Single-cell RNA sequencing reveals the heterogeneity of MYH11+tumour-associated fibroblasts between left-sided and right-sided colorectal cancer

被引:1
作者
Wang, Chao [1 ]
Zhao, Yue [1 ]
Zhang, Sainan [1 ]
Du, Meiyu [1 ]
He, Guanzhi [1 ]
Tan, Senwei [1 ]
Li, Hailong [1 ]
Zhang, Duoyi [2 ]
Cheng, Liang [1 ,3 ]
机构
[1] Harbin Med Univ, Coll Bioinformat Sci & Technol, Harbin, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 2, Harbin, Heilongjiang, Peoples R China
[3] Harbin Med Univ, NHC Key Lab Mol Probe & Targeted Diag & Therapy, Harbin, Heilongjiang, Peoples R China
关键词
colorectal cancer; left-sided and right-sided colorectal cancer; single cell; ISLAND METHYLATOR PHENOTYPE; COLON; EXPRESSION; LANDSCAPE;
D O I
10.1111/jcmm.70102
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Colorectal cancer (CRC) exhibits considerable heterogeneity on tumour location. However, there is still a lack of comprehensive annotation regarding the characteristics and differences between the left-sided (L-CRC) and right-sided (R-CRC) CRC. Here, we performed single-cell RNA sequencing (scRNA-seq) on immune and stromal cells from 12 L-CRC and 10 R-CRC patients. We found that L-CRC exhibited stronger tumour invasion and poor prognosis compared with R-CRC. In addition, functional enrichment analysis of a normal cohort showed that fibroblasts of left colon are associated with tumour-related pathways. This suggested that the heterogeneity observed in both L-CRC and R-CRC may be influenced by the specific location within the colon itself. Further, we identified a potentially novel MYH11+ cancer-associated fibroblast (CAF) subset predominantly enriched in L-CRC. Moreover, we found that MYH11+ CAFs may promote tumour migration via interacting with macrophages, and was associated with poor prognosis in CRC. In summary, our study revealed the crucial role of MYH11+ CAFs in predicting a poor prognosis, thereby contributing valuable insights to the exploration of heterogeneity in L-CRC and R-CRC.
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页数:11
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