Introduction
Acute myeloid leukemia (AML) is a hematologic malignancy characterized by a block of terminal differentiation of the hematopoietic progenitors at early stages in myelopoiesis. AML accounts for ~25% of all leukemias diagnosed in adults and its incidence is stably increasing (1). In the past two decades, there has been little improvement in chemotherapeutic regimens and hence the overall survival for patients with AML remains poor, with a 5-year survival rate of ~20% (2,3) and median survival times of only a few months for elderly patients (4). This is partly due to a higher prevalence of unfavorable cytogenetics and myelodysplasia, a higher incidence of MDR, and more frequent comorbidities that often render them unsuitable for intensive treatment (4,5). Therefore, it is urgent to seek new novel therapeutic agents and strategies with less systemic toxicity for improving the treatment outcomes of elderly patients.
In the past decades, natural products have played a critical role in drug discovery and development. The potential of natural products from plants, notably from traditional Chinese medicine (TCM), has been recognized by the scientific community in the Western world for its low toxicity, and considerable efforts have been made to systematically investigate the active component of TCM for cancer therapy. A series of natural products, such as Homoharringtonine (6), arsenic trioxide (ATO) (7) and paclitaxel (8), have been found and clinically proved for their potential use in leukemia therapy. They demonstrate the translation of basic knowledge of purified agents of complex mixtures from TCM into the clinic. In addition, the successful application of combination of all-trans retinoic acid (ATRA) and ATO therapy in APL demonstrates that the combination of TCM with synthesized compound provides an attractive strategy for the development of novel and improved cancer therapeutics (9,10).
We have focused on studies of TCM treatment in leukemia for decades and have tested more than 10 chemically characterized compounds from TCM treatment in leukemia cell lines and found several active compounds such as icariin (11) and baicalin (12). Baicalin is a flavonoid compound isolated from Scutellaria baicalensis, a Chinese traditional medicinal herb widely used as an anti-inflammatory (13), antibacterial, anxiolytic and hepatoprotective drug (14). Accumulating evidence demonstrates that baicalin exhibits potent antitumor properties by suppressing cell growth, modulating cell cycle, inducing differentiation or apoptosis in leukemia cell lines (15,16), without affecting primary or normal cells (17,18), raising the possibility of treating even older patients with AML.
Hexamethylene bisacetamide (HMBA), a hybrid polar compound, was used in phase I and II clinical trials for the treatment of myelodysplastic syndrome (MDS) and AML (19). Previous studies demonstrated that HMBA exerted dose-dependent dual effects on AML cells. At low concentrations, HMBA induces terminal differentiation in a variety of leukemic cell lines (20,21), while it inhibits cell growth significantly at high concentrations through apoptosis and cell cycle delay rather than through differentiation. Evidence indicates that HMBA induced apoptosis associated with downregulation of Bcl-2 gene expression, upregulation of expression of p21, p53 (22), or HMBA induced the activation of a caspase-independent cell death pathway (23). Additionally, other studies documented that HMBA can be efficacious as an adjunct agent for enhancing the antitumor effects of antineoplastic drugs (24,25). However, some serious side-effects were induced when administered at higher concentrations, such as thrombocytopenia, thereby limiting the utilization of this agent in cancer chemoprevention (21).
It was previously reported that suberoylanilide hydroxamic acid (SAHA) and flavopiridol (FP) interact synergistically to induce mitochondrial damage and apoptosis in human leukemia cells (26,27). In view of the similar molecular structure between SAHA and HMBA, and that between FP and baicalin, together with their potential antileukemic efficacy, the enhancement of baicalin by HMBA in growth arrest and apoptosis induction of AML cells in the present study were detected and the underlying mechanism of their effect was also elucidated.
Materials and methods
Reagents
Baicalin with a purity of up to 99.5% was kindly provided by Professor Xiao Wang (Shandong Analysis and Test Center, Shandong Academy of Sciences) and 10 mg/ml solution dissolved with DMSO was stored at -20°C. HMBA was obtained from Sigma (St. Louis, MO, USA) and 0.5 M stock solution was made by dissolving it in RPMI-1640 medium (Gibco, Grand Island, NY, USA). Propidium iodide (PI), rhodamine 123 (Rh123) were also purchased from Sigma. Hoechst 33342 was obtained from Beyotime Biotechnology, Inc. (Nantong, China). Annexin V fluorescein isothiocyanate (FITC) kit was obtained from BD Biosciences (San Diego, CA, USA). Antibodies for detecting Bax, Bcl-2, cleaved caspase-3, -8, -9, Fas were purchased from Cell Signaling Technology (Beverly, MA, USA). β-actin antibody was purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA, USA). Horseradish peroxidase-labeled IgG anti-mouse and anti-rabbit antibodies were supplied by Zhongshan Golden Bridge Biotechnology Co. (Beijing, China). Cell Counting Kit-8 (CCK-8) was obtained from Dojindo Laboratories (Kumamoto, Japan).
Cell culture
AML cell lines NB4 and THP-1 were purchased from American Type Culture Collection (ATCC, Bethesda, MD, USA); HL-60 cells and K562 cells were conserved by our laboratory. Cells were cultured in RPMI-1640 medium supplemented with 10% heat-inactivated newborn calf serum (NCS), 100 IU/ml penicillin and 100 IU/ml streptomycin at 37°C in an atmosphere with 5% CO2. Logarithmically growing cells were exposed to drugs for the indicated time periods.
Human peripheral blood mononuclear cells (PBMCs) were isolated from heparinized venous blood of healthy volunteers by Ficoll-Paque density gradient centrifugation. After washing with PBS twice, PBMCs were cultured in RPMI-1640 with 10% FCS at 37°C in a humidified atmosphere containing 5% CO2. After incubating on a plastic plate for 6 h, non-adherent cells were collected and used for cytotoxicity assay (18).
Cell viability assay
Cellular viability was detected using CCK-8 according to the manufacturer’s instructions. In brief, logarithmically growing cells were seeded on 96-well plates at a density of 1×104 cells/well in 100 μl of medium in triplicate and treated with baicalin (5, 10, 20, 40, 80 μg/ml) or HMBA (0.5, 1, 2, 4 mM) or in combination. Cells treated with 0.1% (v/v) DMSO or RPMI-1640 medium were used as control. Following incubation for 24 h, 10 μl of CCK-8 solution was added to each well in the assay plate and incubated for an additional 2 h at 37°C. Absorbance was measured at 450 nm using a microplate reader (Model 550; Bio-Rad, USA). Each group had triplicate samples. The inhibition rate was calculated by the following formula: cell inhibition rate (%) = 1 − average absorbance of treated group/average absorbance of control group ×100%. Data were calculated as the means ± SD of triplicate samples and are representative of at least three independent assays.
The cytotoxicity of baicalin and HMBA on PBMCs was assayed by the trypan blue exclusion test. Briefly, PBMCs from two healthy volunteers were cultured with 20 μg/ml baicalin and/or 2 mM HMBA for 3 days, then 1 μl of trypan blue dye was added to cell suspension, mixed and incubated for 2 min. Dye-cell suspension was loaded to a counting chamber and counted under a microscope to determine whether cells take up or exclude dye. Percentage of viable cells was calculated by the following formula: % of viable cells = number of viable cells counted/total number cells counted.
Cell cycle analysis
Following baicalin (20 μg/ml) and/or HMBA (2 mM) treatment for 24 h, HL-60 cells (3×105) were washed twice with ice-cold PBS, and fixed in cold 75% ethanol at 4°C for at least 24 h. Then the cells were rinsed with PBS, resuspended in 1 ml of cell cycle buffer (0.38 mm Na-Citrate, 0.5 mg/ml RNase A and 20 μg/ml PI) at room temperature for 30 min and analyzed using an EPICS XL flow cytometer with EXPO32™ ADC software (Beckman Coulter, Miami, FL, USA).
Morphological assessment of apoptosis
HL-60 cells were plated (3×105 cells/well) after baicalin (20 μg/ml) and/or HMBA (2 mM) treatment for 24 h; cell morphology was observed with light microscopy. For nuclear morphology, cells were washed twice with PBS, fixed with 4% paraformaldehyde for 15 min and stained with Hoechst 33342 (10 μg/ml) for 5 min at room temperature in the dark. After washing three times, cells were resuspended by PBS. Stained nuclei were observed by a Nikon ECLIPSE Ti Fluorescence Microscope (Nikon, Japan) and photographed.
Apoptosis assessment by Annexin V/PI staining
Following drug exposure for 24 h, 3×105 cells were harvested, washed twice with cold PBS and resuspended in 100 μl of 1X binding buffer containing 5 μl Annexin V and 10 μl PI for 15 min at room temperature in the dark. Flow cytometry measurements were made on a Beckman Coulter EPICS XL cytometer.
Assays for analysis of mitochondrial membrane potential (ΔΨm)
ΔΨm was assessed using fluorescent dye Rh123 and flow cytometric analysis. Briefly, following drug treatments for 6 h, the cells were washed twice with PBS; 1×106 cells in different groups were incubated with 10 mg/ml Rh123 for 30 min at 37°C. Following incubation, cells were washed twice and resuspended in PBS followed by flow cytometric analysis. The change in the mean fluorescence intensity reflects the modification of ΔΨm, which drives the uptake and accumulation of Rh123 in the mitochondria.
Reverse transcription (RT)-PCR analysis
Following baicalin (20 μg/ml) and/or HMBA (2 mM) treatment for 24 h, HL-60 cells were collected and total RNA was extracted from each sample of 1×106 cells by TRIzol (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s protocol. The RNA samples were resuspended in RNase-free water and frozen at −80°C until use. RT-PCR was performed as previously described (28). The PCR products were electrophoresed in 1.5% agarose gels. The primers used were all synthesized by Sangon Co., Ltd. (Shanghai, China). The sequences are listed in Table I.
Western blot analysis
After exposing to baicalin (20 μg/ml) and/or HMBA (2 mM) for 24 h, HL-60 cells were washed twice with cold PBS and lysed in extraction buffer (50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1 mM PMSF, 1 mM EDTA, 1% Triton X-100, 0.5% deoxycholate, 1 μg/ml leupeptin, 2 μg/ml aprotinin, 1 mM Na3VO4 and 0.1% SDS) for 30 min on ice. The lysates were centrifuged at 12,000 × g for 15 min and quantified using Bradford protein assay. Proteins were separated by SDS-PAGE and electroblotted onto PVDF membranes. The membranes were blocked with 5% milk for 1 h and incubated with primary monoclonal antibodies against caspase-8 (1:1,000), caspase-9 (1:1,000), cleaved caspase-3 (1:1,000), Fas (1:1,000), Bcl-2 (1:1,000) and Bax (1:1,000) (Cell Signaling Technology) overnight at 4°C followed by incubation with HRP-conjugated secondary antibodies (Zhongshan Golden Bridge Biotechnology Co.) for 1 h. The protein bands were visualized using Immobilon Western Chemiluminescent HRP Substrate (Millipore, Billerica, MA, USA) and pictured by LAS-4000 Mini luminescent image analyzer (Fujifilm, Tokyo, Japan).
Statistical analysis
Data presented are the means ± SD from at least three independent experiments and the significance of difference between two groups was compared by one-way analysis of variance (ANOVA) followed by Tukey’s test using SPSS 13.0 (SPSS, Chicago, IL, USA). P<0.05 was considered to indicate statistically significant differences.
Results
Combined treatment with baicalin and HMBA synergistically inhibits the proliferation of AML cell lines
To determine the optimal combined concentration, HL-60 cells were initially treated with various concentrations of baicalin or HMBA alone. As shown in Fig. 1A, at the indicated concentration scope, baicalin inhibited cell proliferation in a dose-dependent manner. The IC50 value of baicalin was 21.8 μg/ml calculated according to the dose-response curve. At this concentration baicalin showed almost no cytotoxicity in PBMCs even after 5.5 days of culture (18). Therefore, 20 μg/ml was selected for the subsequent analysis. HMBA has been shown to induce differentiation in multiple leukemia types at a concentration of 2–5 mM (29). Thus, the 0–4 mM of HMBA concentration range was selected for cell viability assay. CCK-8 assay indicated that HMBA induced cell growth arrest in a dose-dependent manner, but more mildly than baicalin (Fig. 1B). Based on this growth inhibition of HMBA and the low efficient concentration used in the clinic (30), 2 mM was determined for the combined concentration of HMBA.
Next, studies were performed to detect the inhibitory effect of the combination treatment. Following coadministration of 20 μg/ml baicalin with 2 mM HMBA for 24 h, the inhibition rate strikingly increased from 47.5±6.3 or 22.6±1.5 to 87.4±2.6% (P<0.01), which indicated that combination treatment exerted a synergistic inhibitory effect on the proliferation of HL-60 cells. To determine whether the synergistic effect was restricted to HL-60 cells, parallel studies were performed in other human leukemia cell lines K562, THP-1 and NB4 and the same results were obtained (Fig. 1C). Of these cell lines, the combination treatment showed the most significant inhibitory effect on HL-60 cells. Therefore the following experiments were performed with HL-60 cells.
In order to confirm that the combination of baicalin and HMBA has selectivity for malignant cells, rather than also indiscriminately killing normal cells, PBMCs were separated from healthy volunteers and cultured with baicalin and/or HMBA. The trypan blue staining results demonstrated that single agent or combination treatment had only slight cytotoxicity on PBMCs even after 3 days of culture (Fig. 1D).
Combined treatment with baicalin and HMBA induces a slight G<sub>0</sub>/G<sub>1</sub> arrest in HL-60 cells
To investigate the mechanisms underlying the enhanced growth inhibitory effect of the combination of baicalin and HMBA in HL-60 cells, we performed the cell cycle analysis by flow cytometry. As shown in Fig. 2, no significant changes in cell distribution were observed following exposure of HL-60 cells to 20 μg/ml baicalin or 2 mM HMBA for 24 h, although both cause G0/G1 phase arrest for 48 h or longer (data not shown). However, combined treatment with baicalin and HMBA slightly increased the proportion of cells in the G0/G1 phase from 29.2% in the vehicle-treated cells to 37.6% (P<0.05). The data indicated that a block in the cell cycle may be partly associated with the synergistic inhibitory effect on the proliferation of HL-60 cells after 24 h combined treatment.
Combination of baicalin and HMBA enhances induction of apoptosis in HL-60 cells
To determine whether the synergistic inhibitory effect on combined treatment of HL-60 cells with baicalin and HMBA was due to the induction of apoptosis, cell morphological changes were observed under a light micrograph and under an inverted fluorescence microscope after Hoechst 33342 staining. It was noted that HMBA-treated cells presented no significant morphological changes but only with the numbers decreased compared to control cells. However, after exposure to 20 μg/ml baicalin for 24 h, the number of HL-60 cells significantly decreased and, also, part of the cells exhibited typical morphological characteristics of apoptosis (such as cell shrinkage, membrane blebbing and formation of apoptotic bodies) (Fig. 3A). Combined with HMBA, the phenomenon became stronger. Accordingly, Hoechst 33342 staining results showed that the nuclei of untreated cells and HMBA-treated cells were round and large in size, exhibiting homogeneous blue fluorescence. By contrast, parts of cells treated with baicalin for 24 h were observed with condensed or fragmented nuclei which is characteristic of cell apoptosis. Moreover, the apoptosis events in the combination group were more distinguished than in the baicalin treatment group (Fig. 3B).
To further validate the enhanced effect of combined treatment on cell apoptosis, the extent of apoptosis was evaluated by Annexin V/PI assay. As indicated in Fig. 4, cotreatment with 20 μg/ml baicalin and 2 mM HMBA showed a synergistic effect (34% total apoptotic cells) on the induction of apoptosis in HL-60 cells compared to 24.4 and 7.7% for 20 μg/ml baicalin and 2 mM HMBA treatment alone, respectively. These findings suggest that HMBA enhances apoptosis induced by baicalin on HL-60 cells.
Combined treatment with baicalin and HMBA induces the activation of caspase-3, -8 and -9
The caspase family of cysteinyl-proteases plays the key role in the initiation and execution of programmed cell death (31). Thus, the mRNA expression of caspase-8, caspase-9 was first detected by semiquantitative RT-PCR. As shown in Fig. 5A, baicalin treatment alone caused a 2.82±0.13-fold and 2.29±0.11-fold increase at the transcriptional level of caspase-8 and caspase-9, respectively, as compared with the control group. When combined with HMBA, the mRNA expression of caspase-8, caspase-9 rose to 3.43±0.10-fold and 4.48±0.26-fold, respectively. These data suggest that caspase-8 and caspase-9 may be involved in the apoptosis induced by baicalin/HMBA. To further confirm the involvement of caspases, activation of caspase-8, -9 and -3 was monitored by western blotting. As shown in Fig. 5B, 24 h exposure to 2 mM HMBA failed to increase cleavage and activation of caspase-3 while 20 μg/ml baicalin did. Moreover, combined treatment led to a clear increase in caspase-3 activation which was reflected by the appearance of a 17 kDa caspase-3 cleavage fragment. Similarly, the cleavages of caspase-8 and -9 were significantly enhanced by combined treatment of baicalin and HMBA. These results from RT-PCR and western blot analyses taken together thus indicate that baicalin/HMBA-induced apoptosis is mediated through the activation of caspase-3, -8, and -9.
Combined treatment-induced apoptosis is mediated through both the mitochondrial- and Fas-mediated pathways
Since combination treatment induced the activation of caspase-8 and -9, it suggests that both extrinsic and intrinsic pathways are involved in the apoptosis signaling. To address the intrinsic pathway, ΔΨm was monitored by flow cytometry using Rh123. The reduction of Rh123 fluorescence intensity presented dissipation of ΔΨm. As shown in Fig. 6A, HMBA administered alone for 6 h had little effect on ΔΨm compared with controls, whereas baicalin alone led to a slight reduction of ΔΨm. However, combined treatment of HL-60 cells to baicalin/HMBA resulted in a marked increase in loss of ΔΨm, as compared with either agent alone. These findings were consistent with the activation of caspase-9, which is often the result of disruption of ΔΨm.
To characterize the role of the extrinsic pathway in baicalin/HMBA-induced apoptosis, we detected Fas protein expression by western blot analysis. The results showed that exposure to baicalin or HMBA alone triggered the Fas expression. Moreover, combination treatment significantly increased its expression (Fig. 6B). The data presented herein suggest that activation of the extrinsic Fas-related pathway plays a major role in the enhanced apoptosis observed in baicalin/HMBA-treated cells.
Effect of baicalin and HMBA combined treatment on the mRNA and protein expression of the Bcl-2 family
Proapoptotic and antiapoptotic members of the Bcl-2 family regulate the mitochondrial pathway (32). To further determine whether baicalin/HMBA-induced apoptosis in HL-60 cells is associated with the mitochondrial pathway, the expression of proapoptotic factor Bax, as well as antiapoptotic factor Bcl-2 and Bcl-XL, were tested at the transcriptional and post-transcriptional level. As shown in Fig. 7A, 24 h exposure to either 20 μg/ml baicalin or 2 mM HMBA upregulated the expression of Bax mRNA, while no evident augmentation was observed in the combination group as compared with single agent. In contrast to the increase in the Bax mRNA levels, the mRNA expression of Bcl-2 and Bcl-XL decreased more clearly in combination-treated cells than in single agent-treated cells. Consequently, the ratio of Bcl-2/Bax and the ratio of Bcl-XL/Bax markedly declined. In parallel studies, western blot analysis revealed that the protein expression of Bax and Bcl-2 changed in line with the mRNA expression (Fig. 7B).
Discussion
Similar to previous findings observed in leukemic cells treated with FP in combination with SAHA (26,27), the present study highlighted the synergistic antileukemic effect of baicalin in combination with HMBA in AML cell lines. It was demonstrated for the first time that the administration of a subtoxic concentration of baicalin and a pharmacologically relevant concentration of HMBA results in a synergistic effect in growth inhibition with only slight toxic effect on normal human cells.
To determine whether the synergistic inhibitory effect of the combined treatment of HL-60 cells with baicalin and HMBA is associated with the cell cycle arrest, we performed the cell cycle analysis by flow cytometry. Cell cycle analysis was studied in the way of time course as in our previous study (20), the data confirmed that HMBA alone clearly induced G0/G1 cell cycle arrest after treatment for 48 h or later. Ikezoe et al(33) reported that baicalin arrested G2/M phase in HL-60 cells; however, our results showed that baicalin induced G0/G1 arrest 48 h later. By contrast, a 24-h exposure to 2 mM HMBA or 20 μg/ml baicalin alone had almost no effect on cell cycle distribution, while they could slightly induce G0/G1 arrest, which may at least partly contribute to the synergistical inhibition of cell proliferation (Fig. 2). In general, Cdk inhibitors, including p21waf1 and p27kip1, are involved in G1 to S transition (34). Previous studies demonstrated that baicalin induced expression of p27kip1 as well as slightly upregulated the expression of p21waf1 in HL-60 cells and concomitantly induced differentiation, cell cycle arrest and apoptosis in these cells (33). Buonamici and Aifantis (35) found p21 is also involved in HMBA-induced apoptosis and a short delay in cell cycle. Consistent with the above mentioned studies, herein we also found the upregulation of p21 and p27 in HMBA- or baicalin-treated cells, even more evidently with combination treatment, which may account for the G0/G1 cell cycle arrest (data not shown). However, the result of cell cycle distribution is not fully consistent with the synergistic growth inhibition detected by CCK-8 assay, suggesting that other mechanisms must exist which associate with the antiproliferative effect of drugs in combination.
To confirm whether the synergistic effect on cell growth arrest is associated with apoptosis, cell morphology and Annexin V/PI staining assay were performed. Data showed that treatment of HMBA alone at a concentration of 2 mM had almost no effect on the apoptosis of HL-60 cells. While treatment with baicalin alone induced significant apoptosis. However, the combination treatment of baicalin and HMBA induced more apoptotic cells, which suggested that HMBA may enhance the apoptosis induced by baicalin. This phenomenon is consistent with the pronounced inhibition of cell proliferation (Figs. 3 and 4).
To further delineate the convergence in apoptosis signaling, the caspases, proapoptotic and antiapoptotic proteins were detected in cells with combined treatment of baicalin and HMBA. It is well known that two major apoptotic pathways exist in mammalian cells: the extrinsic death receptor pathway and the intrinsic mitochondrial pathway (36). In the death receptor (extrinsic) pathway, binding of death ligands such as Fas ligand or TNF-α to their cognate death receptors triggers receptor trimerization, recruitment of the adaptor molecule FADD and caspase-8 to the death-inducing signaling complex (DISC). This, in turn, leads to activation of caspase-8, which then either directly cleaves and activates the effector caspase-3 and -7 or cleaves Bid, a Bcl-2 family protein with a BH3 domain only that translocates to mitochondria upon cleavage to initiate a mitochondrial pathway (37). In the mitochondrial (intrinsic) pathway, a variety of extra- and intracellular stresses, including oxidative stress, DNA damage, heat shock and treatment with cytotoxic drugs, converge to induce the release of cytochrome c from the mitochondrial intermembrane space to the cytosol. Cytochrome c cooperates with dATP and Apaf-1 to induce the activation of caspase-9 that can cleave and activate caspase-3 (31), culminating in cell death. Previous studies demonstrated that baicalin acted as a pro-oxidant and induced caspase-3 activation and apoptosis in Jurkat cells (18)or HL-60 cells (15) via the mitochondrial pathway. Recently, the intrinsic (mitochondrial) pathway was confirmed to play a pivotal role in apoptosis induced by baicalin in CA46 Burkitt lymphoma cells (38). Consistent with previous reports, we also observed increase of caspase-3 in cleaved form and caspase-9 mRNA expression in HL-60 cells after exposure to baicalin for 24 h, concomitant with the loss of ΔΨm. Furthermore, 2 mM HMBA failed to induce activation of caspase-9 and -3, although HMBA can do so in P-glycoprotein cells at concentrations as high as 10 mmol/l (23). However, coadministration of baicalin with HMBA resulted in enhanced dissipation of ΔΨm and increased activation of caspase-9, caspase-3 (Figs. 5 and 6A). The data suggested that HMBA lowers the threshold for baicalin-mediated mitochondrial injury and subsequent activation of the caspase cascade, increasing the apoptotic effects induced by baicalin.
The Bcl-2 family proteins are well known for regulating the intrinsic pathway of apoptosis through tightly regulating mitochondrial outer membrane permeabilization (MOMP), which leads to the loss of ΔΨm and therefore the release of proapoptotic molecules, including cytochrome c from mitochondria to the cytosol (39). The family consists of antiapoptotic proteins, such as Bcl-2 and Bcl-XL, as well as proapoptotic members, such as Bax, Bid, Bax and Bak. Accumulating evidence suggests that it is the relative ratio of antiapoptotic and proapoptotic Bcl-2 family proteins rather than the levels of individual proteins that play a major role in determining the survival or death of cells (40). Consistent with previous reports, our data indicated that either baicalin or HMBA induced negative modulation expression of Bcl-2/Bax and Bcl-XL/Bax ratios. Moreover, the ratios decreased more significantly with combination treatment (Fig. 7). Our data suggested that HMBA at a concentration not sufficient to induce cell death per se, reduced the ratio between antiapoptotic and proapoptotic Bcl-2 family members, thereby lowering the threshold for cell death commitment and sensitizing HL-60 cells to the apoptosis induced death by baicalin. This finding is supported by Palumbo et al(24). Collectively, the modification of Bcl-2 family proteins further indicated that the intrinsic apoptotic pathway is involved in baicalin/HMBA-induced apoptosis.
Previous studies had not referred to the effect of baicalin on change of caspase-8 protein. In the present study, RT-PCR and western blot analyses results showed for the first time that the cleavage/activation of caspase-8 increased after exposure to baicalin for 24 h, more significantly in the combination treatment group for 24 h (Fig. 5), which may partly contribute to the increase of caspase-3 activation. Consistent with the above findings, our data also showed that baicalin upregulated the expression of Fas protein (Fig. 6B). However, this is contrary to another report indicating that baicalin had no effect on the expression of Fas protein in TALL cell lines CCRF-CEM (16). The difference is likely due to the specific cell type. Moreover, baicalin markedly elevated the expression of Fas in combination with HMBA. Taking into account the pronounced upregulation of Fas expression and increased activation of caspase-8, we postulate that the extrinsic pathway is likely to be involved in baicalin/HMBA-induced apoptosis in HL-60 cells.
In summary, we showed that the combination of baicalin and HMBA could synergistically inhibit the proliferation of AML cell lines with little toxic effect on normal human cells. In addition, a slight G0/G1 phase arrest and significant apoptosis were observed. The combination treatment triggers apoptosis through the intrinsic pathway, which involves loss of MMP, decreased Bcl-2/Bax ratio and Bcl-XL/Bax ratio, caspase-9 activation, as well as through the extrinsic pathway mediated by Fas and caspase-8 activation. Our results raise the possibility that the novel combination of baicalin and HMBA may be a promising regimen for the treatment of AML.