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pmid:31238980

Long noncoding RNA MYOSLID promotes invasion and metastasis by modulating the partial epithelial-mesenchymal transition program in head and neck squamous cell carcinoma.

Hong-Gang Xiong · Hao Li · Yao Xiao · Qi-Chao Yang · Lei-Lei Yang · Lei Chen · Lin-Lin Bu · Wen-Feng Zhang · Jia-Li Zhang · Zhi-Jun Sun

Journal of experimental & clinical cancer research : CR · 2019 doi:10.1186/s13046-019-1254-4

Paper

complete

Experiment

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Data

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Analysis

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Execution

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pmid:31238980
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2026-11-01T15:40:46Z
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title
Long noncoding RNA MYOSLID promotes invasion and metastasis by modulating the partial epithelial-mesenchymal transition program in head and neck squamous cell carcinoma.
doi
10.1186/s13046-019-1254-4
pmid
31238980
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[0]
Hong-Gang Xiong
[1]
Hao Li
[2]
Yao Xiao
[3]
Qi-Chao Yang
[4]
Lei-Lei Yang
[5]
Lei Chen
[6]
Lin-Lin Bu
[7]
Wen-Feng Zhang
[8]
Jia-Li Zhang
[9]
Zhi-Jun Sun
journal
Journal of experimental & clinical cancer research : CR
year
2019
abstract
BACKGROUND: Partial epithelial mesenchymal transition (p-EMT) was found to play a potential role in the initial stage of metastasis in human head and neck squamous cell carcinoma (HNSCC). Some long noncoding RNAs (lncRNAs) have been reported to function as promoters or inhibitors of cancer metastasis. This study aimed to identify p-EMT-related lncRNAs in HNSCC. METHODS: Differentially expressed lncRNAs (DE-lncRNAs) and mRNAs (DEGs) in HNSCC obtained from The Cancer Genome Atlas (TCGA) were screened out by using the "edgeR" package. DE-lncRNAs in the Oral squamous cell carcinoma (OSCC) lncRNA microarray dataset GSE84805 were screened out by using the "limma" package. Slug-related lncRNAs were determined by Pearson correlation analysis (|Pearson correlation coefficient| ≥ 0.4, p < 0.01) based on TCGA. Survival analysis were performed for the overlapping DE-lncRNAs by using the "Survival" package. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were used to predict the potential functions of MYOSLID. RT-qPCR and In Site Hybridization (ISH) were used to explore the MYOSLID expression and its clinical significance in HNSCC specimens. Immunohistochemical staining, siRNA, wound healing assay, transwell assay, and western blot were used to explore the biological function and potential molecular mechanisms. RESULTS: MYOSLID was identified as a Slug-related lncRNA and with prognostic value among the 9 overlapping DE-lncRNAs. GO and KEGG analyses revealed that MYOSLID was closely related to important biological processes and pathways that regulate cancer metastasis. The results of univariate and multivariate Cox regression analysis based on TCGA and HNSCC tissue microarray data suggested MYOSLID was an independent prognostic factor. MYOSLID expression in HNSCC was closely correlated with Slug, PDPN and LAMB3. The knockdown of MYOSLID in OSCC cell line significantly inhibited cell migration and invasion compared to those in the control cells. In addition, the knockdown of MYOSLID significantly reduced Slug, PDPN and LAMB3 expression levels. However, the knockdown of MYOSLID had no effect on the expression levels of the EMT biomarkers E-cadherin and Vimentin. CONCLUSIONS: Our study revealed that MYOSLID expression was closely related to the p-EMT program in HNSCC, and it might be a new predictive biomarker for aggressive HNSCC.
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Differentially expressed mRNAs and lncRNAs were identified in HNSCC tissues in comparison with normal tissue with data obtained from the TCGA database using the “edgeR” package in R. Differentially expressed lncRNAs were identified in HNSCC tissues in comparison with normal tissues from data obtained from GEO with the accession number GSE84805 using the “limma” package in R.
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sections[5] "Identification of DEGs, DE-lncRNAs and the generation of a Venn diagram" paragraph 2
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Differentially expressed mRNAs and lncRNAs were identified in HNSCC tissues in comparison with normal tissue with data obtained from the TCGA database using the “edgeR” package in R. Differentially expressed lncRNAs were identified in HNSCC tissues in comparison with normal tissues from data obtained from GEO with the accession number GSE84805 using the “limma” package in R.
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All the data and materials supporting the conclusions were included in the main paper.
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Relationship between MYOSLID expression and clinicopathological Characteristics of HNSCC patients based on TCGA (n = 499)
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Survival analysis screening and the assessment of the clinical significance of MYOSLID expression in HNSCC based on the TCGA database
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Survival analysis screening and the assessment of the clinical significance of MYOSLID expression in HNSCC based on the TCGA database
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MYOSLID expression and clinicopathological Characteristics of patients with HNSCC(n = 90)
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Evaluation of the clinical significance of MYOSLID expression in a human HNSCC tissue microarray
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MYOSLID expression and clinicopathological Characteristics of patients with HNSCC(n = 90)
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Univariate and multivariate Cox regression analysis for OS in HNSCC patients (n = 90)
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Evaluation of the clinical significance of MYOSLID expression in a human HNSCC tissue microarray
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Univariate and multivariate Cox regression analysis for OS in HNSCC patients (n = 90)
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0.799
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1.146
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0.403–3.252
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0.985
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1.006
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0.523–1.936
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0.705
[5]
1.189
[6]
0.486–2.905
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0.193
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0.641
[3]
0.328–1.253
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0.228
[5]
0.608
[6]
0.271–1.366
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[0]
Stage
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0.265
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1.601
[3]
0.700–3.659
[4]
0.333
[5]
1.575
[6]
0.628–3.950
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[0]
T
[1]
0.059
[2]
1.426
[3]
0.987–2.060
[4]
0.101
[5]
1.469
[6]
0.928–2.324
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[0]
N
[1]
0.002
[2]
2.981
[3]
1.513–5.875
[4]
0.021
[5]
2.353
[6]
1.136–4.877
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section[24]/table-wrap[2]#Tab4
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asset:data:geo:GSE84805 not downloaded
[1]
asset:data:geo:GSE84805 licence not read
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method-1
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differential_expression
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label
Differential expression analysis
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normalise_counts
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differential_expression_fit
[2]
fdr_bh
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[0]
count_matrix_with_condition
evidence object · 3 fields
score
1
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verbatim
quote
Differentially expressed mRNAs and lncRNAs were identified in HNSCC tissues in comparison with normal tissue with data obtained from the TCGA database using the “edgeR” package in R. Differentially expressed lncRNAs were identified in HNSCC tissues in comparison with normal tissues from data obtained from GEO with the accession number GSE84805 using the “limma” package in R.
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group_comparison
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[0]
group_summary
[1]
welch_t
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0.8
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method-3
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survival_analysis
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Survival analysis
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[0]
survival_km
missing_operations array · 0 items
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[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.8
band
high
quote
Kaplan-Meier
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method-4
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survival_analysis
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cox_proportional_hazards
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Survival analysis
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[0]
cox_ph
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parameters object · 0 fields
data_shapes array · 1 item
[0]
time_to_event_with_censoring
evidence object · 3 fields
score
0.7
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Cox regression
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method-5
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survival_analysis
specific
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Survival analysis
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[0]
logrank_test
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time_to_event_with_censoring
evidence object · 3 fields
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0.8
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log-rank
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method-6
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differential_expression
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limma_voom
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Differential expression analysis
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[0]
normalise_counts
[1]
differential_expression_fit
[2]
fdr_bh
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count_matrix_with_condition
evidence object · 3 fields
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0.7
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limma
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method-7
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correlation_analysis
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pearson
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Correlation analysis
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[0]
pearson_r
missing_operations array · 0 items
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data_shapes array · 1 item
[0]
paired_numeric_columns
evidence object · 3 fields
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0.7
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Pearson correlation
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method-8
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network_analysis
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label
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[0]
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evidence object · 3 fields
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0.7
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pathway enrichment
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method-9
family
contingency_analysis
specific
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label
Categorical (contingency table) analysis
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[0]
chi_square_test
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evidence object · 3 fields
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gaps array · 1 item
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method.reader_differs_from_extractor
capability object · 3 fields
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complete
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capability:computational_analysis
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statistical_regression
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gwas
candidate
Automated Assays Laravel application and simulated adapters
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complete
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nothing:replicable_now
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normalise_counts
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differential_expression_fit
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The paper names the method it used and the corpus's method extractor maps it onto the DSL catalogue: edger.
capability object · 4 fields
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capability:computational_analysis
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owned
basis
The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here.
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tier
R1
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[0]
GSE84805
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[0]
GSE84805
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All the data and materials supporting the conclusions were included in the main paper.
basis
The paper names GSE84805 in Gene Expression Omnibus (GEO) and the accession resolves in the repository. No dataset was downloaded and no licence was read.
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source:pmid:31238980
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asset:table:pmid:31238980:3
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extraction_review
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MiniMax-M3.1-Flash
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minimax
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minimax
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single_reader
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extraction
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pmid:31238980
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source:pmid:31238980
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pmid:31238980
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GEO GSE84805
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agent:corpus-assay-engine
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predict the potential functions of MYOSLID. RT-qPCR and In Site Hybridization (ISH) were used to
[1]
edict the potential functions of MYOSLID. RT-qPCR and In Site Hybridization (ISH) were used to
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99e1195c7d6f
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ts clinical significance in HNSCC specimens. Immunohistochemical staining, siRNA, wound healing assay, transw
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ly correlated with Slug, PDPN and LAMB3. The knockdown of MYOSLID in OSCC cell line significantly i
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those in the control cells. In addition, the knockdown of MYOSLID significantly reduced Slug, PDPN
[2]
PN and LAMB3 expression levels. However, the knockdown of MYOSLID had no effect on the expression l
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SCC specimens. Immunohistochemical staining, siRNA, wound healing assay, transwell assay, and w
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of Medicine [21]. Cal27, SCC4 and SCC9 were cultured in DMEM/high glucose with 10% fetal bovine seru
[1]
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Differentially expressed mRNAs and lncRNAs were identified in HNSCC tissues in comparison with normal tissue with data obtained from the TCGA database using the “edgeR” package in R. Differentially expressed lncRNAs were identified in HNSCC tissues in comparison with normal tissues from data obtained from GEO with the accession number GSE84805 using the “limma” package in R.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:31238980", "kind": "science-record", "revision": 8, "content_hash": "sha256:f621e7b02a4be87d13026ac3be37da801d25725043c986ef56c26038d3bdada3", "created_at": "2026-11-01T15:40:46Z", "updated_at": "2026-11-01T22:44:02Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Long noncoding RNA MYOSLID promotes invasion and metastasis by modulating the partial epithelial-mesenchymal transition program in head and neck squamous cell carcinoma.", "doi": "10.1186/s13046-019-1254-4", "pmid": "31238980", "authors": ["Hong-Gang Xiong", "Hao Li", "Yao Xiao", "Qi-Chao Yang", "Lei-Lei Yang", "Lei Chen", "Lin-Lin Bu", "Wen-Feng Zhang", "Jia-Li Zhang", "Zhi-Jun Sun"], "journal": "Journal of experimental & clinical cancer research : CR", "year": 2019, "abstract": "BACKGROUND: Partial epithelial mesenchymal transition (p-EMT) was found to play a potential role in the initial stage of metastasis in human head and neck squamous cell carcinoma (HNSCC). Some long noncoding RNAs (lncRNAs) have been reported to function as promoters or inhibitors of cancer metastasis. This study aimed to identify p-EMT-related lncRNAs in HNSCC.\nMETHODS: Differentially expressed lncRNAs (DE-lncRNAs) and mRNAs (DEGs) in HNSCC obtained from The Cancer Genome Atlas (TCGA) were screened out by using the \"edgeR\" package. DE-lncRNAs in the Oral squamous cell carcinoma (OSCC) lncRNA microarray dataset GSE84805 were screened out by using the \"limma\" package. Slug-related lncRNAs were determined by Pearson correlation analysis (|Pearson correlation coefficient| ≥ 0.4, p < 0.01) based on TCGA. Survival analysis were performed for the overlapping DE-lncRNAs by using the \"Survival\" package. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses were used to predict the potential functions of MYOSLID. RT-qPCR and In Site Hybridization (ISH) were used to explore the MYOSLID expression and its clinical significance in HNSCC specimens. Immunohistochemical staining, siRNA, wound healing assay, transwell assay, and western blot were used to explore the biological function and potential molecular mechanisms.\nRESULTS: MYOSLID was identified as a Slug-related lncRNA and with prognostic value among the 9 overlapping DE-lncRNAs. GO and KEGG analyses revealed that MYOSLID was closely related to important biological processes and pathways that regulate cancer metastasis. The results of univariate and multivariate Cox regression analysis based on TCGA and HNSCC tissue microarray data suggested MYOSLID was an independent prognostic factor. MYOSLID expression in HNSCC was closely correlated with Slug, PDPN and LAMB3. The knockdown of MYOSLID in OSCC cell line significantly inhibited cell migration and invasion compared to those in the control cells. In addition, the knockdown of MYOSLID significantly reduced Slug, PDPN and LAMB3 expression levels. However, the knockdown of MYOSLID had no effect on the expression levels of the EMT biomarkers E-cadherin and Vimentin.\nCONCLUSIONS: Our study revealed that MYOSLID expression was closely related to the p-EMT program in HNSCC, and it might be a new predictive biomarker for aggressive HNSCC.", "claims": [{"id": "claim-method", "statement": "Differentially expressed mRNAs and lncRNAs were identified in HNSCC tissues in comparison with normal tissue with data obtained from the TCGA database using the “edgeR” package in R. 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Differentially expressed lncRNAs were identified in HNSCC tissues in comparison with normal tissues from data obtained from GEO with the accession number GSE84805 using the “limma” package in R."}], "state": "complete"}, {"id": "claim-data-access", "statement": "All the data and materials supporting the conclusions were included in the main paper.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:31238980", "locator": "sections[37] \"notes\" paragraph 1", "quote": "All the data and materials supporting the conclusions were included in the main paper."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "complete", "objective": null, "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:31238980"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "complete", "blocked_on": null, "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE84805"], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": ["data:geo:GSE84805"], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": []}, "data": {"state": "partial", "assets": [{"id": "source:pmid:31238980", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1186/s13046-019-1254-4", "sha256": 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