[Home ] [Archive]   [ فارسی ]  
:: Main :: About :: Current Issue :: Archive :: Search :: Submit :: Contact ::
Main Menu
Home::
Journal Information::
Editorial Board::
Executive Members::
Instruction to Authors::
Peer Review::
Articles Archive::
Indexing Databases::
Contact Us::
Site Facilities::
::
Search in website

Advanced Search
Receive site information
Enter your Email in the following box to receive the site news and information.
:: Volume 16, Issue 4 (12-2014) ::
J Gorgan Univ Med Sci 2014, 16(4): 80-86 Back to browse issues page
NPM1 and FLT3-(ITD) Gene mutations and laboratory findings in patients with acute myeloid leukemia in Northwest of Iran
Sanaat Z1 , Shams K2 , Nejati B2 , Movasghpour AK2 , Imani V3 , Moghadaszadeh M * 4
1- Associate Professor, Hematology Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
2- Assistant Professor, Hematology Oncology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
3- Resident in Pediatrics, Tabriz University of Medical Sciences, Tabriz, Iran
4- Internist, Department of Internal Medicine, Imam Reza Hospital, Tabriz University of Medical Sciences, Tabriz, Iran , m_moghadaszadeh@hotmail.com
Abstract:   (11962 Views)
Background and Objective: The acute myeloid leukemia (AML) is a malignant disease with an accumulation of the abnormal and undifferentiated blastic myeloid cell in the bone marrow, leading to abnormal hematopoiesis. This study was done to determine the NPM1 and FLT3-(ITD) mutations and laboratory findings in patients with acute myeloid leukemia. Methods: This descriptive-analytic study was carried out on 40 (24 males, 16 females) patients with newly acute myeloid leukemia in Northwest of Iran. The mutation of NPM1 and FLT3-ITD were evaluated using PCR method in 25 patients. In all patients, the flowcytometry findings in the bone marrow, leucocytosis and the LDH levels were evaluated prior to the chemotherapy. Results: The mutation of FLT3-ITD and NPM1 genes was detected in 15 (60%) and 9 (36%) of patients, respectively. FLT3-NPM1+ mutation was seen in 4 (16%) patients. Leukocytosis, LDH level and AML in different classes did no show any significant difference between FLT3-NPM1+ and other gene mutations. Conclusion: The mutation of FLT3-ITD gene was nearly twice than NPM1 in acute myeloid leukemia.
Keywords: Acute myeloid leukemia, NPM1 gene, FLT3-ITD gene, Leukocytosis
Full-Text [PDF 277 kb] [English Abstract]   (17345 Downloads)    
Type of Study: Original Articles | Subject: Oncology
Send email to the article author


XML   Persian Abstract   Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Sanaat Z, Shams K, Nejati B, Movasghpour AK, Imani V, Moghadaszadeh M. NPM1 and FLT3-(ITD) Gene mutations and laboratory findings in patients with acute myeloid leukemia in Northwest of Iran. J Gorgan Univ Med Sci 2014; 16 (4) :80-86
URL: http://goums.ac.ir/journal/article-1-2192-en.html


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
Volume 16, Issue 4 (12-2014) Back to browse issues page
مجله دانشگاه علوم پزشکی گرگان Journal of Gorgan University of Medical Sciences
Persian site map - English site map - Created in 0.04 seconds with 36 queries by YEKTAWEB 4660
Creative Commons License
This work is licensed under a Creative Commons — Attribution-NonCommercial 4.0 International (CC BY-NC 4.0)