- Research article
- Open Access
- Open Peer Review
Leptin as a critical regulator of hepatocellular carcinoma development through modulation of human telomerase reverse transcriptase
© Stefanou et al; licensee BioMed Central Ltd. 2010
- Received: 4 November 2009
- Accepted: 19 August 2010
- Published: 19 August 2010
Numerous epidemiological studies have documented that obesity is associated with hepatocellular carcinoma (HCC). The aim of this study was to investigate the biological actions regulated by leptin, the obesity biomarker molecule, and its receptors in HCC and the correlation between leptin and human telomerase reverse transcriptase (hTERT), a known mediator of cellular immortalization.
We investigated the relationship between leptin, leptin receptors and hTERT mRNA expression in HCC and healthy liver tissue samples. In HepG2 cells, chromatin immunoprecipitation assay was used to study signal transducer and activator of transcription-3 (STAT3) and myc/mad/max transcription factors downstream of leptin which could be responsible for hTERT regulation. Flow cytometry was used for evaluation of cell cycle modifications and MMP1, 9 and 13 expression after treatment of HepG2 cells with leptin. Blocking of leptin's expression was achieved using siRNA against leptin and transfection with liposomes.
We showed, for the first time, that leptin's expression is highly correlated with hTERT expression levels in HCC liver tissues. We also demonstrated in HepG2 cells that leptin-induced up-regulation of hTERT and TA was mediated through binding of STAT3 and Myc/Max/Mad network proteins on hTERT promoter. We also found that leptin could affect hepatocellular carcinoma progression and invasion through its interaction with cytokines and matrix mettaloproteinases (MMPs) in the tumorigenic microenvironment. Furthermore, we showed that histone modification contributes to leptin's gene regulation in HCC.
We propose that leptin is a key regulator of the malignant properties of hepatocellular carcinoma cells through modulation of hTERT, a critical player of oncogenesis.
- HepG2 Cell
- hTERT mRNA
- hTERT Promoter
- hTERT Expression
- STAT3 Binding Site
Obesity is an important risk factor for many types of cancer, including hepatocellular carcinoma (HCC) [1, 2]. Among adipocytokines, that are the main body weight regulators, leptin, the 16-KDa nonglycosylated protein product of the Ob gene, has a central role [3, 4]. It is a multifunctional peptide hormone with a wide range of biological activities including neuroendocrine function , angiogenesis [6, 7], bone formation  and modulation of immune responses [9, 10]. Leptin exerts its actions through its six isoforms of receptors, which are membrane spanning glycoproteins with cytoplasmic domains of varying length .
Leptin's signaling is thought to be transmitted mainly by the Janus-activated Kinase/signal transducers and activators of transcription (JAK/STAT) pathway . Of the seven human STAT genes, STAT3 has been shown to be activated in a wide variety of human tumors and tumor cell lines and its activation is accompanied by increased expression of important cell cycle and survival regulators, such as cyclin D1, c-myc and survivin [13, 14]. Many STAT3 target genes are key components of the regulation of cell cycle progression from G1 to S phase .
At present, a biological explanation for the association between obesity and HCC is not known. It seems that there is a strong relationship between adipocytokines, such as leptin, and HCC but the molecular mechanisms have not been clarified yet. Hepatocarcinogenesis is a multi-step process involving different genetic alterations that ultimately lead to malignant transformation of the hepatocyte [16, 17]. One of the molecular events that underlie the multigenetic process of hepatocarcinogenesis is activation of human telomerase reverse transcriptase (hTERT)/telomerase which is normally suppressed in most human somatic tissues after birth [18, 19].
In the present study we investigated, for the first time, the relationship between leptin, leptin receptors and hTERT mRNA expression in HCC. We also attempted to elucidate on the molecular pathways that may mediate this interaction by investigating the regulation of hTERT gene promoter by histone acetylation status as well as STAT3 and c-myc transcription factors. Finally, the biological effects of leptin in HCC progression through inflammatory cytokines such as IL-1, IL-6, TGF and MMPs were assessed.
The study protocol conformed to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in a priori approval by the local Ethical Committee of the University Hospital of Larissa and by the Institutional Review Board (Institute of Medical Science, University of Tokyo). Specifically, control liver tissue specimens were obtained after oral informed consent from 23 patients (eleven male, twelve female; mean age 54.9 years, range 37-84 years) during an operation that was performed for cholelithiasis (cholecystectomy). All these individuals had apparently no evidence of chronic liver disease and normal ALT (alanine aminotransferase) values (26.6 ± 4.9 U/L), tested negative for HBsAg, anti-HCV and anti-HIV antibodies and denied ever having used hepatotoxic drugs, herbals, or having abused alcohol or injected drugs.
Twenty three liver tissue samples from HCC patients were used in this study, which were purchased from Biomax (US Biomax Inc, MD, USA) and were also provided from the University of Tokyo (thirteen male, ten female; mean age: 58.4 years; range: 45-75 years). Written informed consent was obtained from the patients. The diagnostic criteria for HCC were based on the conclusions of the Barcelona-2000 EASL conference while the histological diagnosis was made according to the AJCC/UICC classification system [20, 21]. From the 23 HCC tissue samples, 8 were due to HBV-related cirrhosis and 15 were due to HCV-related cirrhosis.
Cell cultures, reagents and treatments
HepG2 hepatocellular carcinoma cells were used and were cultured in RPMI 1640 medium (Gibco, Paisley, Scotland, UK) supplemented with 10% fetal bovine serum (Gibco, Paisley, Scotland, UK), L-Glutamine 2 mM (Gibco, Paisley, Scotland, UK), penicillin 100 IU/ml and streptomycin 100 μg/ml (Gibco, Paisley, Scotland, UK), at 37°C in 5% CO2. After 16 hours of serum starvation, the culture media were changed to serum free media containing leptin. Cultures were treated with human recombinant leptin at 25, 50, 100, 200 ng/ml (R&D Systems, Minneapolis, MN, USA). Cell culture supernates were removed, centrifuged and stored at -80°C until assayed. Leptin, TGF-b1, IL-6, IL-1b and IL-1a were measured using commercially available assays according to manufacturers' instructions (R&D Systems, Minneapolis, MN, USA).
RNA isolation and Real-time PCR
Immunohistochemistry for hTERT, leptin and OB-R
Immunohistochemical staining for hTERT and leptin expression was completed using antihuman hTERT antibody (PC563) (EMD Biosciences, Merck KGaA, Darmstadt, Germany), A20 leptin polyclonal Ab (pAb) (Santa Cruz Biotechnology, Santa Cruz, USA), or the M18 ObR pAb, (Santa Cruz Biotechnology) according to standard IHC procedures .
Cell viability was determined with the MTT assay using the TACS MTT kit (R&D Systems, Minneapolis, MN, USA) according to manufacturer's instructions. HepG2 proliferation was assessed in the presence of increasing concentrations of leptin (0-200 ng/ml) or in the absence of leptin (siRNA treatment against leptin). Cell proliferation was examined at 12h, 24h and 48h after addition of leptin.
TRAP (telomeric repeat protocol assay) assay was performed using the TeloTAGGG telomerase PCR ELISA PLUS kit (Roche, Indianapolis, IN, USA) as previously described .
Small interfering RNA treatment
HepG2 cells were transfected with dsRNA oligonucleotides for leptin using Lipofectamine 2000 reagent (Invitrogen, Carlsbad, CA). Different doses of siRNAs were administered at first for either 24, 48, 72 hours, in order to define the optimum dosage and time for a satisfying silencing, controlled by real time RT-PCR and ELISA (cell culture supernates). Negative controls (scrambled) were used in order to verify the absence of toxicity for the different doses administered.
Chromatin Immunoprecipitation was performed using a ChIP assay kit (Upstate USA, Inc., Charlottesville, VA, USA). The immunoprecipitated DNAs were amplified by PCR with the primers indicated below. For leptin promoter (proximal promoter, forward: 5'-CCCTCTAACCCTGGGCTTC-3'; reverse: 5'-ACTATGGCGCAAGGACCAG-3'), for hTERT promoter (set 1 for STAT3, forward: 5'-CCAAACCTGTGGACAGAACC-3'; reverse: 5'-AGACTGACTGCCTCCATCGT-3', set 2 for STAT3, forward: 5'- GGGGTGTCTTCTGGGTATCA-3'; reverse: 5'-AAGGGCTGTGTTTGTGAATTG-3', proximal hTERT promoter, forward: 5'- TGCCCCTTCACCTTCCAGCTC-3'; reverse: 5'- GTGGCCGGGGCCAGGGCTT-3').
Cell cycle distribution was determined by flow cytometry. At least 10.000 events were collected for each sample. Intracellular staining antibodies against MMP-1, MMP-9, proMMP-13 were used for cytometric analysis of HepG2 cells according to manufacturers instructions (R&D Systems, Minneapolis, MN, USA). Effect of leptin treatment (50, 200 ng/ml for 48 h and 100 ng/ml for 2 months) and leptin siRNA on MMP-1, MMP-9 and MMP-13 protein levels were evaluated.
Statistical analysis was performed as previously described .
Leptin, OB-Rl and OB-Rs expression in liver tissues of HCC patients
Correlation of leptin expression with hTERT expression
Interestingly, taking into account our previous findings in chronic viral hepatitis and HCC (altered leptin and hTERT mRNA levels in HCC or chronic viral hepatitis liver samples compared to healthy liver samples), we proceeded to determine whether there is an association between leptin and hTERT mRNA expression [22, 23]. We found a significant association between leptin and hTERT mRNA expression only in HCC livers (r = 0.79, p < 0.05).
Leptin affects hTERT expression levels and TA in HCC cells
The JAK/STAT3 pathway and the Myc/Max/Mad network are important for leptin-mediated up-regulation of hTERT expression
Leptin administration affects cell proliferation and modulates the cell cycle of HCC cells
Leptin could affect tumor progression and invasion dynamics in HCC
Histone H3 modifications contribute to leptin gene regulation in HCC cells
Numerous studies have established a relationship between obesity and various disease states including cancer. Obesity has been suggested as an important risk factor for both cirrhotic and non-cirrhotic hepatocellular carcinoma, which constitutes the third leading cause of cancer death worldwide [2, 26]. It has also been suggested that there is a strong link between leptin and cancer growth and development, with increasing evidence on the involvement of leptin on breast, ovarian, endometrial, colon, and prostate cancer [27–33]. Recently, high leptin and leptin receptor expression levels were correlated with the degree of angiogenesis in human HCC . In addition, leptin-mediated neovascularization showed an effective role of leptin in the development of hepatocarcinogenesis in non-alcoholic steatohepatitis . In the present study, in order to determine the contribution of the leptin system in HCC progression, we investigated the expression of leptin and its receptors in HCC and normal liver tissues. The observed absence of leptin expression in normal liver tissues and it's remarkable presence (78.2%) in HCC liver, accompanied by the elevated OB-Rl and OB-Rs mRNA expression levels in HCC, support the role of leptin system in the development of HCC [36, 37]. As the high expression of leptin and its receptors in HCC liver tissues was not found to be correlated with BMI we could assume that the production of leptin in HCC liver is not directly regulated by the adipose tissue deposit, but also reflects the intricate interactions taking place into the tumorigenic microenvironment.
It has previously been reported that hTERT mRNA overexpression and elevation of TA might be some of the processes involved in tumour initiation and progression in the liver [17, 23, 38]. Our results demonstrate, for the first time to our knowledge, a strong correlation between leptin expression and hTERT levels in HCC liver tissues. Moreover, we found that leptin was capable of a direct beneficent action upon hTERT mRNA and TA in HepG2 cells. The fact that leptin's knockdown by siRNA did not decrease hTERT mRNA levels and TA, suggests that the basal hTERT levels are not only under the control of the leptin system. These findings are in accordance with a very recent study by Ren et al. in MCF-7 cells and reveal that hTERT is probably a target gene for leptin and strengthen the role of leptin as a pivotal factor in HCC .
Previous studies have shown that STAT3 is a key mediator of critical cancer cell processes, as it promotes cell cycle progression and survival, stimulates angiogenesis and generally promotes malignant transformation [13, 14, 40, 41]. Very recently, hTERT has been identified as a direct downstream gene of STAT3 in both tumor and normal cells . Taking into account that STAT3 is downstream of leptin and upstream of hTERT, we investigated the hypothesis that the STAT3 signalling pathway plays a crucial role in leptin-mediated hTERT expression. Our findings showed a recruitment of STAT3 in two binding sites in hTERT promoter under leptin stimulation of HCC cells, supporting the key role of STAT3 signaling in leptin induced hTERT expression.
A number of interesting reports have proposed the identification of the Myc/Max/Mad network, as a molecular switch that either interacts with the core promoter to activate hTERT transcription (Myc/Max) or promotes down regulation of hTERT mRNA production (Mad/Max) [43–45]. In the present study we demonstrated, for the first time, an association between the switch from Mad1/Max to Myc/Max binding and activation of hTERT transcription after leptin treatment of HepG2 cells and additionally an expanded interaction of Myc/Max complex accompanied by an increase in H3 acetylation in hTERT proximal promoter after long term leptin treatment of HCC cells. As the long term leptin treatment of HepG2 cells did not extend further the mRNA production of hTERT and TA, we assume that leptin-mediated hTERT overexpression is also under the consistent control of post-transcriptional regulators.
HCC arises most frequently in the setting of chronic liver inflammation and moreover cytokines, such as IL-6, produced in the inflammatory tumor microenvironment stimulate the growth of cancer cells and tumor invasiveness . In the present study, we demonstrated the ability of leptin to increase IL-6 secretion in HCC cells, suggesting that an alternative indirect and independent of the OB-R presence mechanism might be involved in leptin-mediated hTERT expression through JAK/STAT3 pathway. Furthermore, the fact that leptin repressed the production of TGF-b1, a known negative regulator of hTERT  represents one more step towards the understanding of the molecular mechanism of leptin action in HCC and the proof of power of leptin-hTERT axis in the tumorigenic processes. To gain insight into the biological effects of leptin's action in the progression and invasion of HCC, we next examined leptin's effect in the production of MMP-1, -9, 13 by hepatocarcinoma cells. Many secreted MMPs are nearly absent in healthy, resting tissues, although they are deregulated in active tissues, as in liver fibrosis and tumor metastasis . In our study we observed, for the first time, that leptin is able to suppress MMP-1 expression and trigger MMP-9 and MMP-13 expression in HepG2 cells, and this could contribute to a more favourable environment for invasion and metastasis of HCC in the cirrhotic liver.
In order to elucidate the signalling cascades in liver cancer, the regulatory mechanisms of genes altered in HCC cells need to be determined. In our study, for the first time to our knowledge, we found that the amount of acetylated H3, in HCC cells, interacting with leptin proximal promoter was correlated with the regulation of leptin gene transcription. The importance of this finding lies in the fact that histone acetylation is reversible and thus may have therapeutic potential.
In conclusion, our data revealed, for the first time, that leptin up-regulates hTERT expression and TA and deciphered the molecular mechanisms responsible for their interaction in HCC, thus establishing a clearer view of leptin-mediated HCC cell proliferation and progression.
The authors would like to thank Dr. D. Zacharoulis from the Dept, of Surgery, University of Thessaly, for healthy liver tissue provision.
- Abu-Abid S, Szold A, Klausner J: Obesity and cancer. J Med. 2002, 33: 73-86.PubMedGoogle Scholar
- Nair S, Masson A, Eason J, Loss G, Perrillo RP: Is obesity an independent risk factor for hepatocellular carcinoma in cirrhosis?. Hepatology. 2002, 36: 150-155. 10.1053/jhep.2002.33713.View ArticlePubMedGoogle Scholar
- Morton GJ, Cummings DE, Baskin DG, Barsh GS, Schwartz MW: Central nervous system control of food intake and body weight. Nature. 2006, 443: 289-295. 10.1038/nature05026.View ArticlePubMedGoogle Scholar
- Friedman JM, Halaas JL: Leptin and the regulation of body weight in mammals. Nature. 1998, 395: 763-770. 10.1038/27376.View ArticlePubMedGoogle Scholar
- Huang L, Li C: Leptin: a multifunctional hormone. Cell Res. 2000, 10: 81-92. 10.1038/sj.cr.7290038.View ArticlePubMedGoogle Scholar
- Sierra-Honigmann MR, Nath AK, Murakami C, Garcia-Gardena G, Papapetropoulos A, Sessa WC, et al: Biological action of leptin as an angiogenic factor. Science. 1998, 281: 1683-1686. 10.1126/science.281.5383.1683.View ArticlePubMedGoogle Scholar
- Bouloumie A, Drexler HC, Lafontan M, Busse R: Leptin, the product of ob gene, promotes angiogenesis. Circ Res. 1998, 83: 1059-1066.View ArticlePubMedGoogle Scholar
- La Cava A, Matarese G: The weight of leptin in immunity. Nat Rev Immunol. 2004, 4 (5): 371-379. 10.1038/nri1350. ReviewView ArticlePubMedGoogle Scholar
- Otero M, Lago R, Lago F, Casanueva FF, Dieguez C, Gomez-Reino JJ, et al: Leptin, from fat to inflammation:old questions and new insights. FEBS Lett. 2005, 579: 295-301. 10.1016/j.febslet.2004.11.024.View ArticlePubMedGoogle Scholar
- Fantuzzi G: Adipose tissue, adipokines, and inflammation. J Allergy Clin Immunol. 2005, 115: 911-919. 10.1016/j.jaci.2005.02.023.View ArticlePubMedGoogle Scholar
- Margetic S, Garrela C, Pegg GG, Hill RA: Leptin: a review of its peripheral actions and interactions. Int J Obes. 2002, 26: 1407-1433. 10.1038/sj.ijo.0802142.View ArticleGoogle Scholar
- Ahima RS, Osei SY: Leptin signaling. Physiol Behav. 2004, 81: 223-241. 10.1016/j.physbeh.2004.02.014.View ArticlePubMedGoogle Scholar
- Bromberg J: STAT proteins and oncogenesis. J Clin Invest. 2002, 109: 1139-1142.View ArticlePubMedPubMed CentralGoogle Scholar
- Inghirami G, Chiarle R, Simmons JW, Piva R, Schlessinger K, Levy D: New and old functions of STAT3. A pivotal target for individualized treatment of cancer. Cell Cycle. 2005, 4 (9): 1131-1133. 10.4161/cc.4.9.1985.View ArticlePubMedGoogle Scholar
- Bowman T, Garcia R, Turkson J, Jove R: STATs in oncogenesis. Oncogene. 2000, 19: 2474-2488. 10.1038/sj.onc.1203527.View ArticlePubMedGoogle Scholar
- Caldwell SM, Crespo DM, Kang HS, Al-Osaimi AM: Obesity and hepatocellular carcinoma. Gastroenterology. 2004, 127: 97-103. 10.1053/j.gastro.2004.09.021.View ArticleGoogle Scholar
- Moradpour D, Blum HE: Pathogenesis of hepatocellular carcinoma. Eur J Gastroenterol Hepatol. 2005, 17: 477-483. 10.1097/00042737-200505000-00002.View ArticlePubMedGoogle Scholar
- Nakayama J, Tahara H, Tahara E, Saito M, Ito K, Nakamura H, et al: Telomerase activation by hTERT in human normal fibroblasts and hepatocellular carcinoma. Nat Genet. 1998, 18: 65-68. 10.1038/ng0198-65.View ArticlePubMedGoogle Scholar
- Shimojima M, Komine F, Hisatomi H, Shimiru T, Moriyama M, Arakawa Y: Detection of telomerase activity, telomerase RNA component, and telomerase reverse transcriptase in human hepatocellular carcinoma. Hepatol Res. 2004, 29: 31-38. 10.1016/j.hepres.2004.02.005.View ArticlePubMedGoogle Scholar
- Bruix J, Sherman M, Liovet JM, Beaugrand M, Lencioni R, Burroughs AK, et al: Clinical management of hepatocellular carcinoma. Conclusions of the Barcelona-2000 EASL Conference. J Hepatol. 2001, 35: 421-430. 10.1016/S0168-8278(01)00130-1.View ArticlePubMedGoogle Scholar
- Green FL, Page DL, Fleming ID, Fruitz A, Balch CM, Haller DG, et al: American Joint Committee on Cancer. Liver (including intrahepatic bile ducts). AJCC cancer Staging Handbook. 2002, New York, NY: Springer, 6View ArticleGoogle Scholar
- Stefanou N, Satra M, Papanikolaou V, Kalala F, Gatselis N, Germenis A, et al: Leptin receptor isoforms mRNA expression in peripheral blood mononuclear cells from patients with chronic viral hepatitis. Exp Biol Med. 2006, 231: 1653-1663.Google Scholar
- Satra M, Gatselis N, Iliopoulos D, Zacharoulis D, Dalekos GN, Tsezou A: Real time quantification of human telomerase reverse transcriptase mRNA in liver tissues from patients with hepatocellular cancer and chronic viral hepatitis. Journal of Viral Hepatitis. 2007, 14: 41-47. 10.1111/j.1365-2893.2006.00769.x.View ArticlePubMedGoogle Scholar
- Fiorio E, Mercanti A, Terrasi M, Micciolo R, Remo A, Auriemma A, et al: Leptin/HER2 crosstalk in breast cancer: in vitro study and preliminary in vivo analysis. BMC Cancer. 2008, 8: 305-10.1186/1471-2407-8-305.View ArticlePubMedPubMed CentralGoogle Scholar
- Tsezou A, Oikonomou P, Kollia P, Mademtzis I, Kostopoulou E, Messinis I, et al: The role of human telomerase catalytic subunit mRNA expression in cervical dysplasias. Exp Biol Med. 2005, 230: 263-270.Google Scholar
- Petridou E, Belechri M, Dessypris N, Koukoulomatis P, Diakopoulos E, Spanos E, et al: Leptin and body mass index in relation to hepatocellular carcinoma risk. Ann Nutr Metab. 2002, 46: 147-151. 10.1159/000063081.View ArticlePubMedGoogle Scholar
- Saxena N, Vertino P, Anania F, Sharma D: Leptin-induced growth stimulation of breast cancer cells involves recruitment of histone acetyltransferases and mediator complex to cyclin D1 promoter via activation of STAT3. J Biol Chem. 2007, 282: 13316-13325. 10.1074/jbc.M609798200.View ArticlePubMedPubMed CentralGoogle Scholar
- Yin N, Wang D, Zhang H, Yi X, Sun X, Shi B, et al: Molecular mechanisms involved in the growth stimulation of breast cancer cells by leptin. Cancer Res. 2004, 64 (16): 5870-5875. 10.1158/0008-5472.CAN-04-0655.View ArticlePubMedGoogle Scholar
- Choi JH, Park SH, Leung PC, Choi KC: Expression of leptin receptors and potential effects of leptin on the cell growth and activation of mitogen-activated protein kinases in ovarian cancer cells. J Clin Endocrinol Metab. 2004, 90: 207-210. 10.1210/jc.2004-0297.View ArticlePubMedGoogle Scholar
- Yuan SS, Tsai KB, Chung YF, Chan TF, Yeh YT, Tsai LY, et al: Aberrant expression and possible involvement of leptin receptor in endometrial cancer. Gynecol Oncol. 2004, 92 (3): 769-775. 10.1016/j.ygyno.2003.11.043.View ArticlePubMedGoogle Scholar
- Somansudar P, Frankenberry KA, Skinner H, Vedula G, McFadden DW, Riggs D, et al: Prostate cancer cell proliferation is influenced by leptin. J Surg Res. 2004, 118: 71-82. 10.1016/j.jss.2004.01.017.View ArticleGoogle Scholar
- Garofalo C, Surmacz E: Leptin and cancer. J Cell Physiol. 2006, 207: 12-22. 10.1002/jcp.20472.View ArticlePubMedGoogle Scholar
- Birmingham JM, Busik JV, Hansen-Smith FM, Fenton JI: Novel mechanism for obesity-induced colon cancer progression. Carcinogenesis. 2009, 30 (4): 690-697. 10.1093/carcin/bgp041.View ArticlePubMedPubMed CentralGoogle Scholar
- Ribatti D, Belloni AS, Nico B, Di Comite M, Crivellato E, Vacca A: Leptin-leptin receptor are involved in angiogenesis in human hepatocellular carcinoma. Peptides. 2008, 29 (9): 1596-1602. 10.1016/j.peptides.2008.05.011.View ArticlePubMedGoogle Scholar
- Kitade M, Yoshiji H, Kojima H, Ikenaka Y, Noquchi R, Kaji K, et al: Leptin mediated neovascularization is a prerequisite for progression of non-alcoholic steatohepatitis in rats. Hepatology. 2006, 44: 983-991. 10.1002/hep.21338.View ArticlePubMedGoogle Scholar
- Wang SN, Chuang YT, Yang SF, Chai CY, Chen WT, Kuo KK, et al: Potential prognostic value of leptin receptor in hepatocellular carcinoma. J Clin Pathol. 2006, 59: 1267-1271. 10.1136/jcp.2005.033464.View ArticlePubMedPubMed CentralGoogle Scholar
- Wang SN, Yeh YT, Yang SF, Chai CY, Lee KT: Potential role of leptin expression in hepatocellular carcinoma. J Clin Pathol. 2006, 59 (9): 930-934. 10.1136/jcp.2005.035477.View ArticlePubMedPubMed CentralGoogle Scholar
- Lee CM, Hsu CY, Eng HL, Huang WS, Lu SN, Changchien CS, et al: Telomerase activity and telomerase catalytic subunit in hepatocellular carcinoma. Hepatogastroenterology. 2004, 51: 796-800.PubMedGoogle Scholar
- Ren H, Zhao T, Wang X, Gao Ch, Wang J, Yu M, et al: Leptin upregulates telomerase activity and transcription of human telomerase reverse transcriptase in MCF-7 breast cancer cells. Biochem Bioph Res Co. 2010, 394: 59-63. 10.1016/j.bbrc.2010.02.093.View ArticleGoogle Scholar
- Konnikova L, Kruger MM, Kotecki M, Cochran BH: Knockdown of STAT3 expression by RNAi induces apoptosis in astrocytoma cells. BMC Cancer. 2003, 3: 23-10.1186/1471-2407-3-23.View ArticlePubMedPubMed CentralGoogle Scholar
- Niu G, Wright KL, Huang M, Song L, Haura E, Turkson J, et al: Constitutive Stat3 activity up-regulates VEGF expression and tumor angiogenesis. Oncogene. 2002, 21: 2000-2008. 10.1038/sj.onc.1205260.View ArticlePubMedGoogle Scholar
- Konnikova L, Simeone MC, Kruger MM, Kotecki M, Cochran BH: Signal transducer and activator of transcription 3 (STAT3) regulates human telomerase reverse transcriptase (hTERT) expression in human cancer and primary cells. Cancer Res. 2005, 65 (15): 6516-6520. 10.1158/0008-5472.CAN-05-0924.View ArticlePubMedGoogle Scholar
- Liu L, Lai S, Andrews LG, Tollefsbol TO: Genetic and epigenetic modulation of telomerase activity in development and disease. Gene. 2004, 340: 1-10. 10.1016/j.gene.2004.06.011.View ArticlePubMedGoogle Scholar
- Atkinson SP, Hoare SP, Glasspool RM, Keith NW: Lack of telomerase gene expression in alternative lengthening of telomere cells is associated with chromatin remodelling of the hTR and hTERT gene promoters. Cancer Res. 2005, 65 (17): 7585-7590.PubMedGoogle Scholar
- Iliopoulos D, Satra M, Drakaki A, Poultsides GA, Tsezou A: Epigenetic regulation of hTERT promoter in hepatocellular carcinomas. International Journal of Oncology. 2009, 34: 391-399.PubMedGoogle Scholar
- Lawrence T, Hagemann T, Balkwill F: Sex, cytokines, and cancer. Science. 2007, 317: 51-52. 10.1126/science.1146052.View ArticlePubMedGoogle Scholar
- Li H, Liu JP: Mechanisms of action of TGF-beta in cancer: evidence for Smad3 as a repressor for the hTERT gene. Ann N Y Acad Sci. 2007, 1114: 56-68. 10.1196/annals.1396.016.View ArticlePubMedGoogle Scholar
- Ishii Y, Nakasato Y, Kobayashi S, Yamazaki Y, Aoki T: A study on angiogenesis-related matrix metalloproteinase networks in primary hepatocellular carcinoma. J Exp Clin Cancer Res. 2003, 22: 461-470.PubMedGoogle Scholar
- The pre-publication history for this paper can be accessed here:http://0-www.biomedcentral.com.brum.beds.ac.uk/1471-2407/10/442/prepub
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