-
1
-
-
67650523623
-
Identification of a putative protein profile associated with tamoxifen therapy resistance in breast cancer
-
doi:10.1074/mcp.M800493-MCP200
-
Umar A, Kang H, Timmermans AM, Look MP, Meijer-van Gelder ME, den Bakker MA, Jaitly N, Martens JW, Luider TM, Foekens JA, Pasa-Tolic L (2009) Identification of a putative protein profile associated with tamoxifen therapy resistance in breast cancer. Mol Cell Proteomics 8(6):1278-1294. doi:10.1074/mcp.M800493-MCP200
-
(2009)
Mol Cell Proteomics
, vol.8
, Issue.6
, pp. 1278-1294
-
-
Umar, A.1
Kang, H.2
Timmermans, A.M.3
Look, M.P.4
Meijer-Van Gelder, M.E.5
Den Bakker, M.A.6
Jaitly, N.7
Martens, J.W.8
Luider, T.M.9
Foekens, J.A.10
Pasa-Tolic, L.11
-
2
-
-
1542674446
-
TOR signaling
-
doi:10.1126/stke.2122003re15
-
Harris TE, Lawrence JC, Jr. (2003) TOR signaling. Sci STKE 2003 (212):re15. doi:10.1126/stke.2122003re15
-
(2003)
Sci STKE
, vol.2003
, Issue.212
-
-
Harris, T.E.1
Lawrence Jr., J.C.2
-
3
-
-
77953422867
-
PIK3CA mutations associated with gene signature of low mTORC1 signaling and better outcomes in estrogen receptor-positive breast cancer
-
doi:10.1073/pnas.0907011107
-
Loi S, Haibe-Kains B, Majjaj S, Lallemand F, Durbecq V, Larsimont D, Gonzalez-Angulo AM, Pusztai L, Symmans WF, Bardelli A, Ellis P, Tutt AN, Gillett CE, Hennessy BT, Mills GB, Phillips WA, Piccart MJ, Speed TP, McArthur GA, Sotiriou C (2010) PIK3CA mutations associated with gene signature of low mTORC1 signaling and better outcomes in estrogen receptor-positive breast cancer. Proc Natl Acad Sci USA 107(22):10208-10213. doi:10.1073/pnas.0907011107
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, Issue.22
, pp. 10208-10213
-
-
Loi, S.1
Haibe-Kains, B.2
Majjaj, S.3
Lallemand, F.4
Durbecq, V.5
Larsimont, D.6
Gonzalez-Angulo, A.M.7
Pusztai, L.8
Symmans, W.F.9
Bardelli, A.10
Ellis, P.11
Tutt, A.N.12
Gillett, C.E.13
Hennessy, B.T.14
Mills, G.B.15
Phillips, W.A.16
Piccart, M.J.17
Speed, T.P.18
McArthur, G.A.19
Sotiriou, C.20
more..
-
4
-
-
79957817959
-
Overcoming resistance: Targeting the PI3K/mTOR pathway in endocrine refractory breast cancer
-
doi:10.4161/cbt.11.11.15953
-
Butt AJ (2011) Overcoming resistance: Targeting the PI3K/mTOR pathway in endocrine refractory breast cancer. Cancer Biol Ther 11 (11):947-949. doi:10.4161/cbt.11.11.15953
-
(2011)
Cancer Biol Ther
, vol.11
, Issue.11
, pp. 947-949
-
-
Butt, A.J.1
-
5
-
-
77953717846
-
MCF-7 breast cancer cells selected for tamoxifen resistance acquire new phenotypes differing in DNA content, phospho-HER2 and PAX2 expression, and rapamycin sensitivity
-
Leung E, Kannan N, Krissansen GW, Findlay MP, Baguley BC (2010) MCF-7 breast cancer cells selected for tamoxifen resistance acquire new phenotypes differing in DNA content, phospho-HER2 and PAX2 expression, and rapamycin sensitivity. Cancer Biol Ther 9(9):717-724
-
(2010)
Cancer Biol Ther
, vol.9
, Issue.9
, pp. 717-724
-
-
Leung, E.1
Kannan, N.2
Krissansen, G.W.3
Findlay, M.P.4
Baguley, B.C.5
-
6
-
-
79957818433
-
Comparison of the effects of the PI3K/mTOR inhibitors NVP-BEZ235 and GSK2126458 on tamoxifen-resistant breast cancer cells
-
Leung E, Kim JE, Rewcastle GW, Finlay GJ, Baguley BC (2011) Comparison of the effects of the PI3K/mTOR inhibitors NVP-BEZ235 and GSK2126458 on tamoxifen-resistant breast cancer cells. Cancer Biol Ther 11(11):938-946
-
(2011)
Cancer Biol Ther
, vol.11
, Issue.11
, pp. 938-946
-
-
Leung, E.1
Kim, J.E.2
Rewcastle, G.W.3
Finlay, G.J.4
Baguley, B.C.5
-
7
-
-
70149114591
-
Antiestrogen-resistant subclones of MCF-7 human breast cancer cells are derived from a common monoclonal drug-resistant progenitor
-
doi:10.1073/pnas.0907560106
-
Coser KR, Wittner BS, Rosenthal NF, Collins SC, Melas A, Smith SL, Mahoney CJ, Shioda K, Isselbacher KJ, Ramaswamy S, Shioda T (2009) Antiestrogen-resistant subclones of MCF-7 human breast cancer cells are derived from a common monoclonal drug-resistant progenitor. Proc Natl Acad Sci USA 106 (34):14536-14541. doi:10.1073/pnas.0907560106
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, Issue.34
, pp. 14536-14541
-
-
Coser, K.R.1
Wittner, B.S.2
Rosenthal, N.F.3
Collins, S.C.4
Melas, A.5
Smith, S.L.6
Mahoney, C.J.7
Shioda, K.8
Isselbacher, K.J.9
Ramaswamy, S.10
Shioda, T.11
-
8
-
-
3042755064
-
Genetic variability in MCF-7 sublines: Evidence of rapid genomic and RNA expression profile modifications
-
doi:10.1186/1471-2407-3-13
-
Nugoli M, Chuchana P, Vendrell J, Orsetti B, Ursule L, Nguyen C, Birnbaum D, Douzery EJ, Cohen P, Theillet C (2003) Genetic variability in MCF-7 sublines: evidence of rapid genomic and RNA expression profile modifications. BMC Cancer 3:13. doi:10.1186/1471-2407-3-13
-
(2003)
BMC Cancer
, vol.3
, pp. 13
-
-
Nugoli, M.1
Chuchana, P.2
Vendrell, J.3
Orsetti, B.4
Ursule, L.5
Nguyen, C.6
Birnbaum, D.7
Douzery, E.J.8
Cohen, P.9
Theillet, C.10
-
9
-
-
84875520876
-
Heterogeneity of phenotype in breast cancer cell lines., vol Book 1
-
press, Intech Publishers
-
Baguley BC, Leung E (2011; in press) Heterogeneity of phenotype in breast cancer cell lines., vol Book 1. In Breast Cancer Cells. Intech Publishers
-
(2011)
Breast Cancer Cells
-
-
Baguley, B.C.1
Leung, E.2
-
10
-
-
79151481328
-
Mechanisms for the activity of heterocyclic cyclohexanone curcumin derivatives in estrogen receptor negative human breast cancer cell lines
-
doi:10.1007/s10637-009-9339-0
-
Somers-Edgar TJ, Taurin S, Larsen L, Chandramouli A, Nelson MA, Rosengren RJ (2009) Mechanisms for the activity of heterocyclic cyclohexanone curcumin derivatives in estrogen receptor negative human breast cancer cell lines. Invest New Drugs 29(1):87-97. doi:10.1007/s10637-009-9339-0
-
(2009)
Invest New Drugs
, vol.29
, Issue.1
, pp. 87-97
-
-
Somers-Edgar, T.J.1
Taurin, S.2
Larsen, L.3
Chandramouli, A.4
Nelson, M.A.5
Rosengren, R.J.6
-
11
-
-
0037051106
-
Curcumin exerts multiple suppressive effects on human breast carcinoma cells
-
doi:10.1002/ijc.10183
-
Shao ZM, Shen ZZ, Liu CH, Sartippour MR, Go VL, Heber D, Nguyen M (2002) Curcumin exerts multiple suppressive effects on human breast carcinoma cells. Int J Cancer 98(2):234-240. doi:10.1002/ijc.10183
-
(2002)
Int J Cancer
, vol.98
, Issue.2
, pp. 234-240
-
-
Shao, Z.M.1
Shen, Z.Z.2
Liu, C.H.3
Sartippour, M.R.4
Go, V.L.5
Heber, D.6
Nguyen, M.7
-
12
-
-
0026777116
-
Nuclear type II sites and malignant cell proliferation: Inhibition by 2, 6-bis-benzylide-necyclohexanones
-
Markaverich BM, Schauweker TH, Gregory RR, Varma M, Kittrell FS, Medina D, Varma RS (1992) Nuclear type II sites and malignant cell proliferation: inhibition by 2, 6-bis-benzylide-necyclohexanones. Cancer Res 52(9):2482-2488
-
(1992)
Cancer Res
, vol.52
, Issue.9
, pp. 2482-2488
-
-
Markaverich, B.M.1
Schauweker, T.H.2
Gregory, R.R.3
Varma, M.4
Kittrell, F.S.5
Medina, D.6
Varma, R.S.7
-
13
-
-
1642523505
-
Status of the "protein kinase CK2-HMG14" system in age-related amnesia in rats
-
Reikhardt BA, Kulikova OG, Borisova GY, Aleksandrova IY, Sapronov NS (2003) Status of the "protein kinase CK2-HMG14" system in age-related amnesia in rats. Neurosci Behav Physiol 33 (8):799-804
-
(2003)
Neurosci Behav Physiol
, vol.33
, Issue.8
, pp. 799-804
-
-
Reikhardt, B.A.1
Kulikova, O.G.2
Borisova, G.Y.3
Aleksandrova, I.Y.4
Sapronov, N.S.5
-
14
-
-
34249957508
-
Selective alkylation of imidazole-4(5)-carboxamides
-
doi: 10.1007/bf00497210
-
Piotrovskii LB, Dumpis MA (1990) Selective alkylation of imidazole-4(5)-carboxamides. Chem Heterocycl Compd 26 (4):407-409. doi: 10.1007/bf00497210
-
(1990)
Chem Heterocycl Compd
, vol.26
, Issue.4
, pp. 407-409
-
-
Piotrovskii, L.B.1
Dumpis, M.A.2
-
15
-
-
34347230544
-
Sulforhodamine B colorimetric assay for cytotoxicity screening
-
doi:10.1038/nprot.2006.179
-
Vichai V, Kirtikara K (2006) Sulforhodamine B colorimetric assay for cytotoxicity screening. Nat Protoc 1(3):1112-1116. doi:10.1038/nprot.2006.179
-
(2006)
Nat Protoc
, vol.1
, Issue.3
, pp. 1112-1116
-
-
Vichai, V.1
Kirtikara, K.2
-
16
-
-
33646691757
-
P21CDKN1A allows the repair of replication-mediated DNA double-strand breaks induced by topoisomerase i and is inactivated by the checkpoint kinase inhibitor 7-hydroxystaurosporine
-
doi: 10.1038/sj.onc.1209313
-
Furuta T, Hayward RL, Meng LH, Takemura H, Aune GJ, Bonner WM, Aladjem MI, Kohn KW, Pommier Y (2006) p21CDKN1A allows the repair of replication-mediated DNA double-strand breaks induced by topoisomerase I and is inactivated by the checkpoint kinase inhibitor 7-hydroxystaurosporine. Oncogene 25 (20):2839-2849. doi: 10.1038/sj.onc.1209313
-
(2006)
Oncogene
, vol.25
, Issue.20
, pp. 2839-2849
-
-
Furuta, T.1
Hayward, R.L.2
Meng, L.H.3
Takemura, H.4
Aune, G.J.5
Bonner, W.M.6
Aladjem, M.I.7
Kohn, K.W.8
Pommier, Y.9
-
17
-
-
0034509633
-
Mechanism of action of camptothecin
-
LiuLF, Desai SD, Li TK, Mao Y, Sun M, Sim SP (2000) Mechanism of action of camptothecin. Ann N Y Acad Sci 922:1-10
-
(2000)
Ann N y Acad Sci
, vol.922
, pp. 1-10
-
-
Liulf Desai, S.D.1
Li, T.K.2
Mao, Y.3
Sun, M.4
Sim, S.P.5
-
18
-
-
0036519363
-
DNA and its associated processes as targets for cancer therapy
-
doi:10.1038/nrc749
-
Hurley LH (2002) DNA and its associated processes as targets for cancer therapy. Nat Rev Cancer 2(3):188-200. doi:10.1038/nrc749
-
(2002)
Nat Rev Cancer
, vol.2
, Issue.3
, pp. 188-200
-
-
Hurley, L.H.1
-
19
-
-
0035266161
-
Characterization of a novel topoisomerase i mutation from a camptothecin-resistant human prostate cancer cell line
-
Urasaki Y, Laco GS, Pourquier P, Takebayashi Y, Kohlhagen G, Gioffre C, Zhang H, Chatterjee D, Pantazis P, Pommier Y (2001) Characterization of a novel topoisomerase I mutation from a camptothecin-resistant human prostate cancer cell line. Cancer Res 61(5):1964-1969
-
(2001)
Cancer Res
, vol.61
, Issue.5
, pp. 1964-1969
-
-
Urasaki, Y.1
Laco, G.S.2
Pourquier, P.3
Takebayashi, Y.4
Kohlhagen, G.5
Gioffre, C.6
Zhang, H.7
Chatterjee, D.8
Pantazis, P.9
Pommier, Y.10
-
20
-
-
79952081873
-
Protein kinase CK2 is a central regulator of topoisomerase i hyperphosphorylation and camptothecin sensitivity in cancer cell lines
-
doi:10.1021/bi101110e
-
Bandyopadhyay K, Gjerset RA (2011) Protein kinase CK2 is a central regulator of topoisomerase I hyperphosphorylation and camptothecin sensitivity in cancer cell lines. Biochemistry 50 (5):704-714. doi:10.1021/bi101110e
-
(2011)
Biochemistry
, vol.50
, Issue.5
, pp. 704-714
-
-
Bandyopadhyay, K.1
Gjerset, R.A.2
-
21
-
-
0036074018
-
Mammalian ABC transporters in health and disease
-
doi:10.1146/annurev.biochem.71.102301.093055
-
Borst P, Elferink RO (2002) Mammalian ABC transporters in health and disease. Annu Rev Biochem 71:537-592. doi:10.1146/annurev.biochem.71.102301. 093055
-
(2002)
Annu Rev Biochem
, vol.71
, pp. 537-592
-
-
Borst, P.1
Elferink, R.O.2
-
22
-
-
33746698886
-
BCRP/ABCG2 levels account for the resistance to topoisomerase i inhibitors and reversal effects by gefitinib in non-small cell lung cancer
-
doi:10.1007/s00280-006-0212-y
-
Nagashima S, Soda H, Oka M, Kitazaki T, Shiozawa K, Nakamura Y, Takemura M, Yabuuchi H, Fukuda M, Tsukamoto K, Kohno S (2006) BCRP/ABCG2 levels account for the resistance to topoisomerase I inhibitors and reversal effects by gefitinib in non-small cell lung cancer. Cancer Chemother Pharmacol 58(5):594-600. doi:10.1007/s00280-006-0212-y
-
(2006)
Cancer Chemother Pharmacol
, vol.58
, Issue.5
, pp. 594-600
-
-
Nagashima, S.1
Soda, H.2
Oka, M.3
Kitazaki, T.4
Shiozawa, K.5
Nakamura, Y.6
Takemura, M.7
Yabuuchi, H.8
Fukuda, M.9
Tsukamoto, K.10
Kohno, S.11
-
23
-
-
78649505322
-
A novel DNA topoisomerase i inhibitor with different mechanism from camptothecin induces G2/M phase cell cycle arrest to K562 cells
-
doi: 10.1021/bi1009419
-
Wu N, Wu XW, Agama K, Pommier Y, Du J, Li D, Gu LQ, Huang ZS, An LK (2010) A novel DNA topoisomerase I inhibitor with different mechanism from camptothecin induces G2/M phase cell cycle arrest to K562 cells. Biochemistry 49(47):10131-10136. doi: 10.1021/bi1009419
-
(2010)
Biochemistry
, vol.49
, Issue.47
, pp. 10131-10136
-
-
Wu, N.1
Wu, X.W.2
Agama, K.3
Pommier, Y.4
Du, J.5
Li, D.6
Gu, L.Q.7
Huang, Z.S.8
An, L.K.9
-
24
-
-
0027472338
-
Sequential modifications of topoisomerase i activity in a camptothecin-resistant cell line established by progressive adaptation
-
Madelaine I, Prost S, Naudin A, Riou G, Lavelle F, Riou JF (1993) Sequential modifications of topoisomerase I activity in a camptothecin-resistant cell line established by progressive adaptation. Biochem Pharmacol 45(2):339-348
-
(1993)
Biochem Pharmacol
, vol.45
, Issue.2
, pp. 339-348
-
-
Madelaine, I.1
Prost, S.2
Naudin, A.3
Riou, G.4
Lavelle, F.5
Riou, J.F.6
-
25
-
-
47749138222
-
Mitotic phosphorylation stimulates DNA relaxation activity of human topoisomerase i
-
doi:10.1074/jbc.M802246200
-
Hackbarth JS, Galvez-Peralta M, Dai NT, Loegering DA, Peterson KL, Meng XW, Karnitz LM, Kaufmann SH (2008) Mitotic phosphorylation stimulates DNA relaxation activity of human topoisomerase I. J Biol Chem 283(24):16711-16722. doi:10.1074/jbc.M802246200
-
(2008)
J Biol Chem
, vol.283
, Issue.24
, pp. 16711-16722
-
-
Hackbarth, J.S.1
Galvez-Peralta, M.2
Dai, N.T.3
Loegering, D.A.4
Peterson, K.L.5
Meng, X.W.6
Karnitz, L.M.7
Kaufmann, S.H.8
-
26
-
-
79952006399
-
PKB/Akt promotes DSB repair in cancer cells through upregulating Mre11 expression following ionizing radiation
-
doi:10.1038/onc.2010.467
-
Deng R, Tang J, Ma JG, Chen SP, Xia LP, Zhou WJ, Li DD, Feng GK, Zeng YX, Zhu XF (2011) PKB/Akt promotes DSB repair in cancer cells through upregulating Mre11 expression following ionizing radiation. Oncogene 30(8):944-955. doi:10.1038/onc.2010.467
-
(2011)
Oncogene
, vol.30
, Issue.8
, pp. 944-955
-
-
Deng, R.1
Tang, J.2
Ma, J.G.3
Chen, S.P.4
Xia, L.P.5
Zhou, W.J.6
Li, D.D.7
Feng, G.K.8
Zeng, Y.X.9
Zhu, X.F.10
-
27
-
-
79959840932
-
Evaluation of irinotecan hydrochloride (CPT-11) and trastuzumab combination therapy as salvage treatment in patients with HER2 overexpressing metastatic breast cancer
-
Ikeda M, Kurebayashi J, Sonoo H, Oota Y, Fujii S, Shimo T, Miyake A, Seki M, Souda M, Nomura T, Yamamoto Y, Shiiki S, Nakashima K, Tanaka K (2009) Evaluation of irinotecan hydrochloride (CPT-11) and trastuzumab combination therapy as salvage treatment in patients with HER2 overexpressing metastatic breast cancer. Gan To Kagaku Ryoho 36(5):773-777
-
(2009)
Gan to Kagaku Ryoho
, vol.36
, Issue.5
, pp. 773-777
-
-
Ikeda, M.1
Kurebayashi, J.2
Sonoo, H.3
Oota, Y.4
Fujii, S.5
Shimo, T.6
Miyake, A.7
Seki, M.8
Souda, M.9
Nomura, T.10
Yamamoto, Y.11
Shiiki, S.12
Nakashima, K.13
Tanaka, K.14
|