This article is mentioned in:

Introduction

Among all types of lung cancers, adenocarcinoma accounts for ~40% and generally has both a poor prognosis and increased potential for metastases (1). Currently, surgery is the primary treatment for cancer. However, surgery itself can stimulate cell growth (2), metastasis (3) and recurrence (4) of cancer. Anesthetic agents administered during surgery might influence the cell activities of cancer simultaneously (5).

Propofol (PPF) is a sedative-hypnotic agent, which is widely used in operating rooms and intensive care units (ICU) for smooth induction and rapid recovery from anesthesia. Potential anticancer properties of PPF have been considered. PPF inhibits the invasion and migration of the human lung adenocarcinoma epithelial A549 cell line by regulating matrix metalloproteinases-2 (MMP-2) and p38 MAPK signaling pathways (6). Furthermore, it induces apoptosis in A549 cells through extracellular signal-regulated kinase 1 and 2 (ERK1/2) pathways (7). As a urinary trypsin inhibitor, ulinastatin also has properties that suppress cancer cell growth, proliferation, differentiation and migration (8–13). Studies have shown that the anticancer drugs combined with ulinastatin could offer therapeutic promise for cancer treatment (14–16).

At present, the effects of PPF in combination with ulinastatin on post-perfusion lung syndrome (17) and acute lung injury (18) have been demonstrated. However, antitumor effects associated with different ulinastatin and PPF administration against A549 cells remain unclear and the delivery of PPF (10, 20 and 30 µM) followed by 200 U/ml ulinastatin treatments on cancer cells has not been studied. The aim of this study is to evaluate the synergistic antitumor effect of PPF followed by ulinastatin against A549 cells. The expression of p-ERK1/2 and MMP-2 was detected to identify the mechanisms behind the antitumor effects of PPF (10, 20 and 30 µM) followed by 200 U/ml ulinastatin.

Materials and methods

Cell culture

The A549 cell line was obtained from the Cancer Research Institute of the Southern Medical University (Guangdong, China). Cells were maintained at 37°C in a humidified atmosphere of 95% air and 5% CO2 in DMEM/F-12 with 10% fetal bovine serum (FBS; both Gibco; Thermo Fisher Scientific, Inc., Waltham, MA, USA), 100 units/ml penicillin and 100 ng/ml streptomycin (Sigma-Aldrich; Merck KGaA, Darmstadt, Germany).

Different treatment schedules for A549 cells

To evaluate the antitumor effect of different treatment schedules with PPF (Sigma-Aldrich; Merck KGaA) and ulinastatin (Techpool Bio-Pharma, Guangzhou, China), cells were treated with seven different treatments (Fig. 1A). According to the studies of Kobayashi (8) and Song (7), the concentrations of 800 U/ml ulinastatin and 100 µM PPF were selected as the optimum doses. The control was defined as continuous treatment with serum-free medium for 48 h; 0.1% DMSO was defined as continuous treatment with 0.1% DMSO for 48 h; 800 U/ml ulinastatin was defined as continuous 800 U/ml ulinastatin treatment for 48 h; 100 µM PPF was defined as pretreatment with serum-free medium for 42 h, followed by aspiration, one wash with phosphate buffer saline (PBS), and PPF (100 µM) treatment for 6 h; 800 U/ml ulinastatin +100 µM PPF was defined as pretreatment with 800 U/ml ulinastatin for 42 h, followed by aspiration, one wash with PBS, and concomitant treatment with both 800 U/ml ulinastatin and 100 µM PPF for 6 h; 800 U/ml ulinastatin → 100 µM PPF was defined as pretreatment with 800 U/ml ulinastatin for 42 h, followed by aspiration, one wash with PBS, and 100 µM PPF treatment for 6 h; 100 µM PPF → 800 U/ml ulinastatin was defined as pretreatment with 100 µM PPF for 6 h, followed by aspiration, one wash with PBS, and 800 U/ml ulinastatin treatment for 42 h. The maximum concentration of DMSO (Sigma-Aldrich; Merck KGaA) added to the medium in this study was 0.1%.

Figure 1. Different treatments schedules with PPF and ulinastatin for A549 cells. All compounds were dissolved in the serum-free medium. (A) To evaluate the antitumor effect of different treatment schedules relating to PPF and ulinastatin through high dose treatment, A549 cells were exposed to seven different treatments. 800 U/ml ulinastatin + 100 µM PPF were dissolved in the same serum-free medium. (B) To verify the synergistic antitumor effect of PPF followed by ulinastatin treatments at low concentrations, A549 cells were exposed to nine different treatments. PBS phosphate buffer saline; PPF, propofol.

From the results of the first experimental block, we found that the antitumor of the sequence PPF → ulinastatin at high concentrations was the optimum sequence. To verify the synergistic antitumor effect of PPF → ulinastatin at a low concentration, a concentration gradient of PPF was generated: This increased from 10, 20, 30 µM, while the concentration of ulinastatin was 200 U/ml (Fig. 1B). Control was defined as continuous treatment with serum-free medium for 48 h; 0.1% DMSO was defined as continuous treatment with 0.1% DMSO for 48 h; 200 U/ml ulinastatin was defined as pretreatment with serum-free medium for 6 h, followed by aspiration, one wash with PBS, and 200 U/ml ulinastatin treatment for 42 h; the PPF group was defined as pretreatment with PPF (10, 20, 30 µM) for 6 h, followed by aspiration, one wash with PBS, and incubation in serum-free medium for 42 h; PPF → 200 U/ml ulinastatin groups were defined as pretreatment with PPF (10, 20, 30 µM) for 6 h, followed by aspiration, one wash with PBS, and 200 U/ml ulinastatin treatment for 42 h.

Cell viability inhibition assay

The viability of PPF and ulinastatin against A549 cells was evaluated using the MTT assay. Twenty µl/well of 5 mg/ml MTT solution (Sigma-Aldrich; Merck KGaA) was added to each well and the cultures were further incubated for 4 h. Optical density (OD) was measured at 490 nm on a multimode microplate reader (MDS; SpectraMax M5, San Jose, CA, USA). Viability inhibition rate was calculated as follows: Viability inhibition (%)=[1-(OD490 nm of treated cells-blank/OD490 nm of control cells-blank)] ×100 (19). To determine whether the sequential treatments with ulinastatin and PPF had a synergistic effect, the combination index (CI) of each sequential treatment was analyzed according to the method of Chou and Talaly (20). CI values of <1, 1 and >1 indicate synergistic, additive, and antagonistic effects, respectively. By using CompuSyn 1.0 software (CompuSyn, Inc., Paramus, NJ, USA), the CI value was easily computed.

Cell proliferation cycle detection

A cell proliferation cycle detection kit (KeyGEN Bio TECH Ltd., Nanjing, China) was used to detect the cell proliferation cycle. Pretreated cells were fixed in 70% ethanol at 4°C for 12 h. Cells were aspirated, gently washed twice with ice-cold PBS, centrifuged at 2,000 × g for 5 min at 4°C, aspirated once again, and resuspended in 1 ml PBS containing 50 µg/ml RNase A for 30 min at 37°C. The cells were then incubated with propidium iodide (PI) for 30 min at 4°C in the dark. The percentage of cells with different DNA contents relating to different phases of the cell cycle was measured by fluorescence-activated cell sorting (FACS) analysis.

Trans-well assay for migration

Pretreated A549 cells (100 µl/chamber at a density of 10×106 cells/ml) in serum-free medium were placed in the upper chamber of the trans-well inserts with free Matrigel matrix basement membrane. To attract cells, medium containing 10% FBS was placed in the bottom of the chamber. Cells in the upper membranes were wiped using a cotton swab after incubation for 24 h. Migratory cells were treated with different treatments: Pre-fixation with methanol for 20 min, aspiration, one wash with PBS, followed by 0.1% crystal violet staining for 10 min, before three washes with PBS. Cells were photographed in 9 predetermined fields under an inverted microscope (IX71; Olympus, Center Valley, PA, USA) at magnification, ×200 and images were scored using CompuSyn software.

Trans-well assay for invasion

Falcon cell culture inserts (pore size of 8 µm; Corning Inc., Corning, NY, USA) were pretreated with Matrigel matrix basement membrane (Corning Inc., Corning, NY, USA). Pretreated A549 cells (100 µl/chamber at a density of 10×106 cells/ml) in serum-free medium were placed in the upper chamber of the trans-well inserts. To attract cells, medium containing 10% FBS was placed in the bottom of the chamber. Cells in the upper membrane were wiped using a cotton swab after incubation for 24 h. Invasive cells were treated with different treatments: Pre-fixation with methanol for 20 min, aspiration, one wash with PBS, followed by 0.1% crystal violet staining for 10 min, before three washes with PBS. Cells were photographed in 9 predetermined fields under an inverted microscope (IX71; Olympus, Center Valley, PA, USA) at magnification, ×200 and images were scored using CompuSyn software.

Annexin V-FITC/PI staining assay for apoptosis detection

The Annexin V-FITC apoptosis detection kit (Merck, Darmstadt, Germany) was used to detect apoptosis. Pretreated cells were harvested before centrifugation at 1,000 × g for 5 min at 18–24°C. Then, cells were resuspended in 500 µl 1× binding buffer, before incubation with Annexin V for 15 min at 18–24°C in the dark. The cells were gently resuspended in 500 µl 1X binding buffer. PI was added in the dark. The number of healthy viable cells, apoptotic, and necrotic cells were immediately measured by FACS analysis. The apoptosis rate was calculated as follows: The apoptosis rate (%)=(number of apoptotic cells)/(number of total cells observed) ×100 (21).

Western blot analysis

Pretreated cells were washed three times with ice-cold PBS and lysed with RIPA lysis buffer (1% Triton X-100, 1% sodium deoxycholate, 0.1% sodium dodecyl sulfate, sodium salt, phosphatase inhibitor, and phenylmethanesulfonyl fluoride) (CW2333; CW Bio, Beijing, China). The cell extracts were collected, incubated for 30 min on ice, and centrifuged for 20 min at 12,000 × g at 4°C. The supernatants were used as cell lysates. The cell lysates were subjected to SDS-polyacrylamide gel electrophoresis and transferred to polyvinylidene fluoride (PVDF) membranes after the bicinchoninic acid (BCA) method was used for protein quantification and equitable application of proteins to the gel. The membranes were blocked with 5% bovine serum albumin (BSA) in Tris-buffered saline (TBS) for 1 h at room temperature. After washing 3 times with TBS, the membranes were incubated in rabbit polyclonal antibodies (Cell Signaling Technology, Inc., Danvers, MA, USA) against ERK1/2, p-ERK1/2, and MMP-2 diluted with TBS containing 0.1% Tween-20 with 5% BSA (TBST) before being gently agitated overnight at 4°C. After washing 3 times with TBST, the membranes were incubated in fluorophore-conjugated secondary antibody (LI-COR Biosciences, Nebraska, USA) dilution buffer (TBS containing 0.1% Tween-20 with 5% skimmed dry milk) with gentle agitation for 1 h at room temperature. After washing 3 times with TBST, the Odyssey Infrared Imaging System (Licor, Lincoln, NE, USA) was used to detect proteins. The results were analyzed using ImageJ 1.42q software (Wayne Rasband National Institutes of Health, Bethesda, MD, USA).

Statistical analysis

Data were expressed as mean ± standard deviation (SD) of three independent experiments. After determination of variance homogeneity of variance test, the Least-Significant-Difference and Dunnett' T3 were used to assess statistical significance, with P<0.05 considered to indicate a statistically significant difference

Results

PPF followed by ulinastatin synergistically inhibited the viability of A549 cells

Fig. 2A shows that 100 µM PPF inhibited the viability of A549 cells. However, 800 U/ml ulinastatin had no statistically significant in inhibiting the viability of A549 cells. 100 µM PPF → 800 U/ml ulinastatin was the optimum sequence in inhibiting the viability of A549 cells. There was an antagonistic effect when A549 cells were treated with 800 U/ml ulinastatin → 100 µM PPF, with the CI >1. Furthermore, there was an additive effect when A549 cells were treated with 800 U/ml ulinastatin + 100 µM PPF, with the CI=1. When A549 cells were treated with 100 µM PPF → 800 U/ml ulinastatin, the CI <1, which indicates a synergistic effect.

Figure 2. Viability assay of ulinastatin and PPF in A549 cells. A549 cells were inhibited using different groups and data were obtained from three independent experiments. Data were presented as mean ± SD of three independent experiments, and analyzed by the Least-Significant-Difference. (A) Antitumor effects of different sequential administration with 800 U/ml ulinastatin (UTI800) and 100 µM PPF (PPF100); (B) The synergistic effect of PPF→ulinastatin at clinical concentrations. ΩP<0.05 vs. Control; #P<0.05 vs. UTI800; ΔP<0.05 vs. 200 U/ml ulinastatin (UTI200); &P<0.05 vs. PPF100; ΨP<0.05 vs. 800 U/ml ulinastatin→100 µM PPF (UTI800→PPF100); αP<0.05 vs. 30 µM PPF (PPF30); βP<0.05 vs. 10 µM PPF→200 U/ml ulinastatin (PPF10→UTI200); εP<0.05 vs. 20 µM PPF (PPF20). PPF, propofol.

From the results of the first experimental block, we found that the antitumor effect of the sequence PPF → ulinastatin at high concentration was the optimum sequence. To verify the synergistic antitumor effect of PPF → ulinastatin at low concentration, the results of the second experimental block were as follows. Fig. 2B demonstrates 200 U/ml ulinastatin and PPF groups (10, 20, 30 µM) did not inhibit the viability of A549 cells. 10 µM PPF → 200 U/ml ulinastatin did not significantly inhibit the viability of A549 cells. PPF (20 and 30 µM) → 200 U/ml ulinastatin synergistically inhibited the viability of A549 cells in a dose-dependent manner associated with PPF stimulation. There was a demonstrable antagonistic effect when A549 cells were treated with 10 µM PPF → 200 U/ml ulinastatin, where CI >1, while there was a synergistic effect when A549 cells were treated with 20 µM PPF →200 U/ml ulinastatin and 30 µM PPF→200 U/ml ulinastatin, where CI <1.

PPF followed by ulinastatin synergistically increased the number of S cells and reduced the number of G2/M cells in a PPF dose-dependent manner

There were no statistically significant differences with respect to the number of G0/G1 cells among groups (Fig. 3A). As shown in Fig. 3B, PPF groups (10, 20, 30 µM) and PPF → 200 U/ml ulinastatin groups significantly increased the number of S cells, but 0.1% DMSO and 200 U/ml ulinastatin did not significantly increase the number of S cells. PPF (10, 20 and 30 µM) → 200 U/ml ulinastatin significantly increased the number of S cells respectively compared with PPF (10, 20 and 30 µM) and 200 U/ml ulinastatin in a PPF dose-dependent manner.

Figure 3. A549 cell proliferation cycle of PPF→ulinastatin at clinical concentrations. A549 cells were inhibited using different groups and data were obtained from three independent experiments. Data were presented as mean ± SD of three independent experiments, and analyzed by the Least-Significant-Difference. (A) Percentage of A549 cells in G0/G1 phase; (B) Percentage of A549 cells in S phase; (C) Percentage of A549 cells in G2/M phase. ΩP<0.05 vs. Control; #P<0.05 vs. 10 µM PPF (PPF10); ΔP<0.05 vs. 200 U/ml ulinastatin (UTI200); ΨP<0.05 vs. 20 µM PPF (PPF20); αP<0.05 vs. 30 µM PPF (PPF30); βP<0.05 vs. 10 µM PPF→200 U/ml ulinastatin (PPF10→UTI200); δP<0.05 vs. 20 µM PPF→200 U/ml ulinastatin (PPF20→UTI200). PPF, propofol.

Fig. 3C shows the PPF groups (20, 30 µM) and PPF (10, 20, 30 µM) → 200 U/ml ulinastatin groups significantly reduced the number of G2/M cells. However, 0.1% DMSO and 200 U/ml ulinastatin did not significantly reduce the number of G2/M cells. PPF → 200 U/ml ulinastatin groups synergistically reduced the number of G2/M cells compared with 200 U/ml ulinastatin.

PPF → ulinastatin treatments did not synergistically inhibit the migration and invasion of A549 cells

A549 cells were harvested and assayed for migration (Fig. 4A). 800 U/ml ulinastatin → 100 µM PPF significantly reduced the migration of A549 cells compared with 100 µM PPF, 800 U/ml ulinastatin + 100 µM PPF, and 100 µM PPF→800 U/ml ulinastatin. There was no statistically significant difference in the inhibition of migration of A549 cells treated with 800 U/ml ulinastatin+ 100 µM PPF, 800 U/ml ulinastatin→100 µM PPF, and 100 µM PPF→800 U/ml ulinastatin, compared with 800 U/ml ulinastatin.

Figure 4. Effect of ulinastatin and PPF on invasion and migration of A549 cells. Cells that had migrated (A) and invaded (B) were photographed (magnification, ×200), and photographed in 9 predetermined fields for each treatment. Data were calculated from three independent experiments. Data were presented as mean ± SD of three independent experiments and analyzed by Dunnett' T3. ΩP<0.05 vs. Control; &P<0.05 vs. 100 µM PPF (PPF100); αP<0.05 vs. 800 U/ml ulinastatin +100 µM PPF (UTI800+PPF100); βP<0.05 vs. 100 µM PPF→800 U/ml ulinastatin (PPF100→UTI800). PPF, propofol.

A549 cells were harvested and assayed for invasion (Fig. 4B). The group of 100 µM PPF treated A549 cells (56±5.0) was better than control (70.1±4.4). 800 U/ml ulinastatin→100 µM PPF significantly reduced the invasion of A549 cells compared with 100 µM PPF, 800 U/ml ulinastatin + 100 µM PPF, and 100 µM PPF→ 800 U/ml ulinastatin. 100 µM PPF→ 800 U/ml ulinastatin and 800 U/ml ulinastatin + 100 µM PPF did not significantly reduce the invasion of A549 cells compared with 100 µM PPF and 800 U/ml ulinastatin.

PPF followed by ulinastatin synergistically stimulated late apoptosis or necrosis in A549 cells

As shown in Fig. 5, compared with control, 0.1% DMSO did not significantly stimulate late apoptosis or necrosis in A549 cells. However, 800 U/ml ulinastatin, 100 µM PPF, 800 U/ml ulinastatin + 100 µM PPF, 800 U/ml ulinastatin → 100 µM PPF, and 100 µM PPF → 800 U/ml ulinastatin stimulated apoptosis or necrosis in A549 cells. 800 U/ml ulinastatin + 100 µM PPF and 100 µM PPF → 800 U/ml ulinastatin stimulated late apoptosis or necrosis in A549 cells to a significantly greater extent than 800 U/ml ulinastatin, 100 µM PPF, and 800 U/ml ulinastatin → 100 µM PPF treatments. There were no statistically significant differences on the viability of treated groups with respect to early apoptotic cells.

Figure 5. Effect of ulinastatin and PPF on apoptosis of A549 cells. Annexin V-FITC/PI staining assay. After different treatments, cells were labeled and sorted using flow cytometry. (A) Late apoptotic or necrotic cells in Q2 (B) are depicted in the upper right-hand quadrant of the dot plot; viable cells in Q3 (C) are depicted in the lower left-hand quadrant of the dot plot. Data were calculated from three independent experiments. Data were presented as mean ± SD of three independent experiments and analyzed by the Least-Significant-Difference. For late apoptotic or necrotic cells, ΩP<0.05 vs. Control; #P<0.05 vs. 800 U/ml ulinastatin (UTI800); &P<0.05 vs. 100 µM PPF (PPF100); ΨP<0.05 vs. 800 U/ml ulinastatin→100 µM PPF (UTI800→PPF100). For early apoptotic and viable cells vs. Control, all P-values of treated groups >0.05. PI, propidium iodide; PPF, propofol.

Effects of PPF → ulinastatin at low concentrations on the expression of p-ERK1/2 and MMP-2

The expression of total ERK1/2 was not significantly different among all groups. However, the expression of p-ERK1/2 was different from total ERK1/2 (Fig. 6A). 200 U/ml ulinastatin, 10 µM PPF, and 20 µM PPF did not downregulate the expression of p-ERK1/2 in A549 cells. However, 30 µM PPF and PPF (10, 20, 30 µM) → 200 U/ml ulinastatin significantly reduced the expression of p-ERK1/2. The expression of p-ERK1/2 was synergistically downregulated by PPF (10, 20, 30 µM) → 200 U/ml ulinastatin.

Figure 6. Effects of treatment with ulinastatin, PPF, and PPF → ulinastatin on the protein expression of p-ERK1/2 (A) and MMP-2 (B) in A549 cells. Data were calculated from three independent experiments. Data were presented as mean ± SD of three independent experiments, and analyzed by the Least-Significant-Difference. ΩP<0.05 vs. Control; #P<0.05 vs. 200 U/ml ulinastatin (UTI200); βP<0.05 vs. 10 µM PPF (PPF10); εP<0.05 vs. 20 µM PPF (PPF20); µP<0.05 vs. 30 µM PPF (PPF30). p-ERK, extracellular signal-regulated kinase phosphorylation; MMP, matrix metalloproteinases; PPF, propofol.

0.1% DMSO, 200 U/ml ulinastatin, and PPF groups (10, 20, 30 µM) did not downregulate the expression of MMP-2 (Fig. 6B). Compared with 200 U/ml ulinastatin alone, the expression of MMP-2 was significantly downregulated after cells were treated with PPF (10, 20, 30 µM) →200 U/ml ulinastatin. 10 µM PPF → 200 U/ml ulinastatin downregulated the expression of MMP-2 compared with 10 µM PPF. However, there was no statistically significant difference when cells were treated with 20 µM PPF→200 U/ml ulinastatin or 30 µM PPF→200 U/ml ulinastatin, compared with 20 µM PPF or 30 µM PPF.

Discussion

Among all types of lung cancers, adenocarcinoma accounts for ~40% of cancer and generally has a poor prognosis (1). The A549 cell line is the typical cell line in human lung adenocarcinoma and surgery is the primary treatment for lung cancer. The immunosuppressive effects of surgery are well known with respect to cancer progression (22). Surgery can also generate a microenvironment that is abundant in inflammatory cells and growth factors, including potent angiogenic, lymphangiogenic growth factors, cytokines, and proteases (23). Granov et al found that cancer patients were susceptible in developing acute lung lesions (ALL) and adult respiratory distress syndrome (ARDS) postoperatively (24). Use of ulinastatin and PPF may benefit ARDS patients through different mechanisms (17). PPF exhibits protective effects including an antiinflammatory effect, enhancement of antitumor immunity, reduction of the concentration of cytokines (IL-1, TNF-α and IL-6) and natural killer cell function preservation (25–28). Ulinastatin also improves the immunosuppressive state during surgery for malignancy (29). In view of the clinical translation of our results, the optimum administration protocol (PPF → ulinastatin) may benefit ARDS patients and inhibit lung adenocarcinoma cells, which can improve the postoperative prognosis of lung adenocarcinoma patients. PPF → ulinastatin synergistic antitumor effects may be importantly related to the immune microenvironment. As ERK1/2 phosphorylation is an important step for cytokine secretion such as TNF-α (30) and IL-1β (31), PPF → ulinastatin may synergistically reduce cytokine secretion of TNF-α and IL-1β by inhibiting ERK1/2 phosphorylation in A549 cells.

With respect to clinical application, 100 µM PPF and 800 U/ml ulinastatin was more potent but PPF (6.2–33.7 µM) administered through Target Controlled Infusion (TCI) is widely used in clinical applications (e.g., the maintenance of general anesthesia), and 200 U/ml ulinastatin is introduced in a pharmacy. To verify the synergistic effect of PPF → ulinastatin at a clinical concentration, we tested several concentration gradients of PPF using TCI (10, 20, 30 µM) and a clinical concentration of ulinastatin (200 U/ml). We demonstrated that PPF → ulinastatin treatments effectively inhibited the viability of A549 cells and stimulated late apoptosis or necrosis cells. However, PPF → ulinastatin treatments did not synergistically inhibit the migration and invasion of A549 cells. From the results, we found that the molecular mechanisms regulating the viability and late apoptosis or necrosis of A549 cells might share common properties from which regulating the migration and invasion of A549 cells was different.

In our investigation, the MTT assay clearly indicated that PPF → ulinastatin treatments had a synergistic effect at high and low concentrations in inhibiting A549 cell viability. PPF → ulinastatin synergistically inhibited A549 cell viability, which could be attributed to the different timing events in the cell cycle: PPF → ulinastatin treatments synergistically increased the number of S cells and synergistically reduced the number of G2/M cells in a PPF dose-dependent manner. The G2/M DNA damage checkpoint serves to prevent the cell from entering M-phase, which can result in genomic damage. DNA damage can activate the DNA-PK/ATM/ATR kinases, which result in two parallel cascades that ultimately serve to inactivate the cyclin B-cdc2 kinase. The first cascade rapidly inhibits progression into mitosis: The Chk kinases phosphorylate and inactivate cdc25, which prevents activation of cdc2 (32,33). Phosphorylated ERK1/2 (p-ERK1/2) activates cdc25, which promotes the cell from entering M-phase (34). ERK1/2 is activated through phosphorylation, which plays an important role in the regulation of fundamental cellular processes including proliferation, survival, differentiation, migration (35–37), and apoptosis (38). It has been reported that 100 µM (7) PPF can downregulate the expression of p-ERK1/2 in A549 cells. Liposoluble PPF is liable to pass through the A549 cytomembrane into the cytoplasm and nucleus, which may inactivate ERK1/2 and/or promote DNA damage in A549 cells. This DNA damage may improve the dosing of soluble ulinastatin in the cytoplasm and nucleus of A549 cells, which synergistically inactivate p-ERK1/2, cdc2, and/or cdc25. The DNA-PK/ATM/ATR kinases from DNA damage are inactivated by ulinastatin, which counteracts the DNA damage in A549 cells caused by PPF. We believe these were the reasons why the treatment with PPF → ulinastatin was more effective than both ulinastatin → PPF and the simultaneous combination.

The suppression of ERK1/2 and hypoxia pathways resulted in the suppression of MMP-2, MMP-9, and MMP-7 expression in A549 cell metastasis (39). Metalloproteinases, particularly MMP-2, play an important role in the regulation of fundamental cancer cellular processes including cell growth, invasion, inflammation and angiogenesis (40). PPF suppresses the invasion and migration of A549 human lung adenocarcinoma epithelial cells by downregulating the expression of MMP-2 and p38 MAPK signaling (6). It has been reported that a urinary trypsin inhibitor-like inhibitor can be isolated from human lung cancer tissue (41). In our study, we suspected that ulinastatin did not statistically inhibit the viability of A549 cells because of the presence of the inhibitor from human lung cancer tissues or the low concentration of ulinastatin. Two hundred U/ml of ulinastatin alone did not effectively inhibit the expression of MMP-2 due to the inhibitor or the low concentration of ulinastatin. PPF alone did not effectively inhibit the expression of MMP-2 due to the low concentration of PPF. However, the expression of MMP-2 after PPF → ulinastatin treatment was synergistically downregulated as pretreated A549 cells with PPF could regulate expression of the inhibitor.

In our study, we have partly elucidated the underlying mechanisms of the synergistic antitumor effect of PPF → ulinastatin at clinical concentrations, and detected p-ERK1/2 and MMP-2. DNA-PK/ATM/ATR, Cyclin B-cdc2, and Chk kinases in A549 cells will be detected to verify the mechanism of G2/M DNA damage and how this relates to synergistic suppression of the human lung adenocarcinoma epithelial A549 cell line with PPF treatment followed by ulinastatin.

In summary, we conclude that PPF (20, 30 µM) followed by 200 U/ml ulinastatin treatments synergistically stimulated a significant proportion of A549 cells in S phase, synergistically reduced the percent of A549 cells in G2/M phase, and synergistically suppressed viability, which could possibly be related to regulating the expression of p-ERK1/2 and MMP-2 in A549 cells.

Acknowledgements

Not applicable.

Funding

The present study was supported in part by the Scheme of the Guandong Province Sciences Research (grant no. 2012A030400014).

Availability of data and materials

All data generated or analyzed during this study are included in this published article.

Authors' contributions

PL and PG assisted in the design of the study, conducedt the study, analyze the data and wrote the manuscript. CL assisted in the analysis of the statistics, interpreted the data and graphic illustrations and drafted the manuscript. MH, XZ, CL, JT, WW and WL collaborated in the design of the study and assisted in writing the manuscript. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable.

Patient consent for publication

Not applicable.

Competing interests

The authors declare that they have no competing interests.

References