Evidence map›Paper›PMID 31827398›Full record

ArticleCancer cell international2019

SKA1 promotes malignant phenotype and progression of glioma via multiple signaling pathways.

Xizhao Wang, Yu Zeng, Mingfeng Zhou, Xian Zhang, Anqi Xu, Jie Lin, Zhiyong Wu, Cheng Xie, Jie Luo, Shengfeng Ding and 3 more

Abstract read
In one paragraph

Article in Cancer cell international, 2019. 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
–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

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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.

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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

13 authors.

Xizhao Wang *1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Yu Zeng *1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Mingfeng Zhou *1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Xian Zhang1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Anqi Xu1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Jie Lin1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Zhiyong Wu1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Cheng Xie1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Jie Luo1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Shengfeng Ding1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Zhengming Zhan1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Hao Long1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.
Ye Song1Department of Neurosurgery, Nanfang Hospital, Southern Medical University, Guangzhou, 510515 Guangdong People's Republic of China.ORCID 0000-0003-3101-1143

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSpindle and kinetochore associated protein 1 (SKA1) is a protein involved in chromosome congression and mitosis. It has been found to be upregulated and oncogenic in several human cancers. Herein, we investigated the precise role of SKA1 in the progression and malignant phenotype of human glioma.

methodsBioinformatic analysis was carried out based on the RNA-seq data and corresponding clinical data from GEO, TCGA and CGGA databases. Western blot was performed to analyze the expression of SKA1 in clinical samples and signaling pathway proteins in glioma cells, respectively. CCK8 assay, colony forming assay and EdU assay were performed to assess the cell viability. Cell migration and invasion assays were also performed. Moreover, xenograft model was established and the expression of SKA1 was assessed in the xenograft by immunohistochemistry.

resultsSKA1 expression is positively correlated with glioma grade and could be a promising biomarker for GBM. Moreover, overexpression of SKA1 may lead to poor prognosis in glioma. Downregulation of SKA1 attenuated cell viability, migration, and invasion in U251, U87, LN229 and T98 cells. Furthermore, GSEA analysis demonstrated that SKA1 was involved in the cell cycle, EMT pathway as well as Wnt/β-catenin signaling pathway, which were then confirmed with Western blot analysis.

conclusionSKA1 promotes malignant phenotype and progression of glioma via multiple pathways, including cell cycle, EMT, Wnt/β-catenin signaling pathway. Therefore, SKA1 could be a promising therapeutic target for the treatment of human gliomas.

Indexed as

Cell cycleEMTGliomaMalignant phenotypeSKA1Wnt/β-catenin signaling pathway

Identifiers

PMID31827398
PMCPMC6889600

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