Evidence map›Paper›PMID 34786330›Full record

ArticleJournal of bone oncology2021

BAIAP2L2 promotes the proliferation, migration and invasion of osteosarcoma associated with the Wnt/β-catenin pathway.

Hongting Guo, Jing Peng, Juan Hu, Shichuan Chang, Huawen Liu, Hao Luo, Xiaohua Chen, Haiping Tang, Youhao Chen

Open access · goldAbstract read
In one paragraph

Article in Journal of bone oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 24 citations in OpenAlex.

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  9. Caudatin Inhibits the Proliferation, Invasion, and Glycolysis of Osteosarcoma Cells via the Wnt/Evidence-based complementary and alternative medicine : eCAM · 2022
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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

9 authors.

Hongting GuoOncologe Department, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Jing PengBlood Transfusion Department, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Juan HuDepartment of Anesthesiology, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Shichuan ChangOncologe Department, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Huawen LiuOncologe Department, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Hao LuoDepartment of Orthopaedics, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Xiaohua ChenDepartment of Orthopaedics, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Haiping TangBlood Transfusion Department, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.
Youhao ChenDepartment of Orthopaedics, Chong Qing University Three Gorges Hospital, Chongqing City 404100, PR China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOsteosarcoma is the most common bone cancer that significantly affects the quality of life of patients. Studies have shown that overexpression of BAIAP2L2 elevates the proliferation and growth of some types of cancer cells. However, the role of BAIAP2L2 in osteosarcoma is unclear. This study aimed to investigate the functions of BAIAP2L2 in the development of osteosarcoma.

methodsWe used immunohistochemical and Western blot analysis to determine the expression levels of endogenic BAIAP2L2 in osteosarcoma cells. Cell counting kit-8 assay and colony formation assay were performed to investigate cell proliferation of tumor cells. Transwell assay was performed to detect cell migration. Flow cytometry assay was used to analyze cell apoptosis. The role of BAIAP2L2 in tumor growth was further explored

resultsWe found that BAIAP2L2 was significantly upregulated in human osteosarcoma, and inhibition of BAIAP2L2 suppressed the proliferation of osteosarcoma cells. In addition, down-regulation of BAIAP2L2 could lead to osteosarcoma cancer cell apoptosis, inhibit cell migration and invasion, and induce the inactivation of the Wnt/β-catenin pathway. In addition, down-regulation of BAIAP2L2 inhibited tumor growth

conclusionIn conclusion, down-regulation of BAIAP2L2 inhibited the proliferation, migration, and invasion of osteosarcoma associated with the Wnt/β-catenin pathway.

Indexed as

BAIAP2L2Combinational roleOsteosarcomaWnt/β-catenin pathway

Identifiers

PMID34786330
PMCPMC8577457
OpenAlexW3206860510

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.