نتایج جستجو برای: colo 205

تعداد نتایج: 12324  

Journal: :Annals of oncology : official journal of the European Society for Medical Oncology 2008
A Yada M Yazawa S Ishida H Yoshida K Ichikawa S Kurakata K Fujiwara

BACKGROUND The antitumor activity of CS-1008, a humanized agonistic anti-human death receptor (DR) 5 antibody, was investigated in preclinical models. MATERIALS AND METHODS Cytotoxicity of CS-1008 was evaluated in a several human tumor cell lines as well as primary human hepatocytes in vitro. To evaluate antitumor efficacy, athymic nude mice were inoculated with human colorectal tumor COLO 20...

1999
Shinya Aono Shinichi Nakagawa Albert B. Reynolds Masatoshi Takeichi

p120 ctn binds to the cytoplasmic domain of cadherins but its role is poorly understood. Colo 205 cells grow as dispersed cells despite their normal expression of E-cadherin and catenins. However, in these cells we can induce typical E-cadherin–dependent aggregation by treatment with staurosporine or trypsin. These treatments concomitantly induce an electrophoretic mobility shift of p120 ctn to...

Journal: :The Journal of Cell Biology 1999
Shinya Aono Shinichi Nakagawa Albert B. Reynolds Masatoshi Takeichi

p120(ctn) binds to the cytoplasmic domain of cadherins but its role is poorly understood. Colo 205 cells grow as dispersed cells despite their normal expression of E-cadherin and catenins. However, in these cells we can induce typical E-cadherin-dependent aggregation by treatment with staurosporine or trypsin. These treatments concomitantly induce an electrophoretic mobility shift of p120(ctn) ...

Journal: :Molecular medicine reports 2010
Chun-Yuan Cheng Yi-Hsiang Lin Chin-Cheng Su

Malignant tumors are the leading cause of death in Taiwan; among these, colon cancer ranks third as a cause of cancer-related death. Sann-Joong-Kuey-Jian-Tang (SJKJT), a traditional Chinese medicinal prescription, has been used to treat lymph node diseases and infectious lesions, and exhibits cytotoxic activity in many cancer cell lines. Our previous studies demonstrated that SJKJT inhibits the...

2017
Huan Tong Linhao Zhang Jinhang Gao Shilei Wen Hongying Zhou Shi Feng

It is not established whether de‑methylation of the displacement loop (D‑loop) region if mitochondrial DNA (mtDNA) directly influences mtDNA copy number and further alters the cell cycle, apoptosis and cell proliferation in colorectal cancer. The current study employed cell viability assays, cell cycle analysis, and mtDNA methylation analysis using 5 colorectal cancer cell lines. The present re...

Journal: :Journal of immunology 2010
Fanny Legrand Virginie Driss Marie Delbeke Sylvie Loiseau Emmanuel Hermann David Dombrowicz Monique Capron

Peripheral blood and tissue eosinophilia is a prominent feature in allergic diseases and helminth infections. In cancer patients, tumor-associated tissue eosinophilia is frequently observed. Tumor-associated tissue eosinophilia can be associated with a favorable prognosis, notably in colorectal carcinoma. However, underlying mechanisms of eosinophil contribution to antitumor responses are poorl...

Journal: :Cancer research 1993
D Baeckström O Nilsson M R Price L Lindholm G C Hansson

Earlier studies (Baeckström et al., J. Biol. Chem., 266: 21537-21547, 1991) have revealed that the colon carcinoma cell line COLO 205 produces two different proteins carrying the carcinoma-associated sialyl-Le(a) carbohydrate epitope. One is the MUC1 mucin apoprotein, and the other protein is smaller and has not been characterized in detail. This paper describes a comparison of COLO 205 with th...

Journal: :Molecular cancer therapeutics 2005
Ching-Huai Ko Shing-Chuan Shen Tony J F Lee Yen-Chou Chen

Colorectal carcinoma is a leading cause of human mortality due to its high metastatic ability. Because the activation of matrix metalloproteinases (MMP) is a key factor in the metastatic process, agents with the ability to inhibit MMP activity have potential in the treatment of colorectal carcinoma. In the present study, among 36 flavonoids examined, myricetin was found to be the most potent in...

Journal: :Molecules 2014
Kaiyong Tang Qingqing Huang Jafeng Zeng Guangming Wu Jinwen Huang Junfang Pan Wei Lu

New six C6-celastrol derivatives were designed, synthesized, and evaluated for their in vitro cytotoxic activities against nine human cancer cell lines (BGC-823, H4, Bel7402, H522, Colo 205, HepG2 and MDA-MB-468). The results showed that most of the compounds displayed potent inhibition against BGC823, H4, and Bel7402, with IC50s of 1.84-0.39 μM. The best compound NST001A was tested in an in vi...

Journal: :The Journal of antibiotics 1995
K Ito T Kobayashi Y Moriyama K Toshima K Tatsuta T Kakiuchi M Futai H L Ploegh K Miwa

We screened natural chemical compounds which inhibit the expression of newly-synthesized MHC class II molecules on the cell surface. IFN-gamma stimulates Colo 205 adenocarcinoma cells to induce the expression of MHC class I, MHC class II, and ICAM-1 molecules on the cell surface. We show here that concanamycin B inhibits the expression of MHC class II molecules on Colo 205 cells, whereas it doe...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید