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AIM:To study the expression pattern of ETS2(erythroblastosisvirus oncogene homolog 2)in human esophageal squamouscell carcinoma(ESCC).METHODS:Reverse transcription polymerase chain reaction(RT-PCR)and Northern blot were performed to examinethe expression level of ETS2 mRNA in 37 pairs of ESCCtissue samples.Western blot and immunohistochemistrywere carried out to check the expression level of ETS2 proteinin 30 pairs of ESCC tissue specimens.RESULTS:RT-PCR and Northern blot analysis showed thatETS2 mRNA upregulated in 75.7 %(28/37)examined ESCCtissues relative to matched normal tissues.From those 37cases,14 cases were randomly selected to perform Westernblot and the results revealed that ETS2 protein overexpressedin 71.4 %(10/14)checked ESCC tissues compared with thecorresponding normal tissues.Moreover,the expressionpatterns of ETS2 Protein in those 14 cases were identical tothose of ETS2 mRNA displayed by RT-PCR or Northern Blot.Immunohistochemistry analysis showed that the expressionlevel of ETS2 protein rose in 75 %(12/16)tumor epithelialcells contrasted to the normal cells.Altogether the expressionlevel of ETS2 protein increased in 73.3 %(22/30)checkedESCC tissue samples contrary to their normal counterparts.CONCLUSION:The results suggested that ETS2overexpressed in paired human ESCC tissue samples at bothmRNA and protein levels and may be associated with thetumorigenesis of esophagus.
AIM: To study the expression pattern of ETS2 (erythroblastosis virus oncogene homolog 2) in human esophageal squamous cell carcinoma (ESCC). METHODS: Reverse transcription polymerase chain reaction (RT-PCR) and Northern blot were performed to examinethe expression level of ETS2 mRNA in 37 pairs of ESCCtissue samples. Western blot and immunohistochemistry were carried out to check the expression level of ETS2 proteinin 30 pairs of ESCC tissue specimens. RESULTS: RT-PCR and Northern blot analysis showed that PET2 mRNA upregulated in 75.7% (28/37) to matched normal tissues. Of those 37cases, 14 cases were randomly selected to perform Western blot and the results revealed that ETS2 protein overexpressedin 71.4% (10/14) checked ESCC tissues compared with the same responsive normal tissues. Moreover, the expression patterns of ETS2 Protein in those 14 cases were identical tothose of ETS2 mRNA displayed by RT-PCR or Northern Blot. Immunohistochemistry analysis showed that the expressionl evel of ETS2 protein rose in 75% (12/16) tumor epithelial cells contrasted to the normal cells. Altogether the expression Level of ETS2 protein increased in 73.3% (22/30) checkedESCC tissue samples contrary to their normal counterparts.CONCLUSION: The results suggested that ETS2overexpressed in paired human ESCC tissue samples at both mRNA and protein levels and may be associated with the tumorigenesis of esophagus.