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Introduction

Colorectal cancer (CRC) is a malignant neoplasm arising from the lining of the large intestine (colon and rectum) (1). CRC is the third most common cancer and the third leading cause of cancer-related death in the United States (2). The incidence of CRC in Korea has increased significantly over the past few decades. According to the National Cancer Registry of Korea, age-standardized incidence rates increased from 27.0 to 50.2 per 100,000 for men and from 17.1 to 26.9 per 100,000 for women between 1999 and 2009. The overall incidence of CRC increased by 6.7% annually in men and 5.1% in women from 1999 to 2009, while the incidence rates of the most common cancers, such as stomach and liver cancer, decreased during the same period (3). While more than 50% of CRC patients with surgical resection is cured, 40–50% of these subjects eventually experience recurrences and the possibility of re-operation is very low (4). Because of incomplete therapeutic options for CRC, there is a need to develop novel preventive treatment approaches for this malignancy.

Apoptosis, a controlled and energy-dependent process, is the best-described form of programmed cell death. There are two major apoptotic pathways, which are the extrinsic pathway and the intrinsic pathway (5). The extrinsic pathway is initiated by the binding of transmembrane death receptors [Fas, tumor necrosis factor receptor 1 (TNFR1), TNF-related apoptosis-inducing ligand (TRAIL) receptors] with cognate extracellular ligands (6). Ligand receptors recruit adaptor proteins [TNFR-associated death domain (TRADD) and Fas-associated death domain (FADD)], which interact with and trigger the activation of caspase-8. Activated caspase-8 thereby stimulates the effector caspases-3, -6 and -7 which ultimately execute apoptosis (7). TNF-α is known to trigger apoptotic death via TNFR1 (8). The intrinsic pathway is dominated by the Bcl-2 family of proteins which govern the release of cytochrome c from the mitochondria (9,10). Cytochrome c stimulates the formation of apoptosome (Apaf-1, dATP, cytochrome c and caspase-9) followed by activation of caspase-9, which in turn causes the activation of the ‘executioner’ caspases (-3, -6 and -7) (9,11,12).

Psorospermin, a natural product isolated from the tropical plant Psorospermum febrifugum, consists of a xanthone scaffold and was reported to exhibit potent anticancer activity in vitro and in vivo (13,14). Acronycine, an alkaloid first isolated from Acronychia baueri Schott (Rutaceae) consists of an acridone scaffold and showed a broad spectrum of activity against a variety of solid tumors including sarcoma, myeloma, carcinoma, and melanoma (15). On the basis of the chemical structures of psorospermin with a xanthone template and acronycine derivatives with an acridone template, MHY-449 and MHY-450 (Fig. 1A) constructed on a 1,2-dihydrobenzofuro [4,5-b][1,8]naphthyridin-6(11H)-one scaffold were designed and synthesized as potential anticancer agents (16). Their cytotoxicities were evaluated against five human cancer cell lines, such as prostate cancer cell lines (LNCap, DU145 and PC3) and breast cancer cell lines (MCF-7/ADR and MCF-7). MHY-449 and MHY-450 have shown cytotoxicity against human prostate and breast cancer cells and induction of G2/M phase arrest of the cell cycle in MCF-7/ADR cells, however, the underlying molecular mechanisms of these cytotoxic effects and G2/M phase arrest were not fully elucidated. Therefore, the current study was designed to investigate the effects on HCT116 human colon cancer cells and its mechanisms by which these novel derivatives induce apoptosis and modulation of the cell cycle in HCT116 human colon cancer cells.

Figure 1 Chemical structures and effects of MHY-449 and MHY-450 on the viability of HCT116 cells. (A) MHY-449 [(±)-(R*)-5-methoxy-11-methyl-2-((R*)-2-methyloxiran-2-yl)-1,2-dihydrobenzofuro[4,5-b][1,8]naphthyridin-6(11H)-one] and MHY-450 [(±)-(R*)-5-methoxy-11-methyl-2-((S*)-2-methyloxiran-2-yl)-1,2-dihydrobenzofuro[4,5-b][1,8]naphthyridin-6(11H)-one. (B) One day after seeding, HCT116 cells were treated with incremental concentration of MHY-449 and MHY-450 for 24 h. Proliferation was measured by using the MTT assay. Results are expressed as mean ± SD (n=6). *p<0.05 and **p<0.01 compared between MHY-449 and MHY-450 treated cells.

Materials and methods

Chemicals

The simplified code names and structures of MHY-449 [(±)-(R*)-5-methoxy-11-methyl-2-((R*)-2-methyloxiran-2-yl)-1,2-dihydrobenzofuro[4,5-b][1,8]naphthyridin-6(11H)-one] and MHY-450 [(±)-(R*)-5-methoxy-11-methyl-2-((S*)-2-methyloxiran-2-yl)-1,2-dihydrobenzofuro[4,5-b][1,8]naphthyridin-6(11H)-one] used in this study are shown in Fig. 1. Detailed methods for the design and synthesis of these compounds are described elsewhere (16). They were dissolved in dimethylsulfoxide (DMSO) and stored at −20°C before the experiments and dilutions were made in culture medium. The maximal concentration of DMSO did not exceed 0.1% (v/v) in the treatment range of 0.125-0.5 μM, where there was no influence on the cell growth.

Cell culture and growth study

The human colon cancer HCT116 cells were cultured in RPMI-1640 (Hyclone, Logan, UT, USA) supplemented with 10% fetal bovine serum (FBS, Hyclone), 2 mM glutamine (Sigma-Aldrich Co., St. Louis, MO, USA), 100 U/ml penicillin (Hyclone) and 100 μg/ml streptomycin (Hyclone) at 37°C in a humidified 5% CO2. Cell viability was determined by MTT assay and by trypan blue staining assay. For the MTT assay, HCT116 cells were seeded in a 24-well culture plate at a density of 4×104 cells/well, cultured for 24 h in the growth media and then treated with or without various reagents for the indicated concentrations. The cells were incubated with 0.5 mg/ml MTT [3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] (Sigma-Aldrich) at 37°C for 2 h. The formazan granules generated by the live cells were dissolved in DMSO and the absorbance at 540 nm was monitored by using a multi-well reader. For the trypan blue staining assay, the reagents-treated HCT116 cells were harvested by trypsinization, suspended in phosphate-buffered saline (PBS), stained by trypan blue stain (Gibco, Rockville, MD, USA) solution and the number of viable cells was counted using a hemacytometer.

Nuclear staining with Hoechst 33342

Cells were washed with PBS and fixed with 3.7% paraformaldehyde (Sigma-Aldrich) in PBS for 10 min at room temperature. Fixed cells were washed with PBS and stained with 4 μg/ml Hoechst 33342 for 20 min at room temperature. The cells were washed two more times with PBS and analyzed by a fluorescent microscope.

Assessment of DNA degradation

Cells were lysed in a buffer, containing 5 mM Tris-HCl (pH 7.5), 5 mM EDTA, and 0.5% Triton X-100, for 30 min on ice. Lysates were vortexed and cleared by centrifugation at 27,000 × g for 20 min. Fragmented DNA in the supernatant was treated with RNase, followed by proteinase K digestion, phenol/chloroform/isoamyl alcohol mixture (25:24:1, v/v/v) extraction and isopropanol precipitation. DNA was separated through a 1.5% agarose gel, was stained with 0.1 μg/ml ethidium bromide (EtBr) and was visualized by UV source.

Cell cycle analysis

The DNA content was measured following the staining of the cells with propidium iodide (PI, Sigma-Aldrich). The cells were treated under the appropriate conditions for 24 h, subsequently trypsinized, washed once in cold PBS and then fixed in 70% ethanol at 4°C overnight. The fixed cells were pelleted and stained in cold PI solution (50 μg/ml in PBS) at room temperature for 30 min in the dark. Flow cytometry analysis was performed on a FACScan flow cytometry system (Becton-Dickinson, San Jose, CA, USA).

Caspase activity assay

The cells were harvested and washed with cold PBS. Total cells were lysed with the lysis buffer [40 mM Tris (pH 8.0), 120 mM, NaCl, 0.5% NP-40, 0.1 mM sodium orthovanadate, 2 μg/ml aprotinin, 2 μg/ml leupeptin and 100 μg/ml phenymethylsulfonyl fluoride (PMSF)] at 4°C for 30 min. The lysed cells were centrifuged at 14,000 rpm for 10 min and 100 μg protein was incubated with 100 μl of reaction buffer and 10 μl of colorimetric tetrapeptides, Z-DEVDpNA for caspase-3, Z-IETD-pNA for caspase-8, and Ac-LEHD-pNA for caspase-9, respectively. The reaction mixture was incubated at 37°C for 30 min and liberated p-nitroaniline (pNA) was measured at 405 nm using a multi-well reader.

Annexin V staining

Annexin V-FITC is used to quantitatively determine the percentage of cells within a population that are actively undergoing apoptosis. The cells were treated under the appropriate conditions for 24 h, subsequently harvested, trypsinized, washed once in cold PBS, suspended the cells in 1X binding buffer (Becton-Dickinson, Annexin V-FITC Apoptosis Detection kit). The counted cells were stained in PI and Annexin V-FITC solution (Becton-Dickinson, Annexin V-FITC Apoptosis Detection Kit) at room temperature for 15 min in the dark. The stained cells were analyzed by flow cytometry within 1 h.

Western blot analysis

The cells were treated under the appropriate conditions, harvested and washed with cold PBS. Total cells were lysed in lysis buffer [40 mM Tris (pH 8.0), 120 mM NaCl, 0.5% NP-40, 0.1 mM sodium orthovanadate, 2 μg/ml aprotinin, 2 μg/ml leupeptin and 100 μg/ml phenymethylsulfonyl fluoride (PMSF)]. The supernatant was collected and protein concentrations were then measured with protein assay reagents (Pierce, Rockford, IL, USA). Protein extracts were denatured by boiling at 100°C for 5 min in sample buffer (0.5 M Tris-HCl, pH 6.8, 4% SDS, 20% glycerol, 0.1% bromophenol blue, 10% β-mercaptoethanol). Equal amount of the total proteins were subjected to 6–15% SDS-PAGE and transferred to PVDF. The membranes were blocked with 5% non-fat dry milk in Tris-buffered saline with Tween-20 buffer (TBS-T) (20 mM Tris, 100 mM NaCl, pH 7.5 and 0.1% Tween-20) for 1 h at room temperature. Then, the membranes were incubated for overnight at 4°C with the primary antibodies (Table I). The membranes were washed once for 10 min with 4X TBS-T buffer and incubated for 1 h with horseradish peroxidase-conjugated anti-rabbit or anti-mouse immunoglobin (Santa Cruz Biotechnology Inc., Santa Cruz, CA, USA). The membranes were washed again for 10 min with 4X TBS-T buffer. Antigen-antibody complexes were detected by the enhanced chemiluminescence (ECL) detection system (Amersham Biosciences Co., Little Chalfont, UK).

Table I Primary antibodies used in western blot analysis.

Table I

Primary antibodies used in western blot analysis.

Antibody	2nd antibody	Dilution ratio	Company
Fas	Rabbit	1:1,000	Santa Cruz
Fas-L	Rabbit	1:500	Santa Cruz
TRAIL	Rabbit	1:1,000	Santa Cruz
DR4	Rabbit	1:1,000	Santa Cruz
DR5	Mouse	1:1,000	Santa Cruz
Bax	Rabbit	1:1,000	Santa Cruz
Bcl-2	Mouse	1:500	Santa Cruz
Cdc2	Rabbit	1:1,000	Santa Cruz
Cdc25c	Rabbit	1:1,000	Santa Cruz
Cyclin B1	Mouse	1:1,000	Santa Cruz
Wee1	Mouse	1:500	Santa Cruz
p21	Mouse	1:1,000	Santa Cruz
p27	Mouse	1:1,000	Santa Cruz
p53	Mouse	1:1,000	Santa Cruz
PARP	Mouse	1:1,000	Santa Cruz
Procaspase-3	Mouse	1:1,000	Santa Cruz
Procaspase-8	Rabbit	1:500	Santa Cruz
Procaspase-9	Rabbit	1:500	Santa Cruz
β-actin	Mouse	1:10,000	Sigma-Aldrich

Statistical analysis

Results were expressed as the mean ± SD of three separate experiments and analyzed by Student’s t-test. Means were considered significantly different at *p<0.05 or **p<0.01.

Results

MHY-449 exhibits more potent cytotoxicity than MHY-450 against HCT116 cells

To investigate the effects of MHY-449 and MHY-450 (Fig. 1A), the diastereoisomeric compounds, on the viability of HCT116 cells, the MTT assay was performed. As shown in Fig. 1B, both MHY-449 and MHY-450 showed concentration-dependent cytotoxicity on HCT116 cells. MHY-449, however, exhibited more potent cytotoxicity than MHY-450. Therefore, further experiments were performed only with MHY-449.

MHY-449 inhibits the growth of HCT116 cells

MHY449 showed concentration-dependent cytotoxicity on HCT116 cells. The IC50 value of MHY-449 on HCT116 cells was approximately 0.5 μM (Fig. 2A). Following experiment was performed in order to investigate whether MHY-449 has an anti-proliferation effect on HCT116 cells by using the trypan blue staining assay. As shown in Fig. 2B, MHY-449 showed time-dependent anti-proliferation effect on HCT116 cells.

Figure 2 Concentration- and time-dependent effects of MHY-449 on the viability of HCT116 cells. (A) One day after seeding, HCT116 cells were treated with incremental concentration of MHY-449 for 24 h. Proliferation was measured by using the MTT assay. The results are expressed as mean ± SD (n=6) and as a percentage of vehicle-treated control. *p<0.05 compared between vehicle-treated control and MHY-449 treated cells. (B) To study anti-proliferative effects of MHY-449 on HCT116 cells, cells were treated with incremental concentration of MHY-449 for 24, 48 and 72 h. Proliferation was measured by using the trypan blue staining assay. The results are expressed as mean ± SD (n=3) and as a percentage of vehicle-treated control.

MHY-449 induces apoptosis in HCT116 cells

To investigate whether the growth inhibitory effects of MHY-449 were due to the induction of apoptosis in HCT116 cells, microphotographs were observed. HCT116 cells treated with MHY-449 showed distinct morphological changes compared with control (Fig. 3A upper panel). They were rounded and more dispersed with aggregation in a concentration-dependent manner. Further morphological changes of cellular structures were assessed with Hoechst 33342 staining. As shown in Fig. 3A lower panel, nuclei with chromatin condensation and formation of apoptotic bodies, which are characteristics of apoptosis, were seen in cells cultured with MHY-449 in a concentration-dependent manner, whereas the control cells maintained nuclear structure intact. In addition to this, to confirm the apoptosis of MHY-449 in the HCT116 cells, flow cytometry analysis and DNA fragmentation assay were performed. As shown in Fig. 3B, increases of early apoptosis (lower right quadrant) and late apoptosis/death (upper right quadrant) were clearly observed in concentration-dependent manner. We also analyzed whether DNA fragmentation, another hallmark of apoptosis, was induced by MHY-449 treatment on HCT116 cells. Following agarose gel electrophoresis of HCT116 cells treated with MHY-449 for 24 h, a typical ladder pattern of internucleosomal fragmentation was observed in a concentration-dependent manner (Fig. 3C).

Figure 3 Induction of apoptosis in HCT116 cells by MHY-449. (A) HCT116 cells were treated for 24 h with the indicated concentrations of MHY-449 and morphological changes were observed by phase contrast microscopy at x400 magnification (upper panel). Stained nuclei with fluorescent DNA-binding dye, Hoechst 33342, were then photographed with a fluorescent microscope using a blue filter at x400 magnification (upper panel). Apoptotic cells (arrow). (B) To investigate the effect of MHY-449 on cell death, HCT116 cells were treated for 24 h with the indicated concentrations of MHY-449. Annexin V binding and PI uptake in non-permeabilized cells and analyzed with a flow cytometry. (C) To analyze fragmentation of genomic DNA, cells were treated for 24 h with the indicated concentrations of MHY-449. DNA was extracted and analyzed by 1% agarose gel electrophoresis in the presence of EtBr. A representative blot is shown from three independent experiments. M, marker.

MHY-449 upregulates the expression of apoptosis-related proteins in the extrinsic pathway

The extrinsic pathway of apoptosis in which Fas/FasL system plays a key signaling transduction has been proposed as a therapeutic target in cancer. Thus, involvement of the Fas/FasL system in HCT116 cells treated with MHY-449 was examined. As shown in Fig. 4, the levels of Fas as well as FasL expression were significantly up-reregulated in a concentration-dependent manner. However, the levels of tumor necrosis factor (TNF)-related apoptosis-inducing ligand (TRAIL), DR4, and DR5 were not changed after MHY-449 treatment.

Figure 4 Effect of MHY-449 on the expression levels of proteins involved in extrinsic and intrinsic pathways of apoptosis in HCT116 cells. HCT116 cells were treated for 24 h with the indicated concentrations of MHY-449. The expression levels of proteins involved in extrinsic pathway, such as FasL, Fas, TRAIL, DR4 and DR5 in HCT116 cells were detected by western blot analysis. Proteins were visualized using the ECL detection system. Representative results from three independent experiments are shown. Actin was used as a loading control.

MHY-449 increases caspase activity in HCT116 cells

Significant activation of pro-caspase-3 and -9 were observed and there was little change in pro-caspase-8 (Fig. 5A). Polypeptide degradation, including poly(ADP-ribose) polymerase (PARP), was examined to see the possible involvement of apoptosis-associated protease during the growth inhibition of the colon cancer cells. PARP cleavage was evident by the appearance of the p85 PARP cleavage fragment and clearly observed in the 0.25 μM and 0.5 μM of MHY-449 treatment. In an attempt to further characterize the mechanisms of apoptosis induced by MHY-449, the activities of caspase -3, -8 and -9 were determined by colorimetric assay. The activities of caspase-3, -8 and -9 were increased with the treatment of MHY-449 in concentration-dependent manner (Fig. 5B). Therefore, these results suggested that MHY-449 induce caspase-dependent apoptosis in HCT116 cells.

Figure 5 Effect of MHY-449 on activation of caspase-3, -8, and -9 and degradation of PARP in HCT116 cells. (A) HCT116 cells were treated with indicated concentrations of MHY-449 for 24 h, collected, lysed and then cellular proteins were separated and immunoblotted. The membranes were probed with procaspase-3, pro-caspase-8, procaspase-9 and PARP (116 kDa). Proteins were visualized using the ECL detection system. Representative results from three independent experiments are shown. Actin was used as a loading control. (B) To detect caspase activities, cell lysates from cells treated with MHY-449 for 24 h were assayed for in vitro caspase-3, -8 and -9 activity using Z-DEVD-pNA, Z-IETD-pNA and Ac-LEHD-pNA, respectively, as substrates at 37°C for 1 h. The released fluorescent products were measured. The data represent the mean ± SD values of three independent experiments. The significance was determined by Student’s t-test (*p<0.05 and **p<0.01 vs. vehicle-treated control cells).

MHY-449 modulates the expression levels of apopotosis-related proteins in HCT116 cells

To determine whether the expression levels of apoptosis-related proteins were modulated by MHY-449, western blot analysis was performed. The expression level of Bcl-2 protein was markedly downregulated, while Bax was upregulated in a concentration-dependent manner (Fig. 6A). The ratio between Bcl-2 and Bax has been suggested as a primary event in determining the susceptibility to apoptosis (17). These data suggest that MHY-449 induces apoptosis by the alteration in expression ratio of Bax/Bcl-2 protein (Fig. 6B).

Figure 6 Effects of MHY-449 on the protein expressions of Bax and Bcl-2 in HCT116 cells. (A) HCT116 cells were treated with variable concentrations of MHY-449 for 24 h and total cell lysates were prepared and immunoblotted. The membranes were detected with antibodies against Bax and Bcl-2 and ECL detection. Representative results from three independent experiments are shown. Actin was used as a loading control. (B) Bax/Bcl-2 ratio was presented in the bar graphs.

MHY-449 modulates cell cycle in HCT116 cells

To investigate whether MHY-449 has an effect on the cell cycle, HCT116 cells were treated with various concentrations of MHY-449 for 24 h and analyzed with flow cytometry. As shown in Fig. 7A, the cells treated with MHY-449 were remarkably arrested in the G2/M phase and increased the proportions of sub-G1 phase cells, both in a concentration-dependent manner. A total 41.55% of cells cultured with 0.25 μM MHY-449 were in G2/M phase, compared to 31.35% of control in G2/M phase. In addition, sub-G1 populations were increased from 3.09% in control to 13.24% in cells treated with 0.25 μM MHY-449. These results suggest that MHY-449 retard the growth of HCT116 cells by arresting cell-cycle progression and apoptosis induction.

Figure 7 Effects of MHY-449 on the cell cycle and the levels of cell cycle regulatory proteins. (A) Exponentially growing cells at 60–70% confluence were treated for 24 h with the indicated concentrations of MHY-449. The percentages of cells in sub-G1, G0/G1, S or G2/M phases of cell cycle are indicated within each histogram. (B) To detect the protein levels of cell cycle regulators, the cells were treated with indicated concentrations of MHY-449 for 24 h, collected, lysed and then cellular proteins were separated and immunoblotted. The membranes were probed with indicated antibodies and ECL detection. Representative results from three independent experiments are shown. Actin was used as a loading control.

MHY-449 modulated cell cycle regulatory proteins in HCT116 cells

The western blot analysis was conducted to further characterize the molecular mechanisms whereby MHY-449 inhibit cell growth and modulate the expression of cell cycle regulating proteins. As shown in Fig. 7B, the intracellular protein levels of G2/M phase of cell cycle, such as cyclin B1, Cdc2 and Cdc25c were decreased and Wee1 was increased in HCT116 cells by MHY-449 treatment in a concentration-dependent manner. The induction of p21WAF1/CIP1 causes subsequent arrest in the G0/G1 or G2/M phase of the cell cycle by binding of the cyclin-CDK complex. The protein levels of p21WAF1/CIP1 and p27KIP were increased in HCT116 cells by MHY-449 treatment in a concentration-dependent manner, and the protein level of p53 was also increased. These results suggest that the significant change in the level of p53 by MHY-449 in HCT116 cells leads to the increase in p21WAF1/CIP. Therefore, the induction of p21WAF1/CIP1 in HCT116 cells is assumed to be p53-dependent.

Discussion

This study was conducted to investigate the effects of MHY-449 on HCT116 human colon cancer cells. MHY-449 induced apoptosis and the cell cycle arrest in HCT116 human colon cancer cells. The diastereoisomeric compound, MHY-449 and MHY-450, showed concentration-dependent cytotoxicity on HCT116 cells and MHY-449 exhibited more potent cytotoxicity than MHY-450. Treatment of HCT116 cells with MHY-449 resulted in growth inhibition in a concentration-dependent manner. MHY-449 also resulted in anti-proliferation in a time-dependent manner. Moreover, MHY-449 treatment showed modulation of the cell cycle and induction of apoptosis in HCT116 cells.

The treatment of MHY-449 induced apoptosis as demonstrated by the formation of apoptotic bodies and DNA fragmentation. Apoptosis (programmed cell death), is an important process required for homeostasis (12,18). Apoptosis occurs through two broad pathways: the intrinsic pathway (the mitochondrial pathway) and extrinsic pathway (the death receptor pathway) (19). Death receptors and caspases are key players in the extrinsic pathway, whereas the Bcl-2 family which consists of more than 20 members of pro-apoptotic proteins (including Bax, Bak, Bok, Bad and Bid), and anti-apoptotic proteins (including Bcl-2, Bcl-XL, Mcl-1 and Bfl-1/A1) (20,21) are key players in the intrinsic pathway.

Treatment of HCT116 cells with MHY-449 resulted in increase in expressions of Fas and FasL in a concentration-dependent manner. The activation of initiator caspase-8 and caspase-9 and downstream effector caspase-3, in response to MHY-449 treatment and cleavage of PARP in HCT116 cells were also observed. The ratio between Bcl-2 and Bax has been suggested as a primary event in determining the susceptibility to apoptosis through maintaining the integrity of the mitochondria and inhibiting the activation of caspase cascade (17). In this study, MHY-449 treatment resulted in a significant increase in pro-apoptotic protein Bax and a decrease in anti-apoptotic protein Bcl-2, resulting in a shift in Bax/Bcl-2 ratio in favor of apoptosis.

Different classes of cyclins and their cyclin-dependent kinase (CDK) control cell cycle progression. G2/M transition provides an effective checkpoint in cell cycle progression, which is regulated by cyclin B1, Cdc2 and Cdc25C (22). In this study, flow cytometric analysis revealed that treatment of HCT116 cells with MHY-449 resulted in the arrest of cells in G2/M phase and it seems to be associated with a decrease in the protein levels of cyclin B1, Cdc2 and Cdc25C.

Uncontrolled cell proliferation is the hallmark of cancer, and tumor cells have typically acquired damage to gene that directly regulates their cell cycles. Eukaryotic cell cycle checkpoints involve the regulation of sequential formation, activation and subsequent inactivation of CDKs, the activation of which is dependent upon an association with cyclins (23,24). The G2/M transition in the cell cycle plays a pivotal role at the entry into mitosis, the complex of which is formed by the association of Cdc2 and cyclin B1 (25). Binding to cyclin B and phosphorylation at threonine 161 by CDK activating kinase (CAK) are required to activate Cdc2 during G2 and the Cdc2/cyclin B complex is kept inactive by phosphorylation in tyrosine 15 (Tyr 15) and threonine 14 of Cdc2 by the kinases Wee1 and Myt1, respectively (26,27). CDK-cyclin complexes are regulated by two families of CDK inhibitors (CKIs), the CIP/KIP family (p21WAF/CIP, p27KIP1, and p57KIP2) and INK4 family (p15INK4b, p16INK4a, p18INK4c, and p19INK4d) (28). Members of CIP/KIP family, such as p21WA1F/CIP1, bind to CDK/cyclin complexes and prevent kinase activation, subsequently regulating G2/M-phase transition (29,30) and upregulation in response to the inhibition of cell growth.

p21WAF1/CIP1 is commonly associated with the G1 check point and G2/M phase, and its association with inhibiting the expression of the Cdc2/cyclin B1 complex has been also reported (29,31). p21WAF1/CIP1 transcription can be regulated through either p53-dependent (32) or p53-independent pathways (33). In the present study, p21WAF1/CIP1 was increased by MHY-449 in HCT116 cells, along with significant increase in the protein levels of p53. These results suggest that MHY-449 upregulates p21WAF1/CIP1 expression and thereby leading to G2/M-phase arrest through p53-dependent pathway.

p27KIP1 exerts tumor suppressing function through inhibitory interactions with the cyclin/CDK complexes, and downregulation of p27KIP1 protein is often correlated with poor prognosis in several types of human cancers. Our result showed that p27KIP1 was increased by the treatment of MHY-449. However, p27KIP1 possess oncogenic function as well, and in many cases it is known to be cyclin/CDK independent and attributed to its cytoplasmic localization (34).

In summary, MHY-449 suppressed growth and proliferation of HCT116 cells in a concentration- and time-dependent manner, respectively, by causing G2/M cell cycle arrest and induction of apoptosis. Taken together, these results suggest that novel compound MHY-449 may be useful in the chemo-prevention and/or treatment of colon cancer.

Acknowledgements

This study was supported by National Research Foundation of Korea (NRF) grant funded by the Korea government (MOST) (no. 20090083538). We thank Aging Tissue Bank for providing research information.

References