Background
Squamous cell carcinoma is the most common pathological esophageal cancer in the East [
1], and surgery is still the best curative treatment option [
2]. However, despite having comprehensive staging tests performed to determine which patients are most likely to benefit from potentially curative surgery, many patients develop tumor recurrence after surgery, and the 5-year survival rate is only approximately 42% [
3]. The American Joint Committee on Cancer (AJCC) staging system [
4] is commonly used in the assessment of clinical outcomes in patients with esophageal squamous cell carcinoma (ESCC). However, the system only reflects cancer progression status at the time of diagnosis, and some patients may survive for a long time without recurrence, whereas others with disease in the same tumor-node-metastasis (TNM) stage may have a more unfavorable prognosis due to tumor recurrence and metastasis. These differences are likely attributable to the inherent heterogeneity in the biological behavior of the tumors. Nevertheless, in view of the complexity of cancer progression [
5‐
7], the availability of reliable markers is substantially limited. Thus, the combination of TNM staging with molecular markers and other clinicopathological parameters may be a promising method of selecting the patients with a high risk of postoperative recurrence, for the purpose of guiding tailored therapy.
Cell cycle regulation is critical for cell proliferation and tumorigenesis. One of the key players regulating cell cycle progression is the F-box protein, Skp2 (S-phase kinase–associated protein 2) [
8,
9]. Recent studies reveal that the overexpression of Skp2 is associated with the progression of a variety of human cancers [
10‐
14]. However, the correlation of Skp2 expression with metastasis and prognosis in ESCC is still controversial [
15,
16].
In this study, we first evaluated Skp2 expression in resected ESCC by immunohistochemistry (IHC) using tissue microarrays. The correlation between Skp2 expression and clinicopathological characteristics and survival outcome was determined. We then used ESCC cell lines to further determine the function of Skp2 in the progression of ESCC.
Methods
Patient selection
This study was approved by the medical ethics committee of Sun Yat-sen University Cancer Center. A total of 157 primary ESCC patients who underwent complete resection at the Department of Thoracic Surgery at Sun Yat-sen University Cancer Center between December 1996 and October 2004 were eligible for inclusion in the study. All of the patients included in the study received complete resection and were re-staged according to the seventh edition of the AJCC Cancer Staging Manual [
4]. We applied the definition of complete surgical resection proposed by the International Association for the Study of Lung Cancer (IASLC) Staging Committee [
17].
All patients included in the analysis fit the following criteria: (1) their disease was histologically defined as thoracic squamous cell carcinoma; (2) they underwent complete resection; (3) they had complete information for stage grouping; (4) they fit into pathological AJCC stages I-III; (5) their resections were neither preceded nor followed by adjuvant chemotherapy or radiotherapy (esophagectomy alone); and (6) they had adequate paraffin-embedded cancer tissue samples for use in constructing the tissue microarray.
We excluded the patients with a history of concurrent malignant disease or other previous primary cancers and operative deaths. Operative death is defined as death within 30 days of the operation or any time after the operation if the patient did not leave the hospital alive.
Follow-up of patients
The details of the strategy for patients’ follow-up in the training cohort were described in our previous study [
18].
April 2009 was the last time of contact for the patients. The median time from surgery to the last time of contact for the training cohort was 90.2 months, ranging from 60.7 to 156.1 months.
Tissue microarray construction
For uniform and simultaneous protein expression analysis of multiple tissue samples, we prepared tissue microarrays for IHC staining. Tumor tissue samples were collected, fixed in ethanol, and embedded in paraffin. H&E-stained sections from a single random block from each patient were reviewed by a senior pathologist to define representative tumor regions. For each sample, three tissue cylinders were taken from different representative tumor regions. Tissue cylinders with a diameter of 1 mm were punched from selected areas of each “donor” block using the Manual Tissue Arrayer (Beecher Instruments, Silver Spring, MD, USA) and arrayed into a recipient paraffin block. Serial 4 μm sections were mounted on silane-coated slides for IHC staining. The final IHC staining analyses included cores from 157 ESCC cases.
IHC staining and scoring
IHC staining was performed using tissue microarray sections. The slides were deparaffinized in xylene, rehydrated through graded alcohols to water, heated in boiled EDTA buffer (pH 8.0) for 10 min, and cooled naturally to room temperature. They were subsequently immersed in 3% hydrogen peroxide solution for 10 min to remove endogenous peroxidase activity, blocked with 10% goat serum at room temperature for 30 min, and then incubated with mouse anti-Skp2 (1:40, Invitrogen) overnight (about 16 h) at 4°C. After being washed with PBS, the slides were incubated with secondary antibody (two-step anti-rabbit/mouse universal immunohistochemistry kit, Dako) at room temperature for 30 min and then developed with DAB for 6.5 min. Slides were counterstained with hematoxylin.
Two independent observers who were blinded to the clinicopathological information determined the immunoreactivity score (IRS) for each immunomarker. The staining results were scored based on the following criteria: (a) percentage of positive tumor cells in the tumor tissue: 0 (0%), 1 (1%–10%), 2 (11%–25%), 3 (26%–50%), 4 (51%–75%), or 5 (76%–100%); and (b) signal intensity: 0 (no staining), 1 (weak staining), 2 (moderate staining), or 3 (strong staining) [
10]. IRS was calculated by multiplying the score for the percentage of positive cells by the intensity score (range of 0 to 15) [
19]. The specimens were rescored if the difference between the scores determined by the two pathologists was greater than three [
20]. If the conclusion was still controversial after the specimens were rescored, a third pathologist then intervened and worked collaboratively to find a consensus. The average IRS of each core determined by the two pathologists was assigned as the staining result for the core, and the average IRS of samples for each case was assigned as the staining result for the patient. The patients whose staining IRS were larger than zero were considered as positive expression of Skp2.
Cell culture
ESCC cell lines KYSE30, KYSE140, and KYSE180 were kindly provided by Prof. Xin-Yuan Guan (Sun Yat-sen University Cancer Center). Cells were cultured in DMEM containing 10% fetal bovine serum at 37°C in a humidified atmosphere containing 5% CO2.
Plasmids and siRNA transfection
Transient transfection of 50 nM of Skp2 small interfering RNA (siRNA) or scrambled siRNA was performed using Lipofectamine 2000 (Invitrogen) according to the manufacturer’s instructions. The sequences of the Skp2 siRNA, which were synthesized by the Ribobio Company (Guangzhou, China) as well as the scrambled siRNA (negative control, NC), were 5’-GGUAUCGCCUAGCGUCUGAdTdT-3’ for the sense primer and 5’-UCAGACGCUAGGCGAUACCdTdT-3’ for the anti-sense primer. The sense sequence of the scrambled siRNA was 5'-UUC UCC GAA CGU GUC ACG UTT-3', of which the anti-sense sequence was 5'-ACG UGA CAC GUU CGG AGA ATT-3'. The plasmids of pcDNA3.1-Skp2 and pcDNA3.1 empty vector were constructed in our laboratory and transiently transfected into ESCC cell lines using Lipofectamine 2000 (Invitrogen) according to the manufacturer’s instructions [
21].
Western blot assay
Cells were harvested 24 h after plasmid/siRNA transfection and lysed in a lysis buffer containing a cocktail of protease inhibitors. After centrifugation at 15,000 × g for 15 min at 4°C, supernatants were collected, mixed with dithiothreitol and used for western blotting. Equal amounts of protein extract were electrophoresed and then transferred to nitrocellulose membranes. The membranes were blocked with 3% non-fat milk at room temperature for 1 h, incubated with anti-Skp2 (1:1000, Invitrogen) overnight at 4°C, and incubated with the secondary antibody at room temperature for 1 h. After washing the blots, proteins were visualized by chemiluminescence.
Cell proliferation assay
Cell proliferation was measured by a 3-[4, 5-dimethylthiazol-2-thiazolyl]-2,5- diphenyltetrazolium bromide (MTT) assay. ESCC cells were plated in 96-well plates at a density of 15,000-25,000 cells/mL in triplicate. Four hours before the desired time points, 20μL of 10 mg/mL MTT was added. After incubation for 4 h, the plates were depleted and 150 μL DMSO was added. The optical density (OD) values were determined by spectrophotometry (SpectraMax M5, Molecular Devices).
Briefly, 24 h after plasmid/siRNA transfection, cells were trypsinized, resuspended as single cells, and plated in 6-well plates with 100 cells per well. After 14 days, the colonies were fixed with methanol and stained with crystal violet. Colonies with more than 50 cells were counted under the microscope. The cloning efficiency was calculated using the following formula: colony formation efficiency (%) = (clone number/inoculation cell number) × 100%.
Statistical analysis
The SPSS statistical software package (Standard version 16.0; USA, Chicago, IL) was used for data analysis. The mean values are presented as the mean ± standard deviation (SD). Independent t-tests were used to compare groups of continuous, normally distributed variables. The Pearson chi-square test was used to determine the significant difference between groups for dichotomous variables. All statistical tests were two-tailed, and p < 0.05 was considered statistically significant. Survival time was measured from the date of surgery to the date of event or last follow-up. Patients alive at the end of the study were censored for the purpose of data analysis. Multivariate survival analysis was performed using the Cox regression model.
Discussion
Skp2 was originally identified as an S-phase Kinase Cdk2/Cyclin A-associated protein [
22]. Skp2 is known as a critical component of the Skp2/SCF (Skp1-Cullin1-F-box) complex, which is capable of inducing protein ubiquitination and subsequent proteasome-dependent degradation [
23,
24]. Among the numerous substrates for degradation, many are negative cell cycle regulators, including p27
Kip1, p21
Cip1 and p57
Kip2[
25,
26]. The ubiquitylated p27
Kip1 is then rapidly destroyed by the proteasome, allowing the activity of cyclin E/A-CDK2 and progression to the S phase [
27]. Overexpression of Skp2 significantly promotes the transition from G1 phase to S phase, therefore leading to the accelerated proliferation. In addition, Skp2 may contribute to the resistance to apoptosis induction by DNA damage agents, such as irradiation and doxorubicin [
28].
Previous studies demonstrated that Skp2 was commonly overexpressed and associated with poor prognosis in a variety of human cancers, including gastrointestinal cancer [
27‐
29], breast cancer [
30,
31], prostate cancer [
32,
33], lung cancer [
34,
35] and nasopharyngeal cancer [
14,
21]. However, the prognostic role of Skp2 in ESCC has been seldom investigated and is still controversial. Fukuchi et al. determined the Skp2 expression in a small number (32 cases) of ESCC, in which they suggested that Skp2 might be a prognostic factor in early stage ESCC [
15]. Recently, Wang et al. reported that overexpression of Skp2 correlated with lymph node metastasis and advanced tumor stage in ESCC (140 cases), but unfortunately, the survival prognosis was not determined in their study [
16].
In the present study, we initially showed that high expression of Skp2 in tumor cell nuclei was associated with advanced local invasion of primary carcinoma. Moreover, the positive expression of Skp2 in this study is indicative of unfavorable prognosis. Multivariate Cox proportional hazards analysis further confirmed that high Skp2 expression was an unfavorable prognostic factor independent of conventional prognostic factors, such as T categories and N categories. These results indicated that Skp2 could influence tumor progression of ESCC, and Skp2 could be useful in predicting tumor recurrence for operable ESCC. Our data showed that Skp2 expression did not correlate with lymph node metastasis, but correlated with local tumor invasion. However, Wang et al. reported high expression of Skp2 associated with lymph node metastasis, but not with local tumor invasion [
16], which was contrary to that of our study. The controversy about Skp2 expression and tumor progression also exists in colorectal carcinoma [
10,
27]. These controversies suggest that more studies are warranted for further assessment of the role of Skp2 in cancer progression. A possible mechanism for these controversies is the heterogeneity of cancer. Skp2 is an essential regulator of the cell cycle, probably playing multiple roles in carcinogenesis. In the present study, the case number is much larger than in previous studies [
15,
16]. The large number and multivariate Cox survival analysis make our outcome much more reliable.
Our data from
in vitro experiments, including cell proliferation and colony formation, provided evidence for Skp2’s role in facilitating cancer progression, consistent with the survival analysis results of ESCC patients. In contrast to Wang et al.’s observation that Skp2 may promote ESCC metastasis via inhibiting anoikis [
16], our findings exhibit a possibility that Skp2 directly speeds up the proliferation of ESCC cells. If this is the case, our discovery that Skp2 expression correlates with T stage but not N stage can be explained. Based on this discovery, we did not perform experiments to test the mobility of ESCC cells in which Skp2 was overexpressed or knocked down, since we did not found a correlation between the level of Skp2 expression and lymph node metastasis in our clinicopathological data.
Our data suggests that Skp2 expression might be a new prognostic biomarker for tumor recurrence in ESCC patients. Therefore, the examination of Skp2 expression, detected by IHC, could be used as an additional tool for identifying those patients who are more likely to suffer from recurrence after surgery. Thus, designing an optimized individual adjuvant therapy strategy for resectable ESCC patients will become possible. According to the practice guidelines of the National Comprehensive Cancer Network (NCCN), adjuvant chemotherapy was not recommended for completely resected ESCC [
36]. However, many patients develop local recurrence or metastasis after surgery, and the 5-year survival rate is only about 42% [
3]. For application purposes, if a patient with operable ESCC is with high expression of Skp2, adjuvant chemotherapy can be recommended after surgery; on the contrary, for patients with a low expression of Skp2, observation is preferred. Although further evaluation of this strategy for clinical use will be necessary, it may help clinicians to select the most appropriate therapies for individual ESCC patients in advance.
Despite the finding that Skp2 expression affects the survival of patients with ESCC and the proliferation of ESCC cells, our study has its limitations. On one hand, there is a lack of investigation on the molecular mechanism for the proliferative promotion of Skp2 in ESCC cells. It still remains unclear which signal pathway is involved in the Skp2-dependent regulation of ESCC proliferation. On the other hand, more experiments, such as a tumorigenesis assay in a xenograft model in vivo, are needed to further validate the oncogenic function of Skp2 in ESCC.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
YL, XH and HXY conceived the study, designed, performed and analyzed all experiments and wrote the manuscript. Q. Cui participated in Western blot assays. RZL and JHH participated in IHC studies. TBK, JHF, LJZ and YXZ participated in conceiving the study. All authors read and approved the final version of the manuscript.