Title of article :
SE translocation gene but not zinc finger or X-linked factor is downregulated in gastric cancer
Author/Authors :
Soleimani, Shiva GenIran Lab - Tashkhis Gene Pajohesh - Tehran, Iran , Nasim, Negin GenIran Lab - Tashkhis Gene Pajohesh - Tehran, Iran , Esfandi, Farbod GenIran Lab - Tashkhis Gene Pajohesh - Tehran, Iran , Karimipoor, Morteza Molecular Medicine Department - Biotechnology Research Center - Pasteur Institute of Iran - Tehran, Iran , Kholghi-Oskooei, Vahid Department of Laboratory Sciences - School of Paramedical Sciences - Torbat Heydariyeh University of Medical Sciences - Torbat Heydariyeh, Iran , Naby Gol, Maryam Student Research Committee - Qom University of Medical Sciences - Qom, Iran , Taheri, Mohammad Urogenital Stem Cell Research Center - Shahid Beheshti University of Medical Sickness - Tehran, Iran , Ghafouri-Fard, Soudeh Department of Medical Genetics - Shahid Beheshti University of Medical Sciences - Tehran, Iran
Abstract :
The current study aimed to identify the expression levels of SE Translocation (SET), Zinc Finger, and X-Linked Factor (ZFX)
in gastric cancer tissues and their corresponding adjacent non-cancerous tissues (ANCTs).
Background: SET has been first identified as a component of a fusion protein produced by chromosomal rearrangement in a patient with
acute undifferentiated leukemia. Subsequently, multiple functions have been attributed to this gene in different disorders such as cancer and
Alzheimer’s disease. The expression of SET is regulated by ZFX, a transcription factor which has a potential role in gastric cancer.
Methods: In this case-control study, we evaluated the expression of SET and ZFX in gastric cancer tissues (n=28) and their
corresponding ANCTs (n=28) via quantitative real-time PCR.
Results: SET1 gene was down-regulated in tumoral tissues compared with ANCTs (expression ratio=0.25, P=0.015). However, the
expression of ZFX was similar between tumoral tissues and ANCTs (expression ratio=0.97, P=0.945). We detected a significant
association between the site of primary tumor and SET1 relative expression in tumoral tissues versus ANCTs, where this gene was
down-regulated in all tumors originating from cardia. Based on the area under the receiver operating characteristic curve, the
diagnostic power of transcription levels of SET1 in gastric cancer was 0.68. Finally, we observed remarkable correlations between
expression levels of SET1 and ZFX both in tumoral tissues (R2=0.38, P<0.05) and in ANCTs (R2=0.23, P<0.05).
Conclusion: Overall, our results imply the role of SET1 in gastric cancer and potentially functional associations between this gene
and ZFX in gastric tissues.
Keywords :
Gastric cancer , ZFX , Zinc finger and X-linked factor , SET , SE Translocation
Journal title :
Gastroenterology and Hepatology From Bed to Bench