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Tytuł pozycji:

Survival-associated N 6 -adenosine methyltransferase signatures in lung squamous cell carcinoma and clinical verification.

Tytuł:
Survival-associated N -adenosine methyltransferase signatures in lung squamous cell carcinoma and clinical verification.
Autorzy:
Qu J; Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Science, Jinan, 250117, China.
Wang L; Department of Oncology, Jiujiang University Affiliated Hospital, Jiujiang, 332000, China.
Jiang M; Cancer Precision Medicine Center, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, 266003, China.
Wei Z; Pathology Department, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, 266003, China.
Fu G; Pathology Department, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, 266003, China.
Zhang X; Cancer Precision Medicine Center, The Affiliated Hospital of Qingdao University, Qingdao University, Qingdao, 266003, China. .
Źródło:
BMC cancer [BMC Cancer] 2021 Nov 24; Vol. 21 (1), pp. 1265. Date of Electronic Publication: 2021 Nov 24.
Typ publikacji:
Journal Article
Język:
English
Imprint Name(s):
Original Publication: London : BioMed Central, [2001-
MeSH Terms:
Adenosine/*analogs & derivatives
Carcinoma, Non-Small-Cell Lung/*genetics
Carcinoma, Squamous Cell/*genetics
Lung Neoplasms/*genetics
Methyltransferases/*genetics
Adenine/analogs & derivatives ; Adenine/metabolism ; Adenosine/genetics ; Adenosine/metabolism ; Aged ; Carcinoma, Non-Small-Cell Lung/metabolism ; Carcinoma, Non-Small-Cell Lung/mortality ; Carcinoma, Squamous Cell/metabolism ; Carcinoma, Squamous Cell/mortality ; Databases, Genetic ; Female ; Gene Expression ; Humans ; Immunohistochemistry ; Lung Neoplasms/metabolism ; Lung Neoplasms/mortality ; Male ; Methylation ; Methyltransferases/metabolism ; Middle Aged ; Principal Component Analysis ; Prognosis ; RNA, Messenger/metabolism ; ROC Curve ; Survival Rate ; Time Factors
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Contributed Indexing:
Keywords: Bioinformatic analysis; Epigenetics; Lung squamous cell carcinoma; N6-methyladenine; Prognostic model
Substance Nomenclature:
0 (RNA, Messenger)
103960-10-7 (N(6)-ribosyladenine)
17124-24-2 (N(6)-methoxyadenine)
EC 2.1.1.- (Methyltransferases)
EC 2.1.1.62 (METTL3 protein, human)
JAC85A2161 (Adenine)
K72T3FS567 (Adenosine)
Entry Date(s):
Date Created: 20211124 Date Completed: 20220221 Latest Revision: 20220221
Update Code:
20240105
PubMed Central ID:
PMC8611943
DOI:
10.1186/s12885-021-08939-6
PMID:
34814861
Czasopismo naukowe
Background: N 6 -methyladenine (m 6 A) is the most common modification of mRNA and IncRNA in higher organisms. m 6 A has been confirmed to be related to the formation and progression of tumors and m 6 A-related genes can be used as prognostic biomarkers in a variety of tumors. However, there have been no similar studies on lung squamous cell carcinoma. The main purpose of this study was aimed to explore the differential expression of m 6 A-related genes in lung squamous cell carcinoma tissues and its relationship with patient clinical prognosis.
Methods: We integrated three m 6 A writers that catalyze the methylation of adenine on mRNA molecules. The training set including 501 patients with LUSC was collected from The Cancer Genome Atlas (TCGA) database and the test set including 181 patients with LUSC was collected from the Gene Expression Omnibus (GEO) database. Based on the expression level of the m 6 A methylase gene, we established a tumor subgroup and risk-prognosis model to quantify the risk index and long-term patient prognosis, which were confirmed by principal component analysis (PCA) and receiver operating characteristic (ROC) curve analysis. After lung squamous cell carcinoma tissue specimens were obtained during surgery, immunohistochemistry (IHC) was used to verify the results in vitro.
Results: The results of the study showed that the expression of the three m 6 A methylases in tumor tissues and normal tissues was significantly different (P < 0.05). The survival-prognostic model based on METTL3 gene expression showed better predictive performance (AUC: 0.706). Patients in the high-risk and low-risk groups exhibited significant differences in terms of survival time and 5-year and 10-year survival rates. Immunohistochemistry revealed that patients with high METTL3 expression exhibited a longer survival time than those with low METTL3 expression.
Conclusions: Our study showed that the molecular phenotype based on the expression of METTL3 may be an independent risk factor affecting the prognosis of lung squamous cell carcinoma. These findings not only prove the important role of m 6 A methylase in lung squamous cell carcinoma, but are also expected to provide more accurate prognostic assessment and individualized treatment for patients with lung squamous cell carcinoma.
(© 2021. The Author(s).)
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