Evidence map›Paper›PMID 38714554›Full record

ReviewMedical oncology (Northwood, London, England)2024

The role of IGFBP-3 in tumor development and progression: enlightenment for diagnosis and treatment.

Yudi Wang, He Zhang, Xuehua Zhang, Peizheng Mu, Leilei Zhao, Ruomei Qi, Yurui Zhang, Xiao Zhu, Yucui Dong

Abstract readReview
PubMed Publisher
In one paragraph

Review in Medical oncology (Northwood, London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
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

9 authors.

Yudi Wang *Department of Immunology, Binzhou Medical University, Yantai, China.
He Zhang *Department of Immunology, Qiqihar Medical University, Qiqihar, China.
Xuehua Zhang *Department of Precision Biomedical Laboratory, Liaocheng People's Hospital, Liaocheng, China.
Peizheng MuSchool of Computer and Control Engineering, Yantai University, Yantai, China.
Leilei ZhaoDepartment of Immunology, Binzhou Medical University, Yantai, China.
Ruomei QiDepartment of Immunology, Binzhou Medical University, Yantai, China.
Yurui ZhangDepartment of Immunology, Binzhou Medical University, Yantai, China.
Xiao ZhuSchool of Computer and Control Engineering, Yantai University, Yantai, China. xzhu@ytu.edu.cn.
Yucui DongDepartment of Immunology, Binzhou Medical University, Yantai, China. yucuidong@bzmc.edu.cn.

Funding

National Natural Science Foundation of China 61902094National Natural Science Foundation of China 81402054Natural Science Foundation of Shanghai Municipality ZR2021MH036
6 · The paper itself

Abstract

IGFBP-3 is aberrantly expressed in many tumor types, and its serum and tumor tissue levels provide auxiliary information for assessing the degree of tumor malignancy and patient prognosis, making it a potential therapeutic target for human malignancies and conferring it remarkable clinical value for determining patient prognosis. In this review, we provide a comprehensive overview of the aberrant expression, diverse biological effects, and clinical implications of IGFBP-3 in tumors and its role as a potential prognostic marker and therapeutic target for tumors. In addition, we summarize the signaling pathways through which IGFBP-3 exerts its effects. IGFBP-3 comprises an N-terminal, an intermediate region, and a C-terminal structural domain, each exerting different biological effects in several tumor cell types in an IGF-dependent/non-independent manner. IGFBP-3 shares an intricate relationship with the tumor microenvironment, thereby affecting tumor growth. Overall, IGFBP-3 is an essential regulatory factor that mediates tumor occurrence and progression. Gaining deeper insights into the fundamental characteristics of IGFBP-3 and its role in various tumor types will provide new perspectives and allow for the development of novel strategies for cancer diagnosis, treatment, and prognostic evaluation.

Indexed as

Biomarkers, TumorDisease ProgressionInsulin-Like Growth Factor Binding Protein 3NeoplasmsAnimalsHumansPrognosisSignal TransductionTumor MicroenvironmentBiomarkers, TumorIGFBP3 protein, humanInsulin-Like Growth Factor Binding Protein 3IGFBP-3Signaling pathwaysTargeted therapyTumor microenvironmentTumor progression

Identifiers

What OpenQuestion holds

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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.