Liang Han 1 , Jie Jiang 2 , Mengwen Xue 3 , Tao Qin 1 , Ying Xiao 1 , Erxi Wu 4,5 , Xin Shen 3 , Qingyong Ma 6 , Jiguang Ma 3 . Show Affiliations »
Abstract
BACKGROUND: Many patients with pancreatic cancer (PC) suffer from abdominal pain and back pain. However, the cause of pain associated with PC is largely unclear. In this study, we tested the potential influence of the sonic hedgehog (sHH) signaling pathway on PC pain. METHODS: Substance P (SP) and calcitonin gene-related peptide (CGRP) expression was measured in cultured PC cells and dorsal root ganglions (DRG) by real-time PCR, western blotting analysis and ELISA. Small interfering RNA transfection and plasmid constructs were used to regulate the expression of sHH in the AsPc-1 and Panc-1 cell lines. Pain-related behavior was observed in an orthotopic tumor model in nude mice. RESULTS: In this study, the results show that sHH increased the expression of SP and CGRP in DRGs in a concentration and time-dependent manner. Additionally, sHH secretion from PC cells could activate the sHH signaling pathway and, in turn, increase the expression of nerve growth factor (NGF), P75, and TrkA in DRGs. Furthermore, the sHH signaling pathway and NGF/NGF receptor contributed to pain sensitivity in a nude mouse model. CONCLUSION: Our results demonstrate that PC pain originates from the sHH signaling pathway, and NGF mediates the pain mechanism via regulating SP and CGRP. © American Society of Regional Anesthesia & Pain Medicine 2020. Re-use permitted under CC BY. Published by BMJ.
BACKGROUND: Many patients with pancreatic cancer (PC ) suffer from abdominal pain and back pain . However, the cause of pain associated with PC is largely unclear. In this study, we tested the potential influence of the sonic hedgehog (sHH ) signaling pathway on PC pain . METHODS: Substance P (SP) and calcitonin gene-related peptide (CGRP ) expression was measured in cultured PC cells and dorsal root ganglions (DRG) by real-time PCR, western blotting analysis and ELISA. Small interfering RNA transfection and plasmid constructs were used to regulate the expression of sHH in the AsPc-1 and Panc-1 cell lines. Pain -related behavior was observed in an orthotopic tumor model in nude mice . RESULTS: In this study, the results show that sHH increased the expression of SP and CGRP in DRGs in a concentration and time-dependent manner. Additionally, sHH secretion from PC cells could activate the sHH signaling pathway and, in turn, increase the expression of nerve growth factor (NGF ), P75 , and TrkA in DRGs. Furthermore, the sHH signaling pathway and NGF /NGF receptor contributed to pain sensitivity in a nude mouse model. CONCLUSION: Our results demonstrate that PC pain originates from the sHH signaling pathway, and NGF mediates the pain mechanism via regulating SP and CGRP . © American Society of Regional Anesthesia & Pain Medicine 2020. Re-use permitted under CC BY. Published by BMJ.
Entities: CellLine
Disease
Gene
Species
Keywords:
NGF; pain; pancreatic Cancer; sHH
Year: 2019
PMID: 31792027 DOI: 10.1136/rapm-2019-100991
Source DB: PubMed Journal: Reg Anesth Pain Med ISSN: 1098-7339 Impact factor: 6.288