Invest New Drugs DOI 10.1007/s10637-014-0172-8
PRECLINICAL STUDIES
Novel benzoxazines as inhibitors of angiogenesis Sara Al-Rawi & Terri Meehan-Andrews & Chris Bradley & Jasim Al-Rawi
Received: 23 July 2014 / Accepted: 6 October 2014 # Springer Science+Business Media New York 2014
Summary Dysregulation of angiogenesis has been associated with many pathological disorders, including cancer; where angiogenesis has been found to be critical for the maintenance and metastasis of tumours. One of the pathways involved in the regulation of angiogenesis is the phosphatidylinositol3-kinase (PI3K) signalling pathway. The PI3K family consists of enzymes that phosphorylate the 3-OH of the inositol ring of phosphatidyl inositol. There are four isoforms, PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ, that are signalling intermediaries involved in numerous pathways that sustain and maintain the tumours. In this study, we screened eight novel benzoxazine inhibitors of both PI3K isoforms and the related DNA-PK, for their anti-angiogenic effects. Our findings identified the novel benzoxazine (7, 8 (substituted)-2-morpholino-benz (1,3) oxazine: LTUSI122) to be non-toxic at concentrations up to 5 μM, while exhibiting significant inhibition of various aspects of angiogenesis including endothelial proliferation, migration and tube formation. The molecular mechanisms were examined using an angiogenesis array, revealing inhibition of several proliferative and migratory angiogenic factors, including VEGFR, MMP, IL-8, uPAR and MCP; and stimulation of the endogenous inhibitor, endostatin. We hypothesize that these antiangiogenic effects are mediated by targeting an important signaling intermediary, PI3Kα, and subsequently its action on vascular endothelial growth factor (VEGF, a key
S. Al-Rawi : C. Bradley : J. Al-Rawi School of Pharmacy and Applied Sciences, La Trobe University, Bendigo, VIC, Australia T. Meehan-Andrews (*) La Trobe Rural Health School, La Trobe University, Bendigo, VIC, Australia e-mail:
[email protected]
growth factor in the process of angiogenesis). If used in combination with more targeted therapies, LTUSI122 could reduce tumour growth and increase the efficacy of these treatments. Keywords Angiogenesis . PI3K . Proliferation . Tube formation . Migration . HUVECs
Introduction Cancer develops when a normally tightly regulated cell transforms, due to genetic alterations or other changes, into a cell with uncontrolled proliferative potential. Following transformation of cells into cancer cells at the primary site, the excessive cell growth demands increased blood supply which triggers the release of growth factors that initiate the development of new blood vessels, a process known as angiogenesis. This process is crucial for further growth of the primary tumour, but also facilitates migration of cancer cells to secondary sites, or metastasis [1]. In a cancerous environment, angiogenesis is triggered by cells under hypoxic stress. Subsequent increase in the levels of hypoxia-inducible factors (HIF), induces transcription of several angiogenic proteins; including Vascular Endothelial Growth Factors (VEGF) and Fibroblast Growth Factor (FGF) [2]. Increase in the levels of these factors stimulates the angiogenic cascade, that attracts inflammatory and endothelial cells to the area, and promotes their proliferation and maturation [3], which supplies the cancerous cells with oxygen and nutrients [2]. The angiogenic cascade begins with the degradation of the extracellular matrix, by matrix metalloproteinases (MMPs), and disruption of cell contacts within a mature blood vessel. This is then followed by the generation of “tip cells” at the outgrowth created by the proliferation of endothelial cells.
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These newly proliferated endothelial cells then migrate, driven by chemical gradients, to the site of the cancerous mass. Once enough cells have migrated to the area, they align themselves into tube-like structures and are surrounded by a new basement membrane. Finally, the vessels are stabilized by pericytes and then mature into blood vessels [4, 5]. Inhibition of VEGF signalling, either by neutralising antibodies (e.g. Bevacizunab [6]) or VEGF receptor kinase inhibitors (e.g. Suntinib [7]) has proven to be an effective anti-tumour factor. But these molecules have limited use; limited to cancer type, longevity of results and the potential to accelerate metastasis after short term treatment reduces benefits [8]. Another potential target could be the phosphatidylinositol3-kinase (PI3K) family of enzymes, which are involved in many cellular functions; including cell proliferation, differentiation, motility, survival and intracellular signalling [9]. The PI3K family consists of enzymes that phosphorylate the 3-OH of the inositol ring of phosphatidyl inositol. There are four isoforms, PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ. Among the different PI3K isoforms, PI3Kα plays a major role in cancer. It is frequently mutated and over expressed in many human cancers [10]. PI3Kα is also an intracellular signalling intermediary for VEGF [11]. Previous studies have demonstrated the importance of PI3Kα in angiogenesis in vitro by down regulating its expression via short interfering RNA (siRNA), leading to a reduction in migration. The migration inhibition was also evident in vivo, where PI3Kα knockout mice showed significant delay in migration of endothelial tip cells [9]. Early PI3K inhibitors, LY294002 and wortmannin, both of which have anti-angiogenic activity were not further explored due to their toxic side effects [12]. However, the antiangiogenic effect of LY294002 was found be due to inhibition of VEGF signalling and expression [11]. In this study we screened eight, novel 7-and 7,8 (substituted)-2-morpholinobenz (1, 3) oxazines known to act on different PI3K isoforms and the related DNA-PK with varying IC50s (Table 1, [20, 23]), to determine if they have anti angiogenic effects and the molecular mechanisms underlying these processes. Our results show that the novel benzoaxine, LTUSI122, inhibits proliferation, migration and tube formation of endothelial cells (HUVECs) in vitro; and alters the expression of VEGFR2, TGF- β, thrombopoietin, uPAR, MCP-4, ENA-78, MMP-9, IL8 and endostatin following 24 h exposure.
Materials and methods Compounds and concentrations The novel benzoxazines being tested were prepared and kindly provided by the chemistry team lead by Dr. Jasim Al-Rawi
(Latrobe University, Bendigo, Australia [20, 23]). The PI3Kinhibitor, LY294002, (Cell Signalling, MA) and the DNA-PK inhibitor, NU7026 (Sigma Aldrich, Australia) were included as reference inhibitors. Stock solutions of 1 mM of each test compound were prepared in Dimethyl Sulfoxide (DMSO, Sigma-Aldrich, Australia). Serial dilutions were made from stock solutions to create various concentrations of compounds to be assessed: 0.1 μM, 1 μM and 5 μM. When preparing test compounds dilutions were calculated to ensure that the percentage of DMSO did not exceed the toxic limit 0.5 % v/v. Equivalent concentrations of DMSO were added to the control media. Cell lines and cell culture Human umbilical vein endothelial cells (HUVECs, Merck Millipore) were cultured in sterile growth media composed of phenol red free media (Medium200, Life technologies, Australia) enriched with growth factors, hydrocortisone (1 μg/ml), human epidermal growth factor (10 ng/ml), basic fibroblast growth factor (3 ng/ml), heparin (10 μg/ml) (LSGF kit, Life technologies, Australia) and 10 % foetal bovine serum (FBS, Interpath Services, Australia). Toxicity of compounds Prior to testing the effect of the novel benzoxazines on HUVECs, an initial toxicity profile of these compounds was completed using CellTox Green Cytotoxicity assay™ (Promega). HUVECs were plated at concentration of 8x103 cells per well in a 96 well plate. When confluent, compounds at different concentrations (0.1 μM, 1 μM and 5 μM) were added, along with 1:500 dilution of cyanine dye to measure fluorescence. After 6 and 24 h, fluorescence was read at 485 nm excitation and 520 nm emission (Flex Station 3, Molecular Devices, California), and expressed as % toxicity compared to the media only control. Cell Viability - sulphorhodamine blue assay (SRB) Sulphorhodamine B assay was used to determine compound effect on cell number over time, as described previously with minor alterations [13]. HUVECs were seeded at a concentration of 2x104 cells per well on gelatine coated 24 well plates and allowed to adhere to wells for 24 h. Following incubation, media was removed and cells were resuspended in 1 ml of test media and incubated for a period of 48 h. Control cells where treated with media containing 0.5 % v/v DMSO. Plates were placed in a Flex Station 3 and colour absorbance measured at 540 nm, and expressed as % cell number compared to the media only control.
Invest New Drugs Table 1 Name of novel benzoaxine analogues and the activity in purified enzyme assay for PI3Kα, PI3Kβ, PI3Kγ, PI3Kδ and DNA-PK [20, 23]
Name / IC50 (μM)
PI3Kα
PI3Kβ
PI3Kγ
PI3Kδ
DNA-PK
LTUSI58 LTUSI99 LTUSI122 LTUT1 LTUT3
4.07 7.24 5.20 29.8 11.3
3.35 11.6 14.6 108 24.3
1.44 24.4 18.1 0.33 3.66
0.94 3.78 1.62 0.167 4.55
0.3 1.6 0.62 6.004 14.00
LTUT4 LTUSI118 LTUT5 (negative control)
14.4 0.12 >100
19.9 1.42 >100
0.123 7.21 >100
4.68 2.0 >100
23.10 0.28 >100
Migration - Boyden chamber assay A more quantitative assay to observe the effect of compounds on cell migration is the Boyden chamber. HUVECs were seeded onto cell culture inserts according to manufacturer’s instructions (ThinCertTM, Greiner bio-one Germany) with media containing test compounds and 10 % FBS overnight. Following overnight incubation, cells were harvested and resuspended in low serum supplement media (2 % FBS) to a cell concentration of 106 cells / per ml and added to the culture inserts in the bottom chamber 600 μL/well of media supplemented with the chemo attractant (10 % FBS) and the test compounds at 1 μM or 5 μM. The 24 well plates were then placed in the incubator for 24 h at 37 °C and 5 % CO2. After 24 h, the cell culture medium was removed from each well, and replaced with 450 μl serum-free culture medium containing 8 μM Calcein-AM, and incubated for 45 min. The cell culture inserts were removed, and 200 μl of the solution, now containing the migratory cells, from each well was transferred into a black flat bottom 96 well plate (μ-Clear plate, Interpath, Australia). Fluorescence of Calcein-AM was read using a fluorescence plate reader (Flexstation) at an excitation wavelength of 485 nm and an emission wavelength of 520 nm, and expressed as % migration compared to the media only control.
Tube formation assay Prior to cell culture, plates were pre-coated with Geltrex (Life technologies, Australia). HUVECs were then added to the Geltrex coated 24 well plates (250 μl, 4 to 5×104 cells per well), and 750 μl of test media was added to each well, at either 1 μM or 5 μM. After 24 h exposure, cells were observed and random fields were selected for analysis. Images were captured using a Nikon camera and NIS Elements F 3.0- microscopic imaging software. The number of tubes formed was quantified by counting complete tube-like structures within random fields and
expressed % number of tubes compared to the media only control. Expression of Angiogenic Molecules - Angiogenesis human membrane array Angiogenesis Human Membrane Antibody Arrays (20 and 23 targets, Sapphire Bioscience) were used to determine the effect of LTUSI122 on proteins expressed during angiogenesis. Manufacturer’s instructions were followed with minor alterations [14, 15]. HUVECs were treated with 1 μM LTUSI122 or media only for 24 h. Cells were then detached and washed twice in PBS. After washing in PBS, cells were resuspended at 1x107 cells / ml in lysis buffer, which was then added to the array membrane. After overnight incubation, membranes were washed with wash buffers. Following the final wash, 1 ml biotinconjugated anti-cytokines solution (membrane specific) was added to each membrane and incubated at room temperature for 2 h. Following washes with appropriate wash buffers, 2 ml of HRP-SA (Horse Radish peroxidasestreptavidin) was added to each membrane, and incubated at room temperature for 2 h. After washing with wash buffers, detection buffers were added to membranes, and using CCD camera (G-Box, Syngene) membranes were exposed for 30 s, 1, 2 and 4 min to obtain an image with low background and strong positive control. The results were given as pixel density, which was directly proportional to level of expression of the factors investigated. The pixel density was normalised to each membrane positive controls, which then allowed for a comparison between LTUSI122 treated cells and media only control cells. Statistics and analysis Data was graphed using the Graph pad prism 5.0 statistical package. The statistical significance was determined using one way ANOVA with Newmanns Keuls Post-test and
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Student t-test, with the statistical significance indicated with p values less than 0.05.
benzoxazine analogues had no significant effect on migration. The effect of benzoaxine analogues on tube formation
Results Toxicity of benzoxazine analogues The benzoxazine analogues were chosen as they displayed varying inhibitory activity (IC50) to different members of the PIKK family: DNA-PK, PI3Kα, PI3Kβ, PI3Kγ and PI3Kδ. To ensure the compounds had no detrimental effect on the endothelial cells (HUVECs), the toxicity was determined at concentrations between 0.1 and 5 μM. At these concentrations, the activity of different PIKK members would have been inhibited. Of the eight compounds, seven benzoxazine analogues, LTUSI99, LTUSI122, LTUT1, LTUT3, LTUT4, LTUSI118 and LTUT5, did not have a toxic effect on HUVECs in the in vitro environment (Fig. 1). However, the benzoxazine analogue LTUSI58 was found to be extremely toxic at 5 uM compared to the control treated cells. This was almost twice as toxic as comparative inhibitors, LY294002 and NU7026 after 24 h exposure. Benzoaxine analogues have different effects on cell viability Since endothelial proliferation is important for the formation of new blood vessels, we examined the effect of the benzoaxine analogues on cell number. As LTUSI58 was found to be toxic it was eliminated from any further testing. The remaining seven compounds were tested for their effect on cell number (Fig. 2). After 48 h exposure, LTUSI122 significantly decreased cell number, at 1 μM and 5 μM, when compared to control. The benzoxazine analogues LTUT1, LTUT4 and LTUSI118 caused significant increase in cell number, while NU7026, LTUT3 and LTUSI99 had no effect on cell number. Some of the compounds: LTUT1, LTUT4 LTUSI118 and LTUT3, displayed a different effect on cell number at 5 μM, compared to the trend at the lower concentrations, these cell displayed abnormal morphology (images not shown).
The realignment of endothelial cells into tube like structures is the final process during angiogenesis. We examined the effect of the benzoxaxine analogues using 3-D matrix (Geltrex). After 24 h in the presence of media only (containing growth factors), the HUVECs reorganise into tube-like structures, characterized by the elongation and connection of cells (Fig. 4a). In the presence of 1 μM and 5 μM of the benzoxazine analogue LTUSI122, Fig. 4b and c respectively, there was a reduction in the formation of tube-like structures. Other compounds, for example LTUSI118 at 1 μM and 5 μM, Fig. 4d and e respectively, showed an increase in the formation of tube-like structures. The visual observations were quantified by counting complete (enclosed) tube-like structures. The number of tubes formed in the presence of LTUSI122 was significantly less when compared to control containing media alone (Fig. 4f). LTUT1 and LTUSI118 both stimulated the number of tubes formed, while other benzoxazine analogues had no effect. LTUSI122 alters the expression of several angiogenic molecules Rapid proliferation of cancerous cells, leads to localised hypoxia, in response cells increase the expression of several angiogenic factors, which stimulate endothelial cells during angiogenesis. The novel benzoxazine, LTUSI122, exhibited an inhibitory effect on several stages of angiogenesis: proliferation, migration and tube formation. To determine the molecular pathways involved, or in this case inhibited by LTUSI122, human membrane antibody arrays were used to assess changes in the levels of 43 known angiogenic molecules. Following treatment with 1 μM LTUSI122, only 9 molecules displayed a change in expression (summarised in Table 2). The levels of the angiogenic factors: VEGFR2, TGF-β, Thrombopoietin, uPAR, MMP-9, IL-8, MCP4 and ENA-78 all decreased expression; while there was an increase in the expression of endostatin, an endogenous inhibitor of angiogenesis.
Benzoaxine analogues have different effects on migration Since cell migration is an important process for endothelial cells to form new blood vessels during angiogenesis, we next examined the effect of the benzoaxine analogues on cell migration toward an attractant (10 % FBS) using the quantifiable Boyden chamber assay (Fig. 3). LTUSI122 and LTUT3 significantly inhibited migration of endothelial cells through the gel matrix membrane toward the attractant after treatment for 24 h. All other
Discussion Inhibition of tumor angiogenesis, as a means of reducing the growth of cancers, has become a promising target for adjuvant therapies. In particular, direct inhibition of the VEGF signaling has proven extremely successful, but has limitations [16, 17]. Inhibition of PI3K, which is important for both VEGF
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% Toxicity
150
**
100
*
50
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tr ol U S Ly LT I99 sis U 0 LT SI9 .1µ U 9 M S 1 LT I99 µM U T 5µ LT 4 0 M U .1µ T LT LTU 4 1 M µ U Si T4 M LT 12 5µ M U 2 LT Si1 0.1 U 22 µM Si 1 LT 122 µM U T5 5µM LT 0 U .1 LT T5 µM LT U 1µ U T5 M S 5 LT I58 µM U 0 LT SI5 .1µ LT US 8 1 M U I5 µM 8 S LT I11 5µ M U 8 LT SI1 0.1 U 18 µM SI 1 LT 118 µM U T1 5µM LT 0 U .1 LT T1 µM U 1 LT T1 µM U T3 5µM LT 0 U .1 LT T3 µM N UT 1µ U 70 3 5 M N 26 µM U 0 7 . N 02 1µ LY U7 6 1 M 29 02 µM 5 LY 400 5µ 29 2 0 M LY 4 .1 29 002 µM 40 1 02 µM 5µ M
0
LT
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Fig. 1 Summary of cell toxicity analysis using Cell tox™ green assay. HUVECs were culture in the presence of compounds at varying concentrations (0.1 μM, 1 μM and 5 μM) for 24 h. Graph indicates mean of three replicates ±SEM. (* compound vs. control p
