Semantic Scholar Open Access 2023 8 sitasi

Comparative analysis between high-grade serous ovarian cancer and healthy ovarian tissues using single-cell RNA sequencing

Xiao Zhang Shihao Hong Cheng-Jian Yu Xiaobo Shen Fangying Sun +1 lainnya

Abstrak

Introduction High-grade serous ovarian cancer (HGSOC) is the most common histological subtype of ovarian cancer, and is associated with high mortality rates. Methods In this study, we analyzed specific cell subpopulations and compared different gene functions between healthy ovarian and ovarian cancer cells using single-cell RNA sequencing (ScRNA-seq). We delved deeper into the differences between healthy ovarian and ovarian cancer cells at different levels, and performed specific analysis on endothelial cells. Results We obtained scRNA-seq data of 6867 and 17056 cells from healthy ovarian samples and ovarian cancer samples, respectively. The transcriptional profiles of the groups differed at various stages of ovarian cell development. A detailed comparison of the cell cycle, and cell communication of different groups, revealed significant differences between healthy ovarian and ovarian cancer cells. We also found that apoptosis-related genes, URI1, PAK2, PARP1, CLU and TIMP3, were highly expressed, while immune-related genes, UBB, RPL11, CAV1, NUPR1 and Hsp90ab1, were lowly expressed in ovarian cancer cells. The results of the ScRNA-seq were verified using qPCR. Discussion Our findings revealed differences in function, gene expression and cell interaction patterns between ovarian cancer and healthy ovarian cell populations. These findings provide key insights on further research into the treatment of ovarian cancer.

Topik & Kata Kunci

Penulis (6)

X

Xiao Zhang

S

Shihao Hong

C

Cheng-Jian Yu

X

Xiaobo Shen

F

Fangying Sun

J

Jianhua Yang

Format Sitasi

Zhang, X., Hong, S., Yu, C., Shen, X., Sun, F., Yang, J. (2023). Comparative analysis between high-grade serous ovarian cancer and healthy ovarian tissues using single-cell RNA sequencing. https://doi.org/10.3389/fonc.2023.1148628

Akses Cepat

Lihat di Sumber doi.org/10.3389/fonc.2023.1148628
Informasi Jurnal
Tahun Terbit
2023
Bahasa
en
Total Sitasi
Sumber Database
Semantic Scholar
DOI
10.3389/fonc.2023.1148628
Akses
Open Access ✓