The clinical and prognostic significance of FOXN3 downregulation in acute myeloid leukaemia
Autor: | Yue Wang, Yan Li, Rui Zhang, Jinjing Zhang, Wenbin Mo |
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Rok vydání: | 2019 |
Předmět: |
Oncology
Adult Male medicine.medical_specialty Multivariate analysis Adolescent diagnosis Clinical Biochemistry chemotherapy response FOXN3 Down-Regulation Cell Cycle Proteins 030204 cardiovascular system & hematology Disease-Free Survival 03 medical and health sciences 0302 clinical medicine Downregulation and upregulation Internal medicine White blood cell hemic and lymphatic diseases medicine Humans Clinical significance acute myeloid leukaemia Aged Aged 80 and over business.industry Gene Expression Regulation Leukemic Biochemistry (medical) Complete remission Forkhead Transcription Factors Hematology General Medicine Original Articles Middle Aged Neoplasm Proteins Survival Rate Leukemia Myeloid Acute medicine.anatomical_structure Biomarker (medicine) Female Original Article prognosis Myeloid leukaemia business Chemotherapy response 030215 immunology Follow-Up Studies |
Zdroj: | International Journal of Laboratory Hematology |
ISSN: | 1751-553X |
Popis: | Introduction The expression of forkhead box N3 (FOXN3), also known as checkpoint suppressor 1 (CHES1), is reduced in many types of tumours. However, the clinical significance of FOXN3 and its potential role in acute myeloid leukaemia (AML) remain largely unknown. Methods A total of 117 de novo AML patients newly diagnosed between December 2015 and January 2018 were included in this study. The expression of FOXN3 and its clinical significance were analysed in these AML patients. Results The expression of FOXN3 was significantly downregulated in AML. In addition, lower FOXN3 expression was associated with older age and higher white blood cell counts. Moreover, a close correlation was observed between lower FOXN3 expression and a lower complete remission (CR) rate and shorter overall survival (OS), which was further analysed by multivariate analysis. Conclusion These data suggest that FOXN3 is a novel biomarker in AML and that lower FOXN3 expression predicts poor chemotherapy response and prognosis in AML. |
Databáze: | OpenAIRE |
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