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Xiao Zhang
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P2.04 - Immuno-oncology (ID 167)
- Event: WCLC 2019
- Type: Poster Viewing in the Exhibit Hall
- Track: Immuno-oncology
- Presentations: 1
- Moderators:
- Coordinates: 9/09/2019, 10:15 - 18:15, Exhibit Hall
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P2.04-43 - High Occurrence of LINE-1 Retrotransposition Is Correlated with Smoking History, Local Immunosuppression and Poor Prognosis in LUSC (ID 773)
10:15 - 18:15 | Author(s): Xiao Zhang
- Abstract
Background
Somatic Long Interspersed element-1 (LINE-1) retrotransposition (RT) is a genomic process that relates to gene disruption and tumor occurrence. However, the expression and function of LINE-1 RT in lung squamous cell carcinoma (LUSC) remains unclear.
Method
We analyzed the transcriptomes of paired LUSC samples in The Cancer Genome Atlas (TCGA), to characterize the most common somatic LINE-1 RTs in LUSC, followed by validation in an independent Chinese LUSC cohort and several cancer cell lines. We also analyzed the association between these LINE-1 RTs and clinico-pathology features, as well as the immunocyte content in local LUSC tumor tissues.
Result
We observed LINE-1 RT occurred within 90% of tumor samples in TCGA, among which thirteen LINE-1 RTs were filtered for high occurrence in LUSC. In Chinese cohort, the expression of 13 LINE-1 RTs in LUSC tissues was significantly higher than those in matched adjacent normal tissues. Furthermore, 11 of 13 LINE-1 RTs were exclusively detected in LUSC cell lines rather than normal lung epithelial cells. Further analysis showed 3 LINE-1 RTs, including L1-FGGY, L1-ATP8B1 and L1-SVEP1 were correlated with smoking history, large tumor size, central tumor location, and poorer prognosis. The immunohistochemical staining (IHC) analysis showed that less CD3+ T cells, more CD68+ macrophages and CD33+ myeloid-derived suppressive cells (MDSCs) were detected in LINE-1 RT positive tissues which implied that LINE-1 RT might induce significant immunosuppression in situ.
Conclusion
In conclusion, LINE-1 RT is a frequent genomic event that correlates with smoking-related LUSC development and LUSC immune evasion which might be a promising predictive biomarker of poor prognosis in LUSC.