Magic™ Human OX40L (TNFSF4) Stable Cell Line
- Product Category:
- Membrane Protein Stable Cell Lines
- Subcategory:
- Oncology Cell Lines
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Published Data
Fig.1 Significant inhibition of the expression of BCL-XL, the critical factor responsible for the suppression of tumor cell apoptosis, can be achieved through the blocking of TNFSF4/TNFRSF4 signaling.
Subcutaneous co-implantation of lung adenocarcinoma cells (A549 or SPC-A1, with or without TNFRSF4 knockdown) with fibroblasts (HFL-1) that overexpress TNFSF4 was performed in nude mice. The expression of BCL-XL in A549 or SPC-A1 cells was significantly inhibited by TNFRSF4 knockdown. The observed outcomes indicated notable differences, with **p < 0.01, while NC (negative control) and ns (no significance) were also included in the analysis.
Ref: Li, Yan, et al. "Stress-induced upregulation of TNFSF4 in cancer-associated fibroblast facilitates chemoresistance of lung adenocarcinoma through inhibiting apoptosis of tumor cells." Cancer Letters 497 (2021): 212-220.
Pubmed: 33132120
DOI: 10.1016/j.canlet.2020.10.032
Research Highlights
Xu, Sa. et al. "Construction and validation of a immune-related prognostic gene DHRS1 in hepatocellular carcinoma based on bioinformatic analysis." Medicine, 2023.
A member of the short-chain dehydrogenase/reductase superfamily (DHRS1, SDR19C1) has been identified as a potential predictor of hepatocellular carcinoma (HCC). However, the specific role of DHRS1 in HCC immunity remains unclear. A systematic analysis was conducted using transcriptional and clinical data from the Tumor Immune Estimation Resource and cBioPortal databases to investigate the association between DHRS1 and HCC immunity. Through univariate and multivariate Cox analyses, six DHRS1-associated immunomodulators were found to strongly correlate with survival. These findings were validated using an external validation set and a risk score was created to classify patients into high and low risk categories. Further analyses showed a correlation between DHRS1 gene copy numbers or mRNA levels and immune cell infiltration in HCC. A signature based on these six DHRS1-related immunomodulators was generated and it was found to be an independent indicator of HCC prognosis, with a high predictive accuracy. External validation sets further confirmed the validity of this risk score. In addition, a prognostic nomogram and calibration curve were constructed to predict HCC outcomes. The results suggest that the DHRS1 gene may play a role in regulating HCC immunity and the identified immune signature could be a promising prognostic biomarker for HCC.
Xu, Sa. et al. "Construction and validation of a immune-related prognostic gene DHRS1 in hepatocellular carcinoma based on bioinformatic analysis." Medicine, 2023.
Pubmed:
37861541
DOI:
10.1097/MD.0000000000035268
Yang, Mingyi. et al. "Ferroptosis-related lncRNAs guiding osteosarcoma prognosis and immune microenvironment." Journal of orthopaedic surgery and research, 2023.
This study aims to explore the role of ferroptosis-related long non-coding RNAs (FRLncs) in the prognosis and immune microenvironment of osteosarcoma (OS). A foundational framework will be established to aid in making clinical decisions for OS management.
Yang, Mingyi. et al. "Ferroptosis-related lncRNAs guiding osteosarcoma prognosis and immune microenvironment." Journal of orthopaedic surgery and research, 2023.
Pubmed:
37858131
DOI:
10.1186/s13018-023-04286-3