Evidence map›Paper›PMID 26029998›Full record

ArticleOncotarget2015

Dragon (repulsive guidance molecule b, RGMb) is a novel gene that promotes colorectal cancer growth.

Ying Shi, Guo-Bin Chen, Xiao-Xiao Huang, Chuan-Xing Xiao, Huan-Huan Wang, Ye-Sen Li, Jin-Fang Zhang, Shao Li, Yin Xia, Jian-Lin Ren and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

17 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  6. TGF-β superfamily co-receptors in cancer.Developmental dynamics : an official publication of the American Association of Anatomists · 2022
    Review
  7. Article
  8. Circular RNA_0001073 (Cell journal · 2021
    Article
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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 4 institutions in 1 country.

Ying ShiDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Guo-Bin ChenDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Xiao-Xiao HuangDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Chuan-Xing XiaoDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Huan-Huan WangDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Ye-Sen LiDepartment of Nuclear Medicine, The First Affiliated Hospital of Xiamen University, Xiamen, Fujian Province, China.
Jin-Fang ZhangSchool of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
Shao LiMOE Key Laboratory of Bioinformatics, Tsinghua University, Beijing, China.
Yin XiaSchool of Biomedical Sciences, Faculty of Medicine, The Chinese University of Hong Kong, Shatin, N.T., Hong Kong, China.
Jian-Lin RenDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Bayasi GulengDepartment of Gastroenterology, Zhongshan Hospital, Xiamen University, Xiamen, Fujian Province, China.
Zhongshan Hospital of Xiamen University · CNChinese University of Hong Kong · CNTsinghua University · CNXiamen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the most commonly diagnosed cancers and a major cause of cancer death. However, the molecular mechanisms underlying CRC initiation, growth and metastasis are poorly understood. Dragon (RGMb), a member of the repulsive guidance molecule (RGM) family, has been recently identified as a co-receptor for bone morphogenetic protein (BMP) signaling, but the role of Dragon in CRC development is undefined. Here, we show that Dragon expression was increased in colon cancer tissues compared to control tissues in CAC mouse model and in human patients. Dragon promoted proliferation of CT26.WT and CMT93 colon cancer cells and accelerated tumor growth in the xenograft mouse model. Dragon's action on colon cancer development was mediated via the BMP4-Smad1/5/8 and Erk1/2 pathways. Therefore, our results have revealed that Dragon is a novel gene that promotes CRC growth through the BMP pathway. Dragon may be exploited as a potential therapeutic target for CRC treatment.

Indexed as

AnimalsCell Adhesion Molecules, NeuronalCell ProliferationColorectal NeoplasmsGene Knockdown TechniquesGPI-Linked ProteinsHumansMiceMice, Inbred BALB CMice, Inbred C57BLNerve Tissue ProteinsSignal TransductionXenograft Model Antitumor AssaysCell Adhesion Molecules, NeuronalGPI-Linked ProteinsNerve Tissue ProteinsRGMB protein, humanRgmb protein, mouseBMPcolorectal cancerdragonErk1/2proliferationSmad1/5/8

Identifiers

PMID26029998
PMCPMC4653024
OpenAlexW1591462558

What OpenQuestion holds

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LicenceCC BY
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.