ABSTRACT
Endometrial carcinoma (EnCa) is one of the deadliest gynecological malignancies. The purpose of the current study was to develop an immune-related lncRNA prognostic signature for EnCa. In the current research, a series of systematic bioinformatics analyses were conducted to develop a novel immune-related lncRNA prognostic signature to predict disease-free survival (DFS) and response to immunotherapy and chemotherapy in EnCa. Based on the newly developed signature, immune status and mutational loading between high and lowrisk groups were also compared. A novel 13-lncRNA signature associated with DFS of EnCa patients was ultimately developed using systematic bioinformatics analyses. The prognostic signature allowed us to distinguish samples with different risks with relatively high accuracy. In addition, univariate and multivariate Cox regression analyses confirmed that the signature was an independent factor for predicting DFS in EnCa. Moreover, a predictive nomogram combined with the risk signature and clinical stage was constructed to accurately predict 1-, 2-, 3-, and 5-year DFS of EnCa patients. Additionally, EnCa patients with different levels of risk had markedly different immune statuses and mutational loadings. Our findings indicate that the immune-related 13-lncRNA signature is a promising classifier for prognosis and response to immunotherapy and chemotherapy for EnCa.
Subject(s)
Endometrial Neoplasms/immunology , RNA, Long Noncoding/immunology , Biomarkers, Tumor/genetics , Disease-Free Survival , Female , Gene Expression Profiling , Humans , PrognosisABSTRACT
BACKGROUND: Endometrial cancer (EC) is one of the most common gynecological malignancies worldwide. However, the molecular mechanisms and the prognostic prediction for EC patients remain unclear. METHODS: In the current study, we performed an in-depth analysis of over 500 patients which were obtained from the Cancer Genome Atlas (TCGA) database. The bioinformatics analysis included gene set enrichment analysis (GSEA) and Cox and lasso regression analyses to ensure overall survival (OS)-related genes, moreover, to construct a prognostic model and a nomogram for EC patients. RESULTS: GSEA identified 4 gene sets significantly associated with EC, which are DNA repair, unfolded protein response, reactive oxygen species pathway and UV response up. Twenty-five OS-related DNA repair genes were screened out, after that, a 9-mRNA signature was constructed to measure the risk scores of patients with different outcomes. In addition, a nomogram contained the 9-mRNA model and clinical parameters was also presented to assess the prognosis. Patients with low risk were more likely to have sensitivity to paclitaxel, vinblastine, rapamycin, metformin, imatinib, Akt inhibitor and lapatinib. CONCLUSIONS: The identified highly enriched gene sets may offer a novel insight into the tumorigenesis and treatment of EC. Additionally, the constructed 9-mRNA model and the nomogram have prominent clinical implications for prognosis evaluation and specific therapy guidance for EC patients.
Subject(s)
Biomarkers, Tumor/genetics , DNA Repair Enzymes/genetics , Endometrial Neoplasms/classification , Endometrial Neoplasms/pathology , RNA, Messenger/genetics , Case-Control Studies , Endometrial Neoplasms/genetics , Female , Follow-Up Studies , Gene Expression Profiling , Humans , Middle Aged , Prognosis , Survival RateABSTRACT
The homogeneous surface-enhanced Raman scattering (SERS) active hot spots on a SERS substrate is the most crucial factor in ensuring their application as reproducible and ultrasensitive sensing platforms. In this paper, we report on a simply shaking-assisted liquidliquid (water-chloroform) interfacial assembly process for fabricating aligned Ag nanowire (AgNW) bilayer films on solid substrates. A scalable fabrication process can be easily realized by using a large size of container. These AgNW bilayer films can be used as ideal SERS active substrates for chemical and biomolecular detection with highly sensitivity and excellent reproducibility. Significantly, sensitive and quantitative detection of carbaryl with a detection limit of 0.1 ppm using these SERS substrates to demonstrate potential applications for environmental pollutant analysis.
ABSTRACT
Au-Fe3O4 hybrid hollow spheres have been successfully synthesized by a one-pot process via the hydrothermal treatment of FeCl3, HAuCl4, citrate, urea, and polyacrylamide (PAM). The amount of Au nanoparticles located in the hybrid hollow spheres can be tuned by changing the molar ratio of Au/Fe precursors. A possible synthetic mechanism of the Au-Fe3O4 hybrid hollow spheres has been proposed. The obtained hybrids exhibit not only a superior surface-enhanced Raman scattering (SERS) sensitivity, but also an excellent catalytic activity. The detection limit of the Au-Fe3O4 hybrid hollow spheres (the Au/Fe molar ratio is 0.2, Au-Fe3O4-0.2) for R6G can reach up to 10(-10) M, which can meet the required concentration level for ultratrace detection of analytes using SERS. Furthermore, the catalytic experiments of the Au-Fe3O4-0.2 hybrid hollow spheres demonstrate that the model of 4-nitrophenol (4-NP) molecules can be degraded within 3 min and the catalytic activity can be recovered without sharp activity loss in six runs, which indicates their superior catalytic degradation activity. The reason may be due to the highly efficient partial charge transfer between Au and Fe3O4 at the nanoscale interface. The results indicate that the bifunctional Au-Fe3O4 hybrid hollow spheres can serve as promising materials in trace detection and industrial waste water treatment.