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Ann Greer

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Articles 16
Citations 473
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Recent Articles
1.
Huang F, Chang H, Greer A, Hillerman S, Reeves K, Hurlburt W, et al.
Mol Cancer Ther . 2014 Dec; 14(2):620-30. PMID: 25527633
Insulin-like growth factor receptor 1 (IGF-1R)-targeting therapies are currently at an important crossroad given the low clinical response rates seen in unselected patients. Predictive biomarkers for patient selection are critical...
2.
Ross-Macdonald P, de Silva H, Patel V, Truong A, He A, Neuhaus I, et al.
Bioorg Med Chem . 2011 Dec; 20(6):1961-72. PMID: 22137930
Therapeutic development of a targeted agent involves a series of decisions over additional activities that may be ignored, eliminated or pursued. This paper details the concurrent application of two methods...
3.
Hou X, Huang F, Macedo L, Harrington S, Reeves K, Greer A, et al.
Cancer Res . 2011 Nov; 71(24):7597-607. PMID: 22042792
Insulin-like growth factor (IGF) signaling has been implicated in the resistance to hormonal therapy in breast cancer. Using a model of postmenopausal, estrogen-dependent breast cancer, we investigated the antitumor effects...
4.
Brousseau D, Nimmer M, Yunk N, Nattinger A, Greer A
Pediatrics . 2011 Jan; 127(2):e375-81. PMID: 21242226
Objective: To better understand parental decisions to seek care for their children and physician perceptions of parents' decisions to seek nonurgent emergency-department care. Patients And Methods: In-depth interviews of 26...
5.
Huang F, Hurlburt W, Greer A, Reeves K, Hillerman S, Chang H, et al.
Cancer Res . 2010 Sep; 70(18):7221-31. PMID: 20807811
Agents targeting insulin-like growth factor-I receptor (IGF-IR), including antibodies and small-molecule inhibitors, are currently in clinical development for the treatment of cancers including sarcoma. However, development of resistance is a...
6.
Velaparthi U, Saulnier M, Wittman M, Liu P, Frennesson D, Zimmermann K, et al.
Bioorg Med Chem Lett . 2010 Apr; 20(10):3182-5. PMID: 20399649
A series of 3-[6-(4-substituted-piperazin-1-yl)-4-methyl-1H-benzimidazol-2-yl]-1H-pyridine-2-one were synthesized to modulate CYP3A4 inhibition and improve aqueous solubility of our prototypical compound BMS-536924 (1), while maintaining potent IGF-1R inhibitory activity. Structure-activity and structure-solubility studies...
7.
Carboni J, Wittman M, Yang Z, Lee F, Greer A, Hurlburt W, et al.
Mol Cancer Ther . 2009 Dec; 8(12):3341-9. PMID: 19996272
BMS-754807 is a potent and reversible inhibitor of the insulin-like growth factor 1 receptor/insulin receptor family kinases (Ki, <2 nmol/L). It is currently in phase I development for the treatment...
8.
Wittman M, Carboni J, Yang Z, Lee F, Antman M, Attar R, et al.
J Med Chem . 2009 Sep; 52(23):7360-3. PMID: 19778024
This report describes the biological activity, characterization, and SAR leading to 9d (BMS-754807) a small molecule IGF-1R kinase inhibitor in clinical development.
9.
Huang F, Greer A, Hurlburt W, Han X, Hafezi R, Wittenberg G, et al.
Cancer Res . 2009 Jan; 69(1):161-70. PMID: 19117999
Overexpression and enhanced activity of insulin-like growth factor-I receptor (IGF-IR) in diverse tumor types make it an attractive target for cancer therapy. BMS-536924 is a potent small molecule inhibitor of...
10.
Velaparthi U, Wittman M, Liu P, Carboni J, Lee F, Attar R, et al.
J Med Chem . 2008 Sep; 51(19):5897-900. PMID: 18763755
We previously reported that 1 (BMS-536924), a benzimidazole inhibitor of the insulin-like growth factor-1 receptor, had demonstrated in vivo antitumor activity. This lead compound was found to have potent CYP3A4...