In this paper, Stokes light induced modulation instability (MI) in high power continuous wave (CW) fiber amplifiers is observed. The investigation shows that the Stokes light generated by inter-modal four wave mixing (IMFWM) and stimulated Raman scattering (SRS) in high power fiber amplifiers can be modulated by the signal light through XPM and cause MI. Then, a sideband will be generated around the second-order Raman frequency shift, which is amplified by SRS and shown as a train of pulses in time domain. It is shown that the frequency shift of the sideband will be influenced by IMFWM and SRS. In addition, the sideband was found to be blue-shifted with the increase of the power, which indicates that the frequency shift of the sideband is mainly depended on MI, while SRS plays the role of amplification.
BackgroundOvarian cancer (OC), one of the most prevalent gynecological malignancies, is characterized by late detection and dismal prognosis. Recent studies show that long non-coding RNAs (lncRNAs) in competitive endogenous RNA (ceRNA) networks influence immune infiltration and cancer prognosis. However, the function of lncRNA in OC immune infiltration and prognosis remains unclear.MethodsTranscriptomes of 378 OC samples and clinical data were retrieved from the TCGA repository. Modules related to immune cells were identified using weighted gene co-expression network analysis (WGCNA). Functional enrichment analysis and survival analysis were then performed for the identification of immune-related lncRNAs in the brown module using Cox regression model. Finally, a ceRNA network was constructed by using the lncRNAs and mRNAs from the brown module.ResultsWe found lncRNAs and mRNAs in the brown module to be significantly associated with immune cells in OC and identified 4 lncRNAs as potential OC prognostic markers. We further established that lncRNAs in the ceRNA network influence OC immune infiltration and prognosis by regulating miRNA, ultimately modulating mRNA levels.ConclusionWe have identified 4 lncRNAs as independent immune prognostic factors for OC. Furthermore, our findings offer novel insight into lncRNAs as OC immune and prognostic biomarkers.
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