Background
Hepatocellular carcinoma (HCC) is a major malignancy and the second leading cause of cancer death worldwide [
1,
2]. Due to locally advanced or metastatic disease, the prognosis of HCC is quite poor, and surgery in combination with adjuvant chemotherapy provides a long-term survival possibility for HCC patients [
3]. With the development of regional cancer therapy and multimodality treatments, localized unresectable large HCCs have been transformed to resectable small HCCs [
4]. Transarterial chemoembolization (TACE) is used widely for unresectable HCCs and has been recommended as a standard loco-regional palliative treatment for these patients [
5]. However, not all patients received the same beneficial effect [
6].
Oxaliplatin is one of the first-line drugs used in TACE, and it is widely used in the chemotherapeutic regimes to reduce HCC recurrence and prolong survival. However, due to the development of cellular resistance, its efficacy is limited, which is still a difficult problem for the successful chemotherapy of HCC [
7,
8].
Recent studies suggested that the therapeutic resistance of tumors relies on extrinsic mechanisms represented by the cross-talk between tumor cells and other cellular components of the tumor microenvironment (TME), in particular immune cells [
9]. Tumor-associated macrophages (TAMs) constitute the dominant myeloid cell population in many tumors and play a key role in multiple aspects of TME, including therapeutic resistance [
10‐
12]. In our previous study, we demonstrated that TAMs-secreted IL-8 could induce epithelial-mesenchymal transition in HCC cells by activating the JAK2/STAT3/Snail pathway [
13]. It is also reported that the TAMs density positively correlated with poor prognosis in several types of solid tumor [
12,
14], including HCC [
15,
16]. There is a growing body of evidence that TAM and its products are involved in modulating behavior of cancer cells in chemotherapy [
17‐
19]. However, the relationship between TAMs and chemo-resistance in HCC is still obscure.
In our previous study, it was revealed that autophagy activation in HCC could contribute to the tolerance of oxaliplatin via reactive oxygen species (ROS) modulation [
20]. Interactions between the microenvironment and autophagy have also previously been reported [
21‐
23]. Thus, we presumed that TAMs may induce resistance to oxaliplatin via activating autophagy in HCC cells.
Materials and methods
Patient samples
Patient samples were collected after obtaining informed consent, according to an established protocol approved by the Ethics Committee of Zhongshan Hospital, Fudan University. The data collected does not contain any information that could identify the patients. We collected information on HCC patients who had underwent TACE within 3 months prior to radical resections at the Liver Cancer Institute, Zhongshan Hospital, Fudan University, in 2016. The diagnosis of HCC was confirmed by histological examination. Patients were divided into two groups, according to the tumor growth after receiving TACE (tumor shrinkage vs. tumor non-shrinkage). The tumor size was measured by computed tomography or nuclear magnetic resonance imaging. 9 patients were elected to the tumor shrinkage group and 17 patients were elected to the tumor non-shrinkage group for further research.
Immunohistochemistry
Immunohistochemistry was performed with rabbit anti-human CD68 (1:1000, ab125212, Abcam, Cambridge, UK), using a two-step protocol (Novolink Polymer Detection System, Novocastra, Newcastle, UK), as described previously [
24]. Briefly, after microwave antigen retrieval, tissues were incubated with primary antibodies for 60 min at room temperature and then incubated with secondary antibody (RE7112, Novolink Polymer, Newcastle, UK) for 30 min. The sections were developed in 3,3′-diaminobenzidine solution under microscopic observation and counterstained with hematoxylin. Negative control slides, in which the primary antibodies were omitted, were included in all assays. In each section, staining was captured by Leica QWin Plus version 3 software (Leica Microsystems, Wetzlar, Germany).
Cell preparations and compounds
The human HCC cell lines Huh-7, SMMC-7721 and the human monocyte leukemia cell line THP-1 were purchased from the Institute of Biochemistry and Cell Biology, Chinese Academy of Sciences, Shanghai, China. The 2 HCC cell lines were cultured in Dulbecco’s Modified Eagle Medium (Invitrogen, Carlsbad, CA, USA), and THP-1 cells were cultured in RPMI 1640 Medium (Invitrogen, Carlsbad, CA, USA). Media were supplemented with 10% heat-inactivated fetal bovine serum (FBS) and 100 U/mL penicillin, and 100 mg/mL streptomycin (Invitrogen, Carlsbad, CA, USA). All cell lines were cultured the cells at 37 °C in a humidified atmosphere of 5% CO2.
THP-1 cells were seeded into the upper insert of a 6-well Transwell apparatus (0.4 μm pore size, Corning, Lowell, MA, USA) and treated them with Phorbol myristyl acetate (PMA) (320 nM, P1585, Sigma-Aldrich, St. Louis, MO, USA) for 24 h to obtain PMA-treated macrophages.
Oxaliplatin was purchased from Sigma-Aldrich and dissolved in 100% dimethyl sulfoxide and diluted with DMEM to the desired concentration with a final dimethyl sulfoxide concentration of 0.1% for the in vitro studies.
Establishment of co-culture system with macrophages and HCC cells
After a thorough wash, PMA-treated THP-1 macrophages seeded in upper inserts were co-cultured with HCC cells which were seeded in a 6-well plate (2 × 105 cells per well) without direct contact. After 24 h of co-culture, the upper inserts containing the macrophages were discarded, and HCC cells were washed and used for subsequent experiments.
Assessment of cell viability in vitro
MTT (3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide) kit (Trevigen, Gaithersburg, MD, USA) was used to assess the cell proliferation, according to the manufacturer’s protocol. Cells (5 × 10
3) were plated in 96-well plates, incubated for 24 h at 37 °C, and treated with the specified agents at defined time points. Annexin V- Alexa Fluor 488 assay (Invitrogen, Carlsbad, CA, USA) and propidium iodide (PI) were applied to determine the number of apoptotic cells, according to the manufacturer’s protocol [
25]. Cells were analyzed using a flow cytometer, and data were analyzed using CellQuest software version 3.3 (BD Bioscience, Franklin Lakes, NJ, USA).
Autophagy analysis
The movement of autophagosomes was detected by GFP label. Huh-7 and SMMC-7721 were transfected with a lentivirus plasmid vector containing GFP-LC3 (C3006, Beyotime, Shanghai, China) which targets autophagosomes. Autophagy activity was assessed using GFP-LC3 redistribution and LC3 conversion. Redistribution of GFP-LC3 was detected and the images were captured by using an inverted fluorescence microscope (Carl Zeiss, Dresden, Germany). The average numbers of GFP-LC3—positive dots per cell were determined in 3 independent experiments. Eight randomly selected fields representing 200 cells were counted. For the LC3 conversion assay, cells were lysed with M-PER Mammalian Protein Extraction Reagent (78501, Pierce, MA, USA) and then subjected to westernblot analysis with an antibody against LC3.
RNA interference
Autophagy-related 5 homolog (ATG5) RNA interference was accomplished by transfection of HCC cells with specific small interfering RNA (siRNA) duplexes. Primers for the ATG5 targeting sense and the negative control sense were purchased from GenePharma Company (Shanghai, China). SiRNAs were transfected using the Lipofectamine 2000 transfection reagent (Invitrogen, Carlsbad, CA, USA). Cells were lysed 72 h after transfection, and protein was assayed by western blot analysis.
Western blot analysis
To determine the levels of protein expression, cells were harvested and gently washed with cold phosphate-buffered saline (PBS). Total protein was extracted using RIPA Cell Lysis Buffer (Beyotime, Shanghai, China). For each sample, 50 μg of protein was separated by standard SDS-PAGE and then transferred to polyvinylidene difluoride membranes. The membranes were washed and blocked by 5% nonfat milk powder in TBST buffer for 1 h, and then incubated with specific primary antihuman antibodies against ATG5 (1:1000, #2630, CST, Beverly, MA, USA), LC3B (1:1000, #3868, CST, Beverly, MA, USA) and GAPDH (1:10,000, AP0063, BioWorld, St. Louis Park, MN, USA). After that, the membrane was incubated with horseradish peroxidase–conjugated secondary antibodies. The protein bands were visualized using enhanced chemiluminescence western blotting substrate (Pierce, MA, USA), and captured by ChemiDoc™ XRS + system (Bio-Rad Laboratories, CA, USA) and the densitometry of the protein bands were determined by ImageLab version 3.0 (Bio-Rad Laboratories, CA, USA).
In vivo tumorigenicity
Huh-7 (5 × 10
6) and Huh-7 with THP-1 derived macrophages (5 × 10
6, respectively) were suspended in 100 μL serum-free DMEM and Matrigel (BD Biosciences, CA, USA) (1:1), and then inoculated into the subcutaneous region of the right upper abdomen of nude mice, as described previously [
13]. 3 days later, all the mice were injected intraperitoneally with oxaliplatin 5 mg/kg twice a week. The mice were sacrificed 5 weeks after tumor implantation. At autopsy, the volumes of the largest (a) and smallest (b) tumors were measured and the tumor volume was calculated as: V = a × b
2 × π/6.
Immunohistochemical staining for LC3 expression and hematoxylin and eosin staining in tissues
Xenografts of Huh-7 with THP-1 derived macrophages were fixed with 4% neutral paraformaldehyde. Next, the paraffin-embedded sections (4 μm in thickness) were prepared for hematoxylin and eosin (H&E) staining and immunohistochemical staining of LC3 (ab128025, Abcam, Cambridge, UK). The steps of immunohistochemical staining were described above. The pretreatment of H&E staining was basically the same as the immunohistochemical steps. Sections were treated with hematoxylin reagent for 5 min after deparaffinization and rehydration and then treated with 1% acid–ethanol for 1 s. Subsequently, the sections were stained by eosin reagent for 3 min. The slides were dehydrated and mounted then photographed by microscopy.
TUNEL staining assay for cell apoptosis in vivo
Terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick-end labeling (TUNEL) staining was performed using an In Situ Apoptosis Detection Kit (VB-4005, GeneCopoeia, Rockville, MD, USA), according to the manufacturer’s instructions. Briefly, the tumor slides were incubated with terminal deoxynucleotide transferase (TdT) and a biotinylated nucleotide mixture at 37 °C for 30 min. Subsequently, the endogenous peroxidases was blocked by immersing the slides in 0.3% hydrogen peroxide in PBS for 3–5 min at room temperature. The slides were incubated with streptavidin-HRP and visualized with DAB. Negative controls were set up by substituting distilled water for TdT in the working solution. The results are presented as the ratio of the TUNEL-positive cells to the total number of cells.
Statistical analysis
Statistical analysis was performed using SPSS 22.0 software (IBM, Chicago, IL, USA). Means were compared between two groups using unpaired, two-tailed Student’s t test. The cut-off for statistical significance was P < 0.05.
Discussion
For unresectable HCC, TACE is a well recommended treatment, and it involves catheterization of the tumor supplyinig artery, followed by injection of embolization agents and chemotherapeutics through the catheter [
5]. However, embolization is not always complete, and HCC is generally resistant to chemotherapy. Oxaliplatin is one of the most widely used chemotherapeutic drugs in liver cancer interventional therapy, and oxaliplatin-based chemotherapy is now the most commonly used chemotherapeutic criterion in HCC [
26]. Unfortunately, inoperable HCC patients who develop resistance to oxaliplatin have limited optimal therapeutic strategy [
7]. Our results showed that the density of TAMs in HCC patients with tumor shrinkage after TACE was greater than that in patients without tumor shrinkage. This phenomenon suggested that the macrophages infiltrated in tumor may be associated with drug resistance.
In addition to genetic changes of HCC cells themselves, tumor microenvironment has an important role in chemo-resistance [
27,
28]. In the context of chemotherapy treatment, TAMs have become effective regulators of therapeutic response [
10,
11]. These effector cells can regulate tumor cell survival pathways by providing of cytokines and pro-tumorigenic proteases [
17,
29]. Additionally, TAMs can suppress immune-based mechanisms of cytotoxic chemotherapy [
30,
31]. In the present study, we showed that the HCC cells exhibited enhanced resistance to oxaliplatin after co-culturing with macrophages in vitro and vivo, indicated that TAMs can induced chemo-resistance in HCC.
Autophagy serves as a dynamic recycling system that produces new building blocks and energy for cellular homeostasis and renovation [
32]. It has been demonstrated that autophagy can protect cancer cells against hypoxia, metabolic stress, detachment-induced anoikis and diverse cellular damages, as well as apoptosis or necrosis induced by anti-tumor therapy or other cell death stimuli [
33‐
37]. To directly determine the levels of autophagy occurred in SMMC-7721 and Huh-7 after co-culturing with macrophages, the GFP-LC3 redistribution was observed. The elevated number of GFP-LC3–positive dots per cell in oxaliplatin-treated cells indicated that co-culturing with macrophages could activate autophagy in HCC cells. Similarly, western blotting analysis of LC3 conversion in HCC cells also proved this conclusion. To directly determine the role of autophagy induced by macrophages, RNA interference of the essential autophagy gene ATG5 was used to inhibit autophagy in HCC cell. After co-culturing these HCC cells with macrophages, increased oxaliplatin cytotoxicity was observed in ATG5 siRNA-transfected HCC cells. Moreover, the decreased number of TUNEL-positive HCC cells in THP-1 derived macrophages and HCC cells blended xenografts with simultaneously high level of LC3 expression suggests that macrophages may decrease the anticancer effect of oxaliplatin in vivo by activation of autophagy. These findings indicated that autophagy induced by macrophages in HCC cells may play a vital role in resistance to chemotherapy agents.
There are some limitations to our study. First, TACE is a form of intra-arterial catheter-based chemotherapy that selectively delivers high doses of cytotoxic drug to the tumor bed, combined with the effects of ischemic necrosis induced by arterial embolism. Therefore, we cannot ignore the effect of hypoxia induced by TACE on chemo-resistance. Second, because of the non-contact co-culture system in our study, macrophages may induce autophagy in HCC cells by secretion of certain cytokines. But in vivo, macrophages and HCC cells are in direct contact. Our cell co-culture model cannot perfectly simulate the heterologous and tumor cells in HCC, and more effort should be made to clarify how the macrophages induce autophagy in HCC cells. Third, the detection of cell apoptosis by Annexin V test at the time of no intervention of oxaliplatin involves a problem of spontaneous apoptosis of the cells. Actually, we indeed found that the apoptosis rate of HCC cells at time 0 h oxaliplatin treatment was slightly reduced in co-culture group during the research. The reason we believe in may be associated with the enhanced autophagy or secreted anti-apoptotic factors by co-culturing with macrophages, leading to a decrease in the rate of spontaneous apoptosis. Moreover, the difference in apoptotic rates become more significantly after oxaliplatin treatment. Therefore, in this study, we focused on the reactivity of HCC cells to oxaliplatin before and after co-culture with macrophages. Last, our results only revealed that macrophages could enhance chemo-resistance of HCC cells by activating autophagy in HCC cells. However, TME includes surrounding blood vessels, immune cells, fibroblasts, signaling molecules and the extracellular matrix. Recent studies have shown that the stromal cells in HCC can regulate the response of cancer cells to chemotherapy [
38‐
40]. We hypothesized that macrophages in TME may be affected by other heterogeneous cells in vivo, so further studies to reveal the mechanism will be necessary conducted.
Authors’ contributions
XTF, ZBD and JF conceived and designed the study. XTF, KS drafted the manuscript. JZ, YHS, WRL and QG participated in implementation of the study. GMS and XYW assisted in collecting the data. XTF and ZBD performed the statistical analysis. All authors read and approved the final manuscript.