Dihydropyrimidine dehydrogenase in normal and malignant endometrium: relationship with cell proliferation and thymidine phosphorylase
Dihydropyrimidine dehydrogenase in normal and malignant endometrium: relationship with cell proliferation and thymidine phosphorylase
复制标题
正常和恶性子宫内膜中的二氢嘧啶脱氢酶:与细胞增殖和胸苷磷酸化酶的关系
作者:
R. Fujiwaki;K. Iida;K. Nakayama;H. Kanasaki;T. Ozaki;K. Hata;E. Sakai;K. Miyazaki
Dihydropyrimidine dehydrogenase (DPD) is a pyrimidine salvage enzyme responsible for degradation of thymine, which is produced from thymidine by thymidine phosphorylase (TP). Our purpose was to determine the relationship between DPD, cell proliferation and TP expression in human endometrium. We examined DPD gene expression using reverse transcription-polymerase chain reaction, DPD protein levels using enzyme-linked immunosorbent assay, and DPD protein localization using immunohistochemistry in 58 normal endometria and 28 endometrial cancers. DPD gene expression was then related to the proliferating cell nuclear antigen index and to TP gene expression. DPD gene expression, which was correlated with DPD protein level, was relatively stable throughout various menstrual phases but was significantly elevated in postmenopausal status. It was significantly lower in endometrial cancer than in normal endometrium. Localization analysis revealed that DPD protein was located primarily in epithelial cells, but was also present in stromal cells. DPD gene expression correlated inversely with the PCNA index. TP gene expression pattern contrasted with that of DPD in postmenopausal and malignant endometrium. A high ratio of TP to DPD gene expression was significantly more frequent in endometrial cancer than in normal endometrium in any menstrual phase. DPD may act cooperatively with TP to affect cell function by maintaining the pyrimidine nucleotide pool balance in normal and malignant endometrium.
影响因子:
2
作者:
Ho,DH;Townsend,L;Luna,MA;Bodey,GP
通讯作者:
Bodey,GP
影响因子:
11.2
作者:
Naguib,FN;elKouni,MH;Cha,S
通讯作者:
Cha,S
影响因子:
2.9
作者:
ILTZSCH, MH;ELKOUNI, MH;CHA, S
通讯作者:
CHA, S