Banner

Thrombophilic genes mutations in women with repeated in-vitro fertilization failure‎

• 2011
Back
Publication Information
Authors ‎5-‎ Naglaa Fathy Al Husseini, Ahmad Y. Rezk 1Mosad M. Odah, Shaymaa M. Abd El ‎Rahman and 1Amal idris.‎
Keywords Not Available
Journal Not Available
Publisher Not Available
Volume Not Available
Issue Not Available
Pages Not Available
publication.type International
Paper Link Not Available
Supplementary Materials Not Available
Abstract
Problem statement: Hepatocellular carcinoma will emerge as a major form of malignancy in the coming ‎decades. The continuing high incidence of hepatocellular carcinoma, suggests that this disease will continue ‎to represent a global health problem far into the future. Different genes encode for the various components ‎of the human telomerase complex. These components include the human Telomerase RNA Component ‎‎(hTERC) and the Telomerase Catalytic Subunit (hTERT). Correlation between Telomerase Reverse ‎Transcriptase (hTERT) expression and telomerase activity has been reported in cancer patients. This work ‎aimed to clarify the significance of human Telomerase Reverse Transcriptase (hTERT mRNA) as a potential ‎molecular tumor marker for Hepatocellular Carcinoma (HCC). Approach: The current study included 25 ‎patients of hepatocellular carcinoma (HCC), 30 patients with liver cirrhosis and 25 age and sex matched ‎individuals with normal laboratory and Image findings as a control group. hTERT mRNA was measured in ‎plasma by Real time PCR in all patients samples in comparison with normal healthy controls. Results: The ‎expression of hTERT mRNA by relative unit was 129.10±27.6 with range (67.72-69.6) Vs 5245.87±2382.48 ‎‎(2053-12232.90) Vs 92782.76±16158 (61783.25-118596.47) for control Vs cirrhosis Vs HCC group ‎respectively. The hTERT expression was significantly with 699 and 33 fold increase in HCC and cirrhosis ‎groups correspondingly when compared to that of controls p<0.05. Conclusion: It was suggested that this ‎procedure was highly discriminating between healthy subjects and cancer patients and strongly support the ‎idea that a valuable diagnostic test for cancer might be developed using this genetic marker in plasma. ‎However it needs to be combined with other markers in future studies to be more specific for liver cancer. ‎