The Molecular Membrane Biology (MMB) Program provides a long-standing forum for AECC investigatorswith a primary interest in determining roles in cancer for molecules that function at the cell surface or in thesecretory pathway of mammalian cells. The goals are to determine structure/function relationships ofmolecules that reside in cell membranes or enveloped viruses, and to exploit their properties in cancerdiagnosis, prognosis or treatment. In the past 5 years program members have identified new mechanisms oftumorigenesis, tumor progression, angiogenesis and metastasis and mechanisms of resistance tochemotherapeutic drugs. The group now comprises 18 members, including 4 new primary and one newsecondary member, from 11 departments. Secondary appointees are from the Departments of Medicine,Pediatrics and Oncology. Sadly two members unexpectedly passed away in the last year. Another memberwas not renewed by AECC and one member moved to another cancer center. In the last budget year, MMBmembers were supported by 10 NCI grants ($2.4M direct), a Susan Komen award, and an additional 15 NIHgrants. About a third of the MMB group investigates membrane transporters, including the Na+/l- symporter(NIS), glucose transporters (GLUT4 and GLUTS), folate transporters, the F1/FO ATP synthase, a multi-drugresistance transporter, prostaglandin transporters and the Na+/monocarboxylate transporter (SMCT).Several members investigate mechanisms of membrane trafficking and secretion including two virologistsinvestigating mechanisms of virus assembly and membrane fusion in viruses that either cause cancer, orbelong to a family of viruses that cause cancer. Another focus is on cell surface interactions mediated by Nglycans,Notch receptors, cadherins, and galectins. The group published 189 cancer relevant papers in thelast 5 years; 12% represented intraprogrammatic, and 29% interprogrammatic, collaborations. Future goalsfor the MMB program are to catalyze discoveries of new roles for membrane molecules in cancer diagnosis,prognosis and treatment to clinical applications, to expand the program to include scientists investigatingintegrins and selectins in cancer through new recruitment, and to enhance interactions with the TumorMicroenvironment and Metastasis group in order to expand the scope of cancer research in cell-cellinteractions and membrane-related phenomena.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA013330-35
Application #
7506803
Study Section
Subcommittee G - Education (NCI)
Project Start
2007-09-25
Project End
2012-06-30
Budget Start
2007-09-25
Budget End
2008-06-30
Support Year
35
Fiscal Year
2007
Total Cost
$14,023
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Van Arsdale, Anne R; Arend, Rebecca C; Cossio, Maria J et al. (2018) Insulin-like growth factor 2: a poor prognostic biomarker linked to racial disparity in women with uterine carcinosarcoma. Cancer Med 7:616-625
Ruiz, Penelope D; Gamble, Matthew J (2018) MacroH2A1 chromatin specification requires its docking domain and acetylation of H2B lysine 20. Nat Commun 9:5143
Rohan, Thomas; Ye, Kenny; Wang, Yihong et al. (2018) MicroRNA expression in benign breast tissue and risk of subsequent invasive breast cancer. PLoS One 13:e0191814
Walters, Ryan O; Arias, Esperanza; Diaz, Antonio et al. (2018) Sarcosine Is Uniquely Modulated by Aging and Dietary Restriction in Rodents and Humans. Cell Rep 25:663-676.e6
Racine, Jeremy J; Stewart, Isabel; Ratiu, Jeremy et al. (2018) Improved Murine MHC-Deficient HLA Transgenic NOD Mouse Models for Type 1 Diabetes Therapy Development. Diabetes 67:923-935
Frimer, Marina; Miller, Eirwen M; Shankar, Viswanathan et al. (2018) Adjuvant Pelvic Radiation ""Sandwiched"" Between Paclitaxel/Carboplatin Chemotherapy in Women With Completely Resected Uterine Serous Carcinoma: Long-term Follow-up of a Prospective Phase 2 Trial. Int J Gynecol Cancer 28:1781-1788
Kale, Abhijit; Ji, Zhejun; Kiparaki, Marianthi et al. (2018) Ribosomal Protein S12e Has a Distinct Function in Cell Competition. Dev Cell 44:42-55.e4
Lee, Chang-Hyun; Kiparaki, Marianthi; Blanco, Jorge et al. (2018) A Regulatory Response to Ribosomal Protein Mutations Controls Translation, Growth, and Cell Competition. Dev Cell 46:456-469.e4
Mao, Serena P H; Park, Minji; Cabrera, Ramon M et al. (2018) Loss of amphiregulin reduces myoepithelial cell coverage of mammary ducts and alters breast tumor growth. Breast Cancer Res 20:131
Mocholi, Enric; Dowling, Samuel D; Botbol, Yair et al. (2018) Autophagy Is a Tolerance-Avoidance Mechanism that Modulates TCR-Mediated Signaling and Cell Metabolism to Prevent Induction of T Cell Anergy. Cell Rep 24:1136-1150

Showing the most recent 10 out of 1508 publications