Evidence map›Paper›PMID 31533855›Full record

ArticleJournal of experimental & clinical cancer research : CR2019

UFM1 suppresses invasive activities of gastric cancer cells by attenuating the expres7sion of PDK1 through PI3K/AKT signaling.

Jian-Xian Lin, Xin-Sheng Xie, Xiong-Feng Weng, Sheng-Liang Qiu, Changhwan Yoon, Ning-Zi Lian, Jian-Wei Xie, Jia-Bin Wang, Jun Lu, Qi-Yue Chen and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 67 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 3 institutions in 2 countries.

Jian-Xian LinDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Xin-Sheng XieDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Xiong-Feng WengDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Sheng-Liang QiuDepartment of Pathology, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Changhwan YoonDepartment of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
Ning-Zi LianDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Jian-Wei XieDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Jia-Bin WangDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Jun LuDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Qi-Yue ChenDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Long-Long CaoDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Mi LinDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Ru-Hong TuDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Ying-Hong YangDepartment of Pathology, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China.
Chang-Ming HuangDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China. hcmlr2002@163.com.
Chao-Hui ZhengDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China. wwkzch@163.com.
Ping LiDepartment of Gastric Surgery, Fujian Medical University Union Hospital, Fuzhou, 350001, Fujian Province, China. pingli811002@163.com.
Fujian Medical University · CNUnion Hospital · CNMemorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Hongbiao Carl Lekaye · 1985 to 2026
$347.4M
Minimally Invasive Medical Center of Fujian Province 2011708National Natural Science Foundation of China 81871899NCI NIH HHS P30 CA008748Science Foundation of the Fujian Province 2018J01307Scientific and Technological Innovation Joint Capital Projects of Fujian Province 2016Y9031Scientific and Technological Innovation Joint Capital Projects of Fujian Province 2018Y9008Startup Fund for Scientific Research 2016QH024the Science Foundation of Fujian Province 2016J01463
6 · The paper itself

Abstract

backgroundUFM1 has been found to be involved in the regulation of tumor development. This study aims to clarify the role and potential molecular mechanisms of UFM1 in the invasion and metastasis of gastric cancer.

methodsExpression of UFM1 in gastric tumor and paired adjacent noncancerous tissues from 437 patients was analyzed by Western blotting, immunohistochemistry, and realtime PCR. Its correlation with the clinicopathological characteristics and prognosis of gastric cancer patients was analyzed. The effects of UFM1 on the invasion and migration of gastric cancer cells were determined by the wound and trans-well assays, and the effect of UFM1 on subcutaneous tumor formation was verified in nude mice. The potential downstream targets of UFM1 and related molecular mechanisms were clarified by the human protein kinase assay and co-immunoprecipitation technique.

resultsCompared with the corresponding adjacent tissues, the transcription level and protein expression level of UFM1 in gastric cancer tissues were significantly downregulated (P < 0.05). The 5-year survival rate of gastric cancer patients with low UFM1 expression was significantly lower than the patients with high UFM1 expression (42.1% vs 63.0%, P < 0.05). The invasion and migration abilities of gastric cancer cells with stable UFM1 overexpression were significantly decreased, and the gastric cancer cells with UFM1 stable knockdown showed the opposite results; similar results were also obtained in the nude mouse model. Further studies have revealed that UFM1 could increase the ubiquitination level of PDK1 and decrease the expression of PDK1 at protein level, thereby inhibiting the phosphorylation level of AKT at Ser473. Additionally, the effect of UFM1 on gastric cancer cell function is dependent on the expression of PDK1. The expression level of UFM1 can improve the poor prognosis of PDK1 in patients with gastric cancer.

conclusionUFM1 suppresses the invasion and metastasis of gastric cancer by increasing the ubiquitination of PDK1 through negatively regulating PI3K/AKT signaling.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsBiomarkers, TumorCell Line, TumorEpithelial-Mesenchymal TransitionFemaleHumansMaleMiceMice, Inbred BALB CMice, NudeMiddle AgedNeoplasm InvasivenessNeoplasm MetastasisPhosphatidylinositol 3-KinasesProteinsAKT1 protein, humanBiomarkers, TumorPDK1 protein, humanPhosphatidylinositol 3-KinasesProteinsProto-Oncogene Proteins c-aktPyruvate Dehydrogenase Acetyl-Transferring KinaseUFM1 protein, humanEMTGastric cancerPDK1UFM1

Identifiers

PMID31533855
PMCPMC6751655
OpenAlexW2974842372

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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.