Role of heat shock protein 27 in gemcitabine-resistant human pancreatic cancer: Comparative proteomic analyses
- Authors:
- Published online on: July 31, 2012 https://doi.org/10.3892/mmr.2012.1013
- Pages: 767-773
Abstract
Introduction
Pancreatic cancer is the fourth most common cause of cancer-related mortality worldwide (1). The overall prognosis for patients with pancreatic cancer remains poor; less than 5% of patients with adenocarcinoma of the pancreas survive for more than 5 years following diagnosis (2). Surgical resection is currently the only potentially curative treatment for pancreatic cancer. However, 80–85% patients have advanced unresectable disease at diagnosis (2). Chemotherapy is a very important therapeutic strategy for unresectable cancer patients. Gemcitabine (GEM) and 5-fluorouracil (5-FU) are the common chemotherapy drugs used to treat advanced pancreatic cancer. Gemcitabine (2′-deoxy-2′-difluorodeoxycytidine: Gemzar; GEM) is a deoxycytidine analogue with structural and metabolic similarities to cytarabine. Currently, this nucleoside analogue appears to be the only clinically effective drug for pancreatic cancer, and has shown improvement in overall survival and quality of life (3–6). However, many clinical trials have shown that GEM alone or GEM in combination with other drugs is not likely to achieve marked success and the acquisition of resistance during chemotherapy may further limit the therapeutic success (7,8). Even if a potentially curative surgical resection can be performed, the five-year overall survival is low at 10–25%, mostly due to an almost complete chemoresistance which may be inherent and/or acquired (9,10). Many studies have been directed towards understanding the mechanism of chemotherapy response and resistance, with the ultimate goal of identifying molecular markers that allow the prediction of chemotherapy response. For pancreatic adenocarcinoma, the process of finding new chemotherapeutics has been exceedingly slow and disappointing. To date, there has been no significant breakthrough in the treatment of pancreatic cancer. Therefore, identifying novel molecular markers related to GEM resistance would be helpful to further understand the exact mechanisms of chemoresistance and produce more effective chemotherapy strategies for patients with pancreatic cancer in the future.
Due to intrinsic chemoresistance, chemotherapeutic drugs usually fail to kill all tumor cells at clinically tolerated doses. The presence of surviving cells above a certain threshold following primary therapy increases the relapse occurrence, which may then generate acquired and more complex resistance phenotypes as a result of sequential genetic changes over long periods of time (11,12). These surviving cells may either be pre-existent or may be generated as a direct result of the chemotherapy itself. Recently, we introduced a new model for the study of de novo drug resistance of pancreatic cancer, which involves the utilization of surviving cancer cells following primary drug treatment. The surviving cells are potentially drug-resistant and exhibit similar growth and tumorigenic potentials to their untreated parental cells (13). In this study, we investigated the differential expression of proteins in these stably surviving cells and cells with or without GEM treatment to screen candidate molecules related to intrinsic chemoresistance. In addition, we studied whether these proteins may be used clinically as biomarkers of gemcitabine sensitivity in tumor specimens.
Materials and methods
Cell lines and materials
The pancreatic cancer cell line Capan-1 (ATCC, Manassas, VA, USA) was used in this study. Capan-1 was cultured in IMDM (Gibco, Carlsbad, CA, USA) containing 20% fetal calf serum (Gibco), 100 U/ml penicillin and 100 U/ml streptomycin. The cells were cultured at 37°C, in 5% CO2 and 95% relative humidity. The drug used in this study was GEM (Lilly, France).
Sample preparation and protein extraction
Capan-1 cells were exposed to GEM at a concentration of 2,000 μg/ml (to obtain a cell survival rate of <15%) for 72 h. The cells were then washed twice with phosphate-buffered saline (PBS) solution, and cultured in drug-free media for another 7 days. The surviving cells were then washed twice with PBS, trypsinized and counted. Non-viable cells were excluded using Trypan blue staining. Control cells were counted when the drug treatment was completed. The viable cell rate was calculated as the number of surviving cells divided by the number of control cells ×100%. A ReadyPrep™ Protein Extraction kit (total protein) (Bio-Rad, Hercules, CA, USA) was used for control and surviving cells according to the manufacturer's instructions. The cells were washed 3 times with PBS, centrifuged at 800 rpm for 5 min, the supernatant was discarded, and the cells were lysed to produce protein lysates. The mixture was then sonicated for 30 sec, 3 times (pulse duration of 30 sec on and 15 sec off) in an ice bath sonicator. Finally, the sample was centrifuged at 12,000 rpm at 20°C for 30 min, and the supernatant was collected. The protein cleanup was performed according to the manufacturer's instructions using the ReadyPrep™ 2-D Cleanup kit (Bio-Rad) and the dry proteins were diluted with rehydration buffer (8 M urea, 4% CHAPS). The concentration of the prepared protein samples was determined by the Shanghai Generay Biotech Co., Ltd. (China) BCA protein assay according to the manufacturer's instructions. The samples were stored at −80°C until further analysis.
Two-dimensional gel electrophoresis (2-DE) and silver staining
Firstly, 250 μg protein was diluted with rehydration buffer [8 M urea, 4% CHAPS, 65 mM DTT, 0.2% (w/v) Bio-Lyte (Bio-Lyte 3/10 ampholyte, 40%, Bio-Rad) and 0.001% bromophenol blue] to 350 μl for isoelectric focusing (IEF). IEF was applied on IPG strips (ReadyStrip IPG Strips, pH 3–10, 17 cm, Bio-Rad) with a Protean IEF system (Bio-Rad) according to the following protocol: active hydration (50 V for 14 h), higher voltage liner (250 V for 30 min), rapid cleanup (1,000 V for 1 h), boost voltage (liner, 10,000 V for 5 h) and isoelectric focus (rapidly, 10,000 V for a total 60,000 kVh). Strips were then equilibrated at room temperature for 15 min in 10 ml equilibration solution [6 M urea, 0.375 M pH 8.8 Tris-HCl, 20% glycerol, 2% sodium dodecyl sulfate (SDS), 2% DTT] and incubated for another 15 min in an equilibration solution that was the same as previously used, with the exception of replacement of DTT with 2.5% iodoacetamide. The two-dimensional electrophoresis was performed on 12% SDS gels with a Protean II xi system (Bio-Rad). The SDS-PAGE gels were run at 5 mA/gel (until the proteins had run out of the strips) and then at 25 mA/gel until the bromophenol blue dye front reached the bottom of the gels. Three 2-D gels per sample were run to guarantee reproducibility. Following 2-DE, proteins were visualized by silver-staining according to the manufacturer's instructions (Bio-Rad): Fixing (acetic acid 100 ml, ethanol 400 ml and pure water up to 1,000 ml) for 120 min; incubation (150 ml ethanol, 34 g Na-acetate, 1 g Na2S2O3·5H2O and pure water to 500 ml) for 30 min; washing (pure water) 3×5 min; silvering (AgNO3 0.8 g, add pure water to 500 ml) for 20 min; washing (pure water) 2×1 min; development (12.5 g Na2CO3, 200 μl formaldehyde and pure water to 500 ml) 8–10 min; stopping (200 ml acetic acid and pure water to 500 ml); washing (pure water) 3×5 min; and preserving (4°C, packaged by preservative film).
Visualization and image analysis
The silver-stained gels were scanned using a GS-800™ calibrated densitometer (Bio-Rad) with 300 dpi and analyzed using PDQuest software (version 7.0, Bio-Rad). Protein spots were detected automatically, and manual spot editing or deleting was performed when required. Only those protein spots for which the greatest alterations were >1.5-fold between control cells and the surviving cells after GEM treatment were selected for further characterization using mass spectrometry. The protein spots that were selected were sent to Shanghai Unlimit Biotechnology Co., Ltd. (China) for mass spectrometric analysis.
In-gel digestion
Briefly, spots of interest were excised from the 2-DE gels and were placed in deionized water to soak. After washing with deionized water, the spots of interest were centrifuged, supernatant was absorbed, calcium ammonium nitrate (CAN) was used to condense the gel, and samples were vacuum dried. Then, 45 mM DTT/25 mM NH4HCO3 was added and the mixture was left to react for 1 h at 56°C. Subsequently, the mixture was cooled to room temperature, centrifuged, the supernatant was discarded and the sample was reacted in the dark for 45 min with 100 mM iodoacetoamide/25 mM NH4HCO3. The mixture was then centrifuged, the supernatant was discarded, 25 mM NH4HCO3 was added, then the sample was vibrated for 3–5 min, then centrifuged, the supernatant was discarded, acetonitrile (ACN) was added to condense the gel, the sample was vibrated and vacuum dried. The proteins in-gel were then digested with a tryptic enzyme, firstly at 4°C for 30 min, secondly at 37°C for 12–16 h, and lastly were sonicated for 10 min with 50% ACN/5% formic acid. The sample was then centrifuged, the supernatant was collected in another eppendorf pipe and 50% ACN/5% formic acid was added to the pre-pipe. The sample was sonicated, centrifuged, the supernatant of the pre-pipe was collected and the supernatants were mixed. The supernatants were condensed to 10 μl in a speed-vacuum drier for mass spectrometric analysis.
Liquid chromatography-mass spectrometry detection and analysis
The tryptic peptides were added to an opposite enriching column [(C18, 5 μm, 300 Å, 300-μm inner diameter ×5 mm; Dionex/LC Packings), velocity (10 μl/min), mobile phase (3% ACN, 0.1% FA)]. The enriching column was in series with another opposite analytical column (Dionex/LC Packings, C18, 75-μm inner diameter, 150 mm length). The peptides were eluted using a QStar-XL mass spectrograph (MDS Sciex/Applied Biosystems) with NanoESI ion source at a velocity of 250 μl/min. The liquid phase system of Nano UPLC (Waters) provided gradient elution: mobile phase A, 0.1% formic acid/H2O; and mobile phase B, 0.1% formic acid/acetonitrile. The gradient was 5–50% B (60 min), 50–90% B (30 min) and 90% B (15 min).
The parameter settings of the ion source were voltage 3,000 V, assisting nitrogen 0.2 L/h and temperature 100°C. Chromatography-cascade spectrum acquisition was performed in data dependent acquisition (DDA) mode. There were 8 highest-ionic strength at first level of the spectrum and the 2–4 electrically charged peptides had been selected for cracking. The scanning area of first level of the spectrum was 450–1,800 m/z and the scanning area of the chromatography-cascade spectrum was 50–1,800 m/z.
The chromatography-cascade spectrum searched human protein databases (ftp://ftp.ebi.ac.uk/pub/databases/IPI/Current, version ipi.HUMAN.v3.57.fasta), and the software used for research was Mascot (http://www.matrixscience.com). The quality tolerance of the chromatography-cascade spectrum was 0.3 Da, the maximal enzyme digestion omissive spot was 2, and potential modifiers were carbamoylmethylation of cysteine, oxidize of methionine and phosphatase of serine and tyrosine.
Western blot analysis
Equivalent amounts of total protein (80 μg) and the nuclear and cytoplasm proteins (40 μg respectively, according to the protocol of the extraction of nuclear and cytoplasm protein kit, KeyGen Biotech, China) were loaded in each lane and were fractioned by electrophoresis on 12% (w/v) SDS-PAGE gels (Mini-Protean3, Bio-Rad), then transferred onto a PVDF membrane using Mini Trans-Blot (Bio-Rad) and blocked with TBST containing 5% BSA at 4°C overnight. The PVDF membrane was probed with a 1:2,000 dilution of rabbit anti-heat shock protein B1 (HSP27) polyclonal antibody (ab5579, Abcam, Cambridge, UK). Horseradish peroxidase-conjugated goat anti-rabbit IgG at a dilution of 1:5,000 was used as a secondary antibody. The protein bands were visualized using the ECL system. The same membrane was reblotted with mouse affinity purified anti-GAPDH antibody (Shanghai Kangcheng Biotech Co. Ltd., China) for total protein and cytoplasm protein, and anti-lamin B1 antibody (KeyGen Biotech) for nuclear protein, at a dilution of 1:2,000, to confirm equal loading.
Patients and specimens
The pancreatic ductal adenocarcinoma (PDAC) specimens were collected with informed consent from 47 patients undergoing radical resection of primary PDAC in Changhai Hospital, Second Military Medical University during 2003–2007. The patients were selected based on a distinctive pathological diagnosis of PDAC according to the World Health Organization classification of tumors of the digestive system (2010). All the experimental procedures were approved by the Research Ethics Committee of the Second Military University. The medical records of the patients were retrospectively reviewed, and the demographic, clinicopathological and treatment data were also collected. The tumor location and size were obtained from the surgical report. Patients receiving preoperative chemotherapy or radiotherapy were excluded from the study.
Immunohistochemistry analysis
Tissue microarrays were constructed using the 47 paraffin-embedded tumor tissue specimens by a precision arraying instrument (Beecher Instruments, Silver Spring, MD, USA). In each case, three tumor cores and two surrounding non-tumor tissues were selected. The sections from the tissue microarray blocks were deparaffinized, rehydrated and then heated in 0.01 mol/l sodium citrate buffer (pH 6.0) for 8 min at 95°C. Following incubation with 0.3% hydrogen peroxide in methanol for 15 min at room temperature and treatment with normal goat serum (Invitrogen, Carlsbad, CA, USA), the sections were incubated overnight at 4°C with rabbit anti-HSP27 polyclonal antibody (ab5579, Abcam) at a dilution of 1:250 (Zymed Labroatories, Invitrogen). Slides were rinsed for 10 min in PBS wash solution and incubated for 30 min with the HRP-labeled polymer conjugated secondary antibody (EnVision+; DakoCytomation, Carpintera, CA, USA) was applied according to the manufacturer's instructions. A known positive endometrial cancer tissue biopsy sample was used as the positive control. PBS and non-immune serum were used instead of the primary antibody for the blank control and negative control samples, respectively.
HSP27 protein was stained brown in the cytoplasm of cancer cells. The evaluation of HSP27 staining was carried out by two independent observers, and the staining area and intensity were scored separately. Specifically, a score of 0 was assigned to a staining area with ≤10% of the tumor cells, 1 for an area with 11–25% of the tumor cells, 2 for 26–50% tumor cells, and 3 for >51% tumor cells. For the staining intensity, a score of 0 was assigned for absent/weak staining (negative control), 1 for weak staining markedly stronger than the negative control level, 2 for moderately intense staining, and 3 for intense staining. The final grade of the section was derived from the sum of the staining area and intensity scores. A final score ≥3 was recognized to indicate positive expression. Equivocal stains were considered negative.
Results
Sensitivity of Capan-1 to GEM
As in our previous study, it was necessary to identify doses of GEM (2,000 μg/ml) in vitro that had fewer than 15% viable cells after treatment, and the cell viability rate was 6.03±3.26%. After 7 days of culturing cells in drug-free medium, there was no significant cell mortality. The cells had similar morphology and comparable growth and tumorigenic potential to their untreated parental cells. Repeated subculture affected the cell-cycle profile and growth characteristics of the surviving cells (13). Surviving cells were harvested for protein extraction, at which time the cells were viable, stable, and in some cases, exhibited growth.
Differentially expressed proteins downregulated in the Capan-1 cell line and in stable surviving cells following primary GEM treatment by proteomic analysis
Protein expression was assessed using three samples each of Capan-1 cells cultured under the same conditions. More than 1,000 protein spots were visualized on the 2-DE gels. We adopted a 2-DE analysis to quantitatively compare the protein profiles of the Capan-1 cell line and its stable surviving cells following primary GEM treatment. The differently expressed proteins with more than 1.5-fold changes between the two groups were selected to perform protein identification by liquid chromatography-mass spectrometry analysis. A total of 9 downregulated proteins were successfully identified (Fig. 1). Information on the 9 proteins identified is shown in Table I. Based on their functions, these proteins are mainly involved in signal transduction (guaniune nucleotide-binding protein subunit β-2-like 1 and annexin A1), transport (galectin-3 and hydroxysteroid 17β dehydrogenase-10), metabolism (proline synthetase co-transcribed bacterial homolog protein, proteasome subunit α type-2 and lysophospholipase 1) and as chaperones (heat shock protein B1). There was also one protein with an unknown protein. In this study, we selected HSP27 for further study of intrinsic chemoresistance in pancreatic cancer.
![]() | Table IDifferential expression of proteins between the surviving cells of Capan-1 after primary GEM treatment compared with Capan-1 cells without GEM treatment on proteomic analysis. |
Verification of protein expression by western blot analysis
The differential expression of the Capan-1 cell line and its stable surviving cells following primary GEM treatment identified in the proteomic study were further validated by western blot analysis. As shown in Fig. 2, the surviving cells had a decreased expression level of HSP27 compared to Capan-1 cells, which is consistent with the findings of the proteomic analysis (Fig. 2). The changes of the location of HSP27 indicated that HSP27 decreased in the cytoplasm but increased in the nucleus, compared to Capan-1 cells (Fig. 2).
Immunohistochemistry of HSP27 in pancreatic cancer tissues and the correlation with GEM effects and survival
We further validated the data by examining expression levels of HSP27 at the protein level. Immunoreactivity was detected in the cytoplasm. Adjacent benign pancreatic parenchyma was negative or weakly focally expressed (13%, 6/47). Of the 47 PDAC specimens, 38 (81%) exhibited HSP27 immunoreactivity (Fig. 3). The results of the correlation between tumor HSP27 expression and tumor pathological features are shown in Table II. HSP27 was aberrantly overexpressed in PDACs relative to adjacent non-tumor tissues. However, there was no significant difference between HSP27 levels and other clinicopathological findings such as age, gender, location of tumor, histological grade and perineural invasion in PDAC.
![]() | Table IICorrelation of HSP27 expression with clinicopathological features of pancreatic ductal adenocarcinoma patients. |
Discussion
In this study, we applied 2-DE-based proteomics to identify the differentially expressed proteins of pancreatic carcinoma cells that survived GEM primary treatment in vitro. We successfully identified 9 proteins with significantly altered expression levels. Based on their functions, these proteins are mainly involved in signal transduction, transport, metabolism, and as chaperones. One protein has an unknown function. The expression of HSP27 was decreased in a gemcitabine-resistant pancreatic cancer cell line. HSP27 was aberrantly overexpressed in PDACs relative to adjacent nontumor tissues.
HSP27, an ATP-independent chaperone, is involved in a number of processes such as apoptosis, DNA repair and recombination (14,15). HSP27 is upregulated in many types of cancer, including colorectal (16), breast (17), prostate (18) and pancreatic cancer (19). HSP27 may be expressed in a wide range of human cancers and could be a prognostic marker in many cancers (20–22). HSP27 is associated with poor prognosis in non-small cell lung carcinoma (23) and gastric cancer (24), as well as pancreatic ductal adenocarcinoma (22,25). However, HSP27 is associated with good prognosis in esophageal cancer, oral squamous cell carcinoma and malignant fibrous histiocytoma (23,26). These results suggest that HSP27 may have different functions in various types of cancer. There is evidence that HSP27 is involved in anti-cancer resistance, which is related to its location in many cancer cells. Vargas-Roig et al (27) found that, following drug administration, cytoplasmic HSP27 decreased or disappeared in 5 cases (36%), increased in 5 cases and remained unchanged in 4 cases (28%). Following chemotherapy, HSP27 was expressed in the nuclear compartment in 10 cases (71%); this increase was statistically significant (P=0.007). Increased HSP27 expression is correlated with higher rates of GEM resistance in patients with pancreatic cancer. Furthermore, knock-out of HSP27 reduces chemoresistance (28,29). RP101 (brivudine) may bind to heat shock protein HSPB1 (HSP27) and enhances survival in animals and pancreatic cancer patients (30). As previously shown, HSP27 may be phosphorylated and translocated to the nucleus under different circumstances and exposed to different stresses regulated by multiple steps (31). The phosphorylation status of HSP27 plays a key role in GEM-induced growth suppression of pancreatic cancer, and it could also be a possible biomarker for predicting the response of pancreatic cancer patients to treatment with GEM (32,33). The combination of HSP27 knockdown with OGX-427 and chemotherapeutic agents such as GEM may be a novel strategy to inhibit the progression of pancreatic cancer (34). In our study, we found the downregulation of total HSP27 in pancreatic carcinoma cells survived from GEM treatment. Furthermore, we found that HSP27 was decreased in the cytoplasm and increased in the nucleus, and the nuclear expression of HSP27 was always low in immunostaining of pancreatic cancers, which demonstrated that the expression of HSP27 in pancreatic cancer occurs mainly in the cytoplasm. The results indicated that researching the location of HSP27 was more significant for total HSP27 and the different locations of HSP27 had a correlation with cancer chemotherapy resistance. However, the expression of HSP27 in the nucleus was related to the intrinsic chemoresistance of pancreatic cancer cells.
In conclusion, HSP27 may be important in the intrinsic chemoresistance of pancreatic cancer cells and the location of HSP27 in pancreatic cancer cells was more significant compared to the cytoplasmic location. For therapeutic application, a targeted therapy against HSP27 in the nuclear signaling pathway could be applied to overcome GEM resistance and may be beneficial in the treatment of pancreatic cancer. The mechanisms of HSP27 in pancreatic cancer require further research.
Acknowledgements
This project was supported by the National Key Project of Scientific and Technical Supporting Programs of China (No. 2006BAI02A14) and the National Natural Science Foundation of China (No. 30770996 and No. 81172310).
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