|
|
|
题名
|
作者
|
年代
|
出处
|
被引量
|
| 1 | Secreted protein acidic and rich in cysteine(SPARC)induces epithelial-mesenchymal transition,enhancing migration and invasion,and is associated with high Gleason score in prostate cancer显示文摘Secreted protein acidic and rich in cysteine(SPARC)is a matricellular protein highly expressed in bone tissue that acts as achemoattractant factor promoting the arrival of prostate cancer(PCa)cells to the bone marrow.However,the contribution of SPARCduring the early stages of tumor progression remains unclear.In this study,we show that SPARC is highly expressed in PCa tissueswith a higher Gleason score.Through stable knockdown and overexpression of SPARC in PC3 and LNCaP cells,respectively,here wedem on strate that en doge nous SPARC induces the epithelial-mesenchymal tran sition(EMT),decreasing E-cadheri n and cytokeratin18 and increasing N-cadheri n and vime ntin.Moreover,SPARC in duces the expression of EMT regulatory tran scription factors Snailfamily transcriptional repressor 1(Snail),Snail family transcriptional repressor 2(Slug),and zinc finger E-box binding homeobox 1(Zeb1).In addition,SPARC knockdown in PC3 cells decreases migration and invasion in vitro,without modifying cell proliferation.Our results indicate that SPARC might facilitate tumor progression by modifying the cellular phenotype in cancer cells. | Fernanda Lopez-Moncada Maria Jose Torres Enrique A Castellon Hector R Contreras | 2019 | Asian Journal of Andrology2019，21，6： | 5 |
| 2 | The transcription factor ZEB1 promotes chemoresistance in prostate cancer cell lines显示文摘One of the factors promoting tumoral progress is the abnormal activation of the epithelial-mesenchymal transition(EMT)program which has been associated with chemoresistance in tumoral cells.The transcription factor zinc finger E-box-binding homeobox 1(ZEB1),a key EMT activator,has recently been related to docetaxel resistance,the main chemotherapeutic used in advanced prostate cancer treatment.The mechanisms involved in this protective effect are still unclear.In a previous work,we demonstrated that ZEB1 expression induced an EMT-like phenotype in prostate cancer cell lines.In this work,we used prostate cancer cell lines 22Rvl and DU145 to study the effect of ZEB1 modulation on docetaxel resistance and its possible mechanisms.The results showed that ZEB1 overexpression conferred to 22Rvl cell resistance to docetaxel while its silencing made DU145 cells more sensitive to it.Analysis of resistance markers showed no presenee of ATP-binding cassette subfamily B member 1(MDR1)and no changes in breast cancer resistance protein(BCRP)or ATP-binding cassette subfamily C member 10(MRP7).However,a correlation between ZEB1,multidrug resistance-associated protein 1(MRP1),and ATP-binding cassette subfamily C member 4(MRP4)expression was observed.MRP4 inhibition,using MK571,resensitized cells with ZEB1 overexpression to docetaxel treatment.In addition,modulation of ZEB1 and subsequent change in MRP4 expression correlated with a lower apoptotic response to docetaxel,characterized by lower B-cell lymphoma 2(Bcl2),high BCL2-associated X protein(Bax),and high active caspase 3 expression.The response to docetaxel in our model seems to be mediated mainly by activation of the apoptotic death program.Our results showed that modulation of MRP4 could be a mediator of ZEBl-related resistance to docetaxel in prostate cancer,making it a possible marker for chemotherapy response in patients who do not express MDR1. | Octavio Orellana-Serradell Daniela Herrera Enrique A Castellon Hector R Contreras | 2019 | Asian Journal of Andrology2019，21，5： | 5 |
| 3 | The transcription factor ZEB1 promotes an aggressive phenotype in prostate cancer cell lines显示文摘 | Octavio Orellana-Serradell Daniela Herrera Enrique A Castellon Hector R Contreras | 2018 | Asian Journal of Andrology2018，20，3： | 4 |
| 4 | syndecan-1和-2表达形式的变化可以预测前列腺癌生化复发显示文摘前列腺癌的临床特点不能准确确定患者是否会发生生化复发,因而不适合作为预后和复发的指标。需要新的分子标记物对患者进行适当的术前风险分层。本研究旨在评估syndecan-1和-2的表达改变是否可以预测临床局限性前列腺癌患者行前列腺根治术后的生化复发。取60份局限性前列腺癌患者的石蜡包埋组织标本,采用免疫组化染色检测syndecan-1和-2的表达。取10份良性前列腺增生患者的样本作为非恶性对照。利用半定量分析,对其进行染色评估。为探讨预后效果,用Kaplan—Meier生存曲线进行分析,并进行log—rank检验。在良性前列腺样本中,syndecan-1在基底层上皮细胞中有表达,在上皮分泌细胞的基侧膜上也有表达;syndecan-2则主要但挞底层上皮细胞中表达。前列腺癌样本中,两种syndecan的表达模式都转变成定位在颗粒状细胞质上。生存分析显示,在游离前列腺特异性抗原(fPSA)复发存活曲线中,正常和改变的syndecan-1和-2的表达存在显著差异(P〈0.05)。这些数据表明,syndecan—1和-2可以作为临床局灶性前列腺癌患者预后的标记物,从而改进前列腺特异性抗原(PSA)评估复发风险,增加风险分层。 | Rodrigo Ledezma Federico Cifuentes Ivan Gallegos Juan Fulla Enrique Ossandon Enrique A Castellon Hector R Contreras | 2011 | Asian Journal of Andrology2011，13，3： | 2 |
| 5 | Glutathione peroxidase activity in cell cultures from different regions of human epididymis显示文摘Aim: To study the secretory activity and androgen regulation of glutathione peroxidase (GPx) in epithelial cell cultures from human epididymis. Methods: Tissue was obtained from patients undergoing therapeutic orchidectomy for prostatic cancer. Epithelial cell cultures were obtained from the caput, corpus and cauda epididymides. Enzymatic activity was measured in conditioned media by colorimetric methods in absence or presence of 1, 10 or 100 nmol·L^-1 testosterone. The effect of 1 μmol·L^-1 flutamide was also evaluated. Results: GPx activity was higher in cultures from corpus and cauda than caput epididymidis. The presence of different concentrations of testosterone increase enzyme activity in cell cultures from all epididymal regions. Addition of flutamide reverses the androgen dependent increase of GPx activity. Conclusion: GPx activity is secreted from human epididymal cells in a region dependent manner and is regulated by androgens. | Enrique Castellon Hernan Rioseco Juan Rojas Michel Royer Eduardo Salas Hoctor Contreras Christian Huidobro | 2005 | Asian Journal of Andrology2005，7，1： | 2 |
| 6 | Autoerine activation of an osteopontin- CD44- Rac pathway enhances invasion and transfor- mation by H- RasV12显示文摘 | Teramoto H Castellone MD Malek RL | 2005 | Oncogene2005，24，3： | 1 |
| 7 | Altered frontocortical,cerebellar, and basal ganglia activity in adjuvant-treated breast cancersurvivors 5-10 years after chemotherapy 显示文摘 | Silverman DH Dy CJ Castellon SA | 2007 | Breast Cancer Res Treat2007，103，3： | 1 |
| 8 | Thyroid cancer and inflam- mation显示文摘 | Guarino V Castellone MD Avilla E | 2010 | Mol Cell Endocrinol2010，321，1： | 1 |
| 9 | Use of microencapsulated PCM in concrete walls for energy savings显示文摘 | Luisa F Cabeza Cecilia Castellon | 2007 | Energy and Buildings2007，39，： | 1 |
| 10 | Autocrine activationof an osteopontin-CD44-Rac pathway enhances invasion and trans-formation by H-RasV12显示文摘 | Teramoto H Castellone MD Malek RL | 2005 | Oncogene2005，24，3： | 1 |
| 11 | Robo4 signaling in endothelial cells implies attraction guidance mechanisms显示文摘 | Kaur S Castellone MD Bedell VM | | 0，，： | 1 |
| 12 | Multi-modal medical image integration to optimize radiotherapy planning in lung cancer treatment显示文摘 | Rizzo G Cattaneo GM Castellone P | 2004 | Ann Biomed Eng2004，32，10： | 1 |
| 13 | Autocrine activation of all osteopontin CD44-Rac pathway enhances invasion and transfor mation by H-RasV12显示文摘 | Teramoto H Castellone M D Malek R L | 2005 | Oncogene2005，24，3： | 1 |
| 14 | Functional expression of the CXCR4 chemokine receptor is induced by RET/ PTC oncogenes and is a common event in human papillary thyroid carcinomas显示文摘 | Castellone MD Guarino V De Falco V | 2004 | Oncogene2004，23，35： | 1 |
| 15 | Evaluating scale dependence of ecosystem service valuation:A comparison of NOAA-AVHRR and Landsat TM datasets显示文摘 | KONARSKA K M SUTTON P C CASTELLON M | 2002 | Eeological Econornics2002，41，3： | 1 |
| 16 | Use of microencapsu-lated PCM in concrete walls for energy savings 显示文摘 | Cabeza L F Castellon C Nogues M | 2007 | Energy and Buildings2007，39，2： | 1 |
| 17 | Functional expression of the CXCR4 chemokine receptor is induced by RET/PTC oncogenes and is a common event in human papillary thyroid carcinomas显示文摘 | Castellone MD Guarino V De Falco V | 2004 | Oncogene2004，23，35： | 1 |
| 18 | Layered basic copper anion exchangers : chemical charac- terisation and X-ray absorption study 显示文摘 | LOPEZ A J CASTELLON E R PASTOR P O | 1993 | J Mater Chem1993，，3： | 1 |
| 19 | Neurocognitive performance in breast cancer survivors exposed to adjuvant chemo-therapy and tamoxifen显示文摘 | CASTELLON S A GANZ P A BOWER J E | 2004 | J Clin Exp Neuropsychol2004，26，7： | 1 |
| 20 | Prostaglandin E2 promotes colon cancer cell growth through a gsaxin-beta-catenin signaling axis 显示文摘 | CASTELLONE M D TERAMOTO H WILLIAMS B O | 2005 | Sci2005，310，5753： | 1 |
您所在的机构暂未开通此部分的功能，请联系管理员