Evidence map›Paper›PMID 27391422›Full record

ArticleThe Journal of pathology2016

Serine-arginine protein kinase 1 promotes a cancer stem cell-like phenotype through activation of Wnt/β-catenin signalling in NSCLC.

Liyun Gong, Junwei Song, Xi Lin, Fakai Wei, Cuicui Zhang, Zimei Wang, Jinrong Zhu, Shu Wu, Yu Chen, Jin Liang and 4 more

Abstract read
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In one paragraph

Article in The Journal of pathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 1 synthesis or guideline pooled it, 65 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Review
  6. NCellular & molecular biology letters · 2024
    Article
  7. Review
  8. SRPKs: a promising therapeutic target in cancer.Clinical and experimental medicine · 2023
    Review
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  11. Review
  12. Article
  13. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 6 institutions in 1 country.

Liyun GongKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
Junwei SongKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
Xi LinState Key Laboratory of Oncology in Southern China, Department of Experimental Research, Cancer Center, Sun Yat-sen University, Guangzhou, China.
Fakai WeiKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
Cuicui ZhangKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
Zimei WangKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
Jinrong ZhuDepartment of Biochemistry, Sun Yat-sen University, Guangzhou, China.
Shu WuState Key Laboratory of Oncology in Southern China, Department of Experimental Research, Cancer Center, Sun Yat-sen University, Guangzhou, China.
Yu ChenKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
Jin LiangKey Laboratory of Translational Medicine of Tumor, Department of Biochemistry and Molecular Biology, Health Science Center, Shenzhen University, Shenzhen, China.
XiaoYuan FuThe Affiliated Hospital of Shenzhen University, Shenzhen, China.
Junqiang LuThe Affiliated Hospital of Shenzhen University, Shenzhen, China.
Chunhui ZhouDepartment of Pathology, College of Health Science, Guangzhou Medical University, Guangzhou, Guangdong, China. 2314970312@qq.com.
Libing SongState Key Laboratory of Oncology in Southern China, Department of Experimental Research, Cancer Center, Sun Yat-sen University, Guangzhou, China. songlb@sysucc.org.cn.
Shenzhen University Health Science Center · CNSun Yat-sen University · CNGuangzhou Medical University · CNShenzhen University · CNSun Yat-sen University Cancer Center · CNUniversity of Hong Kong - Shenzhen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer stem cells (CSCs) are commonly associated with cancer recurrence and metastasis that occurs in up to 30-55% of non-small-cell lung carcinoma (NSCLC) patients. Herein, we showed that serine-arginine protein kinase 1 (SRPK1) was highly expressed at both the mRNA and the protein levels in human NCSLC. SRPK1 was associated with the clinical features of human NSCLC, including clinical stage (p < 0.001) and T (p = 0.001), N (p = 0.007), and M (p = 0.001) classifications. Ectopic overexpression of SRPK1 promoted the acquisition of a stem cell-like phenotype in human NSCLC cell lines cultured in vitro. Overexpression of SRPK1 increased sphere formation and the proportion of side-population cells that exclude Hoechst dye. Conversely, SRPK1 silencing reduced the number of spheres and the proportion of side-population cells. Mouse studies indicated that SRPK1 promoted NSCLC cell line tumour growth and SRPK1 overexpression reduced the number of tumour cells required to initiate tumourigenesis in vivo. Mechanistically, gene set enrichment analysis showed that Wnt/β-catenin signalling correlated with SRPK1 mRNA levels and this signalling pathway was hyperactivated by ectopic SRPK1 expression in NSCLC cell lines. Immunofluorescence demonstrated that SRPK1 enhanced β-catenin accumulation in the nuclei of NSCLC cell lines, and inhibition of β-catenin signalling abrogated the SRPK1-induced stem cell-like phenotype. Together, our findings suggest that SRPK1 promotes a stem cell-like phenotype in NSCLC via Wnt/β-catenin signalling. Moreover, SRPK1 may represent a novel target for human NSCLC diagnosis and therapy. Copyright © 2016 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Indexed as

AnimalsCarcinoma, Non-Small-Cell LungCell Line, TumorCell ProliferationHumansLung NeoplasmsMaleMiceNeoplastic Stem CellsPhenotypeProtein Serine-Threonine KinasesWnt Signaling PathwayProtein Serine-Threonine KinasesSRPK1 protein, humanNSCLCSRPK1stem cell-like phenotypeWnt/β-catenin signalling

Identifiers

PMID27391422
OpenAlexW2478611719

What OpenQuestion holds

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Read underepoch 390

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.