Literature DB >> 27179964

Significance of oncogenes and tumor suppressor genes in AML prognosis.

Maria Kavianpour1, Ahmad Ahmadzadeh1, Saeid Shahrabi2, Najmaldin Saki3.   

Abstract

Acute myeloid leukemia (AML) is a heterogeneous disorder among hematologic malignancies. Several genetic alterations occur in this disease, which cause proliferative progression, reducing differentiation and apoptosis in leukemic cells as well as increasing their survival. In the genetic study of AML, genetic translocations, gene overexpression, and mutations effective upon biology and pathogenesis of this disease have been recognized. Proto-oncogenes and tumor suppressor genes, which are important in normal development of myeloid cells, are involved in the regulation of cell cycle and apoptosis, undergo mutation in this type of leukemia, and are effective in prognosis of AML subtypes. This review deals with these genes, the assessment of which can be important in the diagnosis and prognosis of patients as well as therapeutic outcome.

Entities:  

Keywords:  Acute myeloid leukemia; Oncogenes; Tumor suppressor genes

Mesh:

Substances:

Year:  2016        PMID: 27179964     DOI: 10.1007/s13277-016-5067-1

Source DB:  PubMed          Journal:  Tumour Biol        ISSN: 1010-4283


  133 in total

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6.  Diagnostic value of detecting fusion proteins derived from chromosome translocations in acute leukaemia.

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10.  Mutations in the Wilms' tumor gene WT1 in leukemias.

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Journal:  Blood       Date:  1996-03-15       Impact factor: 22.113

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3.  Targeted sequencing reveals genetic variants associated with sensitivity of 79 human cancer xenografts to anticancer drugs.

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Review 6.  Significance of Inactivated Genes in Leukemia: Pathogenesis and Prognosis.

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7.  Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.

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9.  Profiling and functional analysis of circular RNAs in acute promyelocytic leukemia and their dynamic regulation during all-trans retinoic acid treatment.

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10.  Progress in the correlation between PTPN12 gene expression and human tumors.

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