解密肿瘤微环境,阐明卵巢透明细胞癌的癌细胞起源

bioRxiv Pub Date : 2024-08-08 DOI:10.1101/2024.08.06.606821
Uma S Kamaraj, Pradeep Gautam, Terence Cheng, Tham Su Chin, Sun Kuie Tay, Tew Hong Ho, R. Nadarajah, Ronald Chin Hong Goh, Shing Lih Wong, Sangeeta Mantoo, I. Busmanis, Hu Li, Minh TN Le, Qi-Jing Li, Elaine Hsuen Lim, Y. Loh
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摘要

卵巢透明细胞癌(CCC)以东亚人居多。它与子宫内膜异位症有关,子宫内膜异位症是一种良性疾病,即子宫内膜(子宫内膜)组织出现在子宫腔以外的腹腔或盆腔腹膜表面。与其他卵巢癌亚型相比,CCC 对常规化疗的耐药性相对较强,预后较差。在这项研究中,我们招募并获取了 7 名 CCC 患者的肿瘤组织,这些患者均处于 CCC 的四个阶段。我们利用高分辨率 scRNA-seq 对临床 1-4 期的 7 例 CCC 患者的肿瘤和肿瘤微环境(TME)进行了转录谱分析,以深入了解 CCC 的生物学机制。首先,我们建立了CCC肿瘤微环境(TME)的scRNA-seq资源。其次,我们确定了不同细胞类型的比例,并发现 CCC 中存在高水平的免疫浸润。第三,由于 CCC 与子宫内膜异位症有关,我们将 CCC 与两个公开的子宫内膜异位症 scRNA-seq 数据集进行了比较。CCC 恶性细胞与子宫内膜异位症中的腺体分泌细胞和纤毛上皮细胞有相似之处。最后,我们确定了 CCC TME 和子宫内膜异位症中各种细胞类型之间的细胞-细胞通讯差异,以深入了解 CCC 的转变。
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Deciphering tumour microenvironment and elucidating the origin of cancer cells in ovarian clear cell carcinoma
Ovarian clear cell carcinoma (CCC) has an East Asian preponderance. It is associated with endometriosis, a benign condition where endometrial (inner lining of the uterus) tissue is found outside the uterus and on the peritoneal surface, in the abdominal or pelvic space. CCC is relatively more resistant to conventional chemotherapy compared to other ovarian cancer subtypes and is associated with a poorer prognosis. In this study, we recruited and obtained tumour tissues from seven patients across the four stages of CCC. The tumour and the tumour microenvironment (TME) from 7 CCC patients spanning clinical stages 1-4 were transcriptionally profiled using high-resolution scRNA-seq to gain insight into CCC’s biological mechanisms. Firstly, we built a scRNA-seq resource for the CCC tumour microenvironment (TME). Secondly, we identified the different cell type proportions and found high levels of immune infiltration in CCC. Thirdly, since CCC is associated with endometriosis, we compared CCC with two publicly available endometriosis scRNA-seq datasets. The CCC malignant cells showed similarities with glandular secretory and ciliated epithelial cells found in endometriosis. Finally, we determined the differences in cell-cell communication between various cell types present in CCC TME and endometriosis conditions to gain insights into the transformations in CCC.
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