secretase inhibitor DAPT were consistent with the outcomes of PS-1 silencing. PS-1/γ-secretase cleaves E-cadherin and releases its bound protein partner, β-catenin, from the actin cytoskeleton, thereby allowing it to translocate into the nucleus and to activate the TCF/LEF-1 transcriptional activator, which may promote GC invasion and metastasis.In conclusion, PS-1 promotes invasion and metastasis in GC and may represent a novel prognostic biomarker and potential therapeutic target for GC treatment.

Indexed as

Actin CytoskeletonAnimalsbeta CateninCadherinsCell Line, TumorCell MovementCell ProliferationCell Transformation, NeoplasticDiaminesEnzyme ActivationFemaleHumansLymphatic MetastasisLymphoid Enhancer-Binding Factor 1MaleMice24-diamino-5-phenylthiazolebeta CateninCadherinsDiaminesLEF1 protein, humanLymphoid Enhancer-Binding Factor 1Presenilin-1PSEN1 protein, humanTCF Transcription FactorsThiazolesE-cadheringastric cancerPS-1tumorigenicityβ-catenin

Identifiers

PMID26872378
PMCPMC4891148
OpenAlexW2272061662

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.