Differential expression of miRNAs in uterine leiomyoma and adjacent myometrium of different races

نویسندگان

  • Zhaojian Liu
  • Haiyang Guo
  • Jingjing Wu
  • Jiri Zavadil
  • Saleena Ghanny
  • Hong Guo
  • Erica Marsh
  • Serdar Bulun
  • Patricia Soteropoulos
  • Jianjun Wei
چکیده

African American (black) women have a higher rate, larger size and worse morbidity of uterine leiomyomata (fibroids) than white women. The racial difference in gene expression may contribute to the high burden of fibroids in black women. Dysregulated miRNAs have been found to be significantly related to tumorigenesis of fibroids, but racial difference of miRNA expression in fibroids and matched myometrial tissue remains largely unknown. Here, we examined the differential miRNA expression in fibroids and myometrial tissue adjacent to a fibroid from black (n=20) and white (n=20) women. Forty-three miRNAs were significantly different in the fibroids from the two groups. Most importantly, we found that Twenty-three miRNAs were significantly different in myometrial tissues of black and white women. We further determined the expression of the five highly dysregulated miRNAs between the two groups by real-time RT-PCR. We confirmed that miRNAs of miR-10a, miR-10b, miR-21, miR-29b and miR-145 were differentially expressed in both fibroid tissue and adjacent myometrium. Our findings suggested that racial differences in miRNA expression in leiomyoma and adjacent myometrial tissue may have an important role in the tumorigenesis of fibroids.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Differential expression of microRNAs in myometrium and leiomyomas and regulation by ovarian steroids

Given the emerging roles of microRNAs (miRNAs) as key regulator of mRNA stability we assessed their expression profile in paired myometrium and leiomyoma, their isolated smooth muscle cells (MSMC and LSMC), a spontaneously transformed leiomyoma smooth muscle cells (T-LSMC) and SK-LMS-1, a leiomyosarcoma cell line using microarray and real time PCR. Based on global normalization of expression va...

متن کامل

بروز مارکر ایمونوهیستوشیمی p16 در بافت طبیعی و تومورال میومتر در 136 بیمار

Normal 0 false false false EN-US X-NONE AR-SA MicrosoftInternetExplorer4 /* Style Definitions */ table.MsoNormalTable {mso-style-name:"Table Normal" mso-tsty...

متن کامل

Human prolyl hydroxylase expression in uterine leiomyoma during the menstrual cycle

BACKGROUND To investigate the role of prolyl hydroxylase (PH), a key enzyme of collagen synthesis, in human uterine leiomyoma, PH expression was determined in the normal uterine myometrium and the leiomyoma tissues during the menstrual cycle. METHODS The tissues were obtained from 40 regularly cycling women (aged 29 to 53 yr) who were undergoing abdominal hysterectomy for symptomatic uterine ...

متن کامل

Quantification of vascular endothelial growth factor-A in leiomyomas and adjacent myometrium.

Although uterine leiomyomas constitute the commonest benign tumour in women, the regulation of their growth is poorly understood. It is believed that angiogenesis, the process by which new capillaries develop from pre-existing blood vessels, may be involved. We therefore investigated the expression of vascular endothelial growth factor-A (VEGF-A), a primary regulator of angiogenesis, in leiomyo...

متن کامل

Genome-Wide DNA Methylation Indicates Silencing of Tumor Suppressor Genes in Uterine Leiomyoma

BACKGROUND Uterine leiomyomas, or fibroids, represent the most common benign tumor of the female reproductive tract. Fibroids become symptomatic in 30% of all women and up to 70% of African American women of reproductive age. Epigenetic dysregulation of individual genes has been demonstrated in leiomyoma cells; however, the in vivo genome-wide distribution of such epigenetic abnormalities remai...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2015