Evidence map›Paper›PMID 26893686›Full record

ArticleOncology letters2016

Regulation and clinical significance of the hypoxia-induced expression of ANGPTL4 in gastric cancer.

Hiroshi Kubo, Yoshihiko Kitajima, Keita Kai, Jun Nakamura, Shuusuke Miyake, Kazuyoshi Yanagihara, Kiyoto Morito, Tomokazu Tanaka, Masaaki Shida, Hirokazu Noshiro

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 2 pooled it
1.9field-weighted citation impact, top 13% 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

20 citing papers in PubMed, 2 syntheses or guidelines pooled it, 33 citations in OpenAlex.

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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

10 authors at 2 institutions in 1 country.

Hiroshi KuboDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Yoshihiko KitajimaDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan; Department of Surgery, National Hospital Organization Higashisaga Hospital, Saga 849-0101, Japan.
Keita KaiDepartment of Pathology and Biodefense, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Jun NakamuraDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Shuusuke MiyakeDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Kazuyoshi YanagiharaDivision of Translational Research, Exploratory Oncology Research and Clinical Trial Center, National Cancer Center, Kashiwa, Chiba 277-8577, Japan.
Kiyoto MoritoDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Tomokazu TanakaDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Masaaki ShidaDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Hirokazu NoshiroDepartment of Surgery, Saga University Faculty of Medicine, Saga 849-8501, Japan.
Saga University · JPChiba Cancer Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Solid tumors are often exposed to hypoxia. Hypoxia inducible factor (HIF)-1α upregulates numerous target genes associated with the malignant behavior of hypoxic cancer cells. A member of the angiopoietin family, angiopoietin-like protein 4 (ANGPTL4) is a hypoxia-inducible gene. The present study aimed to clarify whether ANGPTL4 is regulated by HIF-1α in gastric cancer cells. The study also assessed whether ANGPTL4 expression is associated with clinicopathological factors or HIF-1α expression in gastric cancer tissues. Hypoxia-induced ANGPTL4 expression was quantitatively analyzed using reverse transcription-quantitative polymerase chain reaction (RT-qPCR) in 10 gastric cancer cell lines. RT-qPCR was further employed to investigate the HIF-1α dependency of ANGPTL4 expression using HIF-1α-knockdown transfectant 58As9-KD and control 58As9-SC gastric cancer cells. The HIF-1α and ANGPTL4 expression levels were immunohistochemically analyzed in 170 gastric cancer tissue specimens and were assessed for any correlations with the clinicopathological factors and/or patient survival. Subsequently, hypoxia-induced ANGPTL4 expression was observed in 7 out of 10 gastric cancer cell lines. The hypoxic induction of ANGPTL4 was almost preserved in the 58As9-KD cells compared with that observed in the 58As9-SC cells, while the induction of known HIF-1α target gene, carbonic anhydrase 9, was completely suppressed in the 58As9-KD cells. In the gastric cancer tissues, ANGPTL4 expression was inversely correlated with the tumor depth, whereas HIF-1α expression was positively correlated with venous invasion. A survival analysis revealed that the expression of ANGPTL4 was significantly correlated with a longer survival time, whereas that of HIF-1α was correlated with a shorter survival time. In conclusion, the present findings indicate that hypoxia-induced ANGPTL4 expression is independent of HIF-1α in hypoxic gastric cancer cells. ANGPTL4 may be a favorable marker for predicting a long survival time, whereas HIF-1α predicts a poor prognosis, in gastric cancer patients. The hypoxic environment independently induces ANGPTL4 and HIF-1α, which are believed to exhibit adverse effects on tumor progression.

Indexed as

ANGPTL4gastric cancerHIF-1hypoxia

Identifiers

PMID26893686
PMCPMC4734226
OpenAlexW2194457498

What OpenQuestion holds

Textmetadata
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.