Prescreening of tumor samples for tumor-centric transcriptome analyses of lung adenocarcinoma

BMC cancer(2022)

引用 0|浏览6
暂无评分
摘要
Background Single-cell RNA sequencing (scRNA-seq) enables the systemic assessment of intratumoral heterogeneity within tumor cell populations and in diverse stromal cells of the tumor microenvironment. Gain of treatment resistance during tumor progression or drug treatment are important subjects of tumor-centric scRNA-seq analyses, which are hampered by scarce tumor cell portions. To guarantee the inclusion of tumor cells in the data analysis, we developed a prescreening strategy for lung adenocarcinoma. Methods We obtained candidate genes that were differentially expressed between normal and tumor cells, excluding stromal cells, from the scRNA-seq data. Tumor cell-specific expression of the candidate genes was assessed via real-time reverse transcription-polymerase chain reaction (RT-PCR) using lung cancer cell lines, normal vs. lung cancer tissues, and lymph node biopsy samples with or without metastasis. Results We found that CEA cell adhesion molecule 5 ( CEACAM5 ) and high mobility group box 3 ( HMGB3 ) were reliable markers for RT-PCR-based prescreening of tumor cells in lung adenocarcinoma. Conclusions The prescreening strategy using CEACAM5 and HMGB3 expression facilitates tumor-centric scRNA-seq analyses of lung adenocarcinoma.
更多
查看译文
关键词
Lung adenocarcinoma,Prescreening strategy,Single-cell RNA sequencing,Tumor cell portions,Tumor-centric analysis
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要