Stephen D. Nimer, MD

Vice Chair, Faculty Development, Department of Medicine; Alfred P. Sloan Chair
Stephen D. Nimer, MD -- Vice Chair, Faculty Development, Department of Medicine; Alfred P. Sloan Chair

I have worked as a hematologist/oncologist for the last 25 years, focusing on the care of patients with hematologic cancers and with bone marrow that does not function normally, such as patients with aplastic anemia and myelodysplastic syndromes. I have led clinical investigations of hematopoietic growth factors and immunosuppressive therapies to try to stimulate the bone marrow of patients with these diseases, and of bone marrow or stem cell transplants (autologous and allogeneic) to eradicate hematologic malignancies or cure bone marrow diseases. More recently, we have used transcriptional modifying therapies like histone deacetylase inhibitors and hypomethylating agents to treat these diseases, and this area of research remains a critical focus of our efforts.

Over the past 18 years while at Memorial Sloan-Kettering, I established the autologous stem cell transplant program for hematologic malignancies. This program focused primarily on treating patients with lymphoma (both non-Hodgkin and Hodgkin lymphoma) and patients with multiple myeloma. In addition to evaluating novel high-dose therapies for these diseases, we established several research programs using investigational agents to target the molecular abnormalities found in myeloid malignancies like acute myelogenous leukemia (AML).

Appointments for New Patients
212-639-5279
Phone
646-888-3120
Education

MD, University of Chicago School of Medicine

Residencies

University of California, Los Angeles, School of Medicine

Fellowships

University of California, Los Angeles, School of Medicine

Board Certifications

Internal Medicine; Medical Oncology; Hematology

Clinical Expertise

Myeloproliferative Disorders; Aplastic Anemia; Myelodysplasia; Acute and Chronic Leukemias; Peripheral Stem Cell Transplantation

See My Colleagues in:
Publications by Stephen D. Nimer

Huang G,  Zhao X, Wang L, Elf S, Xu H, Zhao X, Sashida G, Zhang Y, Liu Y, Lee J, menendez S, Yan Y, Yan X, Zhang P, Tenen DG, Osato M, Hsieh JD, Nimer S. The ability of MLL to gind RUNX1 and methylate H2K4 at Pu.1 regulatory regions is impaired by MDS/AMO-associated RUNX1/AML1 mutations. Blood. 2011, October 19; (e-pub ahead of print)

Wang L, Gural A, Sun XJ, Zhao X, Perna F, Huang G, Hatlen M, Vu L, Liu F, Xu H, Asai T, Xu H, Deblasio T, Mendenz S, Voza F, Jiang Y, Cole P, Zhang J, Melnick A, Roeder R, Nimer SD. The leukemogenicity of AML1-ETO is dependent on sit-specific lysine acetylation. Science. 2011; 765-9.

Moulick M, Ahn JH, Cerchietti L, Beebe K, Smith-Jones P, Perna F, Hatzi K, Vu LP, Zhao X, Zatorska D, Taldone T, Rodina A, Alpaugh M, Gross SS, Larson SM, Levine R, Guzman M, Erdjument-Bromage H, Nimer SD, Melnick A, Neckers L, Chiosis G.  Affinity-based proteomics reveal cancer-specific networks coordinated by Hsp90. Nature Chemical Biology. 2011, Sep 25;7(11):818-26.

Moran-Crusio K, Reavie L, Shih A, Abdel-Wahab O, Ndiaye-Lobry D, Lobry C, Figueroa ME, Vasanthakumar A, Patel J, Zhao X, Perna F, Pandey S, Madzo J, Song C, Dai Q, He C, Ibrahim S, Beran M, Zavadil J, Nimer SD, Melnick A, Godley LA, Aifantis I, Levine RL.  Tet2 loss leads to increased hematopoietic stem cell self-renewal and myeloid transformation. Cancer Cell. 2011 Jul 12;20(1):11-24.

Liu F, Zhao X, Perna F, Wang L, Koppikar P, Abdel-Wahab O, Harr MW, Levine RL, Xu H, Tefferi A, Deblasio A, Hatlen M, Menendez S, Nimer SD. JAK2V617F-mediated phosphorylation of PRMT5 downregulates its methyltransferase activity and promotes myeloproliferation. Cancer Cell 2011; 19 :283-294

Sashida G, Bae N, DiGiandomenico S, Asai T, Gurvich N, Bazzoli E, Liu Y, Huang G, Zhao X, Menendez S, Nimer, SD. The Mef/Elf4 transcription factor fine tunes the DNA damage response. Cancer Research, 2011; 71: 4857-65.

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