PHF19 Gene Expression and EZH2 Gene Deletion as Potential Biomarkers of Acute Myeloid Leukemia

Acute Myeloid Leukemia (AML) is a heterogeneous clonal disorder characterized by immature myeloid cell proliferation and bone marrow failure. Diagnosis of AML is based on morphological diagnosis with proliferation of blast cells ≥ 20% of bone marrow cells, flow cytometric analysis and cytogenetic abnormalities.

The etiological agent and pathogenesis of AML are not entirely clear, only few AML cases can be accurately classified through traditional cellular morphological classification Thus, it is very difficult to judge the disease condition and predict prognosis. Improper expression of specific genes is a common finding in AML and may induce clinically relevant biological subsets. Cytogenetic abnormalities and molecular alterations provide the most powerful prognostic information in AML. Consequently, identification of novel biomarkers which could predict outcome or guide treatment choice will make more contribution to the clinical management of AML.

Gene repression is the deactivation of an active gene that causes shut down of transcription and it represents a powerful tool in controlling gene expression in order to prevent the metabolic dysregulation during the development or the differentiation program Polycomb repressive complex 2 (PRC2) is the sole enzymatic complex capable of establishing gene-repression through high-degree methylation of histone H3 at lysine 27 (H3K27), therefore it plays critical roles in regulation of normal hematopoiesis. Enhancer of Zeste Homolog 2 (EZH2) gene is the catalytic subunit of PRC2, located on chromosome 7q36.1. EZH2 gene encode EZH2 methyltransferase which mediates transcriptional inactivation through trimethylation of lysine 27 of histone H3 (H3K27me3). Methylation activity of EZH2 facilitate heterochromatin formation thereby silences gene function which is important for development, differentiation, and cell fate determination.

Accumulating studies have proved that EZH2 dysregulation is involved in human cancers. EZH2 may have a dual role in cancer development, acting as a tumour suppressor or an oncogene depending on the type of cancer. Overexpression of EZH2 was observed in numerous solid tumours, and targeting EZH2 can cause regression of carcinogenesis.

EZH2 inactivation medicated by mutation or under-expression in myelo-dysplastic syndromes (MDS) or myeloproliferative neoplasms (MPN) can contribute to disease pathogenesis and is associated with a poor prognosis. In AML, EZH2 dysregulation caused by mutation and under-expression may act as potential biomarkers predicting prognosis and guiding the treatment choice between transplantation and chemotherapy. EZH2 was found to have tumor suppressive and oncogenic functions in different phases of AML.