Abstract

Objective To observe the expressions of DNA methyltransferases (DNMTs) 1,3a and 3b in retinoblastoma (RB).Methods Sixty-two RB samples and six normal retinas were studied,including 17 poorly differentiated and 45 well differentiated samples; 16 invasive and 46 non-invasive samples.The expressions of DNMT1,3a,and 3b,and Ki-67 were detected using immunohistochemical analysis.Brown staining of nuclei was considered to represent the positive stain for DNMT1,3a and 3b,and ki-67,blue staining as negative.The level of high expression of nuclear staining was,positive cells in DNMT1≥65 %,in DNMT3a≥60% and in DNMT3b≥40%.The correlations of DNMT1,3a and 3b expression in RB samples,and MIB-1 labeling index were analyzed.Results Viewed under the light microscope,negative expressions of DNMT1,3a and 3b were demonstrated in normal retinas,however,positive expression was observed in RB samples,with 100% in DNMT1,98% in DNMT3a and 92% in DNMT3b.Comparing well differentiated RB samples with poorly differentiated samples,significant differences were found in high expression of DNMT1 (x2 =12.57,P<0.05) and DNMT3a (x2 =10.54,P<0.05) ; also in the positive cells of DNMT1 (U=179,P<0.05) and DNMT3a (U=198,P<0.05).No significant difference was found comparing high expression (x2=1.5,P>0.05) and positive cells (U=307,P>0.05) of DNMT3b.When comparing invasive tumor tissues with non-invasive tumors,significant differences were shown between high expression (x2 =4.72,P<0.05) and positive cells comparing DNMT1 (U=236,P<0.05).No significant difference was shown in high expression (x2=3.53,0.84; P>0.05) in DNMT3a and DNMT3b,or in comparison with positive cells (U=338,257; P>0.05).The expression of DNMTs was positively correlated with the MIB-1 labeling index in RB tissues (R2=0.554,0.376,0.219; P<0.05).Conclusion There are high expressions of DNMT1,3a,and 3b in RB. Key words: Retinoblastoma/enzymology; DNA modification methylases; Tumor makers,biological

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call