Author/Authors :
Nafar, Mohsen Chronic Kidney Disease Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Kalantari, Shiva Chronic Kidney Disease Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Ghaderian, Mohammad Hossein Cellular and Molecular Biology Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Omrani, Mir Davood Urology and Nephrology Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Fallah, Hamid Department of Medical Genetics - Shahid Beheshti University of Medical Sciences, Tehran , Arsang-Jang, Shahram Clinical Research Development Center (CRDU) - Qom University of Medical Sciences , Abbasi, Tahereh Chronic Kidney Disease Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Samavat, Shiva Chronic Kidney Disease Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Dalili, Nooshin Chronic Kidney Disease Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Taheri, Mohammad Urogenital Stem Cell Research Center - Shahid Beheshti University of Medical Sciences, Tehran , Ghafouri-Fard, Soudeh Department of Medical Genetics - Shahid Beheshti University of Medical Sciences, Tehran
Abstract :
Purpose: Long non-coding RNAs (lncRNAs) include a vast portion of human transcripts. They exert regulatory
roles in immune responses and participate in diverse biological functions. Recent studies indicated dysregulation of
lncRNAs in the process of transplant rejection. In the current study, we aimed at identification of the expression of
five lncRNAs (OIP5-AS1, FAS-AS1, TUG1, NEAT1 and PANDAR) in association with the process of transplant
rejection.
Material and Methods: We assessed expression of these lncRNAs in the peripheral blood of 61 kidney transplant
receivers including 29 transplant rejected patients and 32 transplant non-rejected patients using real time PCR
technique.
Results: Expression of FAS-AS1 was significantly higher in rejected group compared to non-rejected group in
males, however, differences between case and control groups were insignificant among females. For other lncRNAs
no significant differences were detected between two study groups. Quantile regression model showed that
patients’ gender was an important parameter in determination of FAS-AS1 expression (Beta = - 9.46, t =- 2.82, P =
0.007) but not for other lncRNAs expressions. Significant pairwise correlations were detected between expression
levels of lncRNAs in a disease related manner.
Conclusion: Based on the higher expression of FAS-AS1 in patients with transplant rejection, this lncRNA might
be associated with the pathogenesis of renal transplant rejection.
Keywords :
kidney transplant , rejection , lncRNA , OIP5-AS1 , FAS-AS1 , TUG1 , NEAT1 , PANDAR