The Molecular Membrane Biology (MMB) Program provides a long-standing forum for AECC investigators with a primary interest in determining roles in cancer for molecules that function at the cell surface or in the secretory pathway of mammalian cells. The goals are to determine structure/function relationships of molecules that reside in cell membranes or enveloped viruses, and to exploit their properties in cancer diagnosis, prognosis or treatment. In the past 5 years program members have identified new mechanisms of tumorigenesis, tumor progression, angiogenesis and metastasis and mechanisms of resistance to chemotherapeutic drugs. The group now comprises 18 members, including 4 new primary and one new secondary 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 member was not renewed by AECC and one member moved to another cancer center. In the last budget year, MMB members were supported by 10 NCI grants ($2.4M direct), a Susan Komen award, and an additional 15 NIH grants. 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-drug resistance transporter, prostaglandin transporters and the Na+/monocarboxylate transporter (SMCT). Several members investigate mechanisms of membrane trafficking and secretion including two virologists investigating mechanisms of virus assembly and membrane fusion in viruses that either cause cancer, or belong 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 the last 5 years; 12% represented intraprogrammatic, and 29% interprogrammatic, collaborations. Future goals for 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 investigating integrins and selectins in cancer through new recruitment, and to enhance interactions with the Tumor Microenvironment and Metastasis group in order to expand the scope of cancer research in cell-cell interactions and membrane-related phenomena.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-36
Application #
7680070
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
36
Fiscal Year
2008
Total Cost
$18,057
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Agalliu, Ilir; Chen, Zigui; Wang, Tao et al. (2018) Oral Alpha, Beta, and Gamma HPV Types and Risk of Incident Esophageal Cancer. Cancer Epidemiol Biomarkers Prev 27:1168-1175
Bhargava, Ragini; Sandhu, Manbir; Muk, Sanychen et al. (2018) C-NHEJ without indels is robust and requires synergistic function of distinct XLF domains. Nat Commun 9:2484
Collu, Giovanna M; Jenny, Andreas; Gaengel, Konstantin et al. (2018) Prickle is phosphorylated by Nemo and targeted for degradation to maintain Prickle/Spiny-legs isoform balance during planar cell polarity establishment. PLoS Genet 14:e1007391
Doyle, Christopher R; Moon, Jee-Young; Daily, Johanna P et al. (2018) A Capsular Polysaccharide-Specific Antibody Alters Streptococcus pneumoniae Gene Expression during Nasopharyngeal Colonization of Mice. Infect Immun 86:
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
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
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
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
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
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

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