Evidence map›Paper›PMID 29720137›Full record

ArticleBMC cancer2018

Upregulation of bone morphogenetic protein 1 is associated with poor prognosis of late-stage gastric Cancer patients.

Yung-Yu Hsieh, Shui-Yi Tung, Hung-Yu Pan, Chih-Wei Yen, Huang-Wei Xu, Yi-Fang Deng, Ying-Jhen Lin, Wan-Ting Hsu, Cheng-Shyong Wu, Chin Li

Abstract read
In one paragraph

Article in BMC cancer, 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
–field-weighted citation impact
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.

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  18. Effects of bone morphogenetic proteins on epithelial repair.Experimental biology and medicine (Maywood, N.J.) · 2021
    Review
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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.

Yung-Yu HsiehDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China.
Shui-Yi TungDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China.
Hung-Yu PanDepartment of Applied Mathematics, National Chiayi University, Chiayi, Taiwan.
Chih-Wei YenDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China.
Huang-Wei XuDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China.
Yi-Fang DengDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China.
Ying-Jhen LinDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China.
Wan-Ting HsuDepartment of Life Science, National Chung Cheng University, 168 University Rd, Minhsiung, Chiayi, 62102, Taiwan, Republic of China.
Cheng-Shyong WuDepartment of Gastroenterology and Hepatology, Chiayi Chang Gung Memorial Hospital, Chiayi, Taiwan, Republic of China. gi0005@cgmh.org.tw.
Chin LiDepartment of Life Science, National Chung Cheng University, 168 University Rd, Minhsiung, Chiayi, 62102, Taiwan, Republic of China. biocl@ccu.edu.tw.

Funding

Chiayi Chang Gung Memorial Hospital CORPG6D0011Chiayi Chang Gung Memorial Hospital CORPG6D0012Chiayi Chang Gung Memorial Hospital CORPG6D0013Chiayi Chang Gung Memorial Hospital CORPG6D0061Chiayi Chang Gung Memorial Hospital CORPG6D0062Chiayi Chang Gung Memorial Hospital CORPG6D0063Chiayi Chang Gung Memorial Hospital CORPG6D0071Chiayi Chang Gung Memorial Hospital CORPG6D0072Chiayi Chang Gung Memorial Hospital CORPG6D0073
6 · The paper itself

Abstract

backgroundGastric cancer is the eighth most common cancer in Taiwan, with a 40% 5-year survival rate. Approximately 40% of patients are refractory to chemotherapy. Currently, the anti-HER2 therapy is the only clinically employed targeted therapy. However, only 7% patients in Taiwan are HER2-positive. Identifying candidate target genes will facilitate the development of adjuvant targeted therapy to increase the efficacy of gastric cancer treatment.

methodsClinical specimens were analyzed by targeted RNA sequencing to assess the expression levels of target genes. Statistical significance of differential expression and correlation between specimens was evaluated. The correlation with patient survival was analyzed as well. In vitro cell mobility was determined using wound-healing and transwell mobility assays.

resultsExpression of BMP1, COL1A1, STAT3, SOX2, FOXA2, and GATA6 was progressively dysregulated through the stages of gastric oncogenesis. The expression profile of these six genes forms an ubiquitously biomarker signature that is sufficient to differentiate cancer from non-cancerous specimens. High expression status of BMP1 correlates with poor long-term survival of late-stage patients. In vitro, suppression of BMP1 inhibits the mobility of the gastric cancer cell lines, indicating a role of BMP1 in metastasis.

conclusionsBMP1 is upregulated in gastric cancer and is correlated with poor patient survival. Suppression of BMP1 reduced gastric cancer mobility in vitro. Our finding suggests that anti-BMP1 therapy will likely augment the efficacy of standard chemotherapy and improve the treatment outcome.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorBone Morphogenetic Protein 1FemaleHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisStomach NeoplasmsUp-RegulationBiomarkers, TumorBMP1 protein, humanBone Morphogenetic Protein 1Bone morphogenetic protein 1Cell mobilityGastric cancer

Identifiers

PMID29720137
PMCPMC5930761

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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.