Evidence map›Paper›PMID 35361764›Full record

ArticleCell death & disease2022

RBMS1 promotes gastric cancer metastasis through autocrine IL-6/JAK2/STAT3 signaling.

Mengyuan Liu, Heming Li, Huijing Zhang, Huan Zhou, Taiwei Jiao, Mingliang Feng, Fangjian Na, Mingjun Sun, Mingfang Zhao, Lei Xue and 1 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 2% 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

57 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

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  12. Role of the RBMS Family in Different Cancers and Research Progress.International journal of medical sciences · 2026
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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

11 authors at 2 institutions in 1 country.

Mengyuan Liu *Department of Gastroenterology, The First Hospital of China Medical University, 110001, Shenyang, China.
Heming Li *Department of Medical Oncology, The First Hospital of China Medical University, 110001, Shenyang, China.ORCID 0000-0002-5702-0147
Huijing ZhangDepartment of Gastroenterology, The First Hospital of China Medical University, 110001, Shenyang, China.
Huan ZhouDepartment of Gastroenterology, The First Hospital of China Medical University, 110001, Shenyang, China.
Taiwei JiaoDepartment of Gastroenterology, The First Hospital of China Medical University, 110001, Shenyang, China.
Mingliang FengDepartment of Gastroenterology, The First Hospital of China Medical University, 110001, Shenyang, China.
Fangjian NaNetwork Information Center, China Medical University, 110122, Shenyang, China.
Mingjun SunDepartment of Gastroenterology, The First Hospital of China Medical University, 110001, Shenyang, China.
Mingfang ZhaoDepartment of Medical Oncology, The First Hospital of China Medical University, 110001, Shenyang, China.
Lei XueDepartment of Oral and Maxillofacial Surgery, School of Stomatology, China Medical University, 110001, Shenyang, China. xuelei4970362@sina.com.
Lu XuDepartment of Medical Oncology, The First Hospital of China Medical University, 110001, Shenyang, China. xulu@cmu.edu.cn.ORCID 0000-0001-7227-2062
First Hospital of China Medical University · CNChina Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metastasis is the most important reason for the poor prognosis of gastric cancer (GC) patients, and the mechanism urgently needs to be clarified. Here, we explored a prognostic model for the estimation of tumor-associated mortality in GC patients and revealed the RNA-binding protein RBMS1 as a candidate promoter gene for GC metastasis by analyzing GOBO and Oncomine high-throughput sequencing datasets for 408 GC patients. Additionally, RBMS1 was observed with overexpression in 85 GC patient clinical specimens by IHC staining and further be verified its role in GC metastasis via inducing EMT process both in in vitro and in vivo experiments. Moreover, we identified that IL-6 was predicted to be one of the most significant upstream cytokines in the RBMS1 overexpression gene set based on the Ingenuity Pathway Analysis (IPA) algorithm. Most importantly, we also revealed that RBMS1 could promote migration and invasion through IL6 transactivation and JAK2/STAT3 downstream signaling pathway activation by influencing histone modification in the promoter regions after binding with the transcription factor MYC in the HGC-27 and SGC-7901 GC cell lines. Hence, we shed light on the potential molecular mechanisms of RBMS1 in the promotion of GC metastasis, which suggests that RBMS1 may be a potential therapeutic target for GC patients.

Indexed as

Interleukin-6Stomach NeoplasmsCell Line, TumorCell MovementDNA-Binding ProteinsGene Expression Regulation, NeoplasticHumansJanus Kinase 2Neoplasm InvasivenessRNA-Binding ProteinsSignal TransductionSTAT3 Transcription FactorDNA-Binding ProteinsInterleukin-6JAK2 protein, humanJanus Kinase 2RBMS1 protein, humanRNA-Binding ProteinsSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID35361764
PMCPMC8971453
OpenAlexW4221006056

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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.