Lin28 regulates BMP4 and functions with Oct4 to affect ovarian tumor microenvironment
Citations Over TimeTop 11% of 2012 papers
Abstract
Emerging evidence suggests that the tumor microenvironment plays a critical role in regulating cancer stem cells (CSCs) and tumor progression through both autocrine and paracrine signaling. Elevated production of bone morphogenetic proteins (BMPs) from human ovarian cancer cells and stroma has been shown to increase CSC proliferation and tumor growth. Here, we report that Lin28, a stem cell factor, binds to BMP4 mRNA in epithelial ovarian carcinoma cells, thereby promoting BMP4 expression at the post-transcriptional level. As co-expression of Lin28 and Oct4 (another stem cell factor) has been implicated in ovarian cancer CSCs, we also determined that high levels of Lin28 are associated with an unfavorable prognosis when co-expressed with high levels of Oct4. Together, these findings uncover a new level of regulation of BMP4 expression and imply a novel Lin28/Oct4/BMP4-mediated mechanism of regulating ovarian tumor cell growth, thus holding potential for the development of new strategies for the diagnosis and treatment of ovarian cancer.
Related Papers
- → Inhibition of both paracrine and autocrine VEGF/ VEGFR-2 signaling pathways is essential to induce long-term remission of xenotransplanted human leukemias(2001)269 cited
- → Computational model and microfluidic platform for the investigation of paracrine and autocrine signaling in mouse embryonic stem cells(2009)40 cited
- → Renal Autocrine and Paracrine Signaling: A Story of Self-protection(2020)27 cited
- → Autocrine/Paracrine Function of Parathyroid Hormone-Related Peptide in Rat Osteoblast-like Cells(1993)16 cited
- The possible role of IL—1 autocrine and paracrine in mesangial cell(MSc)(1992)