RETRACTED: Different docetaxel-induced apoptotic pathways are present in prostate cancer cell lines LNCaP and PC-3 (Retracted Article. See vol 61, pg 1293, 2003)
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作者:
Muenchen, HJ
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机构:Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
Muenchen, HJ
Poncza, PJ
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机构:Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
Poncza, PJ
Pienta, KJ
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机构:Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
Pienta, KJ
机构:
[1] Univ Michigan, Sch Med, Dept Internal Med, Div Hematol Oncol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Surg, Ann Arbor, MI 48109 USA
Objectives. To investigate the molecular machinery of docetaxel (Taxotere)-initiated death signaling on prostate cancer cell lines LNCaP and PC-3. Taxotere is a member of the taxane family of chemotherapeutic agents. It has been shown to disrupt microtubule dynamics causing mitotic arrest, which leads to cell death. Taxotere has demonstrated induction of cell death in LNCaP and PC-3 cells. However, the pathways by which apoptosis occurs differ in each cell line. Methods. The prostate cancer cell lines, LNCaP and PC-3, were treated with 40 nM Taxotere for Various lengths of time (0.5 to 24 hours). Western blot analysis was used for protein analysis. Results. LNCaP cells demonstrated caspase-3 and caspase-7 cleavage, and PC-3 cells demonstrated only caspase-8 and BH3-interacting domain death agonist cleavage. Only LNCaP cells were observed to express clusterin expression; PC-3 cells expressed a novel apoptosis inhibitor, survivin. Conclusions. In this study, we demonstrated two distinctly different Taxotere-induced apoptotic pathways in LNCaP and PC-3 cells that may be of clinical importance when treating prostate cancer. UROLOGY 57: 366-370, 2001. (C) 2001, Elsevier Science Inc.
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Columbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USAColumbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
Schlaberg, Robert
Choe, Daniel J.
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Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USAColumbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
Choe, Daniel J.
Brown, Kristy R.
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Columbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USAColumbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
Brown, Kristy R.
Thaker, Harshwardhan M.
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Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USAColumbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
Thaker, Harshwardhan M.
Singh, Ila R.
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Columbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
Univ Utah, Dept Pathol, Salt Lake City, UT 84112 USAColumbia Univ, Med Ctr, Dept Pathol & Cell Biol, New York, NY 10032 USA
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Univ Salerno, Dept Pharm, I-84084 Fisciano, SA, ItalyUniv Salerno, Dept Pharm, I-84084 Fisciano, SA, Italy
Gangemi, Giuseppina
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Gazzerro, Patrizia
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Fiore, Donatella
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Proto, Maria Chiara
Butini, Stefania
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机构:
Univ Siena, European Res Ctr Drug Discovery & Dev NatSynDrugs, I-53100 Siena, Italy
Univ Siena, Dipartimento Farm Chim Tecnol, I-53100 Siena, ItalyUniv Salerno, Dept Pharm, I-84084 Fisciano, SA, Italy
Butini, Stefania
Gemma, Sandra
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Univ Siena, European Res Ctr Drug Discovery & Dev NatSynDrugs, I-53100 Siena, Italy
Univ Siena, Dipartimento Farm Chim Tecnol, I-53100 Siena, ItalyUniv Salerno, Dept Pharm, I-84084 Fisciano, SA, Italy
Gemma, Sandra
Casagni, Alice
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Univ Siena, European Res Ctr Drug Discovery & Dev NatSynDrugs, I-53100 Siena, Italy
Univ Siena, Dipartimento Farm Chim Tecnol, I-53100 Siena, ItalyUniv Salerno, Dept Pharm, I-84084 Fisciano, SA, Italy