Ion of cyclin D1 have a critical role in cell cycle and HCC. In the present study, we examined the role of bKlotho in hepatocarcinogenesis. Our data showed that bKlotho expression was frequently decreased in primary HCC tissues and was also^2Klotho Suppresses Tumor Growth in HCC Isignificantly down-regulated in HCC cell lines. Furthermore, overexpression of bKlotho into hepatoma cells inhibited their proliferation. The anti-proliferative effect of bKlotho might be linked with G1to S phase arrest, which was mediated by the Akt/ GSK-3b/cyclin D1 pathway. Finally, reintroduction of bKlotho could suppress tumorigenesis in the xenograft mouse model and this effects could be aborted by Akt activity. These findings suggest bKlotho suppresses tumor growth in HCC.Cell lines, Constructs and TransfectionHuman hepatocyte cells (L02) and human hepatoma cell lines (HepG2, Hep3B) were cultured as reported [22]. The other two human hepatoma cell lines, SMMC-7721 and Huh 7, were reported previously [23]. The human bKlotho gene was cloned from L02 cells and using the following primers: forward, 59AATTGCGGCCGCATGAAGCCAGGCTGTGC-39; Fruquintinib chemical information reverse, 59-AATTGGATCCTTAGCTAACAACTCTCTTGCCTT-39. The resulting bKlotho PCR product was digested with NotI and BamHI and ligated into p36FLAG-CMV-7.1 expression vector (Sigma-Aldrich, St. Louis, MO) to obtain the bKlotho expression vector. Constitutively activated myristoylated-Akt (myr-Akt) cDNA expression vector was purchased from Upstate (Charlottesville, VA). All transfections used Lipofectamine 2000 (Invitrogen, Carlsbad, CA) according to the manufacturer’s protocol.Materials and Methods Ethics statementThe study was approval from the Institutional Research Ethics Committees of the third affiliated hospital of Sun Yat-sen university, and written informed consent was obtained from all patients. All animal procedures in this study were approved by the Animal Experimentation Ethics Committee of Lingnan Hospital, Sun Yat-sen University.Immunohistochemistry (IHC)The slides were deparaffinized through xylenes and graded ethyl alcohols and then rinsed in water, followed by quenching of Docosahexaenoyl ethanolamide supplier endogenous peroxidase activity by a 0.3 solution of hydrogen peroxidase in methanol for 30 min. Antigen retrieval was performed by microwave-heating in sodium citrate buffer (10 mM, pH 6.0). Sections were blocked with 1 normal serum in PBS for 1h and then incubated with anti-bKlotho antibody (Abcam, Cambridge, 18325633 MA) overnight at 4uC. Bound anti-body was detected by the avidin-biotin-peroxidase complex method, using the Elite ABC kit (Vector Laboratories, Burlingame, CA) as recommended by the manufacturer.Tissues SamplesSamples of tumor and adjacent non-tumorous liver tissues were obtained from patients who had undergone primary HCC curative hepatic resection at the third affiliated hospital of Sun Yat-sen university, Guangzhou, China. Immediately after resection, all tissues were snap-frozen in liquid nitrogen and stored at 80uC.Figure 1. Decreased expression of bKlotho in HCC tissue and hepatoma cell lines. (A) Immunohistochemical analysis of bKlotho protein expression in non-tumor liver samples and HCC samples. Representative photographs were taken at 6200 or 61000 magnifications. (B) Statistical quantification of relative MOD of bKlotho staining in non-tumor liver samples and HCC samples (47 cases). (C) Western blot analysis and (D) statistical quantification of bKlotho expression in hepatoma cell lines (HepG2, Hep3B, SMMC-7721 and Huh 7) and nor.Ion of cyclin D1 have a critical role in cell cycle and HCC. In the present study, we examined the role of bKlotho in hepatocarcinogenesis. Our data showed that bKlotho expression was frequently decreased in primary HCC tissues and was also^2Klotho Suppresses Tumor Growth in HCC Isignificantly down-regulated in HCC cell lines. Furthermore, overexpression of bKlotho into hepatoma cells inhibited their proliferation. The anti-proliferative effect of bKlotho might be linked with G1to S phase arrest, which was mediated by the Akt/ GSK-3b/cyclin D1 pathway. Finally, reintroduction of bKlotho could suppress tumorigenesis in the xenograft mouse model and this effects could be aborted by Akt activity. These findings suggest bKlotho suppresses tumor growth in HCC.Cell lines, Constructs and TransfectionHuman hepatocyte cells (L02) and human hepatoma cell lines (HepG2, Hep3B) were cultured as reported [22]. The other two human hepatoma cell lines, SMMC-7721 and Huh 7, were reported previously [23]. The human bKlotho gene was cloned from L02 cells and using the following primers: forward, 59AATTGCGGCCGCATGAAGCCAGGCTGTGC-39; reverse, 59-AATTGGATCCTTAGCTAACAACTCTCTTGCCTT-39. The resulting bKlotho PCR product was digested with NotI and BamHI and ligated into p36FLAG-CMV-7.1 expression vector (Sigma-Aldrich, St. Louis, MO) to obtain the bKlotho expression vector. Constitutively activated myristoylated-Akt (myr-Akt) cDNA expression vector was purchased from Upstate (Charlottesville, VA). All transfections used Lipofectamine 2000 (Invitrogen, Carlsbad, CA) according to the manufacturer’s protocol.Materials and Methods Ethics statementThe study was approval from the Institutional Research Ethics Committees of the third affiliated hospital of Sun Yat-sen university, and written informed consent was obtained from all patients. All animal procedures in this study were approved by the Animal Experimentation Ethics Committee of Lingnan Hospital, Sun Yat-sen University.Immunohistochemistry (IHC)The slides were deparaffinized through xylenes and graded ethyl alcohols and then rinsed in water, followed by quenching of endogenous peroxidase activity by a 0.3 solution of hydrogen peroxidase in methanol for 30 min. Antigen retrieval was performed by microwave-heating in sodium citrate buffer (10 mM, pH 6.0). Sections were blocked with 1 normal serum in PBS for 1h and then incubated with anti-bKlotho antibody (Abcam, Cambridge, 18325633 MA) overnight at 4uC. Bound anti-body was detected by the avidin-biotin-peroxidase complex method, using the Elite ABC kit (Vector Laboratories, Burlingame, CA) as recommended by the manufacturer.Tissues SamplesSamples of tumor and adjacent non-tumorous liver tissues were obtained from patients who had undergone primary HCC curative hepatic resection at the third affiliated hospital of Sun Yat-sen university, Guangzhou, China. Immediately after resection, all tissues were snap-frozen in liquid nitrogen and stored at 80uC.Figure 1. Decreased expression of bKlotho in HCC tissue and hepatoma cell lines. (A) Immunohistochemical analysis of bKlotho protein expression in non-tumor liver samples and HCC samples. Representative photographs were taken at 6200 or 61000 magnifications. (B) Statistical quantification of relative MOD of bKlotho staining in non-tumor liver samples and HCC samples (47 cases). (C) Western blot analysis and (D) statistical quantification of bKlotho expression in hepatoma cell lines (HepG2, Hep3B, SMMC-7721 and Huh 7) and nor.
