Mechanisms of resistance and adaptation to thapsigargin in androgen-independent prostate cancer PC3 and DU145 cells.
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Dong I. Lee | D. Ross | G. Inesi | C. Sumbilla | M. Klein | A. Hussain | Myounghee Lee | Chidambaram Natesavelalar
[1] S. Meltzer,et al. Thapsigargin resistance in human prostate cancer cells , 2006, Cancer.
[2] P. Schuff-Werner,et al. Double transfection improves small interfering RNA‐induced thrombin receptor (PAR‐1) gene silencing in DU 145 prostate cancer cells , 2004, FEBS letters.
[3] C. Toyoshima,et al. Specific Structural Requirements for the Inhibitory Effect of Thapsigargin on the Ca2+ ATPase SERCA* , 2004, Journal of Biological Chemistry.
[4] H. Lilja,et al. Prostate-specific antigen-activated thapsigargin prodrug as targeted therapy for prostate cancer. , 2003, Journal of the National Cancer Institute.
[5] J. Montalbano,et al. Effect of Bax deficiency on death receptor 5 and mitochondrial pathways during endoplasmic reticulum calcium pool depletion-induced apoptosis , 2003, Oncogene.
[6] W. El-Deiry,et al. Endoplasmic reticulum calcium pool depletion-induced apoptosis is coupled with activation of the death receptor 5 pathway , 2002, Oncogene.
[7] P. S. Pedersen,et al. The Sarco/Endoplasmic Reticulum Calcium-ATPase 2b Is an Endoplasmic Reticulum Stress-inducible Protein* , 2000, The Journal of Biological Chemistry.
[8] V. Dixit,et al. Characterization of Calcium Release-activated Apoptosis of LNCaP Prostate Cancer Cells* , 2000, The Journal of Biological Chemistry.
[9] M. Yu,et al. Effects of various amino acid 256 mutations on sarcoplasmic/endoplasmic reticulum Ca2+ ATPase function and their role in the cellular adaptive response to thapsigargin. , 1999, Archives of biochemistry and biophysics.
[10] L. Doyle,et al. A multidrug resistance transporter from human MCF-7 breast cancer cells. , 1998, Proceedings of the National Academy of Sciences of the United States of America.
[11] A. Rishi,et al. Gene amplification and transcriptional upregulation of the sarco/endoplasmic reticulum Ca2+ transport ATPase in thapsigargin-resistant hamster smooth muscle cells. , 1998, Nucleic acids research.
[12] A. Rishi,et al. Specific Substitutions at Amino Acid 256 of the Sarcoplasmic/Endoplasmic Reticulum Ca2+ Transport ATPase Mediate Resistance to Thapsigargin in Thapsigargin-resistant Hamster Cells* , 1998, The Journal of Biological Chemistry.
[13] L. Jones,et al. Functional Co-expression of the Canine Cardiac Ca2+Pump and Phospholamban in Spodoptera frugiperda (Sf21) Cells Reveals New Insights on ATPase Regulation* , 1997, The Journal of Biological Chemistry.
[14] S. Bates,et al. Reduced drug accumulation and multidrug resistance in human breast cancer cells without associated P‐glycoprotein or MRP overexpression , 1997, Journal of cellular biochemistry.
[15] T. McCormick,et al. Mouse Lymphoma Cells Destined to Undergo Apoptosis in Response to Thapsigargin Treatment Fail to Generate a Calcium-mediated grp78/grp94 Stress Response* , 1997, The Journal of Biological Chemistry.
[16] A. Campbell,et al. Induction of calreticulin expression in HeLa cells by depletion of the endoplasmic reticulum Ca2+ store and inhibition of N-linked glycosylation. , 1996, The Biochemical journal.
[17] M. Berridge,et al. Capacitative calcium entry. , 1995, The Biochemical journal.
[18] M. F. Schneider,et al. Direct Involvement of Intracellular Ca Transport ATPase in the Development of Thapsigargin Resistance by Chinese Hamster Lung Fibroblasts (*) , 1995, The Journal of Biological Chemistry.
[19] G. Dubyak,et al. Evidence that BCL-2 represses apoptosis by regulating endoplasmic reticulum-associated Ca2+ fluxes. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[20] J. Gutheil,et al. Alterations in Ca2+ transport ATPase and P-glycoprotein expression can mediate resistance to thapsigargin. , 1994, The Journal of biological chemistry.
[21] X. Cao,et al. Transactivation of the grp78 promoter by Ca2+ depletion. A comparative analysis with A23187 and the endoplasmic reticulum Ca(2+)-ATPase inhibitor thapsigargin. , 1993, The Journal of biological chemistry.
[22] A. Duncan,et al. Overexpression of a transporter gene in a multidrug-resistant human lung cancer cell line. , 1992, Science.
[23] S. Mirski,et al. Non-P-glycoprotein-mediated multidrug resistance in a small cell lung cancer cell line: evidence for decreased susceptibility to drug-induced DNA damage and reduced levels of topoisomerase II. , 1991, Cancer research.
[24] J. Putney. Capacitative calcium entry revisited. , 1990, Cell calcium.
[25] A. Fojo,et al. Characterization of adriamycin-resistant human breast cancer cells which display overexpression of a novel resistance-related membrane protein. , 1990, The Journal of biological chemistry.
[26] J. Lytton,et al. Molecular cloning of cDNAs from human kidney coding for two alternatively spliced products of the cardiac Ca2+-ATPase gene. , 1988, The Journal of biological chemistry.
[27] S. Orrenius,et al. 2,5‐Di(tert‐butyl)‐1,4‐benzohydroquinone — a novel inhibitor of liver microsomal Ca2+ sequestration , 1987, FEBS letters.
[28] J. Endicott,et al. Homology between P-glycoprotein and a bacterial haemolysin transport protein suggests a model for multidrug resistance , 1986, Nature.
[29] D. Housman,et al. Isolation and expression of a complementary DNA that confers multidrug resistance , 1986, Nature.
[30] T. Mosmann. Rapid colorimetric assay for cellular growth and survival: application to proliferation and cytotoxicity assays. , 1983, Journal of immunological methods.