Background
According to the tumor data reported in 2019, nearly 529,000 newly diagnosed cases of cervical cancer are reported annually and the mortality of cervical cancer ranks the second in 20- to 39-year-old female cancer patients, with approximately nine cancer patients die of cervical cancer each week [
1]. Cervical cancer is generally treated by surgery, chemotherapy, or radiotherapy alone or in combination [
2]. However, the survival rate of cervical cancer patients remains relatively low. Although the 2-, 4-, and 9-valent human papillomavirus (HPV) vaccines have been shown to prevent cervical cancer, these do not have protective effects on all individuals [
3,
4]. Hence, the development of novel treatments to inhibit tumor invasion and migration and improve the survival rate and quality of life of cervical cancer patients is particularly important.
Metformin is currently the first-line oral drug for the treatment of type 2 diabetes; it is inexpensive and imparts a significant therapeutic effect. Studies have shown that diabetic patients with metformin treatment have a lower incidence of cancer. The antitumor effect of metformin is closely related to mechanistic target of rapamycin complex 1 (mTORC1), a key protein of the PI3K/Akt/mTOR pathway [
5‐
8]. Studies have shown that phosphatidylinositol 3-kinase (PI3K), epidermal growth factor receptor, extracellular signal-regulated kinases, anti-apoptotic B-cell lymphoma 2 (Bcl-2) pathways and proteins play an important role in the development of tumors, particularly solid tumors such as cervical cancer [
9,
10]. These signaling pathways and proteins form the regulatory network of cervical cancer and are ideal targets for the development of antitumor drugs. The PI3K/serine-threonine kinase/rapamycin pathway has recently been shown to be closely related to the growth and proliferation of solid tumor cells, and serine/threonine kinases play a central role in the pathway. PI3K inhibitors inhibit the expression of downstream serine/threonine kinases. In addition, serine/threonine kinase inhibitors suppress tumor cell proliferation [
11,
12].
Natural killer (NK) cells are important immune cells in the body that are involved in antitumor, antiviral infection, and immunomodulation processes. Under specific conditions, NK cells can identify target cells and activate immune cells. NK cells impart broad spectrum antitumor effects and do not show specificity or major histocompatibility complex (MHC) restriction. NK cells have two anticancer effects. First, NK cells can directly kill tumor cells by releasing perforin and granzymes or by death receptor engagement. Second, NK cells can secrete cytokines and chemokines to activate T cells and exert a killing effect [
13]. Studies have shown that valproic acid (VPA) upregulates the expression of human histocompatibility complex class I-related chain A (
MICA) and histocompatibility complex class I-related chain B (
MICB) by activating PI3K/Akt signaling [
14,
15]. The NK group 2D (NKG2D) receptor is an activated receptor for MICA on NK cells that recognizes MHC class I molecules and plays an important role in innate immunity. When MICA on the surface of tumor cells is activated, NK cells can recognize the MICA and initiate the antitumor immune response [
16,
17]. In vitro studies have shown that peripheral blood NK cells (PBNK) are able to kill HPV-infected cell lines [
18]. However, NK cells are often dysfunctional and low in number in cervical cancer patients and thereby unable to mount efficient cytotoxicity against tumors [
19].
Our previous study has shown that metformin disrupts the sponge effect of long non-coding RNA MALAT1/miR-142-3p to activate the expression of the downstream antitumor protein high-mobility group A protein 2 (HMGA2) and exert an anti-cervical cancer effect [
20]. We also found that a combination treatment with metformin and nelfinavir for 12 h significantly upregulated MICA protein expression in SiHa and HeLa cells [
21]. However, the molecular mechanism by which metformin upregulates MICA remains unclear. This study aimed to elucidate the molecular mechanisms by which metformin activates antitumor immunity.
Materials and methods
Cells, reagents, and antibodies
In this study, the human cervical cancer cell lines, SiHa cells and HeLa cells, and the NK-92 cells were from a research laboratory of Foshan Maternity and Child Health Care Hospital, Guangdong Province, China. The SiHa and HeLa cells were cultured in Dulbecco’s modified eagle medium (DMEM) containing 10% fetal bovine serum (Invitrogen, Carlsbad, CA, USA) and 1% streptomycin (Sigma-Aldrich, St. Louis, MO, USA). The NK-92 cells were cultured in alpha-minimum essential medium (ɑ-MEM) containing 100 U/mL interleukin (IL)-2. Dimethyl sulfoxide (DMSO), LY294002, and metformin hydrochloride were purchased from Sigma-Aldrich. Anti-MICA, anti-MICB, anti-ULBP-2/5/6 Phycoerythrin, anti-ULBP-1 Alexa Fluor 488, anti-ULBP-3 Allophycocyanin, anti-DDR-1, anti-HSF-1, anti-PI3K (110ɑ), anti-phospho-PI3Kp55 (Tyr199), anti-Akt, anti-phospho-Akt (ser473), anti- proliferating cell nuclear antigen (PCNA), anti-p53 primary antibodies, and their corresponding secondary antibodies were purchased from Cell Signaling Technology (Beverly, MA, USA).
Analysis of cell proliferation
According to the methods described in a previous study [
22], cells were trypsinized and seeded in 96-well plates (1 × 10
4 cells per well). After the cells were attached, metformin was added at various concentrations (0–400 μM) for 48 h. To analyze cell viability, the cell proliferation assay, cell counting kit-8 (CCK-8), was used to measure the absorbance of the samples using a microplate reader and at a wavelength of 450 nm.
Cell apoptosis assays
According to the methods described in a previous study [
8], Cervical cancer cell lines (HeLa and SiHa) were seeded at a density of 2 × 10
5 cells/well in a 6-well culture plate. The cells were washed twice with cold PBS, and then resuspended in 1× binding buffer. One hundred μl of the cell suspension (1 × 10
5 cells) was transferred to a 5 ml culture tube and mixed with 5 μl of FITC anti-Annexin V and 5 μl PI. The mixture was gently vortexed and incubated for 15 min at RT (25 °C) in the dark. Then, 400 μl of 1× binding buffer was added into each tube. The samples were analyzed by flow cytometry within 1 h. The green fluorescence of Annexin V-FITC was measured at 530 nm, and the red fluorescence of PI was measured at 585 nm. The results were analyzed with FlowJo software.
Cell cycle assays
Cells were harvested in PBS and fixed by addition of ice-cold 70% ethanol with a Pasteur pipette during vortexing, as previously described [
8]. Then, the cells were centrifuged at approximately 2000 rpm for 5 min and washed twice with PBS. Finally, the cell were stained by PI staining solution (Invitrogen) and analyzed by flow cytometry collecting 25,000 events per sample. The results were analyzed with FlowJo software.
According to the methods described in a previous study [
23], cells were washed three times with pre-cooled phosphate buffered saline (PBS) and subsequently scraped off with a cell scraper and collected in a 1.5 mL centrifuge tube. The cells were centrifuged at 1000 rcf, 4 °C, for 3 min. A protease inhibitor, cell lysis buffer, and cell membrane rupture solution were added into the pellet to lyse the cells on ice for 1 h, followed by 1000 rcf centrifugation at 4 °C for 20 min. The supernatant was discarded, and the pellet was then lysed with nuclear extraction lysis buffer on ice for 1 h, with vortexing every 5 h for complete lysis, which was followed by 12,000 rcf centrifugation at 4 °C for 15 min to collect the supernatant (i.e., nuclear protein extract).
Lactate dehydrogenase (LDH) cytotoxicity assay
As described in the methods of a previous study [
21,
23], the human cervical cancer HeLa or SiHa cells were seeded as target cells in 96-well plates (2 × 10
4 cells per well) in a total volume of 100 μL per well. The cells were then divided into five different groups as follows: drug treatment; effector cells (NK-92) with spontaneous LDH efflux; target cells with spontaneous LDH efflux; target cells with maximum LDH efflux; and volume correction (no cells) groups. Approximately 10 μL of lysis buffer (10×) was added to each well of cells and then incubated in a 37 °C incubator with 5% CO
2 atmosphere. After 250×
g centrifugation for 3 min, 50 μL of a reaction solution were added to each well of the 96-well plates, followed by 50 μL stopping solution, with gentle mixing, and then the absorbance at wavelengths of 490 nm and 680 nm were read. The cytotoxicity of different target ratios (%) was calculated using the following formula: Cytotoxicity (%) = (Experimental group − Effector cells with spontaneous LDH efflux group − Target cells with maximum LDH efflux group)/(Target cells with maximum LDH efflux group − Target cells with spontaneous LDH efflux group) × 100.
RNA extraction and quantitative real-time PCR
According to the methods described in a previous study [
20], After transfection for 48 h, total RNA was isolated from SiHa and HeLa using TRIzol reagent (TAKARA, Dalian, China) according to the manufacturer’s instructions. For mRNA quantification, RNA was reverse transcribed into cDNA using the PrimeScript™ RTreagent Kit (Takara, Japan) and then quantified on the CFX96 touch q-PCR system (BIO-RAD, USA) with SYBR Premix Ex Taq Kit (Takara, Japan) according to the manufacturer’s protocols. In this study, GAPDH was used as an internal control for determining the levels of HSP70 and MICA. The primers used for quantitative real-time polymerase chain reaction (qRT-PCR) are listed in Table
1. Reactions were performed using a SYBR Green kit (TAKARA, Dalian, China), according to the manufacturer’s instructions. Each 20-μl reaction mixture included 2 μl of cDNA, 10 μl of SYBR Green Mix, 0.4 μl of forward primer, 0.4 μl of reverse primer, 0.4 μl of RoxReference Dye, and 6.8 μl of RNase-free water. Then, the PCR reactions were performed in the CFX96 touch q-PCR system (BIO-RAD, USA) under the following conditions: 95 °C for 30 s, followed by 40 cycles at 95 °C for 5 s, 60 °C for 30 s, 95 °C for 15 s, and 60°Cfor 60 s. Relative gene expression was determined by using the ΔΔC
t method. Significance was defined according to
P values from the two-tailed t-test. All of the reactions were performed in triplicate.
Table 1
Oligonucleotide primer sequences for qRT-PCR
Western blotting
Western blotting was performed as previously described [
24]. Briefly, the cells were harvested and lysed with RIPA lysis buffer, and the concentration of the collected proteins was determined. Then, 100 μg of the extracted protein was separated in 10, 8%, or 5% SDS-PAGE gel based on the molecular weight of the target protein. The separated protein gel with a pre-stained protein marker was transferred onto a PVDF membrane. Subsequently, the membrane was blocked in a 5% skim milk solution at room temperature for 2 h, followed by incubating with the corresponding primary and secondary antibodies and washing with Tris-buffered saline, 0.1% Tween 20 (TBST) in between. The PVDF membrane was developed using an enhanced chemiluminescence solution (Pierce) and subsequently photographed in a Bio-Rad gel imaging system. The exposure time was adjusted according to the protein bands and background. After selecting the clear protein bands in the image, the gray value of each protein band was analyzed by software and statistical analysis was conducted.
Tumor Xenograft modeling and in vivo experiments
BALB/c nude mice of 4 weeks old (weighing approximately 15–17 g) were purchased from Guangdong Medical Laboratory Animal Center (Guangdong Province, China). All mice were housed and bred in a specific-pathogen-free (SPF) grade animal facility, with 22–25 °C temperature, 40–60% humidity, and 12 h/12 h light/dark cycle. To generate tumor xenograft, 20 mice were used. The skin of the left forelimb near the armpit was disinfected and 0.1 mL SiHa cells suspended in serum-free medium (containing approximately 5 × 106 cells) were injected. After inoculation of the cervical cancer cells, the nude mice were continuously housed under the same conditions. Once the subcutaneous nodules grown to a rice grain size (required approximately a week), the subcutaneous xenograft model of cervical cancer in nude mice was successfully constructed. The subcutaneous tumor size in each nude mouse was measured using a digital vernier caliper. Once the tumor diameter reached approximately 0.3–0.5 cm, the nude mice were numbered, randomly divided into four groups (with five mice per group), namely, control, model, 50 mg/kg/d metformin, and 250 mg/kg/d metformin groups. Metformin was given by gavage. All nude mice were closely monitored for tumor growth, skin condition, and behavior daily and any tumor ulceration or irritation was noted. The longest (A) and the shortest (B) diameters of the subcutaneous tumors were measured with a digital vernier caliper before each metformin administration to calculate the tumor volume (V) using the following formula: V = 0.5 × A × B2. In addition, all nude mice were weighed daily, and their daily food intake was also measured. After the completion of the 23-day metformin administration, all nude mice were sacrificed and placed on ice, their skin was immediately cut open, and the subcutaneous tumor xenografts were collected. After weighing each tumor xenograft on a digital scale, one part of the tumor tissue was dissected and frozen in liquid nitrogen for western blotting. All experimental procedures were approved by the Institutional Animal Care and Use Committee of South Medical University.
Statistical analysis
The SPSS16.0 software (IBM SPSS, Chicago, IL, USA) was used for data analysis in this study. An independent T test was used to compare the results between the two groups. Multivariate ANOVA was used to compare differences between multiple groups, followed by multiple corrections using the Bonferroni’s test. P < 0.05 was considered statistically significant.
Discussion
Classic drug design strategies generally target a single protein or signaling pathway. However, the pathogenesis of most diseases, including cancers, is complex. Thus, it is necessary to develop drugs that target multiple proteins and disease-related signaling pathways. Metformin, a biguanide blood sugar-reducing agent, has been extensively used in clinical practice because of its safety and efficacy profile, as well as being inexpensive. Studies have shown that metformin can target one or more signaling pathways to inhibit tumor cell proliferation, invasion, and migration [
42]. For example, metformin directly activates the AMPK pathway and reduces insulin-like growth factor 1 (IGF-1) expression to inhibit insulin signaling, block the glucose metabolism pathway of tumor, and exert antitumor effect [
43,
44]). A recent study identified AMPK O-GlcNAcylation as anti-proliferative mechanism of metformin in cervical cancer [
45]. Since HeLa cells do not express LKB1 (which phosphorylates AMPK) [
46], it is shown in some studies that this cell line might be resistant to metformin [
47]. However, metformin exhibits a complex anti-tumor mechanism for its small molecular weight (MW: 165.6 )[
48,
49]). In this study, we found that metformin inhibits cervical cancer cell proliferation in a dose-dependent manner through non-AMPK signaling pathways.
P53 is a tumor suppressor. More than 50% of all malignant tumors have
p53 mutation. The protein encoded by
p53 gene is a transcriptional factor called TP53 that controls the initiation of cell cycle. P53 protein is mainly distributed in the nucleoplasm of cells and specifically binds to DNA. Its activity is regulated by post-translational modification, such as phosphorylation, acetylation, methylation, and ubiquitination [
26,
50]. Normal p53 acts as the “guardian of the genome,” screening for sites of DNA damage in the G1 phase and monitoring the integrity of the genome. In the event of DNA damage, p53 prevents DNA replication to provide sufficient time for the repair of the damaged DNA. It triggers apoptosis if the repair of the damaged DNA fails. During the cell cycle, p53 mainly functions in the monitoring of the G1 and G2/M phase check points, and this function is closely related to transcriptional activation. Discoidin domain receptor 1 (DDR1) can activate p53 by binding its receptor. In our present study, we showed the evidence that metformin upregulated DDR-1 expression inhibiting the proliferation of cervical cancer cells, promoting cervical cancer apoptosis and suppress cervical cancer xenograft tumor tissues growth in a dose-dependent manner along with activating p53.
MICA is a member of the MHC class I molecular family and is expressed on the cell surface membranes. Recent research has shown that MICA is associated with the development of a variety of tumors. It is a stress marker and is expressed in pathogenic bacteria, tumors, and organ transplant recipients [
30]. MICA is the receptor of NKG2D, an important activating protein on the NK cell surface, and NK cells play a very important role in tumor innate immunity to kill tumor cells by recognizing tumor cell surface markers and producing a cytotoxic effect [
51]. Previous studies have shown that high glucose protects pancreatic cancer from NK cell-mediated killing through suppressing MICA/B expression. Moreover, high glucose inhibited AMP-activated protein kinase signaling, leading to high expression of Bmi1, a polycomb group (PcG) protein which was found to be up-regulated by high glucose, and mediated the inhibition of MICA/B expression through promoting GATA2 in pancreatic cancer [
52]. AMP-activated protein kinase (AMPK)–histone deacetylase 5 (HDAC5) pathway promoted nuclear accumulation of HIF-1a and functional activation of HIF-1 by deacetylating heat shock protein 70(HSP70) in the cytosol, indicating a novel link between AMPK, HIF-1a, and HSP70 [
53]. HSP70 is not immunogenic but can participate in antigen processing after binding to polypeptides and enhance the immune response. A clinical trial injected purified HSP70 into children with brain cancer and found an antitumor effect and certain feasibility and safety in the antitumor therapy [
54,
55]. Another study has also shown that HSP70 inhibits brain tumor development in a C6 glioblastoma mouse model, which is associated with NK cell and T lymphocyte killing abilities of glioblastoma, as well as increased activities of NK cells and CD81
+ T lymphocytes [
55]. In the present study, we found that metformin increased HSF-1, MICA and HSP70 protein expression in SiHa and HeLa cells and also induced MICA expression on the surface of human cervical cancer cells. However, metformin did not induce MICB, ULBP1, ULBP2/5/6 and ULPB3 expression on the surface of human cervical cancer cells. In addition, the mRNA expression of
HSP70 gene and
MICA gene increased in SiHa and HeLa cells when treated with metformin. We concluded that metformin activated NK cells by regulating MICA though a transcription mechanism to mediate innate immunity. As an immunopotentiator, merformin could upregulate HSF-1, one of the best known activators of HSP70 expression, to activate HSP70 and is involved in specific immune activation in the nude mice and exerted antitumor effect.
In the classic PI3K/Akt/mTOR pathway, PI3K is a family of many lipid kinases consisting of a regulatory subunit, p85, and a catalytic subunit, p110. When a ligand binds to the membrane receptor, the receptor activates p53 and recruits p110, thereby catalyzing the formation of phosphatidylinositol 3-phosphate (PI3P) by phosphatidylinositol 4, 5-bisphosphate (PIP2) on the inner surface of the membrane. PI3P, as a second messenger, further activates Akt and phosphoinositide-dependent kinase 1 (PDK1). Akt, also known as protein kinase B (PKB), is an important downstream molecule of PI3K. Akt immediately attained its activated state by phosphorylation (p-Akt) and activated Akt and mTOR are indicators of poor prognosis in cervical cancer patients. They play an important role in regulating cell growth, proliferation, survival, and glucose metabolism [
56,
57]. A previous study has shown that PI3K is highly expressed in a variety of tumors, including cervical cancer [
56]. When PI3K is inhibited, the corresponding expression of downstream Akt and mTOR is reduced, and the cell signaling pathway is blocked. Therefore, cell proliferation is inhibited. Although Akt is the core molecule of this signaling pathway, only few small-molecule inhibitors directly inhibit Akt by suppressing its phosphorylation. In the present study, we did not block mAbs for NKG2D and /or MICA to demonstrate the specific activity on the NKG2D receptor. However, we used LY294002, a specific PI3K inhibitor, to block the PI3K/Akt pathway. The results showed that combining metformin with LY294002 showed synergistic effect on upregulating MICA in cervical cancer cells. In general, combining two active molecules having the same target in a signal pathway may result in antagonistic effect, while combination of two active molecules having different targets may lead to synergistic effect [
58]. That is to say, metformin directly reduced p-PI3K p85 (Tyr199) and p-Akt (ser473) levels in cervical cancer cells, which probably resulted in the antitumor effect. According with our previous study [
59], metformin did not target PI3Ks or Akt.
According to the clinical application guidelines for metformin [
60], the daily dose of metformin should not exceed 2000 mg/d. Based on the Meeh-Rubner conversion formula and mouse and human bodyweights and specific surface areas as well as previous studies on tumor growth inhibition by metformin, we find the appropriate doses of metformin intraperitoneal injection to be 50–250 mg/kg/d. We selected low and high doses of metformin, 50 mg/k/d and 250 mg/kg/d, respectively, which were equivalent to 384.5 mg/d and 1922.5 mg/d in human, with the high dose nearly matching the highest dose of metformin in clinical practice. This study showed that metformin significantly reduced the tumor xenograft size in the treatment groups, compared with the model group, suggesting that metformin inhibited PI3K/Akt signaling, upregulated p53 signaling, activated MICA protein expression in the tumor cells and inhibited the growth of cervical cancer xenografts in the BALB/c nude mouse model.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.