Year |
Citation |
Score |
2023 |
Lade DM, Agazie YM. Targeting SHP2 with an Active Site Inhibitor Blocks Signaling and Breast Cancer Cell Phenotypes. Acs Bio & Med Chem Au. 3: 418-428. PMID 37876496 DOI: 10.1021/acsbiomedchemau.3c00024 |
0.556 |
|
2022 |
Lade DM, Nicoletti R, Mersch J, Agazie YM. Design and synthesis of improved active-site SHP2 inhibitors with anti-breast cancer cell effects. European Journal of Medicinal Chemistry. 247: 115017. PMID 36584630 DOI: 10.1016/j.ejmech.2022.115017 |
0.499 |
|
2021 |
Martin E, Agazie YM. SHP2 potentiates the oncogenic activity of beta-catenin to promote triple-negative breast cancer. Molecular Cancer Research : McR. PMID 34389690 DOI: 10.1158/1541-7786.MCR-21-0060 |
0.368 |
|
2020 |
Hartman Z, Geldenhuys WJ, Agazie YM. Novel Small-Molecule Inhibitor for the Oncogenic Tyrosine Phosphatase SHP2 with Anti-Breast Cancer Cell Effects. Acs Omega. 5: 25113-25124. PMID 33043190 DOI: 10.1021/acsomega.0c02746 |
0.788 |
|
2020 |
Hartman Z, Geldenhuys WJ, Agazie YM. A specific amino acid context in EGFR and HER2 phosphorylation sites enables selective binding to the active site of Src homology phosphatase 2 (SHP2). The Journal of Biological Chemistry. PMID 32024694 DOI: 10.1074/Jbc.Ra119.011422 |
0.762 |
|
2020 |
Agazie Y, Hartman Z. Abstract P3-10-20: Targeting the tyrosine phosphatase SHP2 is efficacious against HER2-positive breast cancer Cancer Research. 80. DOI: 10.1158/1538-7445.Sabcs19-P3-10-20 |
0.807 |
|
2019 |
Agazie Y, Hartman Z. Abstract P6-20-17: Targeting SHP2 for the treatment of HER2-positive breast cancer Cancer Research. 79. DOI: 10.1158/1538-7445.Sabcs18-P6-20-17 |
0.787 |
|
2018 |
Zhao H, Martin E, Matalkah F, Shah N, Ivanov A, Ruppert JM, Lockman PR, Agazie YM. Conditional knockout of SHP2 in ErbB2 transgenic mice or inhibition in HER2-amplified breast cancer cell lines blocks oncogene expression and tumorigenesis. Oncogene. PMID 30467378 DOI: 10.1038/S41388-018-0574-8 |
0.569 |
|
2016 |
Matalkah F, Martin E, Zhao H, Agazie YM. SHP2 acts both upstream and downstream of multiple receptor tyrosine kinases to promote basal-like and triple-negative breast cancer. Breast Cancer Research : Bcr. 18: 2. PMID 26728598 DOI: 10.1186/S13058-015-0659-Z |
0.597 |
|
2015 |
Zhao H, Agazie YM. Inhibition of SHP2 in basal-like and triple-negative breast cells induces basal-to-luminal transition, hormone dependency, and sensitivity to anti-hormone treatment. Bmc Cancer. 15: 109. PMID 25885600 DOI: 10.1186/S12885-015-1131-2 |
0.591 |
|
2015 |
Farrugia MK, Sharma SB, Lin CC, McLaughlin SL, Vanderbilt DB, Ammer AG, Salkeni MA, Stoilov P, Agazie YM, Creighton CJ, Ruppert JM. Regulation of anti-apoptotic signaling by Kruppel-like factors 4 and 5 mediates lapatinib resistance in breast cancer. Cell Death & Disease. 6: e1699. PMID 25789974 DOI: 10.1038/cddis.2015.65 |
0.497 |
|
2014 |
Zhao H, Agazie YM. Abstract 2014: SHP2 stabilizes EGFR and beta-catenin to promote the transformation and tumorigenic potential of basal-like and triple-negative breast cancer cells Cancer Research. 74: 2014-2014. DOI: 10.1158/1538-7445.Am2014-2014 |
0.578 |
|
2013 |
Hartman ZR, Schaller MD, Agazie YM. The tyrosine phosphatase SHP2 regulates focal adhesion kinase to promote EGF-induced lamellipodia persistence and cell migration. Molecular Cancer Research : McR. 11: 651-64. PMID 23512980 DOI: 10.1158/1541-7786.Mcr-12-0578 |
0.784 |
|
2013 |
Matalka F, Zhao H, Agazie YM. Abstract LB-280: Inhibition of SHP2 in basal-like and triple-negative breast cancer cells induces basal-to-luminal transition, suppresses tumorigenesis, and blocks metastasis. Cancer Research. 73. DOI: 10.1158/1538-7445.Am2013-Lb-280 |
0.604 |
|
2012 |
Hartman Z, Zhao H, Agazie YM. HER2 stabilizes EGFR and itself by altering autophosphorylation patterns in a manner that overcomes regulatory mechanisms and promotes proliferative and transformation signaling. Oncogene. 32: 4169-80. PMID 23027125 DOI: 10.1038/Onc.2012.418 |
0.783 |
|
2012 |
Zhou X, Agazie YM. The signaling and transformation potency of the overexpressed HER2 protein is dependent on the normally-expressed EGFR. Cellular Signalling. 24: 140-50. PMID 21911055 DOI: 10.1016/J.Cellsig.2011.08.015 |
0.557 |
|
2011 |
Matalka F, Hartman Z, Agazie YM. Abstract 238: Inhibition of SHP2 abolishes mammary tumorigenesis in mice Cancer Research. 71: 238-238. DOI: 10.1158/1538-7445.Am2011-238 |
0.797 |
|
2011 |
Matalka F, Agazie Y. Abstract B69: SHP2 as a novel therapeutic target for triple-negative breast cancer Cancer Epidemiology, Biomarkers & Prevention. 20. DOI: 10.1158/1055-9965.Disp-11-B69 |
0.655 |
|
2011 |
Agazie Y, Matalka F, Hartman Z. P3-01-15: The Role of Src Homology Phosphotyrosyl Phosphatase-2 in Basal-Type/Triple-Negative Breast Cancer – Implications for Targeted Therapy. Cancer Research. 71. DOI: 10.1158/0008-5472.Sabcs11-P3-01-15 |
0.814 |
|
2011 |
Hartman Z, Agazie Y. P2-02-05: Molecular Mechanism for Src Homology Phosphotyrosyl Phosphatase 2 Regulation of Cell Motility and Migration. Cancer Research. 71. DOI: 10.1158/0008-5472.Sabcs11-P2-02-05 |
0.804 |
|
2010 |
Zhou X, Ahmed N, Agazie YM. Abstract 3121: A novel molecular mechanism for HER2-induced sustained signaling and transformation Cancer Research. 70: 3121-3121. DOI: 10.1158/1538-7445.Am10-3121 |
0.555 |
|
2009 |
Zhou X, Agazie YM. Molecular mechanism for SHP2 in promoting HER2-induced signaling and transformation. The Journal of Biological Chemistry. 284: 12226-34. PMID 19261604 DOI: 10.1074/Jbc.M900020200 |
0.57 |
|
2008 |
Zhou X, Coad J, Ducatman B, Agazie YM. SHP2 is up-regulated in breast cancer cells and in infiltrating ductal carcinoma of the breast, implying its involvement in breast oncogenesis. Histopathology. 53: 389-402. PMID 18643929 DOI: 10.1111/J.1365-2559.2008.03103.X |
0.484 |
|
2008 |
Zhou XD, Agazie YM. Inhibition of SHP2 leads to mesenchymal to epithelial transition in breast cancer cells. Cell Death and Differentiation. 15: 988-96. PMID 18421299 DOI: 10.1038/cdd.2008.54 |
0.589 |
|
2006 |
Burks J, Agazie YM. Modulation of α-catenin Tyr phosphorylation by SHP2 positively effects cell transformation induced by the constitutively active FGFR3 Oncogene. 25: 7166-7179. PMID 16767162 DOI: 10.1038/Sj.Onc.1209728 |
0.485 |
|
2006 |
Merritt R, Hayman MJ, Agazie YM. Mutation of Thr466 in SHP2 abolishes its phosphatase activity, but provides a new substrate-trapping mutant. Biochimica Et Biophysica Acta. 1763: 45-56. PMID 16413071 DOI: 10.1016/J.Bbamcr.2005.11.013 |
0.373 |
|
2003 |
Agazie YM, Hayman MJ. Molecular mechanism for a role of SHP2 in epidermal growth factor receptor signaling. Molecular and Cellular Biology. 23: 7875-86. PMID 14560030 DOI: 10.1128/Mcb.23.21.7875-7886.2003 |
0.375 |
|
2003 |
Agazie YM, Movilla N, Ischenko I, Hayman MJ. The phosphotyrosine phosphatase SHP2 is a critical mediator of transformation induced by the oncogenic fibroblast growth factor receptor 3. Oncogene. 22: 6909-18. PMID 14534538 DOI: 10.1038/Sj.Onc.1206798 |
0.387 |
|
2003 |
Agazie YM, Hayman MJ. Development of an efficient "substrate-trapping" mutant of Src homology phosphotyrosine phosphatase 2 and identification of the epidermal growth factor receptor, Gab1, and three other proteins as target substrates. The Journal of Biological Chemistry. 278: 13952-8. PMID 12582165 DOI: 10.1074/Jbc.M210670200 |
0.35 |
|
2002 |
Agazie Y, Ischenko I, Hayman M. Concomitant activation of the PI3K-Akt and the Ras-ERK signaling pathways is essential for transformation by the V-SEA tyrosine kinase oncogene Oncogene. 21: 697-707. PMID 11850798 DOI: 10.1038/Sj.Onc.1205115 |
0.306 |
|
1998 |
Wilden PA, Agazie YM, Kaufman R, Halenda SP. ATP-stimulated smooth muscle cell proliferation requires independent ERK and PI3K signaling pathways. American Journal of Physiology. Heart and Circulatory Physiology. 275: H1209-H1215. PMID 29586809 DOI: 10.1152/ajpheart.1998.275.4.H1209 |
0.368 |
|
1996 |
Agazie YM, Burkholder GD, Lee JS. Triplex DNA in the nucleus: Direct binding of triplex-specific antibodies and their effect on transcription, replication and cell growth Biochemical Journal. 316: 461-466. PMID 8687388 DOI: 10.1042/Bj3160461 |
0.583 |
|
1995 |
Latimer LJ, Agazie YM, Braun RP, Hampel KJ, Lee JS. Specificity of monoclonal antibodies produced against phosphorothioate and ribo modified DNAs. Molecular Immunology. 32: 1057-64. PMID 8544855 DOI: 10.1016/0161-5890(95)00086-0 |
0.683 |
|
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