PULMONOLOGY / BASIC RESEARCH
Anti-small cell lung cancer and collagenase inhibition properties of hydroxysafflor yellow A
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1
Department of Respiratory and Critical Care Medicine, Shanxi Provincial People’s Hospital, Taiyuan City, Shanxi, China
2
Department of Chemistry, Turabah University College, Taif University, Taif, Saudi Arabia
3
Department of Thoracic Surgery, Sunshine Union Hospital, Weifang City, Shandong Province, China
Submission date: 2021-05-17
Final revision date: 2021-06-08
Acceptance date: 2021-06-10
Online publication date: 2021-07-09
Corresponding author
Dianxi Yang
Department of Thoracic Surgery, Sunshine Union Hospital, Weifang City,Shandong Province, 261000, China, China
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ABSTRACT
Introduction:
Hydroxysafflor yellow A is the major active chemical ingredient of Carthamus tinctorius L. (safflower), which is widely used in patients with cardiovascular and cerebrovascular diseases in China.
Material and methods:
In our study, the inhibitory effect of hydroxysafflor yellow A on collagenase showed a lower value, IC50 = 78.81 µg/ml. In the cellular and molecular part of the recent study, the cells treated with hydroxysafflor yellow A were assessed by MTT assay for 48 h as regards the cytotoxicity and anti-small cell lung cancer effects on SBC-3, DMS273, and DMS114 cell lines.
Results:
The viability of small cell lung cancer cell lines decreased dose-dependently in the presence of hydroxysafflor yellow A. The IC50 values of hydroxysafflor yellow A were 539, 432, and 416 µg/ml against SBC-3, DMS273, and DMS114 cell lines, respectively. A molecular docking study was carried out for evaluation of the biological activity of hydroxysafflor yellow A against the collagenase H from Clostridium histolyticum.
Conclusions:
The results of the docking calculations revealed the considerable binding affinity of the inhibitor to the enzyme with a docking score of –9.238 (kcal/mol). This remarkable binding affinity could be attributed to the number of hydrogen bonds and hydrophobic contacts, which are 6 and 10, respectively.