Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 20 de 32
Filter
1.
Curr Mol Pharmacol ; 11(4): 316-325, 2018.
Article in English | MEDLINE | ID: mdl-30101722

ABSTRACT

OBJECTIVE: To explore the mechanism by which lobaplatin, as monotherapy and in combination with paclitaxel, inhibits the proliferation of human gastric cancer SGC-7901 cells. METHODS: After treatment, the MTT assay was used to assess cell viability; cell cycle distribution was evaluated flow-cytometrically. Western blot was used to quantitate cyclin D1, E1, B1, and Cdk2/4 protein levels. RESULTS: Lobaplatin and paclitaxel inhibited SGC-7901 cell growth in a concentration and timedependent manner, with IC25 values at 48h of 1.97±0.17µg/ml and 1.98±0.19 ng/ml, respectively. Interestingly, both drugs synergistically inhibited SGC-7901 cells (combination index [CI]<0.95). Lobaplatin did not affect cyclin D1 and CDK4 protein expression, while cyclin E1 and CDK2 levels were significantly increased, with cyclin B1 amounts markedly decreased (p<0.05). More S phase cells were observed after lobaplatin treatment compared with controls (60.03±1.25 vs. 18.69±0.96%; p<0.05). After treatment with paclitaxel, cyclin D1 and CDK4 protein levels were similar to control values; meanwhile, cylinE1 and CDK2 protein amounts were reduced, with increased cyclin B1 levels, compared with control values (p<0.05). More G2/M cells were obtained after treatment with paclitaxel compared with control values (74.54±0.92 vs. 18.62±0.44% (p<0.05). Lobaplatin and paclitaxel combination did not affect cyclin D1 and CDK4 protein levels (p>0.05); meanwhile, cyclin E1 and CDK2 levels were increased, with reduced cyclin B1 amounts, compared with control values (p<0.05). Notably, more S (43.23±0.81 vs. 22.32±0.86%) and G2/M (31.22±0.96 vs. 25.81±2.08%) phase cells were obtained after combined treatment compared with control values. CONCLUSION: Lobaplatin and paclitaxel synergistically inhibit SGC-7901 cells.


Subject(s)
Antineoplastic Agents/pharmacology , Cell Cycle/drug effects , Cell Proliferation/drug effects , Cyclobutanes/pharmacology , Organoplatinum Compounds/pharmacology , Paclitaxel/pharmacology , Stomach Neoplasms/drug therapy , Antineoplastic Agents/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/administration & dosage , Antineoplastic Combined Chemotherapy Protocols/pharmacology , Cell Line, Tumor , Cyclin B1/analysis , Cyclin B1/metabolism , Cyclin E/analysis , Cyclin E/metabolism , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 2/metabolism , Cyclobutanes/administration & dosage , Humans , Oncogene Proteins/analysis , Oncogene Proteins/metabolism , Organoplatinum Compounds/administration & dosage , Paclitaxel/administration & dosage , Stomach Neoplasms/metabolism , Stomach Neoplasms/pathology
2.
Am J Pathol ; 186(7): 1900-1912, 2016 07.
Article in English | MEDLINE | ID: mdl-27182644

ABSTRACT

Cyclin E and its co-activator, phospho-cyclin-dependent kinase 2 (p-CDK2), regulate G1 to S phase transition and their deregulation induces oncogenesis. Immunohistochemical assessments of these proteins in cancer have been reported but were based only on their nuclear expression. However, the oncogenic forms of cyclin E (low molecular weight cyclin E or LMW-E) in complex with CDK2 are preferentially mislocalized to the cytoplasm. Here, we used separate nuclear and cytoplasmic scoring systems for both cyclin E and p-CDK2 expression to demonstrate altered cellular accumulation of these proteins using immunohistochemical analysis. We examined the specificity of different cyclin E antibodies and evaluated their concordance between immunohistochemical and Western blot analyses in a panel of 14 breast cell lines. Nuclear versus cytoplasmic staining of cyclin E readily differentiated full-length from LMW-E, respectively. We also evaluated the expression of cyclin E and p-CDK2 in 1676 breast carcinoma patients by immunohistochemistry. Cytoplasmic cyclin E correlated strongly with cytoplasmic p-CDK2 (P < 0.0001), high tumor grade, negative estrogen/progesterone receptor status, and human epidermal growth factor receptor 2 positivity (all P < 0.0001). In multivariable analysis, cytoplasmic cyclin E plus phosphorylated CDK2 (as one variable) predicted breast cancer recurrence-free and overall survival. These results suggest that cytoplasmic cyclin E and p-CDK2 can be readily detected with immunohistochemistry and used as clinical biomarkers for aggressive breast cancer.


Subject(s)
Biomarkers, Tumor/analysis , Breast Neoplasms/pathology , Cyclin E/analysis , Cyclin-Dependent Kinase 2/analysis , Adult , Aged , Aged, 80 and over , Animals , Blotting, Western , Cell Line, Tumor , Cell Nucleus/chemistry , Cell Nucleus/metabolism , Cytoplasm/chemistry , Cytoplasm/metabolism , Female , Humans , Immunohistochemistry , Mice , Mice, Transgenic , Middle Aged , Tissue Array Analysis
3.
Zhongguo Zhong Yao Za Zhi ; 40(11): 2186-90, 2015 Jun.
Article in Chinese | MEDLINE | ID: mdl-26552178

ABSTRACT

OBJECTIVE: To study the proliferation and apoptosis of tetramethylpyrazine (TMP) on leukemic U937 cells and its possible mechanism. METHOD: The inhibitory effect of TMP on the proliferation of U937 cells was detected by CCK-8 assay. The cell apoptosis and cycle distribution were examined by the flow cytometry. The mRNA expressions of bcl-2 and P27 were determined by the Real-time PCR. Western blot was carried out to detect bcl-2, caspase-3, cyclin E1, CDK2 and P27 expressions. RESULT: TMP inhibited the proliferation of U937 cells in a dose-and-time dependent manner, with IC50 value of 160 mg x L(-1) at 48 h. In addition, TMP could induce the apoptosis of U937 cells and block the cell cycle in G0/G1 phase. According to the results of Real-time PCR and Western blot, TMP could down-regulate the expression of apoptosis-related molecule bcl-2, cycle-related protein cyclin E1 and CDK2 and up-regulate caspase-3 and P27. CONCLUSION: TMP shows the effects in inhibiting the proliferation of leukemic U937 cells and inducing the apoptosis. Its mechanism may be related to the impacts on the cell cycle distribution, down-regulation of the bcl-2 expression, which finally activates caspase-3, starts the apoptosis path and causes the cell apoptosis.


Subject(s)
Apoptosis/drug effects , Cell Proliferation/drug effects , Leukemia/drug therapy , Pyrazines/pharmacology , Cell Cycle/drug effects , Cyclin-Dependent Kinase 2/analysis , Humans , Proto-Oncogene Proteins c-bcl-2/analysis , Pyrazines/therapeutic use , U937 Cells
4.
Ann Surg Oncol ; 21 Suppl 4: S711-20, 2014 Dec.
Article in English | MEDLINE | ID: mdl-24889487

ABSTRACT

BACKGROUND: Attenuated endogenous protein levels of cyclin-dependent kinase 2 associated protein 1 (p12(CDK2AP1)) and its active homodimer p25(CDK2AP1) were found in myxofibrosarcoma-derived cell lines. Clinical and biological significances of this putative tumor suppressor in myxofibrosarcoma were studied. METHODS: Plasmids carrying the CDK2AP1 gene and small hairpin RNA interference (shRNAi) targeting CDK2AP1 were transfected into NMFH-1 and/or OH931 cells to evaluate the effects on the CDK2, active caspase 3 (CASP3), cleaved-CASP8 and -CASP9 levels, cell cycle regulation, and/or apoptotic responses. Immunostaining of p12(CDK2AP1) was interpretable in 102 primary myxofibrosarcomas and correlated with clinicopathological variables, CDK2, Ki-67 and active CASP3 protein levels, and disease-specific survival. RESULTS: Exogenous expression of p12(CDK2AP1) in NMFH-1 and OH931 cells significantly induced G0/G1 cell cycle arrest and down-regulated CDK2 protein level. In NMFH-1 cells, these aspects were reversed by shRNAi targeting CDK2AP1 gene. Increased active CASP3 and cleaved-CASP9, but not -CASP8, were detected after CDK2AP1 overexpression, suggesting the cellular apoptosis were induced through the mitochondrial pathway. Immunostains of p12(CDK2AP1) were aberrantly decreased in 56.9 % of cases; positively and negatively correlated with protein levels of CDK2 (p = 0.023), Ki-67 (p = 0.001) and active CASP3 (p < 0.001), respectively. Following by high histological grades, p12(CDK2AP1) down-regulation was predictive of worse disease-specific survival in univariate (p = 0.003) and multivariate (p = 0.004) analyses. CONCLUSIONS: Through down-regulation of CDK2, high p12(CDK2AP1) level induced cell cycle arrest and the mitochondrial-dependent apoptotic pathway. Low p12(CDK2AP1) level represents a poor prognostic factor in patients with myxofibrosarcoma.


Subject(s)
Fibrosarcoma/enzymology , Fibrosarcoma/genetics , Mitochondria/metabolism , Myxosarcoma/enzymology , Myxosarcoma/genetics , Tumor Suppressor Proteins/genetics , Apoptosis/genetics , Caspase 3/analysis , Caspase 3/metabolism , Caspase 8/metabolism , Caspase 9/metabolism , Cell Cycle Checkpoints/genetics , Cell Line, Tumor , Cell Survival , Chromobox Protein Homolog 5 , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 2/metabolism , Female , Fibrosarcoma/chemistry , Humans , Ki-67 Antigen/analysis , Male , Middle Aged , Mitotic Index , Myxosarcoma/chemistry , Plasmids , RNA, Messenger/metabolism , RNA, Small Interfering/genetics , Survival Rate , Transfection
5.
J Laryngol Otol ; 128(2): 134-41, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24460960

ABSTRACT

OBJECTIVE: The protein 14-3-3 sigma plays a role in cell cycle arrest by sequestering cyclin-dependent kinase 1 cyclin B1 complexes, as well as cyclin-dependent kinases 2 and 4, hence its definition as a cyclin-dependent kinase inhibitor. However, the nature of the interaction between these biological markers in nasopharyngeal carcinoma is unknown. This study aimed to investigate whether altered expression of these markers contributes to nasopharyngeal carcinogenesis. METHODS: The study population consisted of 30 nasopharyngeal carcinoma patients and 10 patients without nasopharyngeal carcinoma. The nasopharyngeal carcinoma cell lines TW02, TW04 and Hone-1 were also assessed. We analysed levels of messenger RNA and protein for the p16 gene and the 14-3-3 sigma, Epstein-Barr nuclear antigen 1, and cyclin-dependent kinase 2 and 4 proteins, in nasopharyngeal carcinoma tissue specimens and cell lines and in normal nasopharyngeal tissue. RESULTS: Protein and messenger RNA levels for cyclin-dependent kinase 2 and Epstein-Barr nuclear antigen 1 were significantly higher in nasopharyngeal carcinoma compared with normal tissue, while levels of cyclin-dependent kinase 4 generally were not; results for 14-3-3 sigma varied. Nasopharyngeal carcinoma patients had diminished p16 gene expression, compared with normal tissue. CONCLUSION: Levels of cyclin-dependent kinase 2 and Epstein-Barr nuclear antigen 1 were significantly higher in nasopharyngeal carcinoma than in normal tissue, while p16 gene expression was diminished. These three proteins may contribute to nasopharyngeal carcinogenesis.


Subject(s)
14-3-3 Proteins/analysis , Biomarkers, Tumor/analysis , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 4/analysis , Epstein-Barr Virus Nuclear Antigens/analysis , Exoribonucleases/analysis , Nasopharyngeal Neoplasms/chemistry , Neoplasm Proteins/analysis , Adult , Aged , Carcinoma , Case-Control Studies , Cell Line, Tumor/chemistry , Cyclin-Dependent Kinase Inhibitor p16 , Female , Humans , Male , Middle Aged , Nasopharyngeal Carcinoma , Nasopharynx/chemistry , Young Adult
6.
Leukemia ; 28(4): 894-903, 2014 Apr.
Article in English | MEDLINE | ID: mdl-23925045

ABSTRACT

Multiple myeloma is a hematological cancer of plasma B cells and remains incurable. Two major subtypes of myeloma, hyperdiploid MM (HMM) and non-hyperdiploid MM (NHMM), have distinct chromosomal alterations and different survival outcomes. Transcription factors (TrFs) have been implicated in myeloma oncogenesis, but their dysregulation in myeloma subtypes are less studied. Here, we developed a TrF-pathway coexpression analysis to identify altered coexpression between two sample types. We apply the method to the two myeloma subtypes and the cell cycle arrest pathway, which is significantly differentially expressed between the two subtypes. We find that TrFs MYC, nuclear factor-κB and HOXA9 have significantly lower coexpression with cell cycle arrest in HMM, co-occurring with their overactivation in HMM. In contrast, TrFs ESR1 (estrogen receptor 1), SP1 and E2F1 have significantly lower coexpression with cell cycle arrest in NHMM. SP1 chromatin immunoprecipitation targets are enriched by cell cycle arrest genes. These results motivate a cooperation model of ESR1 and SP1 in regulating cell cycle arrest, and a hypothesis that their overactivation in NHMM disrupts proper regulation of cell cycle arrest. Cotargeting ESR1 and SP1 shows a synergistic effect on inhibiting myeloma proliferation in NHMM cell lines. Therefore, studying TrF-pathway coexpression dysregulation in human cancers facilitates forming novel hypotheses toward clinical utility.


Subject(s)
Cell Cycle Checkpoints , Estrogen Receptor alpha/physiology , Multiple Myeloma/pathology , Sp1 Transcription Factor/physiology , Bayes Theorem , Cyclin-Dependent Kinase 2/analysis , E2F1 Transcription Factor/physiology , Homeodomain Proteins/physiology , Humans , Interleukin-6/physiology , MAP Kinase Signaling System , Sp1 Transcription Factor/analysis , Transcription Factors/physiology
7.
Tumour Biol ; 35(4): 3355-62, 2014 Apr.
Article in English | MEDLINE | ID: mdl-24297335

ABSTRACT

This study aimed to analyze the expression, clinical significance of cyclin G2 (CCNG2) in esophageal carcinoma, and the biological effect in its cell line by CCNG2 overexpression. Immunohistochemistry and western blot were used to analyze CCNG2 protein expression in 73 cases of esophageal cancer and normal tissues to study the relationship between CCNG2 expression and clinical factors. CCNG2 lentiviral vector and empty vector were respectively transfected into esophageal cancer Eca-109 cell line. Reverse transcription-polymerase chain reaction and western blot were used to detect the mRNA level and protein of CCNG2. MTT assay and cell cycle were also conducted as to the influence of the upregulated expression of CCNG2 that might be found on Eca-109 cell's biological effect. Immunohistochemistry: The level of CCNG2 protein expression was found to be significantly lower in esophageal cancer tissue than normal tissues (P < 0.05). Western blot: The relative amount of CCNG2 protein in esophageal cancer tissue was respectively found to be significantly lower than in normal tissues (P < 0.05). The level of CCNG2 protein expression was not correlated with gender, age, and tumor size (P > 0.05), but it was correlated with lymph node metastasis, clinic stage, and histological grades (P < 0.05). Loss of CCNG2 expression correlated significantly with poor overall survival time by Kaplan-Meier analysis. The result of the biological function showed that Eca-109 cell-transfected CCNG2 had a lower survival fraction, more percentage of the G0/G1 phases (P < 0.05), and lower cyclin-dependent kinase 2 (CDK2) protein expression. CCNG2 expression decreased in esophageal cancer and correlated significantly with lymph node metastasis, clinic stage, histological grade, and poor overall survival, suggesting that CCNG2 may play important roles as a negative regulator to esophageal cancer cell by promoting degradation of CDK2.


Subject(s)
Cyclin G2/physiology , Esophageal Neoplasms/pathology , Adult , Aged , Cyclin G2/analysis , Cyclin G2/genetics , Cyclin-Dependent Kinase 2/analysis , Esophageal Neoplasms/chemistry , Esophageal Neoplasms/mortality , Esophagus/chemistry , Female , Humans , Lymphatic Metastasis , Male , Middle Aged , Neoplasm Staging , Prognosis
8.
Mol Carcinog ; 50(2): 100-12, 2011 Feb.
Article in English | MEDLINE | ID: mdl-21229607

ABSTRACT

3,3'-Diindolylmethane (DIM) is a major in vivo derivative of indole-3-carbinol, which is present in cruciferous vegetables and has been reported to possess anti-carcinogenic properties. In the present study, we examined whether DIM inhibits the development of prostate cancer using the transgenic adenocarcinoma mouse prostate (TRAMP) model. DIM feeding inhibited prostate carcinogenesis in TRAMP mice, reduced the number of cells expressing the SV40 large tumor antigen and proliferating cell nuclear antigen, and increased the number of terminal dUTP nick-end labeling-positive cells in the dorsolateral lobes of the prostate. Additionally, DIM feeding reduced the expression of cyclin A, cyclin-dependent kinase (CDK)2, CDK4, and Bcl-xL, and increased p27 and Bax expression. To assess the mechanisms by which DIM induces apoptosis, LNCaP and DU145 human prostate cancer cells were cultured with various concentrations of DIM. DIM induced a substantial reduction in the numbers of viable cells and induced apoptosis in LNCaP and DU145 cells. DIM increased the cleavage of caspase-9, -7, -3, and poly (ADP-ribose) polymerase (PARP). DIM increased mitochondrial membrane permeability and the translocation of cytochrome c and Smac/Diablo from the mitochondria. Additionally, DIM induced increases in the levels of cleaved caspase-8, truncated Bid, Fas, and Fas ligand, and the caspase-8 inhibitor Z-IETD-FMK was shown to mitigate DIM-induced apoptosis and the cleavage of caspase-3, PARP, and Bid. These results indicate that DIM inhibits prostate carcinogenesis via induction of apoptosis and inhibition of cell cycle progression. DIM induces apoptosis in prostate cancer cells via the mitochondria- and death receptor-mediated pathways.


Subject(s)
Adenocarcinoma/drug therapy , Anticarcinogenic Agents/therapeutic use , Cell Transformation, Neoplastic/drug effects , Indoles/therapeutic use , Prostatic Neoplasms/drug therapy , Animals , Antigens, Polyomavirus Transforming/analysis , Apoptosis/drug effects , Apoptosis Regulatory Proteins , Carrier Proteins/analysis , Caspases/analysis , Cell Line, Tumor , Cyclin A/analysis , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 4/analysis , Cyclin-Dependent Kinase Inhibitor p27/analysis , Cytochromes c/analysis , Disease Models, Animal , Humans , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Mitochondrial Membranes/drug effects , Mitochondrial Proteins/analysis , Oligopeptides/therapeutic use , Peptides , Permeability/drug effects , Poly(ADP-ribose) Polymerases/analysis , Proliferating Cell Nuclear Antigen/analysis , Protein Transport/drug effects , bcl-X Protein/analysis
9.
Environ Mol Mutagen ; 52(2): 145-52, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20839231

ABSTRACT

Human cadmium (Cd) exposure is associated with cancers of the lung and kidney. Using cDNA microarray analysis, we have recently reported that the expression of E2F1 is reduced by Cd in human lung fibroblasts, indicating the possibility of G1-phase arrest. To test this hypothesis, we investigated the effects of Cd on the cyclin-dependent kinase (CDK2) and retinoblastoma protein (Rb) regulatory pathways in WI38 human lung fibroblasts. We demonstrate here that G1-phase accumulation was induced by Cd in WI38 (wild-type for p53 and Rb), but not in the SV40 large T antigen-transformed variant WI38-VA13 (p53- and Rb-defective). Cd-induced cell-cycle arrest was associated with a decrease in CDK2 protein and with increase in p21 expression and p53 phosphorylation. Cd treatment caused a distinct increase in the formation of p21-cyclin E-CDK2 complex, as revealed by immunoprecipitation. The level of Rb-E2F1 complexes was increased, and the translocation of E2F1 to the nucleus was decreased by Cd treatment. Consequently, the transcriptional activity of E2F1 and the expression of the E2F1 target genes were also decreased by Cd. These results clearly demonstrate that Cd-mediated G1 arrest in WI38 cells is associated with the suppression of Rb phosphorylation and with the inhibition of E2F1 transcriptional activity.


Subject(s)
Cadmium/toxicity , E2F1 Transcription Factor/antagonists & inhibitors , G1 Phase/drug effects , Lung/drug effects , Transcription, Genetic/drug effects , Cell Line , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 2/metabolism , Cyclin-Dependent Kinase Inhibitor p21/analysis , Cyclin-Dependent Kinase Inhibitor p21/metabolism , E2F1 Transcription Factor/metabolism , Fibroblasts/drug effects , Humans , Phosphorylation , Retinoblastoma Protein/analysis , Retinoblastoma Protein/metabolism , Tumor Suppressor Protein p53/analysis , Tumor Suppressor Protein p53/metabolism
10.
Surgery ; 149(2): 253-61, 2011 Feb.
Article in English | MEDLINE | ID: mdl-20570301

ABSTRACT

BACKGROUND: Cyclins drive cell-cycle progression by associating with their kinase partners, cyclin-dependent kinases (CDK). We investigated cyclin D1/CDK6, cyclin E/CDK2 complexes, and the cell-cycle negative regulators p15 and p27 in an incisional skin wound model. METHODS: Wounds were produced on the back of female diabetic mice and their normoglycemic littermates. Animals were treated with polydeoxyribonucleotide (PDRN, 8 mg/kg/i.p.), an agonist of adenosine A2(A) receptors, or its vehicle daily. Granulation tissue proliferation by Ki67 immunostaining, cyclin D/CDK6 and cyclin E/CDK2 complexes, and p21 and p16 proteins (Western blot analysis), and the histologic changes were assessed at different days (3, 6, and 12 days after injury). RESULTS: Numerous Ki67 positive cells were observed at day 3 and day 6 in the granulation tissue of normoglycemic mice. Ki67 positive cells were fewer in diabetic than in normoglycemic mice. PDRN increased Ki67 positive cells in diabetic mice. Normoglycemic mice showed the greatest upregulation of cyclin D1, CDK6, cyclin E, and CDK2 at day 6. Diabetic mice had a markedly lower expression of cyclin D1, CDK6, cyclin E, and CDK2 at day 6. They also showed a greater expression of p15 and p27 at day 6. PDRN administration in diabetic mice increased cyclin D1/CDK6 and cyclin E/CDK2 expression and reduced p15 and p27 inhibitors at day 6 after injury; moreover, it improved the impaired wound healing at day 12. CONCLUSION: Our results suggest that adenosine A2(A) receptor activation by PDRN might represent a therapeutic strategy to overcome the diabetes-impaired cell-cycle machinery.


Subject(s)
Cell Cycle , Diabetes Mellitus/physiopathology , Receptor, Adenosine A2A/physiology , Wound Healing/physiology , Animals , Cell Proliferation , Cyclin D1/analysis , Cyclin E/analysis , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 6/analysis , Cyclin-Dependent Kinase Inhibitor p27 , Diabetes Mellitus/pathology , Female , Granulation Tissue/pathology , Intracellular Signaling Peptides and Proteins/analysis , Mice , Mice, Inbred C57BL , Polydeoxyribonucleotides/pharmacology
11.
Cell Cycle ; 9(22): 4533-41, 2010 Nov 15.
Article in English | MEDLINE | ID: mdl-21088490

ABSTRACT

Cyclin E-associated CDK2 activity is required for the initiation of DNA synthesis in human cells. CDK2 activity is tightly regulated; CDK2 must be in the nucleus, bound to a cyclin, phosphorylated on T160, and dephosphorylated on T14/Y15 for complete kinase activation. Nuclear localization exposes CDK2 to activating enzymes (CAK, Cdc25A) in stimulated cells. Previous studies from our lab indicate CDK2 nuclear localization and cyclin E co-expression are insufficient to cause CDK2 activation or T160 phosphorylation in stimulated IIC9 cells; these activities still require serum stimulation and ERK kinase activity. Recent studies have implicated a role for origin of replication (ORC) licensing proteins in the activation of G1/S Cdks. In this study, we show that CDK2 associates with chromatin and Cdc6 in an ERK-dependent manner following stimulation of IIC9 CHEF cells. We show that nuclear-localized CDK2 (CDK2-NLS) ectopically expressed with cyclin E requires mitogenic stimulation and ERK activation for chromatin association, in addition to previously shown kinase activation and T160 phosphorylation in IIC9 cells. Additionally, we show that expression of Cdc6 in stimulated IIC9 cells treated with ERK inhibitor rescues CDK2-NLS chromatin association, kinase activation, and T160 phosphorylation. From the above data, we deduce ERK-dependent CDK2 activation is due in part to ERK-dependent Cdc6 expression. To examine the role of Cdc6 directly in stimulated primary human fibroblasts, we used RNA interference to attenuate the expression of Cdc6. We show that Cdc6 expression is required for CDK2 chromatin association and kinase activation in stimulated primary human fibroblasts. Additionally, we show that Cdc6 expression is required for the initiation of DNA synthesis and S phase entry in stimulated primary human fibroblasts. Ultimately, this data implicates Cdc6 expression as an important mitogen-induced mechanism in the activation of CDK2/cyclin E, the initiation of DNA synthesis, and the regulation of G1-S phase progression.


Subject(s)
Cell Cycle Proteins/metabolism , Cyclin E/metabolism , Cyclin-Dependent Kinase 2/metabolism , Nuclear Proteins/metabolism , Animals , Butadienes/pharmacology , Cell Cycle Proteins/genetics , Cell Line , Chromatin/metabolism , Cricetinae , Cricetulus , Cyclin E/analysis , Cyclin E/genetics , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 2/genetics , Extracellular Signal-Regulated MAP Kinases/antagonists & inhibitors , Extracellular Signal-Regulated MAP Kinases/metabolism , G1 Phase , Humans , Nitriles/pharmacology , Nuclear Proteins/genetics , Phosphorylation , RNA Interference , RNA, Small Interfering/metabolism , S Phase
12.
Oncogene ; 29(50): 6543-56, 2010 Dec 16.
Article in English | MEDLINE | ID: mdl-20818424

ABSTRACT

Tuberous sclerosis complex (TSC) is an autosomally inherited disorder that causes tumors to form in many organs. It is frequently caused by inactivating mutations in the TSC2 tumor-suppressor gene. TSC2 negatively regulates the activity of the GTPase Rheb and thereby inhibits mammalian target of rapamycin complex 1 (mTORC1) signaling. Activation of mTORC1 as a result of lack of TSC2 function is observed in TSC and sporadic lymphangioleiomyomatosis (LAM). TSC2 deficiency has recently been associated with elevated AMP-activated protein kinase (AMPK) activity, which in turn correlated with cytoplasmic localization of p27Kip1 (p27), a negative regulator of cyclin-dependent kinase 2 (Cdk2). How AMPK in the absence of TSC2 is stimulated is not fully understood. In this study, we demonstrate that Rheb activates AMPK and reduces p27 levels in Tsc2-null cells. Importantly, both effects occur largely independent of mTORC1. Furthermore, increased p27 levels following Rheb depletion correlated with reduced Cdk2 activity and cell proliferation in vitro, and with inhibition of tumor formation by Tsc2-null cells in vivo. Taken together, our data suggest that Rheb controls proliferation of TSC2-deficient cells by a mechanism that involves regulation of AMPK and p27, and that Rheb is a potential target for TSC/LAM therapy.


Subject(s)
AMP-Activated Protein Kinases/metabolism , Cell Proliferation , Cell Transformation, Neoplastic/metabolism , Cyclin-Dependent Kinase Inhibitor p27/metabolism , Monomeric GTP-Binding Proteins/metabolism , Neuropeptides/metabolism , Proteins/metabolism , Tumor Suppressor Proteins/metabolism , Animals , Cell Line, Tumor , Colonic Neoplasms/metabolism , Colonic Neoplasms/pathology , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 2/metabolism , Cyclin-Dependent Kinase Inhibitor p27/analysis , Female , Humans , Mechanistic Target of Rapamycin Complex 1 , Mice , Mice, Nude , Multiprotein Complexes , Ras Homolog Enriched in Brain Protein , TOR Serine-Threonine Kinases , Tuberous Sclerosis Complex 2 Protein , Tumor Suppressor Proteins/analysis , Up-Regulation
13.
J Clin Invest ; 120(10): 3594-605, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20811155

ABSTRACT

Platinum-based chemotherapies such as cisplatin are used as first-line treatment for many cancers. Although there is often a high initial responsiveness, the majority of patients eventually relapse with platinum-resistant disease. For example, a subset of testicular cancer patients still die even though testicular cancer is considered a paradigm of cisplatin-sensitive solid tumors, but the mechanisms of chemoresistance remain elusive. Here, we have shown that one key determinant of cisplatin-resistance in testicular embryonal carcinoma (EC) is high cytoplasmic expression of the cyclin-dependent kinase (CDK) inhibitor p21. The EC component of the majority of refractory testicular cancer patients exhibited high cytoplasmic p21 expression, which protected EC cell lines against cisplatin-induced apoptosis via CDK2 inhibition. Localization of p21 in the cytoplasm was critical for cisplatin resistance, since relocalization of p21 to the nucleus by Akt inhibition sensitized EC cell lines to cisplatin. We also demonstrated in EC cell lines and human tumor tissue that high cytoplasmic p21 expression and cisplatin resistance of EC were inversely associated with the expression of Oct4 and miR-106b seed family members. Thus, targeting cytoplasmic p21, including by modulation of the Oct4/miR-106b/p21 pathway, may offer new strategies for the treatment of chemoresistant testicular and other types of cancer.


Subject(s)
Antineoplastic Agents/pharmacology , Cisplatin/pharmacology , Cyclin-Dependent Kinase Inhibitor p21/analysis , Cytoplasm/chemistry , Testicular Neoplasms/drug therapy , Apoptosis/drug effects , Cell Line, Tumor , Chromones/pharmacology , Cyclin-Dependent Kinase 2/analysis , Drug Resistance, Neoplasm , Humans , Male , MicroRNAs/physiology , Morpholines/pharmacology , Octamer Transcription Factor-3/physiology , Proto-Oncogene Proteins c-akt/physiology , Testicular Neoplasms/pathology
14.
Anal Chem ; 82(9): 3531-6, 2010 May 01.
Article in English | MEDLINE | ID: mdl-20394401

ABSTRACT

Proteins mediate the bulk of biological activity and are powerfully assayed in the diagnosis of diseases. Protein detection relies largely on antibodies, which have significant technical limitations especially when immobilized on two-dimensional surfaces. Here, we report the integration of peptide aptamers with extended gate metal-oxide-semiconductor field-effect transistors (MOSFETs) to achieve label-free sub-picomolar target protein detection. Specifically, peptide aptamers that recognize highly related protein partners of the cyclin-dependent kinase (CDK) family are immobilized on the transistor gate to enable human CDK2 to be detected at 100 fM or 5 pg/mL, well within the clinically relevant range. The target specificity, ease of fabrication, and scalability of these FET arrays further demonstrate the potential application of the multiplexable field effect format to protein sensing.


Subject(s)
Biosensing Techniques/methods , Proteins/chemistry , Transistors, Electronic , Cyclin-Dependent Kinase 2/analysis , Humans , Proteins/analysis , Spectroscopy, Fourier Transform Infrared
15.
Methods Mol Biol ; 559: 161-72, 2009.
Article in English | MEDLINE | ID: mdl-19609756

ABSTRACT

Many cell cycle regulatory proteins have been shown to be able to regulate cell death. Activation of Cdk2 has been shown to be necessary for apoptosis of quiescent cells such as thymocytes, neurons, and endothelial cells. This activation is stimulus-specific because it occurs in glucocorticoid and DNA damage but not in CD95-induced apoptosis in thymocytes. Apoptotic Cdk2 activation in lymphoid cells is controlled by a recently identified protein, cyclin O, and its activity is modulated by p53 and members of the Bcl-2 protein family. In this chapter, we describe methods for measuring changes in Cdk2 activity during apoptosis. In addition, we also show the details of the generation of an antibody able to immunoprecipitate the cyclin O complexes from apoptotic cells in native conditions and its use to measure the kinase activity associated with this proapoptotic cyclin.


Subject(s)
Apoptosis , Cyclin-Dependent Kinase 2/metabolism , Immunoprecipitation/methods , Animals , Cell Cycle , Cells, Cultured , Cyclin-Dependent Kinase 2/analysis , Cyclins/immunology , Cyclins/metabolism , Humans , T-Lymphocytes/cytology
16.
J Cell Biol ; 185(5): 797-810, 2009 Jun 01.
Article in English | MEDLINE | ID: mdl-19468068

ABSTRACT

Alternative lengthening of telomeres (ALT) is a recombination-mediated process that maintains telomeres in telomerase-negative cancer cells. In asynchronously dividing ALT-positive cell populations, a small fraction of the cells have ALT-associated promyelocytic leukemia nuclear bodies (APBs), which contain (TTAGGG)n DNA and telomere-binding proteins. We found that restoring p53 function in ALT cells caused p21 up-regulation, growth arrest/senescence, and a large increase in cells containing APBs. Knockdown of p21 significantly reduced p53-mediated induction of APBs. Moreover, we found that heterochromatin protein 1 (HP1) is present in APBs, and knockdown of HP1alpha and/or HP1gamma prevented p53-mediated APB induction, which suggests that HP1-mediated chromatin compaction is required for APB formation. Therefore, although the presence of APBs in a cell line or tumor is an excellent qualitative marker for ALT, the association of APBs with growth arrest/senescence and with "closed" telomeric chromatin, which is likely to repress recombination, suggests there is no simple correlation between ALT activity level and the number of APBs or APB-positive cells.


Subject(s)
Chromosomal Proteins, Non-Histone/physiology , Telomere/metabolism , Tumor Suppressor Protein p53/physiology , Adaptor Proteins, Signal Transducing , Antigens, Viral, Tumor/metabolism , Cell Line , Cellular Senescence/genetics , Cellular Senescence/physiology , Chromobox Protein Homolog 5 , Chromosomal Proteins, Non-Histone/metabolism , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 2/metabolism , Cyclin-Dependent Kinase Inhibitor p21/genetics , Cyclin-Dependent Kinase Inhibitor p21/metabolism , Cyclin-Dependent Kinase Inhibitor p21/physiology , Humans , Nuclear Proteins/analysis , Nuclear Proteins/metabolism , RNA Interference , Telomeric Repeat Binding Protein 1/analysis , Telomeric Repeat Binding Protein 2/analysis , Tumor Suppressor Protein p53/metabolism , Up-Regulation
17.
Arthritis Rheum ; 60(5): 1294-304, 2009 May.
Article in English | MEDLINE | ID: mdl-19404929

ABSTRACT

OBJECTIVE: To elucidate the role of microRNA (miRNA) in the pathogenesis of rheumatoid arthritis (RA), we analyzed synoviocytes from RA patients for their miRNA expression. METHODS: Synoviocytes derived from surgical specimens obtained from RA patients were compared with those obtained from osteoarthritis (OA) patients for their expression of a panel of 156 miRNA with quantitative stem-loop reverse transcription-polymerase chain reaction. The miRNA whose expression decreased or increased in RA synoviocytes as compared with OA synoviocytes were identified, and their target genes were predicted by computer analysis. We used an in vitro system of enhancing the expression of specific miRNA by transfection of precursors into synoviocytes, and then we performed proliferation, cell cycle, and apoptosis assays, as well as enzyme-linked immunosorbent assays for cytokine production. The effects of transfection on predicted target protein and messenger RNA (mRNA) were then examined by Western blot analysis and luciferase reporter assay. RESULTS: We found that miR-124a levels significantly decreased in RA synoviocytes as compared with OA synoviocytes. Transfection of precursor miR-124a into RA synoviocytes significantly suppressed their proliferation and arrested the cell cycle at the G1 phase. We identified a putative consensus site for miR-124a binding in the 3'-untranslated region of cyclin-dependent kinase 2 (CDK-2) and monocyte chemoattractant protein 1 (MCP-1) mRNA. Induction of miR-124a in RA synoviocytes significantly suppressed the production of the CDK-2 and MCP-1 proteins. Luciferase reporter assay demonstrated that miR-124a specifically suppressed the reporter activity driven by the 3'-untranslated regions of CDK-2 and MCP-1 mRNA. CONCLUSION: The results of this study suggest that miR-124a is a key miRNA in the posttranscriptional regulatory mechanisms of RA synoviocytes.


Subject(s)
Arthritis, Rheumatoid/physiopathology , Chemokine CCL2/metabolism , MicroRNAs/physiology , Synovial Membrane/physiopathology , Apoptosis/physiology , Arthritis, Rheumatoid/etiology , Cell Cycle/physiology , Cell Proliferation , Cells, Cultured , Chemokine CCL2/analysis , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinases/analysis , Enzyme-Linked Immunosorbent Assay , Fibroblasts/physiology , Humans , MicroRNAs/analysis , Osteoarthritis/physiopathology , Reverse Transcriptase Polymerase Chain Reaction , Synovial Membrane/cytology , Transfection
18.
Cancer Lett ; 277(1): 91-100, 2009 May 08.
Article in English | MEDLINE | ID: mdl-19138817

ABSTRACT

Human hepatocellular carcinoma (HCC) has an elevated requirement for arginine in vitro, and pegylated recombinant human arginase I (rhArg-PEG), an arginine-depleting enzyme, can inhibit the growth of arginine-dependent tumors. While supplementation of the culture medium with ornithine failed to rescue Hep3B cells from growth inhibition induced by rhArg-PEG, citrulline successfully restored cell growth. The data support the roles previously proposed for ornithine transcarbamylase (OTC) in the arginine auxotrophy and rhArg-PEG sensitivity of HCC cells. Expression profiling of argininosuccinate synthetase (ASS), argininosuccinate lyase (ASL) and OTC in 40 HCC tumor biopsy specimens predicted that 16 of the patients would be rhArg-sensitive, compared with 5 who would be sensitive to arginine deiminase (ADI), another arginine-depleting enzyme with anti-tumor activity. Furthermore, rhArg-PEG-mediated deprivation of arginine from the culture medium of different HCC cell lines produced cell cycle arrests at the G(2)/M or S phase, possibly mediated by transcriptional modulation of cyclins and/or cyclin dependent kinases (CDKs). Based on these results, together with further validation of the in vivo efficacy of rhArg-PEG against HCC, we propose that the application of rhArg-PEG alone or in combination with existing chemotherapeutic drugs may represent a specific and effective therapeutic strategy against HCC.


Subject(s)
Antineoplastic Agents/pharmacology , Arginase/pharmacology , Carcinoma, Hepatocellular/drug therapy , Cell Cycle/drug effects , Liver Neoplasms/drug therapy , Animals , Arginase/therapeutic use , Carcinoma, Hepatocellular/enzymology , Carcinoma, Hepatocellular/pathology , Cell Line, Tumor , Cell Proliferation/drug effects , Citrulline/metabolism , Citrullinemia/epidemiology , Cyclin-Dependent Kinase 2/analysis , Cyclins/analysis , Humans , Liver Neoplasms/enzymology , Liver Neoplasms/pathology , Mice , Ornithine Carbamoyltransferase Deficiency Disease/epidemiology , Recombinant Proteins/pharmacology , Xenograft Model Antitumor Assays
20.
Oncol Res ; 17(4): 175-82, 2008.
Article in English | MEDLINE | ID: mdl-18773862

ABSTRACT

All-trans retinoic acid (ATRA) and sodium butyrate (SB) have shown growth-inhibitory and differentiation-inducing properties to tumor cells when used as single agents or in combination, but the exact molecular mechanism still remains to be determined. In order to determine the mechanism of the synergy in treatment with RA and SB, we evaluated the growth inhibition capability of ATRA and SB, alone or in combination, in human oral squamous carcinoma cell lines SCC-1 and SCC-9, and identified the expression of cell cycle-related genes. ATRA and SB inhibited cell growth and induced cell cycle G1 arrest. The inhibition effect was more pronounced with SB than with ATRA (p = 0.000). There were interactions between ATRA and SB (p = 0.000). Consistent with the inhibition effect and G1 arrest, ATRA and SB, alone or in combination, induced the expression of G1 phase markers cyclin-dependent kinase (CDK) 6, p21, and p27; inhibited the expression of S-G2 phase proteins CDK2; and decreased Rb phosphorylation. Cyclin D1 expression was increased in the SB- and ATRA + SB-treated groups, but inhibited in the ATRA-treated group. Cyclin B1 and cyclin E expression was slightly decreased in the SB- and ATRA + SB-treated groups, but did not change in the ATRA-treated group. These results indicate that the growth inhibition and G1 arrest of oral squamous carcinoma cells in response to ATRA and/or SB correlates with the induction of G1 phase cell cycle regulatory proteins CDK6, p21, and p27 and the inhibition of S-G2 phase cell cycle regulatory protein CDK2.


Subject(s)
Butyrates/pharmacology , Carcinoma, Squamous Cell/drug therapy , Mouth Neoplasms/drug therapy , Tretinoin/pharmacology , Carcinoma, Squamous Cell/pathology , Cell Cycle/drug effects , Cell Proliferation/drug effects , Cyclin-Dependent Kinase 2/analysis , Cyclin-Dependent Kinase 6/analysis , Cyclin-Dependent Kinase Inhibitor p21/physiology , Cyclin-Dependent Kinase Inhibitor p27 , Humans , Intracellular Signaling Peptides and Proteins/physiology , Mouth Neoplasms/pathology
SELECTION OF CITATIONS
SEARCH DETAIL
...