Evaluation of ATG7 and Light Chain 3 (LC3) Autophagy Genes Expression in AML Patients.

AML ATG7 Acute Myeloid Leukemia Autophagy LC3

Journal

Iranian journal of pharmaceutical research : IJPR
ISSN: 1735-0328
Titre abrégé: Iran J Pharm Res
Pays: Netherlands
ID NLM: 101208407

Informations de publication

Date de publication:
2019
Historique:
entrez: 19 9 2019
pubmed: 19 9 2019
medline: 19 9 2019
Statut: ppublish

Résumé

Autophagy, known as cell death type II, is a housekeeping pathway that currently has been worked on in matters of tumorigenesis and leukomogenesis. Therefore, expression levels of ATG7 and LC3 as two key genes in AML patients are targeted in this study. This study was performed on 55 de novo AML patients against 17 healthy volunteers, acquired samples from bone marrow (BM) and peripheral blood (PB) sources in different ages and gender. The evaluation was executed by mRNA extraction, cDNA synthesis, real-time PCR and data was analyzed by SPSS. Analyzed data indicate a significant decrease between expression of ATG7 and LC3 in AML patients against control (Pv < 0.05). Decrease in both genes expression was detected in most of the patients, 81.81% and 75.55%, respectively. Also LC3 overexpression was detected in 11.33% of AML patients. Moreover, a positive significant correlation between ATG7 and LC3 genes was detected (r = 0.481; Pv = 0.001). This study showed that significant reduction of autophagy genes in de novo AML patients is important to overcome this system and initiate leukomogenesis. It seems a new insight is required for new achievements in diagnosis, prognosis, treatment and monitoring AML patients.

Sections du résumé

BACKGROUND AND AIM OBJECTIVE
Autophagy, known as cell death type II, is a housekeeping pathway that currently has been worked on in matters of tumorigenesis and leukomogenesis. Therefore, expression levels of ATG7 and LC3 as two key genes in AML patients are targeted in this study.
MATERIAL AND METHOD METHODS
This study was performed on 55 de novo AML patients against 17 healthy volunteers, acquired samples from bone marrow (BM) and peripheral blood (PB) sources in different ages and gender. The evaluation was executed by mRNA extraction, cDNA synthesis, real-time PCR and data was analyzed by SPSS.
RESULTS RESULTS
Analyzed data indicate a significant decrease between expression of ATG7 and LC3 in AML patients against control (Pv < 0.05). Decrease in both genes expression was detected in most of the patients, 81.81% and 75.55%, respectively. Also LC3 overexpression was detected in 11.33% of AML patients. Moreover, a positive significant correlation between ATG7 and LC3 genes was detected (r = 0.481; Pv = 0.001).
CONCLUSION CONCLUSIONS
This study showed that significant reduction of autophagy genes in de novo AML patients is important to overcome this system and initiate leukomogenesis. It seems a new insight is required for new achievements in diagnosis, prognosis, treatment and monitoring AML patients.

Identifiants

pubmed: 31531087
doi: 10.22037/ijpr.2019.1100682
pmc: PMC6706741
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1060-1066

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Auteurs

Mohamadreza Mohamadimaram (M)

Laboratory Hematology and blood Banking Department, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mehdi Allahbakhshian Farsani (M)

HSCT Research Center, Laboratory Hematology and blood Banking Department, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Amin Mirzaeian (A)

HSCT Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Shaghayegh Shahsavan (S)

HSCT Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Abbass Hajifathali (A)

HSCT Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Sayeh Parkhihdeh (S)

HSCT Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Mohammad Hossein Mohammadi (MH)

HSCT Research Center, Laboratory Hematology and blood Banking Department, School of Allied Medical Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Classifications MeSH