Evidence map›Paper›PMID 32558212›Full record

ArticleOrthopaedic surgery2020

Identification of Lysosome-Associated Protein Transmembrane-4 as a Novel Therapeutic Target for Osteosarcoma Treatment.

Zhe-Xiang Wang, Meng-Yang Guo, Jing Ren, Gui-Shi Li, Xu-Guo Sun

Open access · goldAbstract read
In one paragraph

Article in Orthopaedic surgery, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.4field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

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  6. KIF11 Is a Promising Therapeutic Target for Thyroid Cancer Treatment.Computational and mathematical methods in medicine · 2022
    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

5 authors at 3 institutions in 1 country.

Zhe-Xiang WangSchool of Medical Laboratory, Tianjin Medical University, Tianjin, China.
Meng-Yang GuoSchool of Medical Laboratory, Tianjin Medical University, Tianjin, China.
Jing RenPrecision Medicine Center, Tianjin Medical University General Hospital, Tianjin, China.
Gui-Shi LiDepartment of Joint Orthopaedics, Yantai Yuhuangding Hospital, Yantai, China.
Xu-Guo SunSchool of Medical Laboratory, Tianjin Medical University, Tianjin, China.ORCID https://orcid.org/0000-0002-8017-5403
Tianjin Medical University · CNTianjin Medical University General Hospital · CNYuhuangding Hospital · CN

Funding

National Natural Science Foundation of China 31600761National Natural Science Foundation of China 61703304Natural Science Foundation of Tianjin 16JCYBJC17800
6 · The paper itself

Abstract

objectiveThe aim of the study is to evaluate the expression of lysosome-associated protein transmembrane-4 (LAPTM4B) in human osteosarcoma tissue samples collected in our hospital, and to explore the possible correlations between the clinical pathological features of osteosarcoma patients and LAPTM4B expression.

methodsImmunohistochemical (IHC) assays were performed to detect the expression levels of LAPTM4B in 62 tissue samples of osteosarcoma tissues and corresponding non-tumor tissues. According to LAPTM4B staining intensity in tumor tissues, osteosarcoma patients were classified into LAPTM4B high expression and low expression groups. In addition, the potential correlations between LAPTM4B expression levels and clinical pathological features were evaluated. In addition, we detected the effects of LAPTM4B on the proliferation and invasion of esteosarcoma cells through colony formation assay and transwell assay, respectively. We further explored the potential effects of LAPTM4B on tumor growth and metastasis using in vivo animal model.

resultsWe revealed that LAPTM4B was highly expressed in human osteosarcoma tissues. We determined the significance between LAPTM4B and clinical features, including the tumor size (P = 0.004*) and the clinical stage (P = 0.035*) of osteosarcoma patients. Our results further demonstrated that ablation of LAPTM4B obviously blocked the proliferation and invasion of osteosarcoma cells in vitro and restrained tumor growth and metastasis in mice.

conclusionWe investigated the potential involvement of LAPTM4B in osteosarcoma progression and confirmed LAPTM4B as a novel therapeutic target for osteosarcoma.

Indexed as

AnimalsBiomarkers, TumorBone NeoplasmsCell Line, TumorDisease ProgressionHumansMembrane ProteinsMiceOncogene ProteinsOsteosarcomaTumor BurdenBiomarkers, TumorLAPTM4B protein, humanMembrane ProteinsOncogene ProteinsInvasionLAPTM4BOsteosarcomaProliferationTherapeutic target

Identifiers

PMID32558212
PMCPMC7454209
OpenAlexW3036612594

What OpenQuestion holds

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LicenceCC BY
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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.