نتایج جستجو برای: du145 cell line

تعداد نتایج: 1969409  

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2004
Anthony Raffo Johnathan C Lai C A Stein Paul Miller Steven Scaringe Anastasia Khvorova Luba Benimetskaya

PURPOSE Inhibition of the function of the bcl-2 protein has been postulated to sensitize cells to cytotoxic chemotherapy, and thus provides an attractive target for investigative therapies. G3139, a phosphorothioate antisense oligonucleotide targeted to the initiation codon region of the bcl-2 mRNA, is currently being evaluated in several Phase II and Phase III clinical trials. However, the mec...

Journal: :Anticancer research 2004
P Effert A J Beniers Y Tamimi S Handt G Jakse

BACKGROUND Increased uptake and metabolism of glucose is a characteristic of malignant transformation. Overexpression of glucose transporters, especially Glut-1, is a common event in human malignancies. To date, little is known about the role of Glut-1 in human prostate cancer (PC). The aim of this study was to investigate the expression of Glut-1 both in PC cell lines and clinical specimens of...

Journal: :Cancer investigation 2006
A Drissi H Bennani F Giton Z Charrouf J Fiet A Adlouni

The aim of our study is to evaluate the antiproliferative effect of tocopherols obtained from alimentary virgin argan oil extracted from the endemic argan tree of Morocco and of saponins extracted from argan press cake on three human prostatic cell lines (DU145, LNCaP, and PC3). The results were compared to 2-methoxyestradiol as antiproliferative drug candidates. Cytotoxicity and antiproliferat...

2015
Pedram Kharaziha Dimitris Chioureas George Baltatzis Pedro Fonseca Patricia Rodriguez Vladimir Gogvadze Lena Lennartsson Ann-Charlotte Björklund Boris Zhivotovsky Dan Grandér Lars Egevad Sten Nilsson Theocharis Panaretakis

Autophagy is one of the main cytoprotective mechanisms that cancer cells deploy to withstand the cytotoxic stress and survive the lethal damage induced by anti-cancer drugs. However, under specific conditions, autophagy may, directly or indirectly, induce cell death. In our study, treatment of the Atg5-deficient DU145 prostate cancer cells, with the multi-tyrosine kinase inhibitor, sorafenib, i...

2000
Richard McGowen Hector Biliran Ruth Sager Shijie Sheng

Maspin is a novel serine protease inhibitor (serpin) with tumor suppressive potential in breast and prostate cancer, acting at the level of tumor invasion and metastasis. It was subsequently demonstrated that maspin inhibits tumor invasion, at least in part, by inhibiting cell motility. Interestingly, in cell-free solutions, maspin does not inhibit several serine proteases including tissue-type...

2017
Saima Nawaz Gregory E. D. Mullen Kavitha Sunassee Jayanta Bordoloi Philip J. Blower James R. Ballinger

BACKGROUND Labelling proteins with gallium-68 using bifunctional chelators is often problematic because of unsuitably harsh labelling conditions such as low pH or high temperature and may entail post-labelling purification. To determine whether tris(hydroxypyridinone) (THP) bifunctional chelators offer a potential solution to this problem, we have evaluated the labelling and biodistribution of ...

2018
Shengquan Huang Qian Liu Qianjin Liao Qingjian Wu Bishao Sun Zhenxing Yang Xiaoyan Hu Mingjia Tan Longkun Li

Prostate cancer can progress from androgen dependence to androgen deprivation resistance with some unknown mechanisms. The current study aims to explore the possible role of pituitary tumor transforming gene1 (PTTG1) in castration-resistant prostate cancer (CRPC). Initially, we found that PTTG1 expression was significantly increased in androgen-independent prostate cancer cell lines PC3, DU145 ...

Journal: :Folia histochemica et cytobiologica 2012
Agnieszka Bojko Kinga Reichert Anna Adamczyk Joanna Ligęza Janusz Ligęza Andrzej Klein

We employed two selective EGFR tyrosine kinase inhibitors: AG494 (reversible) and AG1478 (irreversible) for growth regulation of human lung (A549) and prostate (DU145) cancer cell lines, cultured in chemically defined DMEM/F12 medium. Both tested tyrphostins significantly inhibited autocrine growth of the investigated cell lines. The action of AG494 was dose dependent, and at highest concentrat...

2013
Jacqueline Banyard Ivy Chung Arianne M. Wilson Guillaume Vetter Antony Le Béchec Diane R. Bielenberg Bruce R. Zetter

Using an in vivo cycling strategy, we selected metastatic cancer cells from the lymph nodes (LN) of mice bearing orthotopic DU145 human prostate tumors. Repeated rounds of metastatic selection (LN1-LN4) progressively increased the epithelial phenotype, resulting in a new model of tumor cell mesenchymal-epithelial transition (MET). DU145-LN4 showed increased cell-cell adhesions, higher expressio...

Journal: :iranian journal of basic medical sciences 0
seyedeh alia moosavian biotechnology research center, nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran mahmoud reza jaafari biotechnology research center, nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran seyed mohammad taghdisi targeted drug delivery research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran fatemeh mosaffa biotechnology research center, pharmacy school, mashhad university of medical sciences, mashhad, iran ali badiee nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran khalil abnous pharmaceutical research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran

objective(s): development of molecules that specifically recognize cancer cells is one of the major areas in cancer research. human epidermal growth factor receptor 2 (her2) is specifically expressed on the surface of breast cancer cells. her2 is associated with an aggressive phenotype and poor prognosis. in this study we aimed to isolate rna aptamers that specifically bind to her2 overexpressi...

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