2007Zhongguo pu-wai jichu yu linchuang zazhiRequires access

Detection and Significance of β-Glucuronidase mRNA in Human Liver and Kidney Tissues

Zhou Wen-pin

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Abstract

Objective To establish a new method for detection of β-glucuronidase(β-G) mRNA in human liver and kidney tissues.Methods β-G mRNA expression was detected by reverse transcription polymerase chain reaction(RT-PCR) in 10 cases of normal liver tissues,10 cases of normal kidney tissues and 8 cases of hepatocellular carcinoma tissues.Results The expand products of β-G mRNA were expressed in liver and kidney tissues with similar size of 422 bp.The expression contents of β-G mRNA in liver and kidney normal tissues were different(1.71±0.32 vs 1.83±0.22) but without statistical significance(P0.05).However,the expression content of β-G mRNA in hepatocellular carcinoma tissues was 3.88±0.86,which was significantly higher(P0.01) than that in normal liver tissues.Conclusion β-G mRNA determination is feasible by checking β-G gene alignment in gene bank and designing draw matter in the tissue of liver and kidney.It may be very significant to explore the change of β-G mRNA in various tissues in studying of molecular mechanism.

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Objective To establish a new method for detection of β-glucuronidase(β-G) mRNA in human liver and kidney tissues.Methods β-G mRNA expression was detected by reverse transcription polymerase chain reaction(RT-PCR) in 10 cases of normal liver tissues,10 cases of normal kidney tissues and 8 cases of hepatocellular carcinoma tissues.Results The expand products of β-G mRNA were expressed in liver and kidney tissues with similar size of 422 bp.The expression contents of β-G mRNA in liver and kidney normal tissues were different(1.71±0.32 vs 1.83±0.22) but without statistical significance(P0.05).However,the expression content of β-G mRNA in hepatocellular carcinoma tissues was 3.88±0.86,which was significantly higher(P0.01) than that in normal liver tissues.Conclusion β-G mRNA determination is feasible by checking β-G gene alignment in gene bank and designing draw matter in the tissue of liver and kidney.It may be very significant to explore the change of β-G mRNA in various tissues in studying of molecular mechanism.

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Available abstract

Objective To establish a new method for detection of β-glucuronidase(β-G) mRNA in human liver and kidney tissues.Methods β-G mRNA expression was detected by reverse transcription polymerase chain reaction(RT-PCR) in 10 cases of normal liver tissues,10 cases of normal kidney tissues and 8 cases of hepatocellular carcinoma tissues.Results The expand products of β-G mRNA were expressed in liver and kidney tissues with similar size of 422 bp.The expression contents of β-G mRNA in liver and kidney normal tissues were different(1.71±0.32 vs 1.83±0.22) but without statistical significance(P0.05).However,the expression content of β-G mRNA in hepatocellular carcinoma tissues was 3.88±0.86,which was significantly higher(P0.01) than that in normal liver tissues.Conclusion β-G mRNA determination is feasible by checking β-G gene alignment in gene bank and designing draw matter in the tissue of liver and kidney.It may be very significant to explore the change of β-G mRNA in various tissues in studying of molecular mechanism.

Key concepts: Messenger RNA, Hepatocellular carcinoma, Kidney, Biology, Gene expression, Reverse transcription polymerase chain reaction, Real-time polymerase chain reaction, Gene

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