نتایج جستجو برای: drug resistant tumors

تعداد نتایج: 896695  

2017
Xiaoyang Li Jacson K. Shen Francis J. Hornicek Tao Xiao Zhenfeng Duan

Sarcomas are a group of malignant tumors that arise from mesenchymal origin. Despite significant development of multidisciplinary treatments for sarcoma, survival rates have reached a plateau. Chemotherapy has been extensively used for sarcoma treatment; however, the development of drug resistance is a major obstacle limiting the success of many anticancer agents. Sarcoma biology has traditiona...

Journal: :Cancer research 2008
Clara Montagut Sreenath V Sharma Toshi Shioda Ultan McDermott Matthew Ulman Lindsey E Ulkus Dora Dias-Santagata Hannah Stubbs Diana Y Lee Anurag Singh Lisa Drew Daniel A Haber Jeffrey Settleman

Activating BRAF kinase mutations arise in approximately 7% of all human tumors, and preclinical studies have validated the RAF-mitogen-activated protein/extracellular signal-regulated kinase (ERK) kinase-ERK signaling cascade as a potentially important therapeutic target in this setting. Selective RAF kinase inhibitors are currently undergoing clinical development, and based on the experience w...

Journal: :Cancer research 1982
F M Sirotnak D M Moccio L J Goutas L E Kelleher J A Montgomery

The M5076 murine "ovarian" tumor which is naturally refractive to methotrexate was found to be highly responsive to the lipophilic antifolate, metoprine. M5076 cells were markedly deficient in mediated entry of methotrexate. This was in contrast to the L1210 leukemia, a tumor highly responsive to methotrexate but poorly responsive to metoprine. Two L1210 leukemia sublines, with acquired resista...

Journal: :Oncology reports 2008
Iliodora Pop Laurentiu Pop Ellen S Vitetta Maria-Ana Ghetie

The objective of this study was to generate new P-glycoprotein (P-gp)-expressing multidrug resistant (MDR) cell lines by drug selection. Since our previous studies have been carried out with cells infected with a P-gp-containing vector, it was important to confirm our findings in cells generated by drug selection. In this report, we describe three B-lymphoma cell lines which became drug-resista...

A. F. Raja M. Maqbool Z. Ahmad,

Patient noncompliance to current tuberculosis (TB) therapy owing to multidrug administration daily leads to treatment failure and emergence of multidrug resistant and extensively drug resistant TB. To avoid the daily dosing, application of nanotechnology is the only viable solution by virtue of sustained release of drugs. Other potential advantages of the system include the possibility of selec...

Journal: :Blood 1992
T Trippett S Schlemmer Y Elisseyeff E Goker M Wachter P Steinherz C Tan E Berman J E Wright A Rosowsky

Although the mechanisms of resistance to methotrexate (MTX) are known in experimental tumors made resistant to this drug, little information is available regarding acquired resistance to MTX in patients. A competitive displacement assay using the fluorescent lysine analogue of MTX, N-(4-amino-4-deoxy-N10-methylpteroyl)-N epsilon-(4'-fluorescein-thiocarbamyl)-L-lysine (PT430), was developed as a...

Journal: :Acta Biochimica et Biophysica Sinica 2021

Oxaliplatin (OXA) resistance limits the efficiency of treatment for hepatocellular carcinoma (HCC). Studies have shown that PDZ-binding kinase (PBK) plays important roles in tumors. However, role PBK HCC is still a problem. In this study, we explored whether involved chemoresistance to OXA HCC. Expressions six cell lines and one human hepatocytes line were determined by real-time quantitative P...

Journal: :Oncotarget 2015
Neel M Fofaria Dennie T Frederick Ryan J Sullivan Keith T Flaherty Sanjay K Srivastava

Melanoma harboring BRAF mutations frequently develop resistance to BRAF inhibitors, limiting the impact of treatment. Here, we establish a mechanism of resistance and subsequently identified a suitable drug combination to overcome the resistance. Single treatment of BRAF mutant melanoma cell lines with vemurafenib or dabrafenib (BRAF inhibitors) alone or in combination with trametinib (MEK1/2 i...

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