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Implication of metastasis suppressor gene, Kiss-1 and its receptor Kiss-1R in colorectal cancer
© Ji et al.; licensee BioMed Central Ltd. 2014
Received: 2 June 2014
Accepted: 19 September 2014
Published: 27 September 2014
Kiss-1 and Kiss-1R have been suggested as a novel pair of metastasis suppressors for several human solid tumours, however, their role in colorectal cancer remains largely unknown. Therefore, the aim of this study was to investigate the role and signal transduction of Kiss-1 and Kiss-1R in colorectal cancer.
Ribozyme transgenes were used to knockdown high expression of Kiss-1 and Kiss-1R in HT115 and HRT18 cells. The stabilized transfected cells were then used to deduce the influence of Kiss-1 and Kiss-1R on the function of colorectal cancer cells by in vitro assays and ECIS assay. The effect of Kiss-1 on MMPs related to tumour metastasis was also deleted by zymography. The mRNA and protein expression of Kiss-1 and Kiss-1R, and their correlation to the clinical outcome in human colorectal cancer were investigated using real-time PCR and IHC respectively.
Knocking down Kiss-1 resulted in increased invasion and migration of colorectal cancer cells. Kisspeptin-10 decreased cellular migration of colorectal cancer cells and required ERK signaling as shown during the ECIS based analyses. Reduction of MMP-9 was caused by Kisspeptin-10 and ERK inhibitor, shown by zymography. In human colorectal cancer tissues, the mRNA expression level of Kiss-1 had a negative correlation with Dukes staging, TNM staging, tumour size and lymph node involvement. Reduction of Kiss-1R was also linked to poor prognosis for the patients.
The present study has presented evidence that Kiss-1 may be a putative metastasis suppressor molecule in human colorectal cancer.
Colorectal cancer (CRC) is the second most commonly diagnosed cancer and is a major cause for mortality and morbidity globally .
The Kiss-1 gene was identified as a human melanoma metastasis suppressor gene through the analysis of subtractive hybridization in highly metastatic cell lines as compared to non-metastatic cell lines . The Kiss-1 gene encodes a protein of 145-amino-acids, which is subsequently cleaved into a family of Kisspeptins, including Kisspeptin-10, Kisspeptin-13, Kisspeptin-14, Kisspeptin-54 respectively [3–5]. Its receptor, Kiss-1R, also known as G-protein coupled receptor 54 (GPR54) was first discovered and cloned from rat brain in 1999 .
Kiss-1 and Kiss-1R have been suggested as a novel pair of metastasis suppressors in most cancers [5, 7–11]. Correlation between decreased expression of Kiss-1 and poor clinical outcomes has been evident in most malignancies that have been investigated. One possible explanation for the role played by Kiss-1 in cancer biology could be extrapolated from the relationship between Kiss-1 and matrix metalloproteinases (MMPs), whose significance in tumour invasion and metastasis formation is well known . However, few studies have specifically shown a role for Kiss-1 in colorectal cancer as yet.
In this study, we examined the expression of Kiss-1 and Kiss-1R in human colorectal cancer and analyzed the potential clinical and prognostic implications. After that, we investigated their effect on the function of colorectal cancer cells. On the basis of the data from these experiments, Kiss-1 may play a metastasis suppressor role in human colorectal cancer and be linked to the disease progression of patients, by way of aberrant expression and molecular and cellular mechanism (s) that are yet to be identified.
Patients and tissue specimens
Colorectal cancer tissues (n = 94) and normal background tissues (n = 80) were collected immediately after surgery with approval by the South East Wales Local Research Ethics Committee (ref 05/WSE03/92) and patients’ consent. The tissue samples were stored in a deep freezer (−80°C) until further use. Patients were routinely followed after surgery and the median follow up period was 120 months. Tumour tissues and normal tissues (>10 cm away from the tumor margin) were obtained with confirmation by a pathologist.
HT115 and HRT18 cancer cell lines were obtained from the European Collection of Animal Cell Culture (ECACC, Salisbury, England, UK).
Peptide receptors and inhibitors, antibodies
ERK inhibitorII (FR180204) (Calbiochem, Germany), Kisspeptin-10 (No.2570) (Tocris Bioscience, Bristol, UK) and Kisspeptin-234 (Tocris Bioscience, Bristol, UK). Kisspeptin-10, a short peptide of 10 amino acids, is proteolytically processed from Kiss-1 . Kisspeptin-234 is a Kisspeptin-10/Kiss-1R antagonist, which belongs to Kisspeptin-10 analog. Antibodies to Kiss-1 (SC-101246) and Kiss-1R (SC-48220) were purchased from Santa Cruz Biotechnologies Inc., (Santa Cruz, CA, USA).
RNA isolation, cDNA synthesis, RT-PCR, Q-PCR and immunohistochemical staining
Primer sequences used for RT-PCR and Q-PCR in this study
Multivariate analysis for prognostic factors for colorectal related death and incidence (p values)
With colorectal related death
With colorectal related incidence
Real-time quantitative PCR, based on the Amplifluor™ technology, was used to quantify the level of mRNA expression of Kiss-1 and Kiss-1R from the cDNA samples of coloretal tissues and cells, mentioned above. All colorectal cDNA samples were synchronously examined for Kiss-1 and Kiss-1R along with a set of internal controls. Q-PCR primers (Table 1) were designed using Beacon Design software (PREMIER Biosoft, Palo Alto, CA). Real-time PCR was carried out using an IcyclerIQ™ (Bio-Rad, Hemel Hempstead, UK) with the following cycling conditions: 94°C for 5 min, 80–90 cycles of: 94°C for 10 sec, 55°C for 35 sec and 72°C for 20 sec.
Frozen sections of colorectal tumours and adjacent background tissues were sectioned at a thickness of 6 μm using a cryostat . The samples were mounted onto Super Frost Plus microscope slides (Fisher, UK). The samples were fixed in a mixture of 50% acetone and 50% methanol and then air-dried. After rehydration and blocking with 5% horse serum solution, the sections were probed with the appropriate primary antibody and secondary antibodies. Following the instructions, the avidin-biotin complex (Vector Laboratories, Burlingame, CA, USA) was applied before staining with diaminobenzidine chromogen. Nuclei were counterstained in Mayer’s haematoxylin. Sections from fresh frozen human placenta were used as positive controls.
Generation of Kiss-1 and Kiss-1R ribozyme transgenes and stable transfectants
In vitrocell function assays
In vitro cell growth assay
Cells were seeded into 96-well plates at 2,500 cells/well, and cultured using normal media (10% fetal calf serum, 0.1% antibiotics). The cells were cultured in triplicate for 1, 3 and 5 days. After incubation the cells were fixed in 4% formalin and stained with 0.5% crystal violet (w/v). The stained crystal violet was then extracted using 10% (v/v) acetic acid, and the absorbance was determined using a spectrophotometer (Bio-Tek, ELx800) at a wavelength of 540 nm.
In vitro cell adhesion assay
A 96-well plate was precoated with 5 μg of Matrigel (CollaborativeResearch Products, Bedford, Massachusetts, USA) and allowed to air dry. Following rehydration using serum free media, 40,000 cells were seeded into each well. After 40 minutes of incubation, non-adherent cells were washed off using BSS. The adherent cells were then fixed with 4% formalin and stained using 0.5% crystal violet. The number of adherent cells were counted under a microscope.
In vitro invasion assay
Transwell inserts (with 8 μm pore) were precoated with 50 μg of Matrigel and air dried. Following rehydration, 40,000 cells were seeded into each insert. After incubation for three days, cells which had invaded through the matrix and adhered to the other side of the insert were fixed in 4% formalin, and stained with 0.5% (w/v) crystal violet. The number of invaded cells was then counted under a microscope.
In vitro wounding assay for cellular migration
Cells were seeded into a 24-well plate at a density of 200,000 per well and allowed to form a monolayer of cells. The monolayer of cells was then scraped to create a wound. Migration of cells at the wound edges were monitored over a period up to 18 hours. Optimas 6.0 motion analysis (Meyer Instruments, Houston, Texas) was used to track the leading edge of cells to measure the distance of migration.
Electric cell-substrate impedance sensing (ECIS)
The ECIS system (Ztheta, Applied Biophysics Inc., USA) was used to quantify cell migration as previously reported by Jiang et al.. HT115 cells were prepared for six repeats per group and seeded at 40,000 cells per well in 200 μl of DMEM medium alone or medium supplemented with 200 nM ERK small inhibitor, 300 nM Kisspeptin-10 and 300 nM Kisspeptin-234.
Gelatin zymography assay
Cells were counted and 1×106 cells were seeded to a tissue culture flask. After an overnight incubation and 4 hours treatment with appropriate peptide receptor or inhibitor (300 nM Kisspeptin-10, 300 nM Kisspeptin-234 or 200 nM ERK inhibitor), the medium was collected. This method is well established within the laboratory, and has previously been published .
The relationship between the expression of Kiss-1 and Kiss-1R and tumour grade, TNM staging and nodal status was respectively analyzed using Mann–Whitney U test (Tables 2 and 3). Quantitative data of IHC, in vitro assays, ECIS assay and zymography assay was analyzed using the Student’s test, Kruskal-Wallis and chi-squared test, where appropriate. Survival analysis and multivariate analysis were carried out using the SPSS20 software package. Differences were considered to be statistically significant at p < 0.05.
Results and discussion
Kiss-1 and Kiss-1R expression in colorectal adenocarcinoma tissues and the histopathological/clinical characteristics of the disease
Kiss-1 and Kiss-1R expression was analysed in colorectal cancer tissues and adjacent normal tissues using real time PCR (Tables 2 and 3). Decreased levels of Kiss-1 transcript were seen in Dukes B and C tumours compared with Dukes A carcinomas (p < 0.05). The expression level of Kiss-1 decreased as TNM stage progressed, and statistical analysis revealed significant links between TNM stage I and stage III&IV. A significantly decreased expression of Kiss-1R was observed in tumour tissues compared with normal background tissues. Interestingly, Kiss-1R expression in patients undergoing chemo-radio therapy was considerably higher in comparison to that in patients without therapy.
The correlation of mRNA expression of Kiss-1 and clinical parameters
Lymph node involvement
The correlation of mRNA expression of Kiss-1R and clinical parameters
Lymph node involvement
Immunochemical staining was carried out on a portion of paired normal and tumour tissues (n = 23 pairs). Intense expression of Kiss-1 and Kiss-1R was primarily observed in the cytoplasm of epithelial cells in adjacent normal tissues compared with cancer cells (p value < 0.05), as shown in Figure 2A and B.
Knockdown of Kiss-1 and Kiss-1R and the consequent effect on functions of colorectal cancer cells
Analysis of the in vitro function assays revealed cells with Kiss-1 knockdown had significantly increased invasiveness (p = 0.015) and migration (p = 0.0094) compared HT115 pEF cells (Figure 3B and C), but knockdown of Kiss-1 and Kiss-1R did not demonstrate a significant change on cell growth and adhesion of HT115 and HRT18 cells (p > 0.05).
Effect of Kiss-1 and Kiss-1R knockdown on the motility of the cancer cells and the involvement of ERK pathway
MMPs are involved in the regulation downstream of Kiss-1/Kiss-1R and ERK pathway
The expression of Kiss-1 correlated significantly with Dukes classification, TNM staging, tumour stage and lymph node involvement. Interestingly, these stages are classified by the level of tumour invasion and metastasis. Hence, the conclusion from the clinical cohort was consistent with studies in other malignancies. Kiss-1 has a significant, and negative correlation with tumour metastasis and invasion. Loss of Kiss-1R expression was significantly associated with disease free survival, since increased expression of Kiss-1R may have positive correlation with survival. Moreover, high expression of Kiss-1R transcripts was associated with poor prognosis in both overall survival and disease free survival compared with low expression of Kiss-1R. Aberrant Kiss-1 and Kiss-1R expression is definitely a point for consideration. One hypothesis to explain this may be that the inhibitory effect of Kiss-1 on colorectal cancer cells may not solely combine with Kiss-1R, but with other unknown receptors. Navenot et al. reported Kiss-1/Kiss-1R also influenced signaling events by interacting with the chemokine receptor (CXCR4) and the gonadotrophin-releasing hormone receptor . Kiss-1R knockdown has little effect on cell migration compared with the control cells which may support this hypothesis. Finally, a recent report has shown that the reduction/loss of Kiss-1 in colorectal cancer may be the result of hypermethylation of Kiss-1, and this provides a plausible explanation for the reduction of Kiss-1 observed in the current study . It will be interesting to explore the mechanisms by which Kiss-1R is reduced/lost in this cancer type in the future.
Data obtained from the present study suggests that Kiss-1 significantly inhibits the motility and invasion of HT115 and HRT18 colorectal cancer cells, but has no significant effect on the proliferation and adhesion of HT115 and HRT18 cells. Interestingly, no increase in cell migration of Kiss-1R knockdown cells compared with the controls was observed. The motility of Kiss-1R knockdown cells would increase the same as the Kiss-1 knockdown cells did, if Kiss-1 indeed had the inhibitory influence on cell migration through Kiss-1R.
Several studies have suggested the mechanism by which Kiss-1 inhibits metastasis may involve extracellular-regulated kinase 1/2 (ERK1/2) phosphorylation and decreased matrix metalloproteinase-2 (MMP-2) expression [11, 19, 20]. In addition, Yan et al. reported Kisspeptin-10/Kiss-1R activation can dephosphorylate nuclear factor kappa B (NF-Kappa B), and cause it to dissociate from the MMP-9 promoter. This process ultimately results in a decrease of MMP-9 expression in the placenta . It will indeed be very interesting to examine the degradation of NF-Kappa B in response to Kiss-1 signalling in future studies. As a contribution to this endeavor, we have examined the effects of Kisspeptin-10 and ERK inhibitor on the migration ability of HT115 cells using ECIS assays, and found it to suppress the migration of colorectal cancer cells. Addition of ERK inhibitor can diminish the effect of Kisspeptin-10, suggesting the ERK pathway plays an important role in mediating the signaling of Kiss-1/Kiss-1R.
Kiss-1 significantly inhibits the motility and invasion of HT115 cells. It is clear this action is at least partly mediated by regulating the activity of MMP-9. This study further indicates that the effect on MMP-9 is via the ERK pathway rather than the JNK pathway. In summary, it is suggested Kiss-1 inhibits ERK activation and consequently reduces the enzymatic activity of MMP-9 caused by the degradation of NF-κB, which contributes to the suppression of tumour metastasis.
Perhaps the most intriguing property of Kiss-1 is its potential to be exploited clinically. In the future we are interested in investigating the influence of Kisspeptin-10 on tumour growth and metastasis in an in vivo tumour model. Furthermore, Ziegler et al. reported that anti-proliferative function of Kisspeptin-10 was regulated by the expression levels of Kiss-1R . There was no effect on proliferation observed in the breast cancer cells expressing Kiss-1R endogenously, while Kisspeptin-10 caused a significant inhibition of proliferation of transfected neuronal cells over-expressing Kiss-1R . Hence, detecting the influence of Kisspeptin-10 on colorectal cancer through changing Kiss-1R’s expression levels will be the focus of follow-up studies.
In conclusion, the present study has presented evidence that Kiss-1 is a putative metastasis suppressor molecule in human colorectal cancer. This is seen by its inhibitory effect on the migration and invasion of colorectal cancer cells, and on actions achieved by down-regulating the activities of MMP9, via an ERK dependent pathway. The preliminary data from studies on a clinical cohort of colorectal cancer patients support this argument.
The authors would thank the support from Cancer Research Wales and the Albert Hung Foundation.
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