Background
At the time of diagnosis, BTC has often advanced to affect multiple biliary tracts. In many patients, BTC is unresectable and has a poor prognosis [
1,
2]. Chemotherapy is commonly administered to patients with unresectable BTC; however, the most effective regimen confers an overall survival of only 11–15 months [
3‐
7]. Additionally, no specific serum tumour markers are available to diagnose or predict the prognosis of BTC [
8]. Although the sensitivity of CA19-9 for diagnosing BTC was reported to be 71–72% [
9,
10], an elevated CA19-9 level is observed in patients with nonmalignant obstructive jaundice [
11,
12]. Therefore, an appropriate diagnostic or predictive prognostic marker for BTC is needed.
Macrophage inhibitory cytokine-1 (MIC-1) is a member of the TGF-β superfamily [
13]. Elevated serum MIC-1 levels have been observed in patients with several inflammatory diseases and malignant tumours [
14]. In addition, serum MIC-1 levels are markedly higher in patients with pancreatic cancer or BTC than in those with pancreaticobiliary inflammatory diseases or other cancers [
15‐
18]. Although many reports on pancreatic cancer and MIC-1 have been published [
19‐
25], few studies have investigated BTC and MIC-1. A previous study reported that biliary MIC-1 efficiently diagnosed early BTC [
18]. However, the process of bile collection to measure biliary MIC-1 is invasive; thus, a less invasive diagnostic method is desired.
The effect of MIC-1 on each tumour type is different. In BTC, researchers have not determined whether MIC-1 enhances or prevents carcinogenesis. This study aimed to clarify the involvement of MIC-1 in BTC and the efficacy of MIC-1 as a noninvasive biomarker or therapeutic target for BTC.
Methods
This study was approved by the Ethics Committee of Fukushima Medical University (Approval Number: 2387). All procedures were performed according to the manufacturers’ instructions.
Immunostaining of surgical specimens and tissue microarray (TMA)
BTC specimens were immunostained for MIC-1. An anti-GDF-15/MIC-1 polyclonal antibody (Bioss Antibodies Inc., Massachusetts, USA) was used for MIC-1 immunostaining according to the manufacturer’s protocol. The microscope slides were deparaffinized and boiled in 0.01 M sodium citrate buffer (pH 6) at 100 °C for 15–20 min for antigen retrieval. The slides were treated with 3% hydrogen peroxide for 30 min to block endogenous peroxidase activity. Immunostaining was performed using the abovementioned antibody (dilution 1:1000).
BTC specimens were acquired during surgery. Samples from the patients whose surgical specimens were immunostained were included in the in vivo experiments described below. All patients provided written informed consent to participate in this study.
A TMA containing 54 BTC tissues and 25 normal bile duct tissues was purchased from Provitro (catalogue number: 401 22,078, Berlin, Germany). The TMA slides were deparaffinized, rehydrated, and immunostained in the same method used for the immunostaining of surgical specimens. The immunostaining intensity was defined as follows (0: negative, 1: weak, 2: moderate, and 3: strong). Finally, the intensity score was calculated as follows: (1 x % weakly positive cells) + (2 x % moderately positive cells) + (3 x % strongly positive cells). These TMA evaluations were performed at × 400 magnification. The maximum intensity score was defined as 300 [
26,
27].
Cell culture
A commercially available bile duct epithelial cell line (MMNK-1) and BTC cell lines (HuCCT-1 and TFK-1) were used in this study. As described above, BTC sometimes advances to extensively affect multiple biliary tracts. Therefore, TFK-1 cells were used as extrahepatic BTC cells, and HuCCT-1 cells were used as intrahepatic BTC cells. MMNK-1 and HuCCT-1 cells were purchased from JCRB Cell Bank, whereas TFK-1 cells were purchased from the Cell Resource Center for Biochemical Research, Cell Bank, Tohoku University. The MMNK-1 cell line was established from the liver by Maruyama et al
. [
28], the HuCCT-1 cell line was established from malignant ascites by Miyagiwa et al
. [
29], and the TFK-1 cell line was established by Saijyo et al
. [
30] from a common bile duct cancer specimen.
MMNK-1 cells were cultured in DMEM supplemented with 5% foetal bovine serum (FBS) and 1% penicillin–streptomycin in a humidified environment with 5% CO2 at 37 °C. The BTC cell lines were cultured in RPMI medium supplemented with 10% FBS and 1% penicillin–streptomycin in a humidified environment with 5% CO2 at 37 °C. Each cell culture experiment was performed in triplicate.
Western blotting
Western blotting was performed using a previously described protocol [
31]. The seeded cells were removed from the culture dishes and centrifuged, and the resulting cell pellets were lysed in RIPA buffer (Thermo Fisher Scientific, Waltham, MA, USA) supplemented with a protease inhibitor cocktail (Thermo Fisher Scientific). The lysates were mixed with sample buffer (Sigma, St. Louis, MO, USA) at a 1:1 ratio and then resolved on SDS–PAGE gels. After electrophoresis, the proteins were transferred to a PVDF membrane; the membrane was incubated with the primary antibody against GDF15 (1:1000, rabbit monoclonal antibody, no. 8479; Cell Signaling Technology, Beverly, MA, USA) at 4 °C overnight, anti-rabbit IgG secondary antibody (1:1000, no. 7074; Cell Signaling Technology) for one hour at room temperature, and an anti-β-actin polyclonal antibody (MBL, Tokyo, Japan) for one hour at room temperature. Blots were visualized using an Amersham Imager 600 (Cytiva, Tokyo, Japan) and Immobilon Clasico (Sigma–Aldrich, St. Louis, MO, USA). The immunoblots were evaluated by quantifying the band intensity using ImageJ software.
Reverse transcription PCR (RT–PCR)
Total RNA was extracted from MMNK-1, HuCCT-1, and TFK-1 cells using an RNeasy® Mini Kit (Qiagen, Hilden, Germany). The RNA concentration was measured using a NanoDrop 2000 instrument (Thermo Fisher Scientific). The cDNA templates were synthesized using an iScript Advanced cDNA Synthesis Kit for RT–PCR (Bio-Rad, Hercules, CA, USA) and a C1000 Touch™ Thermal Cycler (Bio-Rad). Real-time PCR was performed using QuantStudio 3 (Thermo Fisher Scientific) and TaqMan Gene Expression Assays (Thermo Fisher Scientific) with the following primers: GDF15 Hs00171132_m1 (catalogue no. 4331182) and GAPDH Hs02786624_g1 (catalogue no. 4331182). The mix was heated at 95 °C for 20 s and then amplified at 95 °C for 1 s and 60 °C for 20 s in 40 cycles. The Ct (threshold value) of each sample was obtained according to the threshold cycles with the software provided with the equipment, and the relative expression of the MIC-1 mRNA was renormalized to the expression of the GAPDH mRNA.
Recombinant MIC-1 protein
Recombinant human GDF15/MIC-1 (PeproTech, Cranbury, NJ, USA) was used in all cell culture experiments. In cell proliferation assays, MIC-1 was used at concentrations recommended by both the manufacturer and previous reports [
32,
33]. According to the manufacturer, MIC-1 was used at a concentration of 200 ng/ml. Therefore, the concentration of MIC-1 was diluted from 200 ng/ml to 100, 50, 25, 12.5, and 6.25 ng/ml, which were similar to the concentrations used in previous reports. In the other assays, the lowest effective concentration in the cell proliferation assay was applied.
Cell proliferation assay
HuCCT-1 and TFK-1 cells were seeded in 96-well plates at a density of 5 × 103 cells per well with 100 µl of medium supplemented with 10% FBS. After the plates were incubated overnight, MIC-1 solution (0, 6.25, 12.5, 25, 50, 100, or 200 ng/ml) was added to the cells and incubated for 3–7 days, after which Cell Counting Kit-8 (CCK-8) assays (Dojindo, Kumamoto, Japan) were performed. The absorbance was measured at 450 nm using a Benchmark Plus microplate spectrophotometer (Bio-Rad Laboratories, Hercules, CA).
Cell invasion assay
Cell invasion assays were performed using 24-well Corning BioCoat™ Matrigel Invasion Chambers (Corning, New York, NY, USA) according to the manufacturer’s protocol. Five hundred microlitres of medium containing 10% FBS and MIC-1 were added to the lower chamber, while HuCCT-1 and TFK-1 cells (2.0 × 105 cells/well) were added to the upper chamber in 500 µl of serum-free medium. After 22 h of incubation, cells that did not invade through the membrane were removed from the upper chamber using a cotton swab. The invaded cells were fixed with 4% paraformaldehyde for 20 min and stained with a 1% crystal violet solution for 30 min at room temperature. Three different fields were photographed using a BX41-13 microscope (Olympus, Tokyo, Japan) at 200 × magnification, and invasive cells were counted.
Apoptosis assay
Apoptosis assays were performed using a Caspase-3/7 Fluorescence Assay Kit (Cayman Chemical, Michigan, USA). HuCCT-1 (2.0 × 105 cells/well) and TFK-1 (3.0 × 105 cells/well) cells were seeded in 100 µl of medium supplemented with 10% FBS and incubated overnight. After the medium was removed, the cells were exposed to the MIC-1 solution for three hours. Next, the cells were lysed with cell lysis buffer, after which the levels of active caspase 3 or caspase 7 were measured at an excitation wavelength of 485 nm and an emission wavelength of 535 nm using a Varioskan LUX multimode microplate reader (Thermo Fisher Scientific, MA, USA).
Anticancer drug sensitivity assay
The CCK-8 assay (Dojindo) was performed to determine the effects of MIC-1 and gemcitabine on cell viability and proliferation. First, the effective gemcitabine concentration was determined. HuCCT-1 and TFK-1 cells were seeded in a 96-well plate at a density of 5 × 103 cells/well in medium and incubated for 24 h. After the medium was removed, gemcitabine (Selleck, Houston, TX, USA) was added to each well at the indicated concentration (0, 1, 10, or 100 nmol/L), and the plates were incubated for 7 days. Then, CCK-8 solution was added to each well, and the absorbance was measured at 450 nm using a Benchmark Plus microplate spectrophotometer (Bio-Rad Laboratories). Second, the effect of MIC-1 on gemcitabine toxicity was investigated. Cells were seeded and incubated as described above. The cells were exposed to effective concentrations of gemcitabine and MIC-1 for 7 days. The absorbance was measured after the addition of the CCK-8 solution.
Serum analyses
Serum MIC-1 levels were measured in patients with biliary tract diseases. Serum levels of M30, a selective apoptosis marker, were also measured. The M30 antibody detects cytokeratin-18 fragments that are cleaved during apoptosis, and the presence of M30 in bile duct epithelial and BTC cells was previously reported [
34,
35]. The relationships between MIC-1 and both pathology and serum levels of an apoptotic marker were investigated.
Patients
One hundred eighteen patients with biliary disease who were treated at Fukushima Medical University over a 4-year period were enrolled in this study. The median age of these patients was 72 years. The age range of the patients was 45–101 years. Among these patients, 56 had BTC (intrahepatic BTC: 6, peri-hilar BTC: 23, and extrahepatic BTC: 27), and 62 had benign biliary diseases and participated as control subjects [47 patients with common bile duct (CBD) stones and 15 patients with benign biliary stricture (5 with autoimmune pancreatitis (AIP), 3 with pancreatitis of unknown origin, 3 with chronic pancreatitis, 2 with primary sclerosing cholangitis, 1 with ampullary inflammation, and 1 with intraductal papillary neoplasm (IPMN)]. Patients were diagnosed with BTC using bile/brush cytology, endoscopic biopsy, endoscopic ultrasonography-guided fine needle aspiration, or surgery. Class IV or V cytology was defined as malignant disease. AIP was diagnosed according to the 2010 International Consensus Diagnostic Criteria [
36]. The patient with IPMN presented no worrisome features or high-risk stigmata, as defined by international guidelines [
37], and exhibited no signs of malignancy for more than 1 year of imaging follow-up. Cancer progression was evaluated according to the Union for International Cancer Control (UICC) classification, ver. 8 [
38]. All patients provided written informed consent for participation in this study.
Measurement of serum MIC-1 and M30 levels
Frozen sera were thawed at room temperature. Serum MIC-1 levels were measured using a Quantikine ELISA Human GDF-15 immunoassay kit (R & D Systems, Minneapolis, MN, United States), whereas serum M30 levels were measured using an M30 Apoptosense ELISA kit (VLVbio AB, Nacka, Sweden). Both kits were used according to the manufacturer’s instructions.
Examination items
Serum MIC-1 and M30 levels in patients with BTC were compared with those in control subjects. Additionally, patient characteristics (age and sex) and the levels of several serum markers (AST, ALT, CRP, and CA19-9) were compared. The relationships between serum MIC-1, ALT and M30 levels and cancer progression were investigated. Additionally, the most efficient diagnostic marker for BTC and early BTC (stage I or II) was investigated. The most efficient diagnostic marker was investigated in patients in whom all biomarkers (CA19-9, MIC-1, and M30) were measured. Finally, the prognostic predictive capacities of MIC-1 and M30 for BTC patients were investigated. For the prognostic assessment, disease-free survival (DFS) and overall survival (OS) were evaluated. DFS was examined in patients who underwent surgery and was defined as the period from the date of surgery to the date of recurrence or the last follow-up date. BTC recurrence was confirmed by CT. OS was defined as the period from the date of pretreatment blood sampling for biomarkers to the date of death or the last follow-up date.
Statistical analysis
An unpaired Student’s t test was used to compare data from cell culture experiments. Because the number of subjects was sufficient, an unpaired Student’s or Welch’s t test was also used to compare continuous variables. The Mann–Whitney U test was used to compare continuous variables that did not display a normal distribution. A chi-square test was used to compare categorical variables. Spearman’s rank correlation coefficient was calculated to investigate the correlations between two values. The ability to diagnose BTC using various biomarkers was compared by constructing receiver operating characteristic (ROC) curves. The prognostic assessment was analysed by the log-rank test. All statistical analyses were performed using IBM SPSS Statistics (IBM Corp., Armonk, NY, USA) and the EZR platform (Saitama Medical Center, Jichi Medical University, Saitama, Japan), which is a graphical user interface for R (The R Foundation for Statistical Computing, Vienna, Austria). More precisely, EZR is a modified version of the R commander that was designed to perform functions frequently used in biostatistics [
39].
Discussion
The present study produce the results described below. 1. MIC-1 expression was observed in not only BTC cells but also normal bile duct epithelial cells. However, the intensity of MIC-1 immunostaining detected in the TMA was higher in BTC tissues than in normal tissues. Furthermore, MIC-1 expression was stronger in BTC cells than in normal bile duct epithelial cells, based on western blot and RT–PCR data. On the other hand, MIC-1 expression was detected in normal bile duct epithelial cells using western blotting and RT–PCR. Consequently, the MIC-1 expression levels observed in normal bile duct epithelial cells from surgical specimens were consistent with the western blotting and RT–PCR results. 2. MIC-1 suppressed BTC cell apoptosis and accelerated BTC proliferation and invasion; furthermore, MIC-1 inhibited cellular sensitivity to gemcitabine. 3. The serum levels of MIC-1 and the apoptosis marker M30 were significantly elevated in patients with BTC (all-stage and early BTC) compared with control subjects. Furthermore, serum MIC-1 levels correlated with the tumour stage and serum M30 levels. The combination of MIC-1 and M30 was an efficient diagnostic biomarker for BTC and early BTC. 4. BTC patients with high serum MIC-1 showed poor prognosis.
The function of MIC-1 depends on the tumour location. A summary of reports on the effect of MIC-1 on several cancers is provided in Table
3 [
24,
32,
40‐
65]; however, the relationship between MIC-1 and BTC is unknown. In the present study, MIC-1 suppressed BTC cell apoptosis; therefore, we posit that MIC-1 promotes tumour progression. HuCCT-1 cell proliferation was stimulated by 6.25–50 ng/ml MIC-1 but not by 100–200 ng/ml MIC-1. Previous studies have used several concentrations of MIC-1 in cell proliferation assays; one such report treated cells with 0–40 ng/ml MIC-1 and found that pancreatic cancer cell lines exposed to MIC-1 exhibited a greater increase in proliferation than control cells [
23]. Another previous study used 200 ng/ml MIC-1 [
32], and although MIC-1 was reported to contribute to the maintenance of breast cancer stem-like cells, a breast cancer cell line treated with this concentration of MIC-1 showed less proliferation than the control cells. Based on previous publications and reported physiological concentrations, 100–200 ng/ml MIC-1 might be too high to positively affect the proliferation of cell lines.
Table 3
Reported functions of MIC-1 in several cancer types
Neck Oesophagus | | In vitro | Increases the number of invasive cells |
Urakawa et al ., 2015 [ 40] | In vitro | Associated with cancer growth |
| In vitro In vivo | Induces invasion and metastasis |
Okamoto et al ., 2020 [ 65] | In vitro | Increases proliferation, migration, and invasion |
Lung | | In vitro In vivo | Inhibits proliferation, migration, and invasion |
Breast | | In vitro | Participates in malignant progression |
Sasahara et al ., 2017 [ 32] | In vitro | Maintains cancer stem cell properties |
| In vitro In vivo | Represses metastatic potential |
| In vitro In vivo | Facilitates cancer progression via the GDF15–AKT pathway |
Gkretsi et al ., 2020 [ 62] | In vitro | Suppresses tumour cell invasion |
Liver | | In vitro | Increases viability, invasion, migration, and angiogenesis |
| In vitro | Promotes metastasis |
Stomach | | In vitro | Contributes to cancer progression |
| In vitro | Promotes the apoptosis of gastric cancer cells |
| In vitro | Participates in malignant progression |
| In vitro | Activates apoptosis |
Pancreas | | In vitro In vivo | Promotes cancer progression |
Prostate | | In vitro | Reduces cell adhesion and induces apoptosis |
Senapati et al ., 2010 [ 50] | In vitro In vivo | Induces metastasis |
| In vitro In vivo | Promotes cancer progression |
Husaini et al ., 2015 [ 52] | In vitro In vivo | Promotes local invasion and metastatic spread |
| In vitro In vivo | Inhibits cell proliferation and induces apoptosis |
| In vitro In vivo | Increases IL-8 and IL-6 levels and promotes cancer progression |
Blatter | | In vitro In vivo | Inhibits cell proliferation, invasion and tumorigenesis |
Uterus | | In vitro | Enhances cervical cancer cell proliferation |
Ovary | | In vitro | Promotes cancer cell growth |
Colon | | In vitro | Reduces tumorigenicity |
| In vitro In vivo | Promotes the epithelial–mesenchymal transition and metastasis |
| In vitro | Induces metastasis |
Skin | | In vitro In vivo | Facilitates the development of more aggressive melanoma |
MIC-1 promoted cancer growth by suppressing the apoptosis of BTC cells. Thus, therapeutic agents targeting MIC-1 are a potential approach for treating BTC. A report described that MIC-1 is expressed after bile duct injury and may regulate bile duct proliferation and biliary tumour formation [
67]. However, the detailed mechanism by which MIC-1 suppresses BTC cell apoptosis is unknown. In previous studies, commonalities between the mechanism of BTC progression and the protumorigenic effects of MIC-1 include increases in the activities of the JAK–STAT3 and PI3K–AKT signalling pathways. In a study of the relationship between MIC-1 and tumour progression, MIC-1 was reported to induce tumour progression via STAT3 activation [
68], and STAT-3 signalling was shown to prevent tumour cell apoptosis [
69]. In addition, MIC-1 activates the PI3K–AKT signalling pathway and reduces apoptosis [
70]. Regarding the mechanism of BTC progression, IL-6 was reported to activate the JAK–STAT3 pathway, which promotes tumour cell proliferation and invasion [
71,
72]. In addition, activation of the PI3K–AKT pathway was reported to induce BTC progression [
73‐
75]. In the future, the mechanism by which MIC-1 affects BTC progression may be clarified by investigating cytokines and cytokine-related intracellular signalling pathways.
In the present study, the serum MIC-1 level was a useful diagnostic marker of BTC, and elevated serum MIC-1 levels were also observed in patients with BTC and reflected tumour progression. Moreover, OS was significantly shorter in BTC patients with high serum MIC-1. Therefore, the serum MIC-1 level has potential as a useful prognostic biomarker of BTC. In addition, the combination of serum MIC-1 levels and serum levels of the apoptosis marker M30 was effective at diagnosing BTC. As described above, a previous study reported the efficacy of biliary MIC-1 levels in diagnosing individuals with BTC (cut-off value: 58.2 × 10
–2 ng/ml, AUC 0.77, sensitivity 71.4%, specificity 82.8%) [
18]; however, this method is limited by the invasive nature of measuring biliary MIC-1 levels. The application of serum MIC-1 and M30 levels overcomes this limitation and was superior to the diagnostic ability of biliary MIC-1 levels (the combination of serum MIC-1 and M30 levels for diagnosing BTC: AUC 0.813, sensitivity 80%, specificity 74.4%). Additionally, the serum MIC-1 level was positively correlated with the serum M30 level, a finding that differed from the cell culture experiment findings. One potential explanation for this discrepancy might be that MIC-1 increases tumour volume, and consequently, the apoptosis of tumour cells increases. The serum M30 level properly reflects tumour size [
76]; therefore, the serum M30 level increases with cancer progression. Notably, the M30 level showed a positive correlation with the BTC stage (Fig.
3D; r = 0.37; P < 0.01, Spearman’s rank correlation coefficient).
The present study has several limitations. First, this study included a relatively small sample size and employed a single-centre design. However, the difference in serum MIC-1 levels between the two groups was 150.8 × 10
–2 ng/ml, and the standard deviation for the comparison between two groups was 191.7 × 10
–2 ng/ml. Thus, the total sample size necessary to achieve an α error of 5% and a β value of 0.2 was 52 cases. When serum MIC-1 levels were determined to be the main outcome, the minimum number of necessary cases was collected. Second, MIC-1 immunostaining was performed on surgical specimens from only two patients; then, MIC-1 expression was determined using western blotting and RT–PCR and compared between a normal bile duct epithelial cell line and BTC cell lines. Third, the diagnostic specificity of serum MIC-1 levels for BTC was insufficient. However, serum MIC-1 levels are higher in patients with pancreaticobiliary cancer than in patients with other cancers or pancreaticobiliary inflammatory disease [
15,
17]. In addition, the specificity was improved by combination with a serum apoptosis biomarker.
Conclusions
In summary, previous reports have analysed MIC-1 in several types of cancer. However, serum MIC-1 levels were shown to be elevated to a greater extent in patients with pancreaticobiliary cancer than in patients with other types of cancer. Although MIC-1 and pancreatic cancer have been the focus of several previous studies, the effect and efficacy of MIC-1 have not been investigated in BTC. We previously reported the efficacy of evaluating biliary MIC-1 levels in diagnosing BTC. However, bile collection is an invasive procedure. The novelty of this study is the documentation of the effect of MIC-1 on BTC and the establishment of a new, noninvasive diagnostic method for BTC. Moreover, BTC patients with high serum MIC-1 had a poor prognosis. In conclusion, MIC-1 suppresses BTC cell apoptosis and promotes BTC progression. Additionally, the serum MIC-1 level reflects BTC progression, apoptosis, and prognosis of BTC patients. The ability to diagnose BTC is improved using the combination of serum MIC-1 and M30 levels, which is also useful for diagnosing early BTC. Therefore, MIC-1 might be a useful biomarker, prognostic marker, and therapeutic target in BTC.
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