Background
Extranodal natural killer (NK)/T-cell lymphoma (ENKL) is a distinct subtype of non-Hodgkin’s lymphoma, with a geographical predilection for Asian population [
1]. ENKL predominantly occurs in the nasal or paranasal areas, and exhibits aggressive clinical features, characterized primarily by local indeterminate growth and destructive invasion [
2]. Epstein–Barr virus (EBV) is usually detected in ENKL cells and plays an important role in lymphomagenesis. In most ENKL cases, the disease leads to significant chemotherapy resistance and poor clinical outcomes, probably due to the expression of multidrug-resistant genes and close association with EBV infection [
3,
4]. Treatment regimens containing
l-asparaginase (
l-ASP) or pegaspargase have elicited promising responses [
5,
6]. Hematopoietic cell transplantation (HCT) and targeted therapy have shown potential for clinical application [
7,
8]. However, the therapeutic effect and prognosis of ENKL is still relatively poor compared with other types of lymphoma, and recurrent or refractory phenomenon usually emerges in the process of treatment. The fundamental reasons include lack of insight into biological characteristics of ENKL, such as cytological heterogeneity, multidrug resistance, EBV infection/latency/reactivation, and more importantly, the interaction between different factors.
Side population (SP) cell sorting, initially used for the identification of primitive hematopoietic stem cells, has been applied to enrich stem cell compartments in diverse tissues and organs [
9]. SP cells are determined by their efflux of the fluorescent dye, Hoechst 33342 through an adenosine triphosphate (ATP)-binding cassette (ABC) membrane transporter. To elucidate the drug resistance and heterogeneous characteristics of nasal NK/T-cell lymphoma cells, we developed a doxorubicin-resistant cell line of ENKL known as SNK-6/ADM and identified the SP cells. Surprisingly, these cells exhibited conserved biological features and stronger chemotherapy resistance suggesting that human ENKL cells comprise heterogeneous populations of malignant NK cells, which may play an important role in the treatment of nasal NK/T-cell lymphoma.
Materials and methods
Doxorubicin-resistant cell lines
The EBV-positive ENKL cell line, SNK-6, established from primary lesions with nasal NK-cell lymphoma [CD3ε+, CD20−, CD56+, CD3(Leu4)−, EBER(+)] [
10], was kindly provided by Dr. Norio Shimizu and Yu Zhang of Chiba University. Cells were cultured in RPMI 1640 supplemented with 10% heat-inactivated human serum and 700 U/mL recombinant human interleukin 2, 2M glutamine, 100 IU/mL penicillin, and 100 g/mL streptomycin sulfate in a 5% CO
2-containing atmosphere.
Resistance to doxorubicin (ADM) was induced in SNK-6 by gradually increasing the concentration of doxorubicin in the culture medium with 2 μg/mL initial concentration. The resistance index (RI) was evaluated as follows: RI = IC50 (SNK-6)/IC50 (SNK-6/ADM). SNK-6/ADM cells were cultured in a medium containing 6 μg/mL ADM or without ADM 48 h before experiments.
Methylthiazole tetrazolium (MTT) assay
Cells (4 × 104 per well) seeded in 96-well plates were cultured in 180 μL medium, supplemented with 20 μL of chemotherapeutic drug (doxorubicin, cytarabine, cisplatin, gemcitabine, l-asparaginasum) in each well with a concentration gradient for 48 h. MTT (20 μL, 5 mg/mL) was added to each well, and incubated for 4 h at 37 °C in a 5% CO2-containing atmosphere. The absorbance at 490 nm (A) was measured with a spectrophotometer. The inhibition ratio was measured as a percentage of untreated controls. Measurements were conducted in duplicate and experiments were repeated at least three times. Inhibition rate (%) = (Control OD value − Experiment OD value/Control OD value) × 100%. IC50 was finally calculated by linear regression method.
Side population (SP) cells
SP cells of SNK-6 and SNK-6/ADM were sorted by Hoechst33342 assay with flow cytometry as described previously [
11]. We designated SP cells of SNK-6/ADM as SNK-6/ADM-SP. The SP cells of SNK-6 were not sorted due to small sample size.
Cell transfection
For transfection, SNK-6/ADM and SNK-6/ADM-SP cells were cultured at 50–70% confluency without antibiotics. The short-hairpin RNA plasmids directly knocking down ABCC4 (sh-ABCC4), ABCG2 (sh-ABCG2) or the non-targeting sequence (sh-control) were chemically synthesized by Sangon (Shanghai, China). Plasmid transfection into SNK-6/ADM-SP cells was performed using Lipofectamine 2000 (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s protocol.
Western blot
Cell protein extracts were immunoblotted with a primary antibody followed by a secondary antibody. Primary antibodies (P-gp, ABCG2, ABCC4, LMP1) were used at a diluted concentration of 1:2000 while the secondary antibody was used at 1:10,000. Protein bands were visualized with enhanced chemiluminescence. Equal protein loading was confirmed with anti-β-actin antibody, which was diluted as recommended by the manufacturer.
Cell cycle assay
Cells were collected, and fixed with 70% cold ethanol. The fixed cells were treated with 50 μg/mL of DNase-free RNase and 20 μg/mL of propidium iodide. A total of 10,000 cells were analyzed by FACScan. Cell cycle was detected, and cells in G0/G1, S, and G2/M phases were evaluated.
Expression of surface markers
Cells were analyzed by two-color immunofluorescence using flow cytometry to determine the expression of surface markers. The following antibodies conjugated with fluorescein isothiocyanate (FITC) were used: anti-CD16, -CD25, -CD56, -CD34, -CD117, and -CD122.
IL-15 sensitive assay
SNK-6, SNK-6/ADM and SNK-6/ADM-SP cells (4 × 104 per well) were treated with 10 ng/mL IL-15 for 48 h, stained with 20 μL MTT (5 mg/mL) and subsequently dissolved in 100 μL of DMSO. The final cell activity was determined by MTT assay.
EBV-DNA
We examined the concentration of EBV DNA in the EBV-positive ENKL cell lines, SNK-6, SNK-6/ADM and SNK-6/ADM-SP cells. First, we treated cells with histone deacetylase (HDAC) inhibitor (Epidaza) for 72 h for EBV reactivation until the virus titer was detected. The EBV DNA copy number was measured in the cell culture supernatants using quantitative PCR.
Statistical analysis
All the experiments were performed in triplicate. All the data were analyzed with SPSS 17.0 software and expressed as mean ± standard deviation (SD). Statistical significance of differences was determined by Student’s t-test. A P value of less than 0.05 was considered significant.
Discussion
ENKL is a distinct clinicopathological entity and EBV-associated disease that is highly aggressive, with a geographic predilection for Asia, Central and South America [
12,
13]. Current treatment strategies are not effective and chemoresistance leads to poor prognosis [
5,
14]. The mechanism of oncogenesis and biological characteristics of ENKL which provide important insights into potential therapeutic options is not clear [
4].
The origin and differentiation of lymphatic leukemia and B cell lymphomas are well described. Previous studies have suggested that oncogenesis of hematological malignancy occurs via two principal mechanisms: transformation of hematopoietic stem cells and progenitor cells committed to tumor-initiating cells, and differentiation along the original lineage. Most lymphomas are more likely to originate from normal lymphocytes during specific developmental stages [
15‐
17]. However, the oncogenic features of ENKL lymphomas and even normal NK cells are less clear. The current hypothesis is that traditional NK cells originate in the bone marrow from a common T cell/NK cell progenitor, and develop to maturity [
18,
19]. Nevertheless, the NK cell phenotype and function in mucous and other extranodal tissues vary from that of traditional NK cells [
20]. The origin and relationship with local microenvironment remain to be elucidated. Thus, ENKL cells manifest distinct biology and clinicopathology that distinguish them from other T cell or NK cell-derived hematological malignancies. Perhaps, this cellular heterogeneity is a major factor underlying the unique biological characteristics and elusive response to chemotherapy of ENKL.
In the previous study, we developed a doxorubicin-resistant ENKL cell line known as SNK-6/ADM based on classical ENKL cell line SNK-6 [CD3ε+, CD20−, CD56+, CD3(Leu4)−, EBER(+)] [
3]. We originally scheduled to sort the SP cells to investigate the oncogenesis of ENKL. However, we could hardly found SP cells among normal SNK-6 cells. Fortunately, SP cells varied from approximately 1% to 2% of SNK-6/ADM cells were successfully enriched and designated as SNK-6/ADM-SP. Due to the abundance of studies reporting SNK-6 phenotype, we identified the origin of these SP cells by evaluating CD56, CD16, CD34 and CD117 expression. Results showed that SNK-6/ADM-SP cells originated from mature NK cells, which were similar to normal SNK-6 and SNK-6/ADM cells. We further evaluated the sensitivity of chemotherapy drugs of three cell lines, and results showed that ENKL cells were originally not sensitive to traditional chemotherapy drugs doxorubicin and cytarabine with higher IC50s. Furthermore, the resistence indexes of doxorubicin, cytarabine and cisplatin in SNK-6/ADM and SNK-6/ADM-SP cells were significantly increased, especially in the SNK-6/ADM-SP cells. That means SNK-6/ADM-SP cells have stronger multidrug resistance even than doxorubicin-resistant ENKL cell line. In contrast, IC50s of gemcitabine and
l-asparaginasum among three cell lines were had almost no change. Moreover, gemcitabine also showed a wonderful sensitivity to normal or resistant ENKL cells. These results were exactly consistent with our latest advances of clinical trial [
5,
6].
Consequently, we developed some further studies in order to explore the biological characteristics and mechanism of drug-resistance of SNK-6/ADM-SP cells. Morphological and proliferation assays showed that SNK-6/ADM-SP cells manifested indolent status, mostly were restricted to stationary phase. The control SNK-6 cells showed effective proliferation. These preliminary observations suggested that SNK-6/ADM-SP possess distinct biological characteristics as independent cell populations. SP cells were separated from many tissues including malignant tumors by sorting cancer stem cells [
11]. One study [
21] found that a low concentration of doxorubicin increased the proportion of SPs in acute leukemia cell line HL60. Further studies [
22] demonstrated that the efflux of Hoechst 33342 by SP cells was mainly mediated by ATP-binding cassette sub-family G member 2 (ABCG2), one of the ATP-binding cassette (ABC)-type transporters. They displayed stem cells-like features. However, a few other studies indicated that SP cells might be a subgroup of heterologous cell populations with ‘SP phenotype’, with stem cell characteristics, multidrug resistance or other potential [
23,
24]. In our study, we did not consider SNK-6/ADM-SP as cancer stem-like cells because of their mature NK cell-derived phenotype and indolent cellular characteristics but as potentially super multidrug resistant cells. Therefore, the expression of ABCB1, ABCG2 and ABCC4 was detected in SNK-6, SNK-6/ADM, and SNK-6/ADM-SP cells. The results showed that the expression of ABCC4 in SNK-6/ADM and SNK-6/ADM-SP were both higher than that in SNK-6, while the ABCG2 expression was significantly increased in SNK-6/ADM-SP cells. What was more, we considered that the main factor underlying SNK-6/ADM drug resistance was ABCC4 and ABCG2 rather than P-gp, which is the most classic MDR protein, and consistent with recent studies [
4,
25] suggesting the absence of absolute correlation between P-gp and chemotherapy resistance. Further results showed that the doxorubicin resistance in SNK-6/ADM-SP cells transfected with shRNAs targeting ABCC4, ABCG2 and ABCC4 + ABCG2 was significantly decreased compared with the sh-control groups, indicating the vital roles of ABCC4 in drug resistance and ABCG2 in conservative characteristics of SNK-6/ADM-SP cells.
Previous studies elucidating the process of normal NK-cell development provide comparative support for investigations into the differentiation patterns of ENKL [
26,
27]. Studies [
28,
29] reported that IL-15 plays an important role in the survival of human natural killer (NK) cells. In human bone marrow and secondary lymphoid tissue (SLT), CD34+ hematopoietic stem cells and hematopoietic progenitor cells differentiate into cytolytic NK cells after stimulation with either IL-2 or IL-15 [
30]. We investigated the role of IL-15 in the proliferation of three cell lines SNK-6, SNK-6/ADM, SNK-6/ADM-SP. Cells cultured in a medium containing IL-2 over several generations were not evaluated for IL-2. Based on our analysis, we found that SNK-6/ADM-SP showed an obvious reduction in sensitivity to IL-15. Detection of CD122 (IL-2/15R-β) showed that downregulation of expression resulted in poor sensitivity of SNK-6/ADM-SP cells to IL-15. These phenomena also suggested that SNK-6/ADM-SP cells might be a subgroup of indolent or conservative population of cells.
Nasal ENKL is characterized by EBV infection. SNK-6 cell line is representative of EBV-positive ENKL cell origin. EBV infects more than 90% of the population and mostly exhibits latency following infection. However, EBV is reactivated from the latent phase to the lytic phase and produces infectious viral progeny under changing external conditions. A recent study has revealed that the HDAC inhibitor could reactivate EBV in SNK-6 cell line [
31]. In our study, SNK-6 cells and other cell lines were not analyzed for EBV DNA possibly because of the latent infection leading to extremely low virus load. After treatment with HDAC inhibitor (Epidaza), we found EBV-DNA (approximately 3.0 − 4.5 × 10
3 copies/μL) in SNK-6 and SNK-6/ADM, but rarely in SNK-6/ADM-SP cells. We speculated that the decreased EBV DNA was associated with the conservative characteristics of SNK-6/ADM-SP cells. The following analysis of LMP1 expression suggested that EBV-related protein decreased in SNK-6/ADM-SP cells, further suggesting that SNK-6/ADM-SP cells exhibited a conservative virus inhibition. Maybe self-protection mechanism in the evolution process of lymphocyte was involved in this phenomenon.
Authors’ contributions
Conception and design: XZ, XF, and MD. Development of methodology: MM and ZL. Acquisition of data: XW, LL, FN, and JY. Analysis and interpretation of data: XL, ZS, and YC. Administrative, technical, or material support: ZY and SW. Writing, review, and/or revision of the manuscript: XZ and YM. Study supervision: MZ and QC. All authors read and approved the final manuscript.