The intensity of staining was divided into 10 units. Bisulfite sequencing Genomic DNA extracted from ovarian cancer and normal ovarian tissue with a TIANamp Genomic DNA kit (Tiangen Biotech, Beijing, China) was subjected to bisulfite conversion using the EZ DNA Methylation-Direct kit (Zymo Research, Orange, USA) following the manufacturer’s instructions. https://www.selleckchem.com/products/jph203.html The conversion efficiency was estimated to be at least 99.6%. The DNA was then amplified by nested PCR. After gel purification, cloning, and transformation into Escherichia coli Competent Cells JM109 (Takara, Tokyo, Japan), 10 positive clones of each sample were sequenced to ascertain

the methylation patterns of each CpG locus. The following primers were used: round I, 5′-TTGTAGTTTTTTTAAAGAGT-3′ (F) and 5′-TACTACCTTTACCCAAAACAAAA-3′ MK5108 in vivo (R); and round II, 5′-GTAGTTTTTTTAAAGAGTTGTA-3′ (F) and 5′-ACCTTTACCCAAAACAAAAA-3′ (R). The conditions were as follows: 95°C for 2 min, 40 cycles of 30 s at 95°C, 30 s at 56°C, and 45 s at 72°C, then 72°C for 7 min. Statistical analysis The data are presented as mean ± standard deviation (SD). Statistical differences in the data were evaluated by a Student’s t-test or one-way analysis of variance (ANOVA) as appropriate, and were

considered significant at P < 0.05. Results Differences in expression patterns of EGFR in non-mutated and BRCA1- or BRCA2-mutated ovarian cancer Real-time PCR and immunohistochemical analysis showed that the levels of EGFR mRNA and protein were increased in non-mutated 4��8C and BRCA1-mutated ovarian cancer compared with their selleck screening library adjacent normal tissue. It is interesting to note that BRCA1-mutated ovarian cancer showed dramatically increased expression of EGFR compared with the remaining three groups (Figure  1A and B). However, although the levels of EGFR mRNA and protein were increased in non-mutated and BRCA2-mutated ovarian cancer compared with their adjacent normal tissue, there was no significant difference in the expression of EGFR between the non-mutated and BRCA2-mutated groups, including ovarian cancer and normal ovarian tissue (Figure  1C and D). Figure 1 EGFR

expression patterns in non-mutated and BRCA1- or BRCA2-mutated ovarian cancer. A and C, relative EGFR mRNA levels were measured in non-mutated and BRCA1- or BRCA2-mutated ovarian cancer, and their adjacent normal tissue. Bar graphs show mean ± SD. B and D, EGFR protein levels assessed by immunohistochemistry in non-mutated and BRCA1- or BRCA2-mutated ovarian cancer, and their adjacent normal tissue. The intensity of staining was divided into 10 units. Reduced expression of BRCA1 mediated by BRCA1 promoter hypermethylation is inversely correlated with EGFR levels In mammals, promoter methylation is an epigenetic modification involved in regulating gene expression [13]. Consistent with this idea, we showed that ovarian cancer tissue with a hypermethylated BRCA1 promoter (Figure  2B and D, P < 0.05) displayed reduced expression of BRCA1 (Figure  2E, P < 0.