Pancreatic Cancer Cell-Derived Exosomes Promote Lymphangiogenesis by Downregulating ABHD11-AS1 Expression.
Xulin ZhouFengyun ZhongYongmin YanSihui WuHuizhi WangJunqiang LiuFeifan LiDawei CuiMin XuPublished in: Cancers (2022)
Research on pancreatic cancer microbiomes has attracted attention in recent years. The current view is that enriched microbial communities in pancreatic cancer tissues may affect pancreatic cancer metastasis, including lymph node (LN) metastasis. Similar to carriers of genetic information between cells, such as DNA, mRNA, protein, and non-coding RNA, exosomes are of great importance in early LN metastasis in tumors, including pancreatic cancer. Our previous study showed that the long non-coding RNA ABHD11-AS1 was highly expressed in tissues of patients with pancreatic cancer, and was correlated with patient survival time. However, the role of ABHD11-AS1 in pancreatic cancer LN metastasis has rarely been studied. Hence, in this paper we confirmed that exosomes derived from pancreatic cancer cells could promote lymphangiogenesis in vitro and in vivo, and that the mechanism was related to the downregulation of ABHD11-AS1 expression in lymphatic endothelial cells, and to the enhancement of their ability to proliferate, migrate, and form tubes. These findings preliminarily show a new mechanism by which pancreatic cancer cells regulate peripheral lymphangiogenesis, providing a new therapeutic strategy for inhibiting LN metastasis in pancreatic cancer.
Keyphrases
- long non coding rna
- poor prognosis
- lymph node
- mesenchymal stem cells
- endothelial cells
- stem cells
- gene expression
- signaling pathway
- squamous cell carcinoma
- dna methylation
- healthcare
- cell proliferation
- small molecule
- early stage
- cell free
- radiation therapy
- health information
- cell cycle arrest
- bone marrow
- circulating tumor
- rectal cancer
- drug induced
- circulating tumor cells