Complexity in regulation of microRNA machinery components in invasive breast carcinoma.

Pathol Oncol Res

Department of Pathology, School of Medicine, Keimyung University, 1095 Dalgubeoldaero, Dalseo-Gu, Daegu, 704-701, South Korea.

Published: July 2014

AI Article Synopsis

  • The study investigates the expression of key microRNA machinery components (Drosha, DGCR8, Dicer, and AGO2) in invasive breast carcinoma (IBC) tissues and their potential implications for cancer progression.
  • Researchers found decreased levels of these components in tumor samples compared to non-cancerous tissues, suggesting a link between their reduced expression and IBC.
  • The findings also reveal that altered levels of DGCR8 and AGO2 are associated with clinical factors like estrogen receptor status and cancer stage, highlighting their potential role in breast cancer diagnostics and treatment strategies.

Article Abstract

Altered expression of microRNA (miRNA) machinery components may play an important role in breast cancer progression. The objective of the current study was to evaluate Drosha, the DiGeorge syndrome critical region gene 8 (DGCR8), Dicer, and Argonaute 2 (AGO2) mRNA expression in invasive breast carcinoma (IBC) and to assess the value of clinical parameters on their expression. By using quantitative real-time PCR, we examined the expression of the four miRNA machinery components in 52 breast tumor tissues which are diagnosed as invasive ductal carcinoma and adjacent non-neoplastic tissues. In the present study, decreased mRNA expression levels of major miRNA machinery components were observed in IBC. The altered mRNA expression levels of DGCR8 and AGO2 are positively correlated with to each other. This study revealed for the first time that expression alterations of DGCR8 are significantly associated with estrogen receptor and Ki-67 status in IBC. Moreover, AGO2 mRNA expression level was significantly correlated with N stage. These results provided evidences that down-regulated the four miRNA machinery components may play an important role in breast pathobiology and that DGCR8 and AGO2 might be associated with important clinical factors.

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Source
http://dx.doi.org/10.1007/s12253-014-9750-5DOI Listing

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