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pmid:37679666

Analysis of myosin genes in HNSCC and identify MYL1 as a specific poor prognostic biomarker, promotes tumor metastasis and correlates with tumor immune infiltration in HNSCC.

Ce Li · Rui Guan · Wenming Li · Dongmin Wei · Shengda Cao · Fen Chang · Qun Wei · Ran Wei · Long Chen · Chenyang Xu · Kainan Wu · Dapeng Lei

BMC cancer · 2023 doi:10.1186/s12885-023-11349-5

Paper

complete

Experiment

complete

Data

partial

Analysis

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Execution

absent

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pmid:37679666
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title
Analysis of myosin genes in HNSCC and identify MYL1 as a specific poor prognostic biomarker, promotes tumor metastasis and correlates with tumor immune infiltration in HNSCC.
doi
10.1186/s12885-023-11349-5
pmid
37679666
authors array · 12 items
[0]
Ce Li
[1]
Rui Guan
[2]
Wenming Li
[3]
Dongmin Wei
[4]
Shengda Cao
[5]
Fen Chang
[6]
Qun Wei
[7]
Ran Wei
[8]
Long Chen
[9]
Chenyang Xu
[10]
Kainan Wu
[11]
Dapeng Lei
journal
BMC cancer
year
2023
abstract
Head neck squamous cell carcinoma (HNSCC) is one of the most common malignant tumors which ranks the sixth incidence in the world. Although treatments for HNSCC have improved significantly in recent years, its recurrence rate and mortality rate remain high. Myosin genes have been studied in a variety of tumors, however its role in HNSCC has not been elucidated. GSE58911 and GSE30784 gene expression profile analysis were performed to detect significantly dys-regulated myosin genes in HNSCC. The Cancer Genome Atlas (TCGA) HNSCC database was used to verify the dys-regulated myosin genes and study the relationship between these genes and prognosis in HNSCC. The results showed that MYL1, MYL2, MYL3, MYH2, and MYH7 were down-regulated, while MYH10 was up-regulated in patients with HNSCC. Interestingly, MYL1, MYL2, MYH1, MYH2, and MYH7 were shown to be unfavorable prognostic markers in HNSCC. It is also worth noting that MYL1 was a specific unfavorable prognostic biomarker in HNSCC. MYL1, MYL2, MYL3, MYH2, MYH7, and MYH10 promoted CD4 + T cells activation in HNSCC. MYL1 was proved to be down-regulated in HNSCC tissues compared to normal tissues at protein levels. MYL1 overexpression had no effect on proliferation, but significantly promoted migration of Fadu cells. MYL1 increased EGF and EGFR protein expression levels. Moreover, there is a positive correlation between MYL1 expression and Tcm CD8 cells, Tcm CD4 + cells, NK cells, Mast cells, NKT cells, Tfh cells and Treg cells in HNSCC. Overall, MYL1 facilitates tumor metastasis and correlates with tumor immune infiltration in HNSCC and these effects may be associated with the EGF/EGFR pathway.
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Gene expression profiles (GSE58911 and GSE30784) analysis was performed to detect significantly up-regulated and down-regulated genes in HNSCC by using R studio 4.1.1 and limma package.
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Gene expression profiles (GSE58911 and GSE30784) analysis was performed to detect significantly up-regulated and down-regulated genes in HNSCC by using R studio 4.1.1 and limma package.
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Overall, MYL1 facilitates tumor metastasis and correlates with tumor immune infiltration in HNSCC and these effects may be associated with the EGF/EGFR pathway.
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Overall, MYL1 facilitates tumor metastasis and correlates with tumor immune infiltration in HNSCC and these effects may be associated with the EGF/EGFR pathway.
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Overall, MYL1 facilitates tumor metastasis and correlates with tumor immune infiltration in HNSCC and these effects may be associated with the EGF/EGFR pathway.
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Gene expression profiling of oral squamous cell carcinoma (OSCC)
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an interactive web server for analyzing the RNA sequencing expression data of 9,736 tumors and 8,587 no
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ion analysis option using data from Clinical Proteomic Tumor Analysis Consortium (CPTAC) and the In
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Gene expression profiles (GSE58911 and GSE30784) analysis was performed to detect significantly up-regulated and down-regulated genes in HNSCC by using R studio 4.1.1 and limma package.
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Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:37679666", "kind": "science-record", "revision": 4, "content_hash": "sha256:556c487f164cfb9b435c4a93e4237a42a1fdc6c715270d801f5a0f705b4805e0", "created_at": "2026-11-01T19:02:28Z", "updated_at": "2026-11-01T22:52:39Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Analysis of myosin genes in HNSCC and identify MYL1 as a specific poor prognostic biomarker, promotes tumor metastasis and correlates with tumor immune infiltration in HNSCC.", "doi": "10.1186/s12885-023-11349-5", "pmid": "37679666", "authors": ["Ce Li", "Rui Guan", "Wenming Li", "Dongmin Wei", "Shengda Cao", "Fen Chang", "Qun Wei", "Ran Wei", "Long Chen", "Chenyang Xu", "Kainan Wu", "Dapeng Lei"], "journal": "BMC cancer", "year": 2023, "abstract": "Head neck squamous cell carcinoma (HNSCC) is one of the most common malignant tumors which ranks the sixth incidence in the world. Although treatments for HNSCC have improved significantly in recent years, its recurrence rate and mortality rate remain high. Myosin genes have been studied in a variety of tumors, however its role in HNSCC has not been elucidated. GSE58911 and GSE30784 gene expression profile analysis were performed to detect significantly dys-regulated myosin genes in HNSCC. The Cancer Genome Atlas (TCGA) HNSCC database was used to verify the dys-regulated myosin genes and study the relationship between these genes and prognosis in HNSCC. The results showed that MYL1, MYL2, MYL3, MYH2, and MYH7 were down-regulated, while MYH10 was up-regulated in patients with HNSCC. Interestingly, MYL1, MYL2, MYH1, MYH2, and MYH7 were shown to be unfavorable prognostic markers in HNSCC. It is also worth noting that MYL1 was a specific unfavorable prognostic biomarker in HNSCC. MYL1, MYL2, MYL3, MYH2, MYH7, and MYH10 promoted CD4 + T cells activation in HNSCC. MYL1 was proved to be down-regulated in HNSCC tissues compared to normal tissues at protein levels. MYL1 overexpression had no effect on proliferation, but significantly promoted migration of Fadu cells. MYL1 increased EGF and EGFR protein expression levels. Moreover, there is a positive correlation between MYL1 expression and Tcm CD8 cells, Tcm CD4 + cells, NK cells, Mast cells, NKT cells, Tfh cells and Treg cells in HNSCC. 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