Background:
Cancer continues to pose a great problem and burden on society despite new
treatment options. While surgery, radiotherapy, and chemotherapy have led to major improvements in
patient prognosis, newer treatments are needed to more effectively manage this disease in its advanced
stage. Epidermal growth factor receptor (EGFR) is a receptor tyrosine kinase (RTK), which is catalytically
active and under tight regulatory control. Dysregulation of its activity is strongly associated with
tumorigenesis and cancer patients with altered EGFR activity tend to have a more aggressive disease,
associated with a poor clinical prognosis. The family of EGFR has been intensively studied due to its
strong influence on the formulation and deterioration of carcinoma. Thus, it is a good strategy that design
anticancer agents by inhibiting the EGFR pathway.
Methods:
We group to obtain the six series compounds (8a-f, 9a-f, 10a-f, 11a-f, 12a-b and 13a-d). Hence
we disclosed the design, synthesis and antitumor activity of novel quinazoline analogues against EGFR
overexpression cancer cells A549 (human lung cancer), HepG-2 (human liver cancer), MCF-7 (human
breast cancer) and PC-3 (human prostate cancer) and as well as the inhibitory on EGFR kinase. Moreover,
apoptosis by acridine orange single staining and docking studies were presented in this paper as well.
Results:
Six series of quinazoline derivatives bearing 2,3-dihydro-indole or 1,2,3,4-tetrahydroquinoline
(8a-f, 9a-f, 10a-f, 11a-f, 12a-b and 13a-d) were designed, synthesized and evaluated for the half maximal
inhibitory concentration (IC50) values against four cancer cell lines (A549, HepG-2, MCF-7 and
PC-3). Thirty target compounds showed moderate to excellent (1.49 - 50 µM) cytotoxicity activity against
one or several cancer cell lines. The compound 13a showed the best activity against A549, HepG-
2, MCF-7 and PC-3 cancer cell lines, with the IC50 values of 1.49 ± 0.17 µM, 2.90 ± 0.24 µM, 1.85 ±
0.19 µM, 3.30 ± 0.22 µM, respectively. What’s more, the secondary amines were introduced to the
target compounds to improve the water-soluble. The results showed that the compounds were beneficial
to the cytotoxicity activity. Furthermore, the results prompted us that this series of compounds may be a
kind of potential epidermal growth factor receptor (EGFR) kinase inhibitors.
Conclusion:
Six series of quinazoline derivatives bearing 2,3-dihydro-indole or 1,2,3,4-
tetrahydroquinoline moiety (8a-f, 9a-f, 10a-f, 11a-f, 12a-b and 13a-d) were designed, synthesized and evaluated
for the IC50 values of cytotoxicity against four cancer cell lines (A549, HepG-2, MCF-7 and PC-3).
Thirty synthesized compounds showed moderate to excellent cytotoxicity activity against the different
cancer cells. Especially, the compound 13a exerted antitumor effects in a dosage-dependent manner and
the IC50 values of compound 13a were 1.49 µM, 2.90 µM, 1.85 µM and 3.30 µM against A549, HepG-2,
MCF-7 and PC-3, respectively. From the antitumor activity data show that the compounds possessed selectivity
for A549 and MCF-7 cancer cell lines. It meant that the compounds had better treatment effect on
lung cancer and breast cancer. On the whole, the compounds substituted by 1,2,3,4-tetrahydroquinoline at
C-4 position of quinazoline and (S)-tetrahydrofuran-3-ol at C-8 position of quinazoline were beneficial to
the cytotoxicity activity. From the result of acridine orange (AO) single staining which indicated the compound
13a could induce apoptosis of A549 cells. From the result of Docking Studies, we hypothesized that
the C-4 position of quinazoline were substituted by 2,3-dihydro-indole or 1,2,3,4-tetrahydroquinoline with
the equal influence of the cytotoxicity activity. Overall, the results prompted us that this series of compounds
may be a kind of potential EGFR kinase inhibitors.
One-pot biosynthesis of CdS quantum dots through in vitro regeneration of hairy roots of Rhaphanus sativus L. And their apoptosis effect on MCF-7 and AGS cancerous human cell lines
