Overview
The Means laboratory is interested in the study of cell signaling cascades that regulate cell proliferation, differentiation or function and how alterations in these pathways contribute to disease states. It is hoped that an understanding of these pathways may provide clues to novel targets that may be amenable to the drug discovery process. Current major research projects under investigation include:
1. The cellular mechanisms that govern regulation of CaMKIV, the CaM cascade, which includes CaMKK, CaMK1, CaMKIV and AMPK, and how these calcium-mediated signaling cascade affects cell function fate decisions. Examples of current studies include apoptosis, differentiation, self-renewal of stem cells and central regulation of energy balance.
2. Evaluating the pathways that are involved in regulating cell migration and invasiveness. One project investigates the protein kinase MLK3 and how it is involved in the cascade of events by which small G proteins such as Cdc42, Rac and Rho control directed cell movements via changes in the cytoskeleton.
3. Examining the role of the prolyl isomerase Pin1 in oncogenesis. Studies are focused on the Ras-mediated pathways involving Pin1 that control accumulation of oncoproteins such as Myc and cyclin E and how these pathways participate in human cell transformation and tumorigenesis.
1. The cellular mechanisms that govern regulation of CaMKIV, the CaM cascade, which includes CaMKK, CaMK1, CaMKIV and AMPK, and how these calcium-mediated signaling cascade affects cell function fate decisions. Examples of current studies include apoptosis, differentiation, self-renewal of stem cells and central regulation of energy balance.
2. Evaluating the pathways that are involved in regulating cell migration and invasiveness. One project investigates the protein kinase MLK3 and how it is involved in the cascade of events by which small G proteins such as Cdc42, Rac and Rho control directed cell movements via changes in the cytoskeleton.
3. Examining the role of the prolyl isomerase Pin1 in oncogenesis. Studies are focused on the Ras-mediated pathways involving Pin1 that control accumulation of oncoproteins such as Myc and cyclin E and how these pathways participate in human cell transformation and tumorigenesis.
Current Appointments & Affiliations
Nanaline H. Duke Distinguished Professor Emeritus of Pharmacology, in the School of Medicine
·
2011 - Present
Pharmacology & Cancer Biology,
Basic Science Departments
Professor Emeritus of Pharmacology & Cancer Biology
·
2012 - Present
Pharmacology & Cancer Biology,
Basic Science Departments
Recent Publications
Hypothalamic CaMKK2 contributes to the regulation of energy balance.
Journal Article Cell Metab · May 2008 Featured Publication Detailed knowledge of the pathways by which ghrelin and leptin signal to AMPK in hypothalamic neurons and lead to regulation of appetite and glucose homeostasis is central to the development of effective means to combat obesity. Here we identify CaMKK2 as ... Full text Link to item CiteDegradation of the tumor suppressor PML by Pin1 contributes to the cancer phenotype of breast cancer MDA-MB-231 cells.
Journal Article Mol Cell Biol · February 2008 Featured Publication Promyelocytic leukemia protein (PML) is an important regulator due to its role in numerous cellular processes including apoptosis, viral infection, senescence, DNA damage repair, and cell cycle regulation. Despite the role of PML in many cellular functions ... Full text Link to item CiteCalmodulin-dependent kinase IV links Toll-like receptor 4 signaling with survival pathway of activated dendritic cells.
Journal Article Blood · January 15, 2008 Featured Publication Microbial products, including lipopolysaccharide (LPS), an agonist of Toll-like receptor 4 (TLR4), regulate the lifespan of dendritic cells (DCs) by largely undefined mechanisms. Here, we identify a role for calcium-calmodulin-dependent kinase IV (CaMKIV) ... Full text Link to item CiteRecent Grants
NCI Clinical Trials Reporting (CTRP) - Early Adaptors
ResearchPrincipal Investigator · Awarded by National Institutes of Health · 2010 - 2014Hormonal regulation of a Ca2+/AMPK signaling pathway
ResearchPrincipal Investigator · Awarded by National Institutes of Health · 1984 - 2011CaM Kinase Cascades in Endocrine Cells
ResearchPrincipal Investigator · Awarded by National Institutes of Health · 1997 - 2011View All Grants
Education, Training & Certifications
University of Texas, Austin ·
1967
Ph.D.
Oklahoma State University, Stillwater ·
1964
M.S.
Oklahoma State University, Stillwater ·
1963
B.S.