Evidence map›Paper›PMID 37658049›Full record

ArticleCell death & disease2023

IGF2BP3 promotes the progression of colorectal cancer and mediates cetuximab resistance by stabilizing EGFR mRNA in an m

Li-Jie Chen, Hui-Ye Liu, Zhi-Yuan Xiao, Ting Qiu, Dan Zhang, Ling-Jie Zhang, Fang-Yi Han, Guo-Jun Chen, Xue-Mei Xu, Jiong-Hua Zhu and 4 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 43 citations in OpenAlex.

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  14. World journal of gastroenterology · 2025
    Article
  15. Targeting of the mNature communications · 2025
    Article
  16. Review
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  18. The mMolecular biomedicine · 2025
    Review
  19. 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

14 authors at 2 institutions in 1 country.

Li-Jie Chen *Department of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Hui-Ye Liu *Department of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0001-9893-2241
Zhi-Yuan Xiao *Department of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Ting QiuDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Dan ZhangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.ORCID 0000-0001-5376-0124
Ling-Jie ZhangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Fang-Yi HanDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Guo-Jun ChenDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Xue-Mei XuDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Jiong-Hua ZhuDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Yan-Qing DingDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Shu-Yang WangDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China.
Ya-Ping YeDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China. yeyp1980@126.com.ORCID 0000-0002-2008-6046
Hong-Li JiaoDepartment of Pathology, Nanfang Hospital, Southern Medical University, Guangzhou, China. 25048195@qq.com.ORCID 0000-0003-2554-8868
Key Laboratory of Guangdong Province · CNJinan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin-like growth factor 2 mRNA-binding protein 3 (IGF2BP3), an RNA-binding protein, is associated with tumorigenesis and progression. However, the exact molecular mechanisms of IGF2BP3 in colorectal cancer (CRC) oncogenesis, progression, and drug resistance remain unclear. This study found that IGF2BP3 was upregulated in CRC tissues. Clinically, the elevated IGF2BP3 level is predictive of a poor prognosis. Functionally, IGF2BP3 enhances CRC tumorigenesis and progression both in vitro and in vivo. Mechanistically, IGF2BP3 promotes epidermal growth factor receptor (EGFR) mRNA stability and translation and further activates the EGFR pathway by serving as a reader in an N6-methyladenosine (m

Indexed as

Colorectal NeoplasmsErbB ReceptorsAntibodiesCarcinogenesisCell Transformation, NeoplasticCetuximabHumansRNA-Binding ProteinsRNA, MessengerAntibodiesCetuximabEGFR protein, humanErbB ReceptorsIGF2BP3 protein, humanRNA-Binding ProteinsRNA, Messenger

Identifiers

PMID37658049
PMCPMC10474290
OpenAlexW4386348856

What OpenQuestion holds

Textmetadata
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.