LncRNA HCG18 suppresses CD8+ T cells to confer resistance to cetuximab in colorectal cancer via miR-20b-5p/PD-L1 axis.
Yan-Jie XuJie-Min ZhaoXue-Feng NiWei WangWen-Wei HuChang-Ping WuPublished in: Epigenomics (2021)
Aim: We aimed to explore the effect of long noncoding RNA HCG18 in colorectal cancer (CRC). Materials & methods: Relative gene and protein expression were screened. Colony formation and flow cytometry assays were performed to determine proliferation and apoptosis. Dual luciferase and RNA immunoprecipitation assays were conducted to validate the interaction between indicated molecules. Xenograft in nude mice was applied to verify the conclusion in vivo. Results: HCG18 and PD-L1 were upregulated while miR-20b-5p was downregulated in CRC tissue. Functional analysis revealed that lncRNA HCG18 promoted proliferation, migration and resistance to cetuximab of CRC cells via the miR-20b-5p/PD-L1 axis. Conclusion: HCG18 facilitated progress of the tumor, conferred to cetuximab resistance and suppressed CD8+ T cells via the miR-20b-5p/PD-L1 axis.
Keyphrases
- long noncoding rna
- flow cytometry
- signaling pathway
- cell cycle arrest
- wild type
- induced apoptosis
- metastatic colorectal cancer
- locally advanced
- high throughput
- oxidative stress
- cell death
- endoplasmic reticulum stress
- long non coding rna
- squamous cell carcinoma
- genome wide
- type diabetes
- single cell
- metabolic syndrome
- radiation therapy
- insulin resistance
- genome wide identification