- Open Access
Overexpression of Klotho suppresses liver cancer progression and induces cell apoptosis by negatively regulating wnt/β-catenin signaling pathway
- Huidong Sun†1, 3,
- Yanchao Gao†1,
- Kemei Lu2,
- Guimei Zhao1,
- Xuehua Li1,
- Zhu Li1 and
- Hong Chang3Email author
© Sun et al. 2015
- Received: 29 April 2015
- Accepted: 5 October 2015
- Published: 24 October 2015
Klotho is a discovered aging suppressor gene, and its overexpression in mice extends the life span of the animal. Recently, Klotho is also identified as a tumor suppressor gene in variety of tumors; however, the potential role and the antitumor mechanism remain unclarified in liver cancers.
RT-PCR and western blotting analysis were used to detect the expression of Klotho, β-catenin, C-myc, and Cyclin D1. MTT assay was used to detect the survival rates of HepG2 and SMMC-7721 cells. Colony formation assay was used to test the proliferation ability in Klotho transfected cells. FACS was used to detect the cell apoptosis rate in different groups.
The results showed that lower expression of Klotho were found in liver cancer cell lines than the immortalized liver cell L02. Also, MTT assay results found that overexpression or recombinant Klotho administration suppressed the proliferation of liver cancer cells HepG2 and SMMC-7721. Moreover, the colony formation assay results showed that the number of colonies was significantly lower in the cells with transfection with pCMV-Klotho than the controls. Thus, functional analysis demonstrated that Klotho expression inhibited the proliferation of liver cancer cells and Klotho worked as an important antitumor gene in tumor progression. Next, the mechanism was partly clarified that Klotho expression induced cell apoptosis in HepG2 and SMMC-7721 cells, and this phenomenon was mainly involved in the Wnt/β-catenin signaling pathway. The western blotting analysis revealed that overexpression or recombinant administration of Klotho obviously decreased the expression levels of β-catenin, C-myc, and Cyclin D1 in HepG2 cells. Most importantly, the antitumor mechanism for Klotho due to that overexpression of Klotho not only decreased the endogenous β-catenin levels but also inhibited the nuclear translocation of β-catenin to delay the cell cycle progression.
Klotho was a tumor suppressor gene, and overexpression of Klotho suppressed the proliferation of liver cancer cells partly due to negative regulation of Wnt/β-catenin signaling pathway. So, Klotho might be used as a potential target, and the study will contribute to treatment for therapy of liver cancer patients.
- Liver cancer
Liver cancer is one of the most lethal cancers in the world, and its mortality ranks the third in cancer deaths [1, 2]. Each year, about 60 million people worldwide die of liver cancer, and this has a growing trend. Primary liver cancers mainly include two types: hepatocellular carcinoma (HCC) and intrahepatic bile duct cancer . In the developing countries, hepatitis B and hepatitis C are the risk factors responsible for most cases of primary liver cancer [4, 5]. Although the risk factors are preventable, the incidence of liver cancer is actually rising in many developing countries. The most common risk factor in the USA is alcohol abuse, followed by obesity and diabetes [6, 7]. The incidence has gotten over 30,000 cases each year in the USA. Thus, it is very important to elucidate the mechanism for the occurrence and development of hepatocellular carcinoma.
Klotho was a new identified aging suppressor gene, which is highly conserved between human and mouse, with 86 % amino acid identity . The gene encoded a membrane protein and defect in Klotho gene expression in the mouse that causes a syndrome of aging, including a short lifespan . Recently, the relationship of Klotho expression and cancer progression has been studied [10–12]; however, the role and mechanism in a variety of cancers remain unclear. Lu et al. had a clinical follow-up study of 189 epithelial ovarian cancer patients, which demonstrated that high expression of secreted Klotho was associated with increased risk of disease progression and death and positively correlated with the expression of IGF-I and IGFBP-3 but not with IGF-II . However, Wang et al. reported that Klotho, as a novel tumor suppressor gene, was epigenetically inactivated and silenced through promoter hypermethylation in gastric cancer, and the promoter methylation of Klotho could be used to predict the prognosis of gastric cancer patients . In human colon cancers, expression of Klotho was downregulated and correlated with tumor invasion and Dukes staging, while overexpression of Klotho inhibited cell proliferation and invasion through inhibition of IGF1R-mediated PI3K/AKT pathway in colon cancer cells . Moreover, Klotho inhibited the capacity of cell migration and invasion in cervical cancer, in vitro restoration of Klotho expression in SiHa cells resulting in a decreased cell motility and invasiveness through upregulation of E-cadherin, downregulation of N-cadherin, and reduced expression of MMP-7 and MMP-9 .
However, the relationship and association between the expression of Klotho and primary liver cancers is not clarified till now . In the present study, we explored the effects and possible mechanisms relating to Klotho in human liver cancer cell lines, and the clarification of the association and mechanism would contribute to treatment for therapy of liver cancer patients.
Agent and cell lines
Recombinant human Klotho (rKlotho) is a 65–70 kDa glycoprotein containing 516 amino acid residues. The protein of rKlotho was obtained from Sigma Corporation (cat. SRP3102). The myc-tagged Klotho expression vector (pCMV6-Klotho) and the control vector (pCMV6) were designed and obtained from OriGene corporation (Rockville, MD, USA). The liver cancer cell lines HepG2, SMMC-7721, and BEL-7404 were obtained from American Type Culture Collection (ATCC, Rochville, MD. USA). The normal liver cancer cells L02 was purchased from Junrui Coporation (Shanghai, China). The liver cancer cells were cultured in DMEM medium (GIBCO, Gaithersburg, MD, USA) supplemented with 10 % fetal bovine serum and cultured at 37 °C with 5 % CO2 in a humidified atmosphere.
Cell proliferation is tested by MTT assay. Generally, the human liver cancer cells HepG2 and SMMC-7721 cells were planted into 48-well plates. Then, the cells were cultured for 8 h and transfected with p CMV6-Klotho and p CMV-6 vector for 24, 48, 72, and 96 h. Finally, MTT agent was added into the medium, and the purple crystals were dissolved with DMSO. The liquid was transferred into 96-well plates and read on a microplate reader at a test wavelength of 490 nm and a reference wavelength of 570 nm.
The RNApure kit (Bioteke, Beijing, China) was used to extract total RNA, and reverse transcriptase (RT) SuperScript III (Invitrogen BV, Carlsbad, CA) was used to transcript the cDNA. The primer sequences were as follows: for glyceraldehyde-3-phosphate dehydrogenase (GAPDH), 5′-GAAGGTGAAGGTCGGAGTC-3′ (sense) and 5′-GAAGATGGTGATGGGATTTC-3′ (antisense) and for Klotho, 5′-ACCTGGTGGCGCACAACC-3′(sense) and 5′-TTGGCAAACCAACCTAGTACA-3′. The Klotho PCR reaction condition is that 94 °C 5 min, followed by 30 cycles of 94 °C for 30 s, 55 °C for 30 s, and 72 °C for 30 s, and finally, elongation is 72 °C for 10 min. The GAPDH reaction condition is similar to Klotho but for the annealing temperature it is 55 °C for 30 s.
Colony formation assay
The liver cancer cells were transfected with pCMV6-Klotho and pCMV-6 vector for stable cell lines. For colony formation assay, the cells were plated into 6-well plate. After 8 h, the cells transfected with Klotho or control vector were cultured for 14 days, and the medium was refreshed every 3 days. Then, methanol was used to fix the colonies (≥50 cells per colony). They were stained with 1.25 % crystal violet and counted under a light microscope.
Flow cytometric analysis
Annexin V-FITC/PI dual staining analysis is used for detection of the apoptosis rates in human lung cancer cells according to the kit protocols (Santacruz, USA). Briefly, the liver cancer cells (4 × 105 cells/well) were plated into 6-well plate and transfected with pCMV6-Klotho and pCMV6 vector for 48 h. Then, the cells were washed with ice PBS buffer for three times and resuspended in binding buffer with HEPES–NaOH 10 mM pH 7.4, 25 mM CaCl2, and 144 mM NaCl. At last, the staining dye of Annexin V (0.1 μg/μl) and PI (0.05 μg/μl) were added for incubation in the dark for 30 min on ice, and the cells were subjected to FACS analysis.
Western blot analysis
The liver cancer cells were plated into 48-well plates and cultured for 8 h for adherence. Then, the cells were transfected with pCMV6-Klotho and p CMV-6 vector for 48 h. The pCMV6 vector was used as the control. The other treatment was that the cells were treated with rKlotho or BSA at the concentration of 250 ng/mL. BSA was used as the negative control. Next, the cells were washed with ice-cold PBS buffer, and cell lysates were prepared for PAGE. The primary antibodies used were included; the anti-beclin 1, anti-LCI, anti-LC-II, anti-C-myc, anti-Cyclin D1, and anti-GAPDH were all purchased from Santa Cruz biotechnology. The primary antibodies of β-tublin (ab6046), lamin B1(ab16048), and Anti-Klotho (ab18131) were obtained from Abcam corporation. The horseradish peroxidase-conjugated goat anti-mouse secondary antibody was purchased from Abgent Corporation.
All of the data was analyzed using SPSS software. All of the experiments were repeated three times in duplicates. Student’s t test was used to assess the significance of the data, and all of the data are showed as mean ± SD. P < 0.01 means that there is significant difference.
Low level of Klotho is detected in liver cancer cell lines
Overexpression or recombinant Klotho administration suppresses the proliferation of liver cancer cells
Klotho expression suppresses liver cancer cell growth by colony formation assay
Klotho expression induces cell apoptosis in human liver cancer cells
Klotho levels negatively correlate with Wnt/β-catenin signaling pathway in HepG2 cells
Overexpression of Klotho decreases endogenous β-catenin level and inhibits its nuclear translocation
Primary hepatocellular carcinoma is a common malignancy in the world . With the emergence of the problem, such as an aging population and environmental pollution, the incidence of liver cancer arises rapidly and liver cancer has become the second killer in China [18, 19]. It not only gives the pain and psychological burden for patients but also gives serious economic burden to the family and the community [20, 21]. Thus, it has become the focus of medical research and hotspots in China to investigate the molecular mechanisms of the development and progression of liver cancer, which could give some new clues for the prognosis and treatment on hepatocellular carcinoma.
Klotho has been newly identified as an antiaging gene that is involved in the suppression of several aging phenotypes [22–25]. But the potential role and the antitumor mechanism remains unclear in human liver cancers. In the present study, we first explored the expression levels in a panel of three liver cancer cell lines, HepG2, SMMC-7721, and Bel-7404, and the normal liver cell L02. As expected, the expression levels of Klotho in three liver cancer cell lines were obviously decreased than those in L02 cells. The MTT assay proved that overexpression or recombinant Klotho administration in liver cancer cells significantly suppressed the proliferation of cancer cells. This was consistent with the results from the colony formation assay. Moreover, FACS analysis results demonstrated that overexpression of Klotho induced cell apoptosis in HepG2 and SMMC-7721 cells. All of the data revealed that Klotho worked as an important antitumor gene in liver cancer progression although some other paper found that high levels of Klotho promoted cancer progression. One of the probable reasons is that Klotho may have different role in the progression and development of various tumors.
Then, we further explore the mechanism of Klotho involving in the progression of liver cancers. It has reported that overexpression of Klotho inhibits growth and invasion through inhibition of IGF1R-mediated PI3K/AKT pathway in colon cancer cells . In lung cancer cells, Klotho, as a novel secreted Wnt antagonist, could inhibit activation of Wnt /beta-catenin signaling pathway, in a dose-dependent manner . As we know, Wnt/β-catenin signaling pathway is essential for development and tumorigenesis, and this signaling pathway is abnormally activated in the progress of hepatocellular carcinoma. Beta-catenin is an important component in Wnt/β-catenin pathway by being a coactivator of LEF/TCF transcription factors. In pathological conditions, cytoplasmic β-catenin leads to its nuclear accumulation and form the complex with LEF/TCF transcription factors. Then, the LEF/TCF target genes are transactivated, such as C-myc and Cyclin D1, which promote cell cycle progression.
Here, we also detected the association of Klotho expression with Wnt/β-catenin signaling pathway. The western blotting analysis showed that high levels of Klotho were associated with decreased levels of β-catenin. Importantly, the nuclear translocation of β-catenin was also suppressed in HepG2 cells. Additionally, the target genes of the downstream (C-myc and Cyclin D1) were downregulated. All of the data demonstrated that overexpression of Klotho suppressed the proliferation of liver cancer cells and promoted cell apoptosis partly due to negative regulation of Wnt/β-catenin signaling pathway. Thus, Klotho might be used as a potential target, and the study will contribute to treatment for therapy of liver cancer patients.
Klotho was a tumor suppressor gene and overexpression of Klotho suppressed the proliferation of liver cancer cells partly due to negative regulation of Wnt/β-catenin signalling pathway. So, Klotho might be used as a potential target and the study will contribute to treatment for therapy of liver cancer patients.
We thank Qun Chen for helping us analyze the data.
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