Background
Lung cancer is highly aggressive and is the leading cause of cancer-related mortality worldwide. Non-small cell lung cancer, which comprises 80–85% of all lung cancer cases, is also one of the most common malignancies overall, with adenocarcinoma as the main histological type [
1]. Since the discovery of epidermal growth factor receptor (EGFR) activating mutations in non-small cell lung cancer, and the subsequent success of EGFR tyrosine kinase inhibitors, treatment of advanced cases has shifted from chemotherapy to molecular-targeted therapy, especially in Asians, females, never smokers, and/or patients with adenocarcinoma, of whom about 40–50% harbor a mutation in the tyrosine kinase domain in EGFR [
2]. Indeed, EGFR tyrosine kinase inhibitors, which suppress cancer cell proliferation and induce apoptosis, cell cycle arrest, and senescence, are now standard therapy for advanced cases with activating EGFR mutations. Nevertheless, progression-free survival is less than 1 year for patients treated with these inhibitors [
3,
4], and mechanisms of resistance remain obscure despite extensive research.
Annexin A5 (ANXA5), which contains a very short unphosphorylated N-terminus in comparison to other annexins, regulates cell proliferation, signal transduction, and coagulation [
5‐
7]. In particular, ANXA5 binds to cell membranes rich in phosphatidylserine or in response to a Ca
2+ burst, and promotes membrane resealing by forming two-dimensional arrays at the site of membrane damage [
8,
9]. Strikingly, ANXA5 is overexpressed in many cancers, including renal cell cancer, hepatocellular carcinoma, colorectal cancer, and breast cancer [
10‐
13]. Intriguingly, Lu et al. found that the natural product berberine may target ANXA5 in ovarian cancer, and, conversely, ANXA5 may block the antitumor activity of berberine [
14]. However, the role of ANXA5 in non-small cell lung cancer, and especially in resistance to EGFR tyrosine kinase inhibitors, is poorly understood.
We now report that ANXA5 is upregulated in gefitinib-resistant cell lines, as well as in clinical specimens resistant to EGFR tyrosine kinase inhibitors. In particular, ANXA5 promotes gefitinib resistance by inhibiting apoptosis and cell cycle arrest. Indeed, knockdown of ANXA5 from gefitinib-resistant cells restores sensitivity to the drug. Taken together, the data highlight ANXA5 as a mediator of resistance to EGFR tyrosine kinase inhibitors.
Methods
Cell culture
PC9 and H4006 human lung adenocarcinoma cells were purchased from American Type Culture Collection (Manassas, VA, USA), and cultured as monolayers at 37 °C in a humidified atmosphere of 5% CO2, and in Roswell Park Memorial Institute 1640 medium (RPMI-1640, Thermo Fisher Scientific, Waltham, MA, USA) supplemented with 10% heat-inactivated fetal bovine serum and 100 U/mL penicillin/streptomycin. Cells were exposed to escalating doses of gefitinib (Selleckchem, Houston, TX, USA) to induce resistance, and then routinely cultured in 1 μM gefitinib to maintain resistance.
Lentivirus construction and infection
Short hairpin RNA (shRNA) against ANXA5 was obtained from RNAi Consortium (Broad Institute, Cambridge, MA, USA). Lentiviral plasmids (GV112) expressing shANXA5 or negative control shRNA were obtained from GeneChem (Shanghai, China). Lentiviral vector (GV358) overexpressing human EGFR (EGFR-over) (GenBank: NM_005228) was purchased from GeneChem. PC9R and H4006 cells grown to 50–70% confluence in 6-well plates were then infected at multiplicity of infection 10 with lentiviral particles produced in HEK 293 T cells and suspended in 4 μg/mL polybrene. After 24 h, cells were exposed to an escalating dose of gefitinib.
Cell proliferation
Cells were seeded in 96-well plates at approximately 1000 cells/well in 200 μL culture medium. After 24 h, cells were stained for 1 h at 37 °C with 10 μL CCK8 reagent (Dojindo Laboratories, Kumamoto, Japan), and assayed at 450 nm on a Multiskan microplate reader (Thermo Fisher Scientific).
EdU incorporation
PC9R and H4006R cells were incubated with 10 μM EdU (Thermo Fisher Scientific) for 4 h, fixed for 15 min at 20–25 °C with 3.7% formaldehyde in phosphate-buffered saline (PBS), processed according to the manufacturer’s instructions, counterstained with Hoechst 33,342, and imaged on an A1R confocal laser scanning microscope (Nikon, Tokyo, Japan). The total number of cells, as well as the number of EdU-stained cells, was determined in ImageJ v. 1.42 (National Institutes of Health, Bethesda, MD, USA).
Detection of apoptotic cells by flow cytometry
Infected PC9R cells were seeded in 6-well plates at 5 × 105 cells/well, treated with 1 μM gefitinib, digested with trypsin-EDTA (Thermo Fisher Scientific), washed three times with PBS, resuspended in 500 μL binding buffer, stained for 15 min at room temperature in the dark with 5 μL FITC-conjugated annexin V and 3 μL propidium iodide (Thermo Fisher Scientific), and sorted on a FACS Aria II flow cytometer (BD Biosciences, Franklin Lakes, NJ, USA).
Cell cycle analysis
Infected PC9R cells were seeded in 6-well plates at 5 × 105 cells/well, treated with 1 μM gefitinib, harvested, washed with PBS, fixed for 24 h at 4 °C in 70% ethanol, stained with propidium iodide for 30 min at room temperature in the dark, and analyzed by flow cytometry.
Measurement of mitochondrial membrane potential
Mitochondrial membrane potential was measured using MitoProbe, which is based on tetraethylbenzimidazolylcarbocyanine iodide (JC-1) (Thermo Fisher Scientific), a compound that forms aggregates emitting red fluorescence at 590 nm in intact mitochondria, but is a monomer emitting green fluorescence at 490 nm in depolarized mitochondria. Thus, an increase in green fluorescence, as measured by flow cytometry, is indicative of mitochondrial damage.
qPCR
Total RNA was extracted using TRIzol (Thermo Fisher Scientific), and reverse transcribed into cDNA using a reverse transcriptase (Toyobo, Osaka, Japan). Subsequently, 20 ng cDNA was used as qPCR template to quantify ANXA5 with 5’-ACCCTCTCGGCTTTATGATG-3′ and 5’-GATGGCTCTCAGTTCTTCAGG-3′, BIRC5 with 5’-AGAGTCCCTGGCTCCTCTA-3′ and 5’-CCCGTTTCCCCAATGACTTA-3′, PLK1 with 5’-GACAAGTACGGCCTTGGGTA-3′ and 5’-GTGCCGTCACGCTCTATGTA-3′, TOP2α with 5’-AGCAGATTAGCTTCGTCAACAGC-3′ and 5’-ACATGTCTGCCGCCCTTAGA-3′, CDK1 with 5’-TAGCGCGGATCTACCATACC-3′ and 5’-CATGGCTACCACTTGACCTG-3′, EGFR with 5′- TGTCCCCACGGTACTTACTCC-3′ and 5’-CCAAATGCTGATGAATCCAATG-3′, and β-actin with 5’-CTGGCACCCAGCACAATG-3′ and 5’-CCGATCCACACGGAGTACTTG-3′. Targets were amplified over 40 cycles at 95 °C for 15 s, 60 °C for 15 s, and 72 °C for 45 s. Gene expression was normalized to β-actin according to the cycle threshold (2−ΔΔCT) method.
Western blotting
Total protein was extracted in radioimmunoprecipitation buffer (Beyotime Institute of Biotechnology, Shanghai, China), separated on polyacrylamide gels, transferred to polyvinylidene difluoride, and probed overnight at 4 °C with antibodies against ANXA5 (Abcam, Cambridge, UK), EGFR, PLK1, cyclin-dependent kinase (CDK)1, topoisomerase 2α (TOP2α), and baculoviral inhibitor of apoptosis repeat-containing 5 (BIRC5, also called survivin), cleaved caspase-3 (Asp175), cleaved PARP (Asp214), and actin (Cell Signaling Technology, Danvers, MA, USA). Membranes were then labeled at room temperature for 1 h with goat anti-rabbit or anti-mouse immunoglobulin G conjugated to horseradish peroxidase, visualized by enhanced chemiluminescence (Pierce, Rockford, IL, USA), and analyzed in Quantity One v.4.6 (Bio-Rad, Hercules, CA, USA).
cDNA array screening
Total RNA was extracted using RNeasy Plus Mini Kit (Qiagen, Valencia, CA, USA) from PC9R cells expressing shANXA5 or negative control shRNA, reverse transcribed, and amplified using OneArray Plus RNA Amplification Kit (Phalanx Biotech Group, Taiwan). Cy5-labeled amplicons were hybridized to Human Whole Genome OneArray (Phalanx Biotech Group), imaged on a G2505C Agilent Microarray Scanner (Agilent Technologies, Santa Clara, CA, USA), and analyzed in Resolver (Rosetta Biosoftware, Seattle, WA, USA).
Tumorigenicity
Animal experiments were approved by the Institutional Animal Care and Use Committee at Zhongshan Hospital of Fudan University, China. Male BALB/c nude mice 4–6 weeks old were obtained from Shanghai Experimental Animal Center, Chinese Academy of Sciences (Shanghai, China), and were subcutaneously injected in the right flank with PC9R cells. Tumor volume was calculated as volume = (length × width2)/2. After 1 month, tumors were dissected, weighed, sectioned in paraffin, and analyzed by immunohistochemistry for Ki67 to detect proliferating cells. Ki67-stained cells in randomly selected fields from each tissue section were quantified in ImageJ.
Pleural effusion sample collection
A total of 27 lung adenocarcinoma patients, including 18 who were sensitive to and nine who had acquired resistance to EGFR TKIs, were enrolled in the study at the Department of Pulmonary Medicine, Zhongshan Hospital, Fudan University. All study participants provided informed consent and the study protocol was approved by the institutional ethics committee (approval number B2016-154R). All patient managements and pleural effusion sample collection were carried out in accordance with the relevant guidelines. Pleural effusions were collected and centrifuged at 1000×g for 10 min. Cell pellets were washed twice with PBS and total RNA was extracted from cells using TRIzol reagent (Invitrogen). ANXA5 mRNA level was quantitated by qPCR.
Statistical analysis
Data are reported as mean ± standard deviation (SD) of at least three independent experiments with three replicates. Differences among multiple groups were evaluated by one-way analysis of variance followed by Bonferroni’s multiple comparisons test, while Student’s t test was used to compare two groups. Differences were considered statistically significant at P < 0.05.
Discussion
First-generation EGFR tyrosine kinase inhibitors, including gefitinib and erlotinib, are the first-line treatment against advanced non-small cell lung cancers with EGFR activating mutations, especially in Asians, females, never smokers, and/or patients with adenocarcinoma [
16]. However, resistance to such inhibitors is a serious issue, with approximately 20–30% of patients unresponsive to treatment. Even among patients who show initial improvement, progressive disease eventually develops about 1 year after treatment [
17]. Therefore, understanding the mechanisms of resistance is essential to improve efficacy. A few such mechanisms have been identified, including a secondary T790 M mutation in exon 20 of EGFR, amplification of the
MET proto-oncogene, and overexpression of hepatocyte growth factor [
18‐
20]. Nevertheless, approximately 25% of resistant cases are not due to these mechanisms. We now report that ANXA5 is significantly upregulated in gefitinib-resistant cells, and that it promotes gefitinib resistance by inhibiting apoptosis and G2/M arrest via polo-like kinase 1.
EGFR activation promotes cancer cell division, survival, metastasis, and cellular repair. The major downstream signaling route includes Ras/Raf/mitogen-activated protein kinase, Janus kinase/signal transducer and activator of transcription, and phosphoinositide 3-kinase/AKT/mammalian target of rapamycin. EGFR tyrosine kinase inhibitors efficiently block these cascades and induce cell cycle arrest and cell apoptosis [
21,
22]. Thus, escape from cell cycle arrest and apoptosis is an important feature of resistance to EGFR tyrosine kinase inhibitors.
ANXA5 is an important cell membrane protein that reseals damaged membranes by forming two-dimensional arrays at high Ca
2+ concentrations [
9]. As EGFR tyrosine kinase inhibitors may damage membranes via release of apoptotic proteins and induction of immunity [
23], ANXA5 may confer resistance through membrane repair. Accordingly, gefitinib causes mitochondrial degradation in cells that were already resistant to EGFR tyrosine kinase inhibitors but were then depleted of ANXA5. ANXA5 knockdown also significantly enhanced apoptosis, consistent with the model that failure of membrane repair eventually causes apoptosis [
24]. Moreover, we found that ANXA5 knockdown represses G2/M proteins, and thereby induces cell cycle arrest. For example, PLK 1, which promotes transition from G2 to mitosis by phosphorylating cell division control protein 25 and Wee1 kinase, was downregulated along with cyclin-dependent kinase 1, which is activated further downstream [
25]. Loss of cyclin-dependent kinase 1 also downregulated its substrates BRIC5 and TOP 2α [
26,
27], of which the former regulates microtubule dynamics at G2/M. Ultimately, loss of BRIC5 induces G2 arrest, activates caspase-3, and elicits apoptosis, as we observed [
28,
29]. On the other hand, TOP 2α is abundantly expressed at G2/M to promote chromosome replication, and its loss potently triggers G2/M arrest [
30,
31]. Collectively, our data show that ANXA5 knockdown induces G2/M arrest and apoptosis by suppressing polo-like kinase 1 signal pathwayin cells resistant to EGFR tyrosine kinase inhibitors.