Affiliation:
1. Department of Oncology, Chongqing University Fuling Hospital, No. 2, Gaosuntang Road, Fuling District, Chongqing, 408000, China
Abstract
Background:
Osteolytic bone metastasis is a common complication of Non-Small Cell
Lung Cancer (NSCLC), resulting in bone pain, hypercalcemia, and fractures that severely reduce
the quality of life and survival time of patients. Semaphorins 3A (Sema3A) is one of the isoforms
of the Semaphorins family, which is important in a variety of physiological and pathological processes,
such as angiogenesis, immune regulation, and tumorigenesis. However, the role of Sema3A
in the development of osteolytic bone metastasis in NSCLC is unknown.
Methods:
In this study, we established in vitro models simulating NSCLC cells in regulating the
differentiation and maturation of osteoblast and osteoclast precursors and observed the differentiation
of osteoblasts and osteoclasts.
Results:
The results demonstrated that the expression of Sema3A inhibited the proliferation, migration,
and invasion of NSCLC cells, as well as promoted the differentiation of osteoblasts and inhibited
the differentiation of osteoclasts, suggesting that Sema3A can inhibit the occurrence and
development of osteolytic bone metastasis of NSCLC.
Conclusion:
This study provides a new idea for the clinical treatment of osteolytic bone metastasis
in NSCLC.
Publisher
Bentham Science Publishers Ltd.