Honokiol is an active compound purified from magnolia that has been shown to induce cell differentiation, apoptosis, and anti-angiogenesis effects, as well as an enhancement in tumor growth delay in combination with chemotherapeutic agents in several mouse xenograft models. Our goal was to investigate the radiosensitization effect of honokiol on lung carcinoma. The radiosensitization effect of liposomal honokiol in Lewis lung carcinoma cells (LL/2) was analyzed using an in vitro clonogenic survival assay. For an in vivo study, Lewis lung carcinoma-bearing C57BL/6 mice were treated with either liposomal honokiol at 25 mg/kg or 5 Gy of single tumor radiation, or a combination of both over 12 days of treatment. The tumor growth delay and the survival time were evaluated. In addition, histological analysis of tumor sections was performed to examine changes by detecting the microvessel density and apoptosis in tumor tissues. In the clonogenic survival assay, LL/2 cells treated with IC50 Lipo-HNK for 24 h showed a radiation enhancement ratio of 1.9. After 12 days of combination treatment, the tumor volume decreased 78% and produced an anti-tumor activity 1.3-fold greater than a predicted additive effect of honokiol and radiation alone. This combination treatment also caused an 8.7 day delay in tumor growth. The cell cycle distribution and histological analysis demonstrated that liposomal honokiol has an anti-tumor effect via inducing apoptosis and inhibiting angiogenesis. Liposomal honokiol can enhance tumor cell radiosensitivity in vitro and in vivo, indicating that radiotherapy combined with liposomal honokiol can lead to greater anti-tumor efficacy.
Lung cancer is a leading cause of death worldwide. Despite aggressive approaches in the treatment of lung cancer in the past few years, the five year survival rate is still less than 15% (Belinsky et al., 2006) and about 90% of deaths from lung cancer are thought to result from metastasis (Yano et al., 1997). Concurrent or sequential combinations of radiotherapy or chemotherapy with antiangiogenic therapy have been suggested as promising alternatives to single-agent therapies. Recent reports from experimental and clinical studies have proposed that such combinations have shown greater than additive effects due to apparent mutual reinforcement of these approaches (Bello et al., 1999; Abdollahi et al., 2003; Burdelya et al., 2006). Irradiation induces the production of VEGF or PDGF, which may promote tumor regrowth after irradiation (Gorski et al., 1999; Abdollahi et al., 2003; Colevas et al., 2003; Huber et al., 2005) and result in protection of vessels from radiation-induced cell damage. Thus, the rationale for this combination involves killing endothelial cells with radiotherapy and preventing their regrowth using an anti-angiogenesis inhibitor, which may act as a radiosensitizing compound to increase the deleterious effects of X-rays on tumor cells.
Honokiol is an active compound purified from magnolia that has drawn much attention for its anti-angiogenisis, cell differentiation, and apoptotic properties. Previous reports have demonstrated that honokiol can induce apoptosis in numerous cell lines, including murine endothelial SVR cells (Bai et al., 2003), human leukemia MOLT 4B cells (Hibasami et al., 1998), human colorectal carcinoma RKO cells (Wang et al., 2004), and human squamous lung cancer CH27 cells (Yang et al, 2002). The mechanism of anti-angiogenesis is down-regulation of the phosphorylation of vascular endothelial growth factor 2 (VEGFR2) (Bai et al., 2003). Differences in the action mechanisms and toxicity profiles of honokiol and radiotherapy indicate that the combination treatment has clinical potential.
We evaluated the ability of honokiol to enhance radiation-induced cytotoxity in the LL/2 cell line. The anti-tumor effects of a combination consisting of liposomal honokiol and radiotherapy were systematically investigated both in vitro and in vivo. The combined mechanisms underlying the antitumor effects were investigated by observing the microvessel density and apoptosis in tumor tissues. Honokiol was encapsulated with liposome due to poor water solubility.
Materials and Methods
High-purity soybean phosphatidyl choline, polyethylene glycol 4000 (PEG 4000), and cholesterol were purchased from Sigma Chemical Co, Inc. (St. Louis, MO). Honokiol was obtained from Chengdu Sikehua Biotechnology Co. Ltd. (Chengdu, China). Mouse monoclonal antibodies against human CD31 antibodies were purchased from BD Biosciences Co. (Dako LSAB kit, Dako). Biotinylated goat anti-rabbit IgG and biotinylated goat anti-rat IgG were obtained from Vector Laboratories. DAB coloring reagent, HRP labeled rabbit anti-mouse antibodies, and goat anti-rabbit were obtained from Beijing Zhongshanjinqiao Biotechnology Co. Ltd. (Beijing, China).
Cell culture, tumor model, and irradiation
The human lung cancer cell lines SPC-A1 and A549, and the Lewis mouse lung cancer cell line LL/2 were purchased from American Type Culture Collection, ATCC. SPC-A1, and A549 cells were incubated in RPMI-1640 medium (GIBICO) and LL/2 cells were incubated in DMEM medium (GIBICO). Cells were supplemented with 10% heat-inactivated FCS, 100 units/ml of penicillin, and 100 units/ml of streptomycin at 37℃ with 95% relative humidity under 5% CO2. Cell concentrations were determined by counting trypsinized cells using a hemocytometer. For combination experiments, LL/2 cells were used for proliferation and clonogenic survival assays based on pilot experiments.
The LL/2 bearing-tumor model was established in C57BL/6N mice (female; 18-20 g body weight; 8 weeks old). These mice were inoculated s.c. in the right posterior limb area with LL/2 cells (5 × 105). All mice were purchased from Sichuan University Animal Center (Chengdu, China). Photon irradiation was administered using a digital linear accelerator (Elekta Instrument AB, Sweden) at 6 MV at a dose rate of 2.4 Gy/min. All animals used in the experiments were treated humanely in accordance with Institutional Animal Care and Use Committee guidelines.
Preparation of liposomal honokiol
Liposomal honokiol (Lipo-HNK) was prepared in our lab. Lecithin, cholesterol, PEG4000, and honokiol were mixed in weight ratios of 3:3:6:4 and dissolved in 15 ml of chloroform/methanol at a ratio of 3:2 (v/v). The mixture was gently warmed to 40℃ in a round-bottomed flask, and the solvent was evaporated under a vacuum in a rotary evaporator until a thin lipid film was formed. The dried lipid films were left overnight and sonicated in 5% glucose solution, followed by concentration and lyophilization. The preparation of empty liposome (Lipo-null) was the same as Lipo-HNK without addition of honokiol. The final Lipo-HNK and Lipo-null were small multilamellar liposomes in a size range of 130 ± 20 nm and 100 ± 20 nm, respectively. The unencapsulated drug was separated by passing the liposome preparation through a sterile Sephadex G-75 column (Pharmacia) eluted with PBS buffer at pH 7.4. The preparation was then filter sterilized by passage through a 0.22 µm Millex filter. Lyophilized Lipo-HNK and Lipo-null were dissolved in NS for in vitro and in vivo studies.
Cell growth inhibitory activities
The cell growth-inhibitory activities of Lipo-HNK for SPC-A1, A549, and LL/2 cells were evaluated using an MTT assay (Zhang et al., 2005). SPC-A1, A549, and LL/2 cells were seeded in a 96-well plate at a plating density of 0.5-1 × 104/ml, and cultured for 24 h. Harvested cells were exposed to either Lipo-null or Lipo-HNK at various doses in fresh DMEM or RPMI-1640 medium at the indicated dosages. Free honokiol was dissolved in DMSO (the final concentration of DMSO did not exceed 0.1%). Four replicates of one well each for each treatment dose were performed. The control groups were treated with Lipo-null that contained an equivalent dose of the polyethylene glycol liposomes of Lipo-HNK. Four to six wells were left as blanks. The plate was placed at 37℃ in 5% CO2 for various times (12 h, 24 h, 36 h, 48 h), and then cells were added to 20 µl of MTT (5 mg/ml) for 3 h at 37℃. After incubation, the supernatant was removed, the plate was reloaded with 0.15 ml of DMSO, and the absorbance was measured at 570 nm using a Spectramax M5 Microtiter Plate Luminometer (Molecular Devices). The absorbance value of untreated cells was considered to be 100%. IC50 was defined by the concentration that caused a 50% absorbance decrease in drug-treated cells compared with untreated cells.
Clonogenic survival assay
After treatment with drugs and irradiation, cells were harvested and plated in triplicate in 6 cm dishes with densities varying from 200 to 10,000 cells/dish, depending on the radiation dose that the cells received (Xu et al., 2005). The cells were then cultured in a 37℃, 5% CO2 incubator for 14 days. The culture dishes were stained with crystal violet. Colonies with more than 50 cells were scored as positive and the surviving fraction was determined. Radiation survival data were corrected using Lipo-HNK-treated only cells as a control. Cell survival curves were constructed using the one-hit multi-target equation. The radiation enhancement ratio (RER) was defined as RER = mean inactivation dose (radiotherapy)/mean inactivation dose (drug+radiotherapy). A RER value of > 1 was indicative of radiosensitization (Supiot et al, 2005).
Flow cytometry and apoptosis analyses
Evaluation of the cell cycle phase distribution was done using flow cytometry. LL/2 cells were seeded in a 6-well plate and treated with 18 µg/ml of Lipo-HNK, Lipo-null that contained an equivalent dose of the polyethylene glycol liposomes of Lipo-HNK, 5 Gy of radiation, or 18 µg/ml of Lipo-HNK + 5 Gy of radiation. Cells were then collected, washed with PBS, and suspended in 1 ml hypotonic fluorochrome solution that contained 50 µg of propidium iodide/ml in 0.1% sodium citrate plus 0.1% Triton X-100. The cells were analyzed using a flow cytometer (ESP Elite, Beckman-Coulter, Miami, FL). The numbers of apoptotic cells appearing in the cell cycle distribution were estimated using Listmode software.
In vivo anti-tumor efficacy
Tumor-bearing C57BL/6 mice were coded and divided randomly into 5 groups (n = 10 each group). Treatment was initiated at fifteen days when the tumor volume was approximately 500 mm3. The five groups of mice bearing tumors were treated with i.p. axenic NS (0.5 ml each), Lipo-HNK at 25 mg/kg, Lipo-null at 37.5 mg/kg, radiotherapy (RT, 5 Gy each), and Lipo-HNK combined with radiotherapy. The first three groups were given treatment every day for 10 days. The RT group was given treatment at a dose of 5 Gy every day for 5 days. In the combination treatment, mice were given a dose of 5 Gy/day for five days after treatment with Lipo-HNK for 40 min, and then treated with Lipo-HNK for five days. Survival times and tumor volumes were observed. The tumor size was determined by measuring the largest and the perpendicular diameters every three days. Tumor volumes were calculated according to the formula V = a × b2 × 0.52, where a is the largest superficial diameter and b is the smallest superficial diameter. To detect necrosis, apoptosis, and the microvessel density, tumor tissues were excised, fixed in 10% formalin, and frozen at -80℃.
Immunohistochemistry for microvessel, cell apoptosis, and proliferation analyses
Tumor tissues were fixed in a 10% neutral buffered formalin solution and embedded in paraffin. Sections 3-5 µm thick were stained with hematoxylin and eosin (H&E) for detection of necrosis. Induced apoptosis was evaluated by a TUNEL assay using an in situ cell death detection kit (Roche Molecular Biochemicals) following the manufacturer's protocol (Xiao et al., 2002). Cells undergoing apoptosis and necrosis were identified per one high-power microscope field. The anti-angiogenesis activity of Lipo-HNK was detected using frozen sections fixed in acetone and incubated with monoclonal rat anti-mouse CD31. After washing in PBS, sections were treated with secondary biotinylated goat anti-rat antibody. The sections were then stained with labeled streptavidin biotin reagents. The vessel density was determined by counting the number of microvessels per one high-power field (Blezinger et al., 1999; Lu et al., 2003).
Statistical comparisons were made with one-factor analysis of variance (ANOVA) and a two-tailed t test. For the survival time of animals, Kaplan-Meier curves were established for each group, and survival was compared using a log rank test. Differences between means or ranks as appropriate were considered significant when yielding a P < 0.05. Results are presented as means ± SD. Experiments were performed at least in triplicate.
Tumor cell proliferation due to Lipo-HNK treatment
Before testing the effect of Lipo-HNK on the radiosensitivity of tumor cells, we first investigated the effects of free honokiol and Lipo-HNK alone on LL/2, A549, and SPC-A1 cell proliferation in a 24 h test with MTT. Lipo-HNK reduced the cell number with an IC50 of 17.7 ± 0.8 µg/ml for LL/2, an IC50 of 19.9 ± 1.2 µg/ml for A549, and an IC50 of 19.7 ± 1.1 µg/ml for SPC-A1. The cell killing effects of Lipo-HNK and free HNK for all of the three cell lines were dose and time-dependent (Figure 1). LL/2 cells were found to be more sensitive than other cells and were used for further experiments. Although free honokiol exhibited a slightly stronger effect in killing tumor cells than Lipo-HNK, there was no significant difference between them. In order to raise the water solubility and depress the toxicity towards normal organs, Lipo-HNK was used for in vivo experiments.
Radiosensitization assessed by a clonogenic survival assay
Clonogenic cell survival was assayed to determine whether Lipo-HNK increases the sensitivity of tumor cells to radiation. According to the results with MTT, the doses of Lipo-HNK 6 µg/ml (IC10), 12 µg/ml (IC30), and 18 µg/ml (IC50) were used to explore the sensitivity to radiation-induced cytotoxicity. LL/2 cells were irradiated after incubation with Lipo-HNK for 24 h and the survival at 6 µg/ml was not significantly different from untreated cell survival. The enhancement ratio (RER) was 1.09 ± 0.07 (P > 0.05). Both the 12 µg/ml and 18 µg/ml concentrations of Lipo-HNK produced a significant increase in radio sensitization with RER values of 1.44 ± 0.11 (P < 0.05) and 1.93 ± 0.12 (P < 0.05), respectively (Figure 2A). This combination resulted in synergistic effects compared to Lipo-HNK and irradiation alone.
We then examined the effect of the timing of irradiation during exposure to Lipo-HNK. LL/2 cells were incubated with Lipo-HNK at 6 µg/ml (IC10), 12 µg/ml (IC30), and 18 µg/ml (IC50) for a total of 24 h. The cells were also irradiated either 2 h before drug addition or 2 h, 12 h, or 24 h following Lipo-HNK addition. The greatest irradiation enhancement ratio was obtained when cells were incubated for 24 h prior to irradiation (Table 1). There was no difference between irradiation either 2 h before or after Lipo-HNK addition.
In order to assess whether the radiosensitivity enhancement effect of Lipo-HNK was time-depended, LL/2 cells were exposed to 6 µg/ml (IC10), 12 µg/ml (IC30), and 18 µg/ml (IC50) of Lipo-HNK for 2 h, 12 h, or 24 h, then the drugs were washed out prior to treatment with 1-8 Gy of radiation. The ability of Lipo-HNK to enhance the sensitivity of LL/2 cells increased with time (Figure 2B). When LL/2 cells were treated with 12 µg/ml of Lipo-HNK, the radiation enhancement ratio was 1.13 ± 0.09, for 12 h of incubation, and 1.44 ± 0.11 for 24 h of incubation. When LL/2 cells were treated with 18 µg/ml of Lipo-HNK for 24 h, the radiation enhancement ratio was 1.93 ± 0.12, which was almost 2-fold greater than the 1.09 ± 0.07 value for 2 h of incubation. Our results demonstrated that Lipo-HNK increased the sensitivity to radiation-induced cytotoxicity in both a dose and time-dependent manner.
Effect of Lipo-HNK and/or radiation on the cell cycle distribution
To determine the effect of Lipo-HNK and IR on the cell cycle distribution, LL/2 cells were seeded in a 6 well plate. The Lipo-HNK treated group was incubated with 18 µg/ml (IC50) of Lipo-HNK for 24 h and/or 5 Gy of radiation. The cell cycle and apoptosis were analyzed by flow cytometry after 24 h. LL/2 cells accumulated in the G0/G1-phase after treatment with Lipo-HNK alone (> 60%), with a corresponding decrease in the S-phase, compared with a control and with Lipo-null treatment results. The increase in the G0/G1 phase and the decrease in the S-phase indicated that the cells were blocked in the G0/G1 phase. At 24 h after a 5 Gy dose of ionizing radiation, more than 20% of cells were in the G2/M phase and the percentage of cells in the S-phase was decreased to nearly half the value of the control. The Lipo-HNK and radiation combination in LL/2 cells produced a conspicuous S-phase decrease that was only 0.3-fold of the control and 0.5-fold of the Lipo-HNK and radiation treatment results alone. More than 70% of cells were in the G0/G1-phase (Figure 3).
Apoptosis was measured using the sub-G1 DNA content determined via flow cytometry. Cells in the sub-G1 phase were considered to be apoptotic. The apoptosis rates in non-treated, Lipo-null-treated, 18 µg/ml Lipo-HNK-treated, and 5 Gy radiation-treated cells were 4.8 ± 1.3%, 6.1 ± 2.2%, 29.7 ± 4.6%, and 24.4 ± 6.2%, respectively. The apoptosis rate in the combination treatment was 48.2 ± 7.4%, which was nearly 2-fold greater than for the Lipo-HNK or radiation treatments alone (Figure 3). This was confirmed by a TUNEL assay.
Combination of honokiol and irradiation synergistically inhibits tumor growth
Single Lipo-HNK significantly inhibited tumor growth in LL/2-bearing C57BL/6N mice compared with NS and Lipo-null control (P > 0.05) groups. However, the combination treatment group showed more significant tumor growth inhibition compared with both radiotherapy and liposomal honokiol treatments alone. After 12 days of combination treatment, the tumor volume was 734.4 ± 256.1 mm3, which was decreased 78% compared with the untreated tumor volume. The single Lipo-HNK and radiotherapy treatments only reduced the tumor sizes by 42% (1,707.6 ± 523.1 mm3 and 1694.1 ± 291.1 mm3, respectively) compared with the untreated tumor volume (2,947.3 ± 1,330.0 mm3) (Figure 4A). On day 12 after the combination treatment, the synergistic ratio reached a value of 1.34, showing that Lipo-HNK synergistically (ratio > 1) enhances the antitumor efficacy of radiation (Table 2). However, on day 15 after the combination treatment, the ratio was decreased to 1.02, showing only an additive effect. The combination treatment resulted in a significant improvement in the survival time (Figure 4B). The Lipo-HNK/radiotherapy combination treatment resulted in an 8.7 day delay in tumor growth to reach a volume of 1,000 mm3. In contrast, Lipo-HNK and radiotherapy treatments alone resulted in 2.7 and 3.2 day delays in tumor growth to reach the same volume. The delay time of tumor growth was defined as the average difference in time for the tumor volume to reach 1,000 mm3 between the treated group and the NS control group. The average time was 6.5 days for the NS control group.
Synergistic induction of apoptosis
DNA fragmentation determined by TUNEL detection revealed differences between groups. Although treatment with either Lipo-HNK or irradiation increased apoptosis compared to the untreated groups, the combination treatment induced more significant apoptosis. Significant increases in the number of TUNEL-positive nuclei were found for the combined treatment compared with the Lipo-HNK and irradiation treatments alone (Figure 5A-E).
H&E staining was performed to measure necrosis and the number of blood vessels in paraffin sections. Tissue sections of Lipo-HNK and radiotherapy treatment specimens exhibited significant necrosis, but less than for the combination of Lipo-HNK and radiotherapy treatments. NS and Lipo-null control group specimens exhibited little necrosis and some of the tumor cells showed active proliferation (Figure 5F-J).
Synergistic inhibition of angiogenesis
Angiogenesis within tumor tissues was estimated in tumor sections stained with an antibody reactive to CD31 and quantified as described in Materials and Methods. Compared to untreated groups, both liposomal honokiol and irradiation treatments resulted in apparent inhibition of angiogenesis in tumors. The average numbers of blood vessels observed at a magnification of 200× in tumors treated with NS, Lipo-null, Lipo-HNK, irradiation, and the combination of Lipo-HNK and irradiation were 55.8 ± 5.7, 57.2 ± 4.3, 33.7 ± 4.1, 38.6 ± 4.5, and 16.2 ± 3.4, respectively. The combination of Lipo-HNK and irradiation resulted in enhanced inhibition of angiogenesis and revealed a synergistic effect in the tumor MVD (Figure 6A-F) (the synergistic index was 1.44). Significantly reduced numbers of blood vessels in tumors treated with a combination in comparison with Lipo-HNK and radiation alone (P < 0.01) indicated that a reduction in tumor vascularity contributes to enhanced tumor regression.
All groups of mice tolerated Lipo-HNK and no gross signs of cumulative adverse consequences were observed, such as huddling, weight loss, ruffling of fur, reduced life span, unusual behavior, and unusual feeding habits. Furthermore, no pathologic changes in the liver, lung, kidney, spleen, brain, heart, pancreas, intestines, or bone marrow were found under microscopic examination. In order to measure the systemic toxicity of the treatments, pathologic inspection was assessed by hematoxylin & eosin staining of sections. No pathologic changes in the liver, lung, kidney, spleen, brain, heart, pancreas, intestines, or bone marrow were found under microscopic examination (data not shown).
Anti-angiogenesis therapy has become a novel method for the treatment and prevention of tumors by restraining or destroying tumor vessels (Marshall et al., 1998; Mauceri, 1998; Marx, 2000, 2003; Rakhmilevich et al., 2004; Garkavtsev et al., 2004). However, this therapy can not lead to complete regression of the tumor. Continued medication is usually required to prevent dormant tumor growth. Previous research has indicated that the content of VEGF in the blood of tumor patients is significantly heightened during radiotherapy treatment, and there is a correlation between the expression level of VEGF and the prognosis after radiotherapy. Radiation can induce the creation of VEGF by the MAPK pathway, so that tumor vessels form and degrade the therapeutic effect of the radiotherapy. Hence, angiogenesis inhibitors have shown a fairly strong synergistic effect when combined with radiotherapy (Huber et al., 2005).
Honokiol has been reported to have anti-angiogenesis effects (Yang et al., 2002) and can induce apoptosis in many tumor cells (Hibasami et al., 1998; Chen et al., 2004; Wang et al., 2004; Ishitsuka et al., 2005). The mechanism of its anti-angiogenesis effect is interference with the phosphorylation of vascular endothelial growth factor 2 (VEGFR2) (Bai et al., 2003). A recent study has confirmed that honokiol can inhibit vasiformation in the microenvironment of the bone marrow and kill tolerated multiple myeloma cells (Ishitsuka et al., 2005).
This study demonstrated for the first time that liposomal honokiol enhances the radiation response of LL/2 cells in in vitro and in in vivo in tumor xenograft models. In a clonogenicity assay, Lipo-HNK exhibited an enhancement to radiosensitization in LL/2 cells in both a dose and time-dependent manner. Cell cycle studies showed that honokiol combined with radiotherapy can induce LL/2 cells to arrest in the G0/G1 phase with a corresponding decrease in the S-phase, indicating that radiation combined with honokiol interrupts tumor cell division. CD31 staining of blood vessel endothelial cells to visualize the microvessel density in the combination treatment group showed significant inhibition of tumor vessel formation. Honokiol combined with radiotherapy apparently reduced the vessel number compared with NS and Lipo-HNK treatments alone. H&E and TUNEL staining indicated that honokiol has the effect of inducing apoptosis in LL/2 tumor cells, and can enhance the effect of inducing apoptosis when combined with radiotherapy.
We investigated the dose-effect relationship of Lipo-HNK in vivo (Liu et al.) using four doses of honokiol from 5 mg/kg to 50 mg/kg and found that 25 mg/kg presented a favorable therapeutic efficacy. In order to mimic the frequently used clinical method, we applied a routine divided method for radiotherapy. The RT group was administered a dose of 5 Gy every day for 5 days and the combination group was administered a dose of 5 Gy/day for five days after treatment with Lipo-HNK for 40 min, followed by continued treatment with Lipo-HNK for five days. This combination treatment significantly improved the survival time versus other groups and resulted in a delay in tumor growth compared with liposomal honokiol and radiotherapy treatments alone. A synergistic relationship in tumor volume, angiogenesis, apoptosis, and proliferation was demonstrated according to a combined index calculation. Our findings indicate that angiogenesis inhibitors have a fairly strong synergistic effect on a combination therapy with radiotherapy. It should be pointed out that the total irradiation dose and the total dosage time for the mice in our study were deficient compared with clinical therapies. Better therapeutic efficacy may be obtained if the irradiation dose is increased and the time is lengthened.
Previous in vitro and in vivo studies have shown that encapsulating antitumor agents with liposome is an effective way to avoid rapid clearance and short circulation time in order to significantly prolong the plasma residence time of drugs (Boman et al., 1995; Emerson et al., 2000; Tardi et al., 2000; Lee et al., 2002). As previously reported (Yi Liu et al., Fan et al., 1995), defects in the capillary endothelium of tumor vasculature are typically in the size range of 400-600 nm. Liposomes, having a diameter smaller than 400 nm, can efficiently accumulate within the tumor interstitial space. In a previous study, we developed honokiol encapsulated with liposomes to overcome problems of water insolubility and toxicity towards normal organisms (Liu et al., 2008). We found the toxicity of free honokiol towards mice is strong and water insolubility hampers honokiol application for intravenous injection. MTT results indicated that tumor cytotoxicity is not significantly different between free honokiol and Lipo-HNK. Encapsulating honokiol with liposome does not degrade the effect on tumor cells. Our experiments demonstrated that there are no significant differences for both tumor growth and mouse life span between Lipo-null and NS control groups, and no visible side effects of Lipo-null were observed. Thus, the use of a liposomal formulation is feasible.
The data presented in this report indicate that liposomal honokiol combined with RT mediates a potent inhibition of Lewis lung cancer tumor growth and prolongs the survival time of tumor-bearing mice. In addition, a combination treatment results in significantly increased necrosis and a synergistic decrease in tumoral blood vessels and angiogenesis. Honokiol encapsulated with liposome presents the favorable effect of radiosensitization and organism tolerance. Our findings support the design of treatment strategies that combine IR with liposomal honokiol, a potent anti-angiogenesis inhibitor. Further exploration of the potential application of this combined approach in the treatment of lung cancer is indicated.
This work was supported by the National Basic Research Program of China (2004CB518800 and 2004CB518706), the National 863 Program, the National Natural Science Foundation of China, and the New Century Talent Foundation of the Ministry of Education of China (2005).
hematoxylin and eosin
radiation enhancement ratio
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Bioorganic & Medicinal Chemistry (2019)