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
Stepankova, Martina; Bartonkova, Iveta; Jiskrova, Eva et al. (2018) Methylindoles and Methoxyindoles are Agonists and Antagonists of Human Aryl Hydrocarbon Receptor. Mol Pharmacol 93:631-644
Anayannis, Nicole V; Schlecht, Nicolas F; Ben-Dayan, Miriam et al. (2018) Association of an intact E2 gene with higher HPV viral load, higher viral oncogene expression, and improved clinical outcome in HPV16 positive head and neck squamous cell carcinoma. PLoS One 13:e0191581
Ingram, Jessica R; Blomberg, Olga S; Rashidian, Mohammad et al. (2018) Anti-CTLA-4 therapy requires an Fc domain for efficacy. Proc Natl Acad Sci U S A 115:3912-3917
Maggi, Elaine C; Gravina, Silvia; Cheng, Haiying et al. (2018) Development of a Method to Implement Whole-Genome Bisulfite Sequencing of cfDNA from Cancer Patients and a Mouse Tumor Model. Front Genet 9:6
Chen, Zigui; Schiffman, Mark; Herrero, Rolando et al. (2018) Classification and evolution of human papillomavirus genome variants: Alpha-5 (HPV26, 51, 69, 82), Alpha-6 (HPV30, 53, 56, 66), Alpha-11 (HPV34, 73), Alpha-13 (HPV54) and Alpha-3 (HPV61). Virology 516:86-101
Dulyaninova, Natalya G; Ruiz, Penelope D; Gamble, Matthew J et al. (2018) S100A4 regulates macrophage invasion by distinct myosin-dependent and myosin-independent mechanisms. Mol Biol Cell 29:632-642
Kunnath-Velayudhan, Shajo; Porcelli, Steven A (2018) Isolation of intact RNA from murine CD4+ T cells after intracellular cytokine staining and fluorescence-activated cell sorting. J Immunol Methods 456:77-80
Heo, Moonseong; Kim, Namhee; Rinke, Michael L et al. (2018) Sample size determinations for stepped-wedge clinical trials from a three-level data hierarchy perspective. Stat Methods Med Res 27:480-489
Sparano, Joseph A (2018) Prognostic gene expression assays in breast cancer: are two better than one? NPJ Breast Cancer 4:11
Zamurrad, Sumaira; Hatch, Hayden A M; Drelon, Coralie et al. (2018) A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5. Cell Rep 22:2359-2369

Showing the most recent 10 out of 1508 publications