Evidence map›Paper›PMID 26423399›Full record

ArticleTumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine2016

Repression of PES1 expression inhibits growth of gastric cancer.

Jieping Li, Xiaodong Zhou, Xiaopeng Lan, Guobin Zeng, Xuping Jiang, Zongming Huang

Abstract read
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In one paragraph

Article in Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine, 2016. 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
0.4field-weighted citation impact, top 39% 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, 21 citations in OpenAlex.

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  5. PES1 reduces CD8Journal of biomedical science · 2023
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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

6 authors at 2 institutions in 1 country.

Jieping LiDepartment of Clinic Medical Laboratory, General Hospital of Fujian Corps of CAPF, Fuzhou, 350003, China. liejieping@hotmail.com.
Xiaodong ZhouDepartment of Gastroenterology, The First Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Xiaopeng LanInstitute of Clinic Laboratory Medicine, Fuzhou General Hospital of Nanjing Military Command, PLA, Fuzhou, 350003, China. lanxp@sina.com.
Guobin ZengDepartment of Clinic Medical Laboratory, General Hospital of Fujian Corps of CAPF, Fuzhou, 350003, China.
Xuping JiangDepartment of Clinic Medical Laboratory, General Hospital of Fujian Corps of CAPF, Fuzhou, 350003, China.
Zongming HuangDepartment of Pathology, General Hospital of Fujian Corps of CAPF, Fuzhou, 350003, China.
Fuzhou General Hospital of Nanjing Military Command · CNNanchang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer is one of the leading causes of cancer death worldwide. However, precise molecular mechanisms underlining its development are far from clear. We recently reported that PES1 promoted development of breast cancer and ovarian cancer as an oncogene. In this study, we reported that ablation of endogenous PES1 resulted in significant suppression of cell proliferation and growth and led to cell cycle arrest in G2 or G1 phase, respectively, in two gastric cancer cell lines (AGS and N87) in vitro. Meanwhile, silencing of PES1 obviously decreased expressions of cyclin D1, HIF-1α, and vascular endothelial growth factor (VEGF) expressions and increased p21WAF1 expression. Re-expression of PES1 in these two kinds of PES1 knockdown cells rescued these effects. In vivo, repression of endogenous PES1 expression suppressed gastric tumor growth in nude mice. In addition, 40.7 % (24/59) of gastric cancer tissues showed PES1 expression via immunohistochemical (IHC) staining. However, there were not any positive PES1 stainings in matched adjacent tissues. Our results demonstrated that repression of PES1 changed expressions of some cell proliferation- and angiogenesis-related genes and inhibited gastric cancer growth, and PES1 expression increased in gastric cancer tissues. These results suggest that PES1 may play an important role in development of gastric cancer. PES1 may be a potential target for gastric cancer therapy.

Indexed as

AnimalsCell Line, TumorCell ProliferationHumansMiceMice, Inbred BALB CProteinsRNA-Binding ProteinsStomach NeoplasmsPES1 protein, humanProteinsRNA-Binding ProteinsGastric cancerPES1

Identifiers

PMID26423399
OpenAlexW1630802974

What OpenQuestion holds

Textmetadata
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.