Protective effect of ulinastatin on acute lung injury after radiotherapy in patients with lung cancer and the related molecular mechanism
Objective: To analyze the protective effect of ulinastatin on acute lung injury after radiotherapy in patients with lung cancer and the related molecular mechanism. Methods: A total of 78 patients who received radiotherapy and developed acute lung injury in our hospital between December 2013 and...
Main Author: | |
---|---|
Format: | Article |
Language: | English |
Published: |
Editorial Board of Journal of Hainan Medical University
2016-12-01
|
Series: | Journal of Hainan Medical University |
Subjects: | |
Online Access: | http://www.hnykdxxb.com/PDF/201624/30.pdf |
Summary: | Objective: To analyze the protective effect of ulinastatin on acute lung injury after radiotherapy
in patients with lung cancer and the related molecular mechanism. Methods: A total of 78
patients who received radiotherapy and developed acute lung injury in our hospital between
December 2013 and December 2015 were randomly divided into observation group and control
group, control group received symptomatic treatment, observation group received symptomatic
+ ulinastatin treatment, and the content of growth factors, inflammatory factors, disease-related
proteins in serum as well as the expression of P38MAPK signaling pathway molecules in
alveolar lavage fluid were compared between two groups of patients after treatment. Results:
Ten days after treatment, HGF, KGF, VEGF, IL-1β, IL-8, IL-10, IL-18, IL-13, PCT, S100A8,
S100A9 and SP-D content in serum of observation group were significantly lower than those
of control group while Clara cell protein content was significantly higher than that of control
group; phosphorylated p38MAPK, MAPK, MKK3/6 and ATF-2 protein expression levels
in alveolar lavage fluid were significantly lower than those of control group. Conclusions:
Ulinastatin can alleviate the overall condition in patients with acute lung injury after
radiotherapy, and the specific mechanism is associated with P38MAPK signaling pathway. |
---|---|
ISSN: | 1007-1237 1007-1237 |