-
1
-
-
0037097863
-
Mammalian cell size is controlled by mTOR and its downstream targets S6K1 and 4EBP1/eIF4E
-
Fingar DC, Salama S, Tsou C, Harlow E, Blenis J. Mammalian cell size is controlled by mTOR and its downstream targets S6K1 and 4EBP1/eIF4E. Genes Dev 2002;16:1472-87.
-
(2002)
Genes Dev
, vol.16
, pp. 1472-1487
-
-
Fingar, D.C.1
Salama, S.2
Tsou, C.3
Harlow, E.4
Blenis, J.5
-
2
-
-
20044392290
-
Atrophy of S6K1(-/-) skeletal muscle cells reveals distinct mTOR effectors for cell cycle and size control
-
Ohanna M, Sobering AK, Lapointe T, Lorenzo L, Praud C, Petroulakis E, et al. Atrophy of S6K1(-/-) skeletal muscle cells reveals distinct mTOR effectors for cell cycle and size control. Nat Cell Biol 2005;7:286-94.
-
(2005)
Nat Cell Biol
, vol.7
, pp. 286-294
-
-
Ohanna, M.1
Sobering, A.K.2
Lapointe, T.3
Lorenzo, L.4
Praud, C.5
Petroulakis, E.6
-
3
-
-
77950516104
-
mTOR signaling and drug development in cancer
-
Dancey J. mTOR signaling and drug development in cancer. Nat Rev Clin Oncol 2010;7:209-19.
-
(2010)
Nat Rev Clin Oncol
, vol.7
, pp. 209-219
-
-
Dancey, J.1
-
4
-
-
0036632368
-
The phosphatidylinositol 3-Kinase AKT pathway in human cancer
-
Vivanco I, Sawyers CL. The phosphatidylinositol 3-Kinase AKT pathway in human cancer. Nat Rev Cancer 2002;2:489-501.
-
(2002)
Nat Rev Cancer
, vol.2
, pp. 489-501
-
-
Vivanco, I.1
Sawyers, C.L.2
-
5
-
-
70349696530
-
EGFR-dependent and independent activation of Akt/mTOR cascade in bone and soft tissue tumors
-
Dobashi Y, Suzuki S, Sato E, Hamada Y, Yanagawa T, Ooi A. EGFR-dependent and independent activation of Akt/mTOR cascade in bone and soft tissue tumors. Mod Pathol 2009;22:1328-40.
-
(2009)
Mod Pathol
, vol.22
, pp. 1328-1340
-
-
Dobashi, Y.1
Suzuki, S.2
Sato, E.3
Hamada, Y.4
Yanagawa, T.5
Ooi, A.6
-
6
-
-
33750068623
-
mTOR, translation initiation and cancer
-
Mamane Y, Petroulakis E, LeBacquer O, Sonenberg N. mTOR, translation initiation and cancer. Oncogene 2006;25:6416-22.
-
(2006)
Oncogene
, vol.25
, pp. 6416-6422
-
-
Mamane, Y.1
Petroulakis, E.2
LeBacquer, O.3
Sonenberg, N.4
-
7
-
-
84898821195
-
Activation of the Akt/mammalian target of rapamycin pathway in myxofibrosarcomas
-
Takahashi Y, Kohashi K, Yamada Y, Endo M, Setsu N, Ishii T, et al. Activation of the Akt/mammalian target of rapamycin pathway in myxofibrosarcomas. Hum Pathol 2014;45:984-93.
-
(2014)
Hum Pathol
, vol.45
, pp. 984-993
-
-
Takahashi, Y.1
Kohashi, K.2
Yamada, Y.3
Endo, M.4
Setsu, N.5
Ishii, T.6
-
8
-
-
84857995538
-
The Akt/mammalian target of rapamycin pathway is activated and associated with adverse prognosis in soft tissue leiomyosarcomas
-
Setsu N, Yamamoto H, Kohashi K, Endo M, Matsuda S, Yokoyama R, et al. The Akt/mammalian target of rapamycin pathway is activated and associated with adverse prognosis in soft tissue leiomyosarcomas. Cancer 2012;118:1637-48.
-
(2012)
Cancer
, vol.118
, pp. 1637-1648
-
-
Setsu, N.1
Yamamoto, H.2
Kohashi, K.3
Endo, M.4
Matsuda, S.5
Yokoyama, R.6
-
9
-
-
34250013899
-
The AKT-mTOR pathway plays a critical role in the development of leiomyosarcomas
-
Hernando E, Charytonowicz E, Dudas ME, Menendez S, Matushansky I, Mills J, et al. The AKT-mTOR pathway plays a critical role in the development of leiomyosarcomas. Nat Med 2007;13:748-53.
-
(2007)
Nat Med
, vol.13
, pp. 748-753
-
-
Hernando, E.1
Charytonowicz, E.2
Dudas, M.E.3
Menendez, S.4
Matushansky, I.5
Mills, J.6
-
10
-
-
84869505772
-
Alterations of the p53 and PIK3CA/AKT/mTOR pathways in angiosarcomas: A pattern distinct from other sarcomas with complex genomics
-
Italiano A, Chen CL, Thomas R, Breen M, Bonnet F, Sevenet N, et al. Alterations of the p53 and PIK3CA/AKT/mTOR pathways in angiosarcomas: a pattern distinct from other sarcomas with complex genomics. Cancer 2012;118:5878-87.
-
(2012)
Cancer
, vol.118
, pp. 5878-5887
-
-
Italiano, A.1
Chen, C.L.2
Thomas, R.3
Breen, M.4
Bonnet, F.5
Sevenet, N.6
-
11
-
-
34248216623
-
Phosphoprotein pathway mapping: Akt/mammalian target of rapamycin activation is negatively associated with childhood rhabdomyosarcoma survival
-
Petricoin EF III, Espina V, Araujo RP, Midura B, Yeung C, Wan X, et al. Phosphoprotein pathway mapping: Akt/mammalian target of rapamycin activation is negatively associated with childhood rhabdomyosarcoma survival. Cancer Res 2007;67:3431-40.
-
(2007)
Cancer Res
, vol.67
, pp. 3431-3440
-
-
Petricoin, E.F.1
Espina, V.2
Araujo, R.P.3
Midura, B.4
Yeung, C.5
Wan, X.6
-
12
-
-
84884908724
-
Prognostic impact of the activation status of the Akt/mTOR pathway in synovial sarcoma
-
Setsu N, Kohashi K, Fushimi F, Endo M, Yamamoto H, Takahashi Y, et al. Prognostic impact of the activation status of the Akt/mTOR pathway in synovial sarcoma. Cancer 2013;119:3504-13.
-
(2013)
Cancer
, vol.119
, pp. 3504-3513
-
-
Setsu, N.1
Kohashi, K.2
Fushimi, F.3
Endo, M.4
Yamamoto, H.5
Takahashi, Y.6
-
13
-
-
84872546604
-
Prognostic significance of AKT/mTOR and MAPK pathways and antitumor effect ofmTORinhibitor in NF1-related and sporadic malignant peripheral nerve sheath tumors
-
Endo M, Yamamoto H, Setsu N, Kohashi K, Takahashi Y, Ishii T, et al. Prognostic significance of AKT/mTOR and MAPK pathways and antitumor effect ofmTORinhibitor in NF1-related and sporadic malignant peripheral nerve sheath tumors. Clin Cancer Res 2013;19:450-61.
-
(2013)
Clin Cancer Res
, vol.19
, pp. 450-461
-
-
Endo, M.1
Yamamoto, H.2
Setsu, N.3
Kohashi, K.4
Takahashi, Y.5
Ishii, T.6
-
14
-
-
84867505054
-
PTEN promoter methylation and activation of the PI3K/Akt/mTOR pathway in pediatric gliomas and influence on clinical outcome
-
Mueller S, Phillips J, Onar-Thomas A, Romero E, Zheng S, Wiencke JK, et al. PTEN promoter methylation and activation of the PI3K/Akt/mTOR pathway in pediatric gliomas and influence on clinical outcome. Neuro Oncol 2012;14:1146-52.
-
(2012)
Neuro Oncol
, vol.14
, pp. 1146-1152
-
-
Mueller, S.1
Phillips, J.2
Onar-Thomas, A.3
Romero, E.4
Zheng, S.5
Wiencke, J.K.6
-
15
-
-
84865722534
-
PDGF receptor alpha is an alternative mediator of rapamycin-induced Akt activation: Implications for combination targeted therapy of synovial sarcoma
-
Ho AL, Vasudeva SD, Lae M, Saito T, Barbashina V, Antonescu CR, et al. PDGF receptor alpha is an alternative mediator of rapamycin-induced Akt activation: implications for combination targeted therapy of synovial sarcoma. Cancer Res 2012;72:4515-25.
-
(2012)
Cancer Res
, vol.72
, pp. 4515-4525
-
-
Ho, A.L.1
Vasudeva, S.D.2
Lae, M.3
Saito, T.4
Barbashina, V.5
Antonescu, C.R.6
-
16
-
-
0033179378
-
Expression of insulin-like growth factor-1 receptor in synovial sarcoma: Association with an aggressive phenotype
-
Xie Y, Skytting B, NilssonG, Brodin B, LarssonO. Expression of insulin-like growth factor-1 receptor in synovial sarcoma: association with an aggressive phenotype. Cancer Res 1999;59:3588-91.
-
(1999)
Cancer Res
, vol.59
, pp. 3588-3591
-
-
Xie, Y.1
Skytting, B.2
Nilsson, G.3
Brodin, B.4
Larsson, O.5
-
17
-
-
0028328655
-
Rapamycin selectively inhibits the growth of childhood rhabdomyosarcoma cells through inhibition of signaling via the type I insulin-like growth factor receptor
-
Dilling MB, Dias P, Shapiro DN, Germain GS, Johnson RK, Houghton PJ. Rapamycin selectively inhibits the growth of childhood rhabdomyosarcoma cells through inhibition of signaling via the type I insulin-like growth factor receptor. Cancer Res 1994;54:903-7.
-
(1994)
Cancer Res
, vol.54
, pp. 903-907
-
-
Dilling, M.B.1
Dias, P.2
Shapiro, D.N.3
Germain, G.S.4
Johnson, R.K.5
Houghton, P.J.6
-
18
-
-
33744829237
-
CCI-779 inhibits rhabdomyosarcoma xenograft growth by an antiangiogenic mechanism linked to the targeting of mTOR/Hif-1alpha/VEGF signaling
-
Wan X, Shen N, Mendoza A, Khanna C, Helman LJ. CCI-779 inhibits rhabdomyosarcoma xenograft growth by an antiangiogenic mechanism linked to the targeting of mTOR/Hif-1alpha/VEGF signaling. Neoplasia 2006;8:394-401.
-
(2006)
Neoplasia
, vol.8
, pp. 394-401
-
-
Wan, X.1
Shen, N.2
Mendoza, A.3
Khanna, C.4
Helman, L.J.5
-
19
-
-
70449450426
-
Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models
-
Taylor JGt, Cheuk AT, Tsang PS, Chung JY, Song YK, Desai K, et al. Identification of FGFR4-activating mutations in human rhabdomyosarcomas that promote metastasis in xenotransplanted models. J Clin Invest 2009;119:3395-407.
-
(2009)
J Clin Invest
, vol.119
, pp. 3395-3407
-
-
Taylor, J.Gt.1
Cheuk, A.T.2
Tsang, P.S.3
Chung, J.Y.4
Song, Y.K.5
Desai, K.6
-
20
-
-
84880506610
-
Synthetic lethal interaction between PI3K/Akt/mTOR and Ras/MEK/ERK pathway inhibition in rhabdomyosarcoma
-
Guenther MK, Graab U, Fulda S. Synthetic lethal interaction between PI3K/Akt/mTOR and Ras/MEK/ERK pathway inhibition in rhabdomyosarcoma. Cancer Lett 2013;337:200-9.
-
(2013)
Cancer Lett
, vol.337
, pp. 200-209
-
-
Guenther, M.K.1
Graab, U.2
Fulda, S.3
-
21
-
-
84887065790
-
Dual blockade of the PI3K/AKT/mTOR (AZD8055) and RAS/MEK/ERK (AZD6244) pathways synergistically inhibits rhabdomyosarcoma cell growth in vitro and in vivo
-
Renshaw J, Taylor KR, Bishop R, Valenti M, De Haven Brandon A, Gowan S, et al. Dual blockade of the PI3K/AKT/mTOR (AZD8055) and RAS/MEK/ERK (AZD6244) pathways synergistically inhibits rhabdomyosarcoma cell growth in vitro and in vivo. Clin Cancer Res 2013;19:5940-51.
-
(2013)
Clin Cancer Res
, vol.19
, pp. 5940-5951
-
-
Renshaw, J.1
Taylor, K.R.2
Bishop, R.3
Valenti, M.4
De Haven Brandon, A.5
Gowan, S.6
-
22
-
-
84856555606
-
Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcomaand neuroblastoma withmutated genes in growth signaling pathways
-
Shukla N, Ameur N, Yilmaz I, Nafa K, Lau CY, Marchetti A, et al. Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcomaand neuroblastoma withmutated genes in growth signaling pathways. Clin Cancer Res 2012;18:748-57.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 748-757
-
-
Shukla, N.1
Ameur, N.2
Yilmaz, I.3
Nafa, K.4
Lau, C.Y.5
Marchetti, A.6
-
23
-
-
84901687144
-
A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations
-
Kohsaka S, Shukla N, Ameur N, Ito T, Ng CK, Wang L, et al. A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations. Nat Genet 2014;46:595-600.
-
(2014)
Nat Genet
, vol.46
, pp. 595-600
-
-
Kohsaka, S.1
Shukla, N.2
Ameur, N.3
Ito, T.4
Ng, C.K.5
Wang, L.6
-
24
-
-
84896691170
-
Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors
-
Shern JF, Chen L, Chmielecki J, Wei JS, Patidar R, Rosenberg M, et al. Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors. Cancer Discov 2014;4:216-31.
-
(2014)
Cancer Discov
, vol.4
, pp. 216-231
-
-
Shern, J.F.1
Chen, L.2
Chmielecki, J.3
Wei, J.S.4
Patidar, R.5
Rosenberg, M.6
-
25
-
-
34548700597
-
Rapamycin: Something old, something new, sometimes borrowed and now renewed
-
Hartford CM, Ratain MJ. Rapamycin: something old, something new, sometimes borrowed and now renewed. Clin Pharmacol Ther 2007;82:381-8.
-
(2007)
Clin Pharmacol Ther
, vol.82
, pp. 381-388
-
-
Hartford, C.M.1
Ratain, M.J.2
-
26
-
-
72049117072
-
Mammalian target of rapamycin: Discovery of rapamycin reveals a signaling pathway important for normal and cancer cell growth
-
Gibbons JJ, Abraham RT, Yu K. Mammalian target of rapamycin: discovery of rapamycin reveals a signaling pathway important for normal and cancer cell growth. Semin Oncol 2009;36 Suppl 3:S3-S17.
-
(2009)
Semin Oncol
, vol.36
, pp. S3-S17
-
-
Gibbons, J.J.1
Abraham, R.T.2
Yu, K.3
-
27
-
-
32944457518
-
mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt
-
O'Reilly KE, Rojo F, She QB, Solit D, Mills GB, Smith D, et al. mTOR inhibition induces upstream receptor tyrosine kinase signaling and activates Akt. Cancer Res 2006;66:1500-8.
-
(2006)
Cancer Res
, vol.66
, pp. 1500-1508
-
-
O'Reilly, K.E.1
Rojo, F.2
She, Q.B.3
Solit, D.4
Mills, G.B.5
Smith, D.6
-
29
-
-
84862777192
-
The translational landscape of mTOR signalling steers cancer initiation and metastasis
-
Hsieh AC, Liu Y, Edlind MP, Ingolia NT, Janes MR, Sher A, et al. The translational landscape of mTOR signalling steers cancer initiation and metastasis. Nature 2012;485:55-61.
-
(2012)
Nature
, vol.485
, pp. 55-61
-
-
Hsieh, A.C.1
Liu, Y.2
Edlind, M.P.3
Ingolia, N.T.4
Janes, M.R.5
Sher, A.6
-
30
-
-
84875219652
-
Efficacy of the investigationalm TOR kinase inhibitor MLN0128/INK128 in models of B-cell acute lymphoblastic leukemia
-
Janes MR, Vu C, Mallya S, Shieh MP, Limon JJ, Li LS, et al. Efficacy of the investigationalm TOR kinase inhibitor MLN0128/INK128 in models of B-cell acute lymphoblastic leukemia. Leukemia 2013;27:586-94.
-
(2013)
Leukemia
, vol.27
, pp. 586-594
-
-
Janes, M.R.1
Vu, C.2
Mallya, S.3
Shieh, M.P.4
Limon, J.J.5
Li, L.S.6
-
31
-
-
84860532107
-
Dual mTORC1/2 and HER2 blockade results in antitumor activity in preclinical models of breast cancer resistant to anti-HER2 therapy
-
Garcia-Garcia C, Ibrahim YH, Serra V, Calvo MT, GuzmanM,Grueso J, et al. Dual mTORC1/2 and HER2 blockade results in antitumor activity in preclinical models of breast cancer resistant to anti-HER2 therapy. Clin Cancer Res 2012;18:2603-12.
-
(2012)
Clin Cancer Res
, vol.18
, pp. 2603-2612
-
-
Garcia-Garcia, C.1
Ibrahim, Y.H.2
Serra, V.3
Calvo, M.T.4
Guzman, M.5
Grueso, J.6
-
32
-
-
84878759479
-
Investigational drug MLN0128, a novel TORC1/2 inhibitor, demonstrates potent oral antitumor activity in human breast cancer xenograft models
-
Gokmen-Polar Y, Liu Y, Toroni RA, Sanders KL, Mehta R, Badve S, et al. Investigational drug MLN0128, a novel TORC1/2 inhibitor, demonstrates potent oral antitumor activity in human breast cancer xenograft models. Breast Cancer Res Treat 2012;136:673-82.
-
(2012)
Breast Cancer Res Treat
, vol.136
, pp. 673-682
-
-
Gokmen-Polar, Y.1
Liu, Y.2
Toroni, R.A.3
Sanders, K.L.4
Mehta, R.5
Badve, S.6
-
33
-
-
84895921712
-
Preclinical trial of a new dual mTOR inhibitor, MLN0128, using renal cell carcinoma tumorgrafts
-
Ingels A, Zhao H, Thong AE, Saar M, Valta MP, Nolley R, et al. Preclinical trial of a new dual mTOR inhibitor, MLN0128, using renal cell carcinoma tumorgrafts. Int J Cancer 2014;134:2322-9.
-
(2014)
Int J Cancer
, vol.134
, pp. 2322-2329
-
-
Ingels, A.1
Zhao, H.2
Thong, A.E.3
Saar, M.4
Valta, M.P.5
Nolley, R.6
-
34
-
-
84902689895
-
Sustained inhibition of receptor tyrosine kinases and macrophage depletion by PLX3397 and rapamycin as a potential new approach for the treatment of MPNSTs
-
Patwardhan PP, Surriga O, Beckman MJ, de Stanchina E, Dematteo RP, Tap WD, et al. Sustained inhibition of receptor tyrosine kinases and macrophage depletion by PLX3397 and rapamycin as a potential new approach for the treatment of MPNSTs. Clin Cancer Res 2014;20:3146-58.
-
(2014)
Clin Cancer Res
, vol.20
, pp. 3146-3158
-
-
Patwardhan, P.P.1
Surriga, O.2
Beckman, M.J.3
De Stanchina, E.4
Dematteo, R.P.5
Tap, W.D.6
-
35
-
-
34547102253
-
Gene expression profiling of liposarcoma identifies distinct biological types/subtypes and potential therapeutic targets in well-differentiated and dedifferentiated liposarcoma
-
Singer S, Socci ND, Ambrosini G, Sambol E, Decarolis P, Wu Y, et al. Gene expression profiling of liposarcoma identifies distinct biological types/subtypes and potential therapeutic targets in well-differentiated and dedifferentiated liposarcoma. Cancer Res 2007;67:6626-36.
-
(2007)
Cancer Res
, vol.67
, pp. 6626-6636
-
-
Singer, S.1
Socci, N.D.2
Ambrosini, G.3
Sambol, E.4
Decarolis, P.5
Wu, Y.6
-
36
-
-
0037507252
-
The mammalian target of rapamycin (mTOR) partner, raptor, binds the mTOR substrates p70 S6 kinase and 4E-BP1 through their TOR signaling (TOS) motif
-
Nojima H, Tokunaga C, Eguchi S,Oshiro N, Hidayat S, Yoshino K, et al. The mammalian target of rapamycin (mTOR) partner, raptor, binds the mTOR substrates p70 S6 kinase and 4E-BP1 through their TOR signaling (TOS) motif. J Biol Chem 2003;278:15461-4.
-
(2003)
J Biol Chem
, vol.278
, pp. 15461-15464
-
-
Nojima, H.1
Tokunaga, C.2
Eguchi, S.3
Oshiro, N.4
Hidayat, S.5
Yoshino, K.6
-
37
-
-
0025776523
-
Targets for cell cycle arrest by the immunosuppressant rapamycin in yeast
-
Heitman J, Movva NR, Hall MN. Targets for cell cycle arrest by the immunosuppressant rapamycin in yeast. Science 1991;253:905-9.
-
(1991)
Science
, vol.253
, pp. 905-909
-
-
Heitman, J.1
Movva, N.R.2
Hall, M.N.3
-
38
-
-
33646023695
-
Prolonged rapamycin treatment inhibits mTORC2 assembly and Akt/PKB
-
Sarbassov DD, Ali SM, Sengupta S, Sheen JH, Hsu PP, Bagley AF, et al. Prolonged rapamycin treatment inhibits mTORC2 assembly and Akt/PKB. Mol Cell 2006;22:159-68.
-
(2006)
Mol Cell
, vol.22
, pp. 159-168
-
-
Sarbassov, D.D.1
Ali, S.M.2
Sengupta, S.3
Sheen, J.H.4
Hsu, P.P.5
Bagley, A.F.6
-
39
-
-
75749105049
-
mTORC1-activated S6K1 phosphorylates Rictor on threonine 1135 and regulatesm TORC2 signaling
-
Julien LA, Carriere A, Moreau J, Roux PP. mTORC1-activated S6K1 phosphorylates Rictor on threonine 1135 and regulatesm TORC2 signaling.Mol Cell Biol 2010;30:908-21.
-
(2010)
Mol Cell Biol
, vol.30
, pp. 908-921
-
-
Julien, L.A.1
Carriere, A.2
Moreau, J.3
Roux, P.P.4
-
40
-
-
58649092475
-
mTOR complex 2 (mTORC2) controls hydrophobic motif phosphorylation and activation of serum- and glucocorticoid-induced protein kinase 1 (SGK1)
-
Garcia-Martinez JM, Alessi DR. mTOR complex 2 (mTORC2) controls hydrophobic motif phosphorylation and activation of serum- and glucocorticoid-induced protein kinase 1 (SGK1). Biochem J 2008;416:375-85.
-
(2008)
Biochem J
, vol.416
, pp. 375-385
-
-
Garcia-Martinez, J.M.1
Alessi, D.R.2
-
41
-
-
23844438209
-
Activation of Akt and eIF4E survival pathways by rapamycin-mediated mammalian target of rapamycin inhibition
-
Sun SY, Rosenberg LM, Wang X, Zhou Z, Yue P, Fu H, et al. Activation of Akt and eIF4E survival pathways by rapamycin-mediated mammalian target of rapamycin inhibition. Cancer Res 2005;65:7052-8.
-
(2005)
Cancer Res
, vol.65
, pp. 7052-7058
-
-
Sun, S.Y.1
Rosenberg, L.M.2
Wang, X.3
Zhou, Z.4
Yue, P.5
Fu, H.6
-
42
-
-
77953763269
-
Rictor phosphorylation on the Thr-1135 site does not require mammalian target of rapamycin complex 2
-
Boulbes D, Chen CH, Shaikenov T, Agarwal NK, Peterson TR, Addona TA, et al. Rictor phosphorylation on the Thr-1135 site does not require mammalian target of rapamycin complex 2. Mol Cancer Res 2010;8:896-906.
-
(2010)
Mol Cancer Res
, vol.8
, pp. 896-906
-
-
Boulbes, D.1
Chen, C.H.2
Shaikenov, T.3
Agarwal, N.K.4
Peterson, T.R.5
Addona, T.A.6
-
43
-
-
33747598681
-
Expression and genomic status of EGFR and ErbB-2 in alveolar and embryonal rhabdomyosarcoma
-
Ganti R, Skapek SX, Zhang J, Fuller CE, Wu J, Billups CA, et al. Expression and genomic status of EGFR and ErbB-2 in alveolar and embryonal rhabdomyosarcoma. Mod Pathol 2006;19:1213-20.
-
(2006)
Mod Pathol
, vol.19
, pp. 1213-1220
-
-
Ganti, R.1
Skapek, S.X.2
Zhang, J.3
Fuller, C.E.4
Wu, J.5
Billups, C.A.6
-
44
-
-
56249147509
-
Rapamycin differentially inhibits S6Ks and 4E-BP1 to mediate cell-type-specific repression of mRNA translation
-
Choo AY, Yoon SO, Kim SG, Roux PP, Blenis J. Rapamycin differentially inhibits S6Ks and 4E-BP1 to mediate cell-type-specific repression of mRNA translation. Proc Natl Acad Sci U S A 2008;105:17414-9.
-
(2008)
Proc Natl Acad Sci U S A
, vol.105
, pp. 17414-17419
-
-
Choo, A.Y.1
Yoon, S.O.2
Kim, S.G.3
Roux, P.P.4
Blenis, J.5
-
45
-
-
0029103330
-
Control of p70 s6 kinase by kinase activity of FRAP in vivo
-
Brown EJ, Beal PA, Keith CT, Chen J, Shin TB, Schreiber SL. Control of p70 s6 kinase by kinase activity of FRAP in vivo . Nature 1995;377:441-6.
-
(1995)
Nature
, vol.377
, pp. 441-446
-
-
Brown, E.J.1
Beal, P.A.2
Keith, C.T.3
Chen, J.4
Shin, T.B.5
Schreiber, S.L.6
-
46
-
-
0032520009
-
4E-BP1, a repressor of mRNA translation, is phosphorylated and inactivated by the Akt(PKB) signaling pathway
-
Gingras AC, Kennedy SG, O'Leary MA, Sonenberg N, Hay N. 4E-BP1, a repressor of mRNA translation, is phosphorylated and inactivated by the Akt(PKB) signaling pathway. Genes Dev 1998;12:502-13.
-
(1998)
Genes Dev
, vol.12
, pp. 502-513
-
-
Gingras, A.C.1
Kennedy, S.G.2
O'Leary, M.A.3
Sonenberg, N.4
Hay, N.5
-
47
-
-
84894095058
-
Adaptation to mTOR kinase inhibitors by amplification of eIF4E to maintain cap-dependent translation
-
Cope CL, Gilley R, Balmanno K, Sale MJ, Howarth KD, Hampson M, et al. Adaptation to mTOR kinase inhibitors by amplification of eIF4E to maintain cap-dependent translation. J Cell Sci 2014;127:788-800.
-
(2014)
J Cell Sci
, vol.127
, pp. 788-800
-
-
Cope, C.L.1
Gilley, R.2
Balmanno, K.3
Sale, M.J.4
Howarth, K.D.5
Hampson, M.6
-
48
-
-
75149112670
-
AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity
-
Chresta CM, Davies BR, Hickson I, Harding T, Cosulich S, Critchlow SE, et al. AZD8055 is a potent, selective, and orally bioavailable ATP-competitive mammalian target of rapamycin kinase inhibitor with in vitro and in vivo antitumor activity. Cancer Res 2010;70:288-98.
-
(2010)
Cancer Res
, vol.70
, pp. 288-298
-
-
Chresta, C.M.1
Davies, B.R.2
Hickson, I.3
Harding, T.4
Cosulich, S.5
Critchlow, S.E.6
-
49
-
-
80051590039
-
Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2: Distinct from rapamycin
-
Bhagwat SV, Gokhale PC, Crew AP, Cooke A, Yao Y, Mantis C, et al. Preclinical characterization of OSI-027, a potent and selective inhibitor of mTORC1 and mTORC2: distinct from rapamycin. Mol Cancer Ther 2011;10:1394-406.
-
(2011)
Mol Cancer Ther
, vol.10
, pp. 1394-1406
-
-
Bhagwat, S.V.1
Gokhale, P.C.2
Crew, A.P.3
Cooke, A.4
Yao, Y.5
Mantis, C.6
-
50
-
-
33749076673
-
SIN1/MIP1 maintains rictor-mTOR complex integrity and regulates Akt phosphorylation and substrate specifi city
-
Jacinto E, Facchinetti V, Liu D, Soto N, Wei S, Jung SY, et al. SIN1/MIP1 maintains rictor-mTOR complex integrity and regulates Akt phosphorylation and substrate specifi city. Cell 2006;127:125-37.
-
(2006)
Cell
, vol.127
, pp. 125-137
-
-
Jacinto, E.1
Facchinetti, V.2
Liu, D.3
Soto, N.4
Wei, S.5
Jung, S.Y.6
|