Depiction of the genomic and genetic landscape identifies CCL5 as a protective factor in colorectal neuroendocrine carcinoma

生物 转录组 癌症研究 基因组DNA 遗传学 基因 基因表达
作者
Dong Chen,Xuanwen Bao,Ruyi Zhang,Yongfeng Ding,Min Zhang,Benfeng Li,Hangyu Zhang,Xiaolin Li,Zhou Tong,Lulu Liu,Xiaohu Zhou,Saisai Wang,Xiaofei Cheng,Yi Zheng,Jian Ruan,Weijia Fang,Peng Zhao
出处
期刊:British Journal of Cancer [Springer Nature]
卷期号:125 (7): 994-1002 被引量:21
标识
DOI:10.1038/s41416-021-01501-y
摘要

Colorectal neuroendocrine carcinomas (CRNECs) are highly aggressive tumours with poor prognosis and low incidence. To date, the genomic landscape and molecular pathway alterations have not been elucidated. Tissue sections and clinical information of CRNEC (n = 35) and CR neuroendocrine tumours (CRNETs) (n = 25) were collected as an in-house cohort (2010–2020). Comprehensive genomic and expression panels (AmoyDx® Master Panel) were applied to identify the genomic and genetic alterations of CRNEC. Through the depiction of the genomic landscape and transcriptome profile, we compared the difference between CRNEC and CRNET. Reverse transcription-polymerase chain reaction and immunofluorescence staining were performed to confirm the genetic alterations. High tumour mutation load was observed in CRNEC compared with CRNET. CRNECs showed a “cold” immune landscape and increased endothelial cell activity compared with NETs. Importantly, PAX5 was aberrantly expressed in CRNEC and predicted a poor prognosis of CRNECs. CCL5, a factor that is considered an immunosuppressive factor in several tumour types, was strongly expressed in CRNEC patients with long-term survival and correlated with high CD8+ T cell infiltration. Through the depiction of the genomic landscape and transcriptome profile, we demonstrated alterations in molecular pathways and potential targets for immunotherapy in CRNEC.
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