|Table of Contents|

Expression and clinical significance of Myo1E in pancreatic ductal adenocarcinoma tissues

Journal Of Modern Oncology[ISSN:1672-4992/CN:61-1415/R]

Issue:
2024 22
Page:
4323-4328
Research Field:
Publishing date:

Info

Title:
Expression and clinical significance of Myo1E in pancreatic ductal adenocarcinoma tissues
Author(s):
ZHU Xiaojing1SHI Jiawen2GUO Wenwen1WANG Yan1
1.Department of Pathology,the Second Affiliated Hospital of Nanjing Medical University,Jiangsu Nanjing 210009,China;2.Pathology Teaching and Research Unit,School of Medicine,Nantong University & Department of Clinical Biobank,Nantong University Affiliated Hospital,Jiangsu Nantong 226001,China.
Keywords:
pancreatic ductal adenocarcinomaMyo1EPD-L1prognosis
PACS:
R735.9
DOI:
10.3969/j.issn.1672-4992.2024.22.017
Abstract:
Objective:Analysis of the expression and clinical significance of myosin 1E (Myo1E) in pancreatic ductal adenocarcinoma (PDAC) tissues.Methods:The expression level of Myo1E mRNA in PDAC tissues and its relationship with prognosis and immune checkpoints were analyzed using the next-generation sequencing data of PDAC in the online cancer genome mapping database,and the clinical significance of Myo1E protein expression and its correlation with the immune checkpoint PD-L1 were analyzed by immunohistochemistry staining using PDAC microarray.Results:The expression of Myo1E mRNA and protein in PDAC tissues was significantly higher than that in benign pancreatic tissues,and was related to the poor prognosis of patients.Myo1E protein expression was associated with tumor diameter (P=0.004),lymph node metastasis (P<0.001),invasion of surrounding tissues (P=0.008),clinical stage (P<0.001).Survival analysis showed that Myo1E protein was expressed in PDAC tissues and was an independent risk factor for patient prognosis (HR:1.686,P=0.010),and was linearly positively correlated with the expression of PD-L1 (r=0.388,P<0.001).Conclusion:Myo1E is an independent risk factor for patient prognosis in PDAC tissues and may be a potential target for immunotherapy.

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