o 7th INTERNATİONAL CONGRESS OF THE MOLECULAR BİOLOGY, İstanbul, Türkiye, 27 - 29 Eylül 2019, cilt.5, sa.43, ss.53
Aim: Apoptosis is a programmed cell death, a physiological event that regulates the homeostasis of the organism by the destruction of unnecessary/damaged cells without an inflammatory response. The BID (BH3 Interacting Domain Death Agonist) protein, encoded by the BID gene, is a member of the BCL2 family that regulates apoptosis by activating the mitochondrial death pathway via Caspase 8, allowing cytochrome C to be released. In the literature, increased expression levels of BID gene have been observed in glioma, lymphoma, colon, prostate and cervical cancers; while in Hepatitis B Virus (HBV) infected hepatocellular carcinoma, its decreased expression levels have been reported. In our study (I.U.BAP-ONAP-42152), we aimed to investigate the differentially expressed levels of BID gene in Turkish larynx cancer patients and to reveal the clinical significance.
Methods: The expression status of BID was analyzed in tumor and matched-normal tissue samples of 50 larynx cancer patients using LightCycler 480 by the quantitative real-time polymerase chain reaction method. The results were compared with clinicopathological data.
Results: BID and the reference gene expression status were analyzed by calculating the threshold cycle numbers (Ct) as fold changes using the 2-ΔΔCt method. After evaluation of the expression levels, we selected the ratio of >=2 as the threshold for the differentially expressed BID. The increased expression levels of BID were observed in 46% (23/50) of tumor samples compared with matched normal tissue, whereas the expression levels were decreased in 28% (14/50) of patients. The statistical significanceswere observed between the increased expression levels of BIDwith recurrence (p=0.024) and anatomical region (p=0.018).
Conclusion: The increase in the expression level of the BID gene is thought to be associated with the development and recurrence of larynx cancer.
Keywords: Larynx cancer, expression, BID gene