It is suggested that IFN-γ +874 AA genotype and A allele are risk factors for developing brucellosis infection in Iranian subjects. “
“Citation Morales-Prieto
DM, Schleussner E, Markert UR. Reduction in miR-141 is Induced by Leukemia Inhibitory Factor and Inhibits Proliferation in Choriocarcinoma Cell line JEG-3. Am J Reprod Immunol 2011; 66 (Suppl. 1): 57–62 Starting from the peri-implantation period, leukemia inhibitory factor (LIF) is a major regulator of trophoblast functions. Micro-RNAs (miRNA) are short non-coding RNA sequences, which regulate expression of genes at post-transcriptional level. The influence of LIF on miRNA expression in trophoblastic cells has not yet been analyzed and was focus of this investigation. JEG-3 choriocarcinoma cells have been stimulated with LIF for 1, 2, 4, 6, and 24 hr. The expression of miR-9, miR-141, miR-21, miR-93, GSK2118436 in vivo and let-7g has been analyzed by real-time PCR. Subsequently, miR-141 has been silenced and over-expressed to test its role in the proliferation of JEG-3 cells after 24 and 48 hr. MiR-141 has been significantly downregulated by more than 50% after LIF stimulation, while miR-21 and miR-93 expression has been significantly upregulated. Silencing of miR-141 completely inhibited the proliferation
Palbociclib nmr of JEG-3 cells, while over-expression had no effect. LIF regulates expression of miRNA in trophoblastic ADAMTS5 cells, which may be responsible for several functional effects induced by LIF. Leukemia inhibitory factor (LIF) induces tyrosine phosphorylation of signal transducer and activator of transcription 3 (STAT3) in several trophoblast
and choriocarcinoma cell types and lines (summarized in1). This event triggers several trophoblastic functions, such as migration, invasion or induction and suppression of expression of a variety of genes.2,3 Because functional effects have been observed after several days, it cannot be excluded that parts thereof are secondary or indirectly induced. We argue that micro-RNA (miRNA) may be involved in the regulation of these previously observed LIF-induced functions. For this reason, we have selected a panel of five miRNAs which have been described to influence STAT3 expression or which are known to be expressed on full activation of STAT3. MiRNAs constitute a novel group of regulatory molecules that play a pivotal role in the control of gene expression at post-transcriptional level. The number of miRNAs described thus far arises approximately 1000 (MiRBase V16), which may regulate up to 30% of the human genome.4 The signature of miRNA expression is regulated in a tissue- and developmental stage-specific manner, and thereby, it may be used as a biomarker for the identification of certain physiological or pathological events including malignancies.
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