Zena Werb, Ph.D, “Queen of the Matrix”: in Memoriam (1945–2020) Shahin Rafii1 and David Lyden2
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WMIC 2015 Plenary Speaker Zena Werb, Ph.D., Professor University Of
WMIC 2015 Plenary Speaker Zena Werb, Ph.D., Professor University of California, San Francisco San Francisco, California, USA, Focus of WMIC 2015 Plenary Talk: Intravital Imaging Reveals Properties of Cancer Progression, Mestastasis and Response to Therapy Zena Werb, Ph.D. Dr. Zena Werb received her B.Sc. in Biochemistry from the University of Toronto, and her Ph.D. in Cell Biology from Rockefeller University, New York. After postdoctoral studies at the Strangeways Research Laboratory in Cambridge England, she was recruited to the faculty of the University of California, San Francisco, where she is currently Professor and Vice‐Chair of Anatomy. Her honors include the Charlotte Friend Award of the American Association for Cancer Research, the Alexander von Humboldt Research Award and the Colin Thomson Memorial Medal from the Association for International Cancer Research. Dr. Werb has been elected to the National Academy of Sciences, the Institute of Medicine, and the American Academy of Arts and Sciences. She has published more than 400 papers. Dr. Werb is recognized internationally for her fundamental discoveries about the molecular and cellular bases of extracellular matrix proteolysis by matrix metalloproteinases and their roles in the normal functioning and pathogenesis of tissues. Her studies have led to new paradigms about the role of the cellular microenvironment and intercellular communication in breast development and breast cancer. Her current research uses mouse models of breast cancer and patient‐derived breast cancer xenografts to study normal mammary development and its perturbation during tumor progression and metastasis. . -
An Interview with Zena Werb
Disease Models & Mechanisms 3, 513-516 (2010) doi:10.1242/dmm.006338 © 2010. Published by The Company of Biologists Ltd A MODEL FOR LIFE The extracellular matrix and disease: an interview with Zena Werb Zena Werb’s pioneering efforts brought recognition to the idea that the extracellular matrix has a profound influence in determining cell fate. Here, she discusses how a ‘rocky’ start in geophysics led her to a career that is changing the way we think about cancer. I started college. Ironically, earthquakes veryone is influenced by what became an important part of my life as a goes on around them, and cells resident of San Francisco, but I didn’t realise are much the same. The signalling this would be the case then. Back in college, Emolecules and support structures I wanted to go on a summer geology field of the extracellular matrix (ECM) course to the Rockies. I was one of the top direct many aspects of normal cell two students in my class, but they wouldn’t behaviour, including shape, migration and let me go because I was female – they said survival. However, the ECM can also play that there were not the proper facilities on a role in the development and progression the site for women. Instead, I found a DMM of disease. For example, a cell does not summer job in the field and actually got become cancerous on its own – together paid for the experience I gained, which with intrinsic changes, oncogenesis is would not have happened if I’d been encouraged by cues from the surrounding allowed into the course. -
Extracellular Matrix Degradation and Remodeling in Development and Disease
Downloaded from http://cshperspectives.cshlp.org/ on September 30, 2021 - Published by Cold Spring Harbor Laboratory Press Extracellular Matrix Degradation and Remodeling in Development and Disease Pengfei Lu1,2, Ken Takai2, Valerie M. Weaver3, and Zena Werb2 1Breakthrough Breast Cancer Research Unit, Paterson Institute for Cancer Research and Wellcome Trust Centre for Cell Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester M20 4BX, United Kingdom 2Department of Anatomy and Program in Developmental Biology, University of California, San Francisco, California 94143-0452 3Department of Surgery and Center for Bioengineering and Tissue Regeneration, University of California, San Francisco, California 94143 Correspondence: [email protected] The extracellular matrix (ECM) serves diverse functions and is a major component of the cellular microenvironment. The ECM is a highly dynamic structure, constantly undergoing a remodeling process where ECM components are deposited, degraded, or otherwise modified. ECM dynamics are indispensible during restructuring of tissue architecture. ECM remodeling is an important mechanism whereby cell differentiation can be regulated, including processes such as the establishment and maintenance of stem cell niches, branch- ing morphogenesis, angiogenesis, bone remodeling, and wound repair. In contrast, abnor- mal ECM dynamics lead to deregulated cell proliferation and invasion, failure of cell death, and loss of cell differentiation, resulting in congenital defects and pathological processes including tissue fibrosis and cancer. Understanding the mechanisms of ECM remodeling and its regulation, therefore, is essential for developing new therapeutic inter- ventions for diseases and novel strategies for tissue engineering and regenerative medicine. he extracellular matrix (ECM) forms a milieu versatile and performs many functions in addi- Tsurrounding cells that reciprocally influ- tion to its structural role. -
Fire Focus:The Newsletter of the New Jersey Division of Fire Safety
Excellence in Public Safety Lt. Governor Sheila Y. Oliver, Commissioner New Jersey Department of Community Affairs Richard Mikutsky, Director and State Fire Marshal New Jersey Division of Fire Safety Spring 2020-2021 Volume 16 Issue 6 A Message from New Jersey Division of Fire Safety Director and State Fire Marshal Richard Mikutsky This space is usually reserved for briefing the state fire service on issues important to them, so though we begin the new year with a similar set of challenges we confronted in the year just past, we see no weakening of the resolve shown by front line responders and Division staff. A heartfelt thank you goes to all of you. Please continue your work in our common cause by clicking on the graphic below to assist your fellow first responders and the public you continue to selflessly serve. IN THIS POSTING... GUEST ARTICLE: NJ RISE FOR FIREFIGHTERS NTSB ELECTRIC VEHICLE FIRES ADVISORY EMS CRISIS HOTLINE BILL MOVES FORWARD FIRE SERVICE STIMULUS BILL DETAILS BRAIN INJURY RESPONSE TRAINING IN MEMORIAM 1 FIRE FOCUS:THE NEWSLETTER OF THE NEW JERSEY DIVISION OF FIRE SAFETY (Our Guest Correspondent is These pillars have been established with the goal Firefighter Oscar Morales Peer of supporting our first responders with aid in their Support Specialist III, RISE NJ First time of need, much like a RIC team during a Responder COVID Hope & MAYDAY call. Healing Program at Rutgers University Behavioral Health According to the Department of Defense Centers of Center) Excellence (DCOE) and the Department of Health and Human Services (DHHS), peer support can offer the following benefits: foster social “Mayday, Mayday, Mayday…” networking, improve quality of life, promote wellness, improve coping skills, support acceptance A call for help that no first responder ever wants of illness/situation, improve compliance, reduce to hear, but a call which we are ALWAYS concerns, and increase satisfaction with health prepared for. -
Testimony of Paul Berg, Ph.D. Chair, Public Policy Committee The
THE AMERICAN SOCIETY FOR OFFICERS SUZANNE PFEFFER CELL President BIOLOGY HARVEY LODISH President-Elect GARY BORISY NATIONAT. OFFICE: 8120 Woodmont Avenue, Suite 750 Bethesda, Maryland 20814-2762 Past-President TEL: 301/347-9300 FAX: 301/347-9310 E-MAIL: [email protected] www.ascb.org LAWRENCE S. B. GOLDSTEIN Secretary GARY WARD Treasurer ELIZABETH MARINCOLA Testimony of Executive Director COUNCIL HELEN BLAU Paul Berg, Ph.D. ANTHONY BRETSCHER KEVIN P. CAMPBELL Chair, Public Policy Committee PIETRO DE CAMILLI ALAN RICK HORWITZ The American Society KATHRYN E, HOWELL for Cell Biology SANDRA L. SCHMID JEAN SCHWARZBAUER W. SUE SHAFER JANET SHAW to the JULIE THERIOT PETER WALTER COMMITTEE CHAIRS Senate Judiciary Committee DON CLEVELAND Constitution & By-Laws KENNETH R. MILLER Education United States Senate GARY WARD Finance ENRIQUE RODRIGUEZ-BOULAN International Affairs MATTHEW WELCH Local Arrangements LAWRENCE S. B. GOLDSTEIN March 19, 2003 Mentbership DONELLA J. WILSON Minorities Affairs RICHARD HYNES Nominating KATHERINE L. WILSON Public Information PAUL BERG Public Policy VIVEK MALHOTRA Scientific Meetings ZENA WERB Women in Cell Biology CELL BIOLOGY EDUCATION A, MALCOLM CAMPBELL Co-Editor-in-Chief SARAH C. R. ELGIN Co-Editor-in-Chief MOLECULAR BIOLOGY OF THE CELL KEITH R. YAMAMOTO Editor-in-Chief Statement of Paul Berg Robert and Vivian Cahill Professor, Emeritus of Cancer Research and Biochemistry Director, Emeritus of the Beckman Center for Molecular and Genetic Medicine, Stanford University Medical Center Chair, Public Policy Committee, The American Society for Cell Biology Mr. Chairman, Members of the Committee, thank you for inviting me to testify on this most important issue. I have followed the debate on the cloning questions we will address today and | welcome the opportunity to submit my own views on the matter. -
2. Sara Salazar Hughes, “Domesticity & Diasporic Homeland: Constructing 'Home' in West Bank Settlements”
Triennial Preliminary SWG Triennial Schedule May 26-May 29, 2017 2:00-4:00 pm SWG Board Meeting 3:00-5:00 pm Registration Hub open with SWG information, and authors’ tables and books 5:00 pm Welcome Reception 6:30 pm Welcome Dinner 7:45 pm Tanya Atwater, “The California Coast,” SWG Gold Medal Recipient 2005, retired geophysicist and marine geologist, specializing in plate tectonics, UC Santa Barbara Saturday, May 27 7:30 am Breakfast 9:00 am Welcome by President, Director, Triennial Committee Chair 9:15 am Keynote: Mechtild Rössler, “World Heritage under threat: from Bamiyan to Palmyra,” UNESCO, Director of the Division for Heritage and the World Heritage Centre (Paris) 10:00 am Keynote: Kathryn Sullivan, “Looking at Earth,” Lindbergh Fellow in Aerospace History, National Air & Space Museum; former NASA Astronaut and NOAA scientist and administrator (McLean, VA) 10:45 am Coffee break 11 am Art Interlude: Susan Leonard, “The Beauties of the Reef: What We May Lose,” SWG NY Chair 11:15 am Panel: "Living and working in the 'Anthropocene,'" Tanya Atwater, Mechtild Rössler, and Kathryn Sullivan; Sandy Nichols, Moderator; in dialogue with each other and the audience 12 noon Lunch; In Memoriam; Annual Meeting of the Members 1:30 pm Beach, dune, and pine forest walk with ranger 3:00-4:10 pm Emerging Research in Geography UCLA Graduate Student Panel on Emerging Research in Geography: why research matters, to the individuals and to the world, women making a difference 1. Ashley Fent, “Regionalizing Resistance: Zircon Mining in the Context of the Casamance Conflict (Senegal)” 2. -
Metastasis and Invasion 3 – Metastasis Science Cancer
CANCER SCIENCE 3 Cancer Science 3 – Metastasis and Invasion 3 – Metastasis Science Cancer www.ipsen.com 2FI 0069 Metastasis and Invasion Tuscany, May 20-23, 2007 24, rue Erlanger – 75016 Paris – Tel.: 33(0)1 44 96 10 10 – Fax: 33(0)1 44 96 11 99 COLLOQUES MÉDECINE ET RECHERCHE Fondation Ipsen SCIENTIFIC REPORT BY APOORVA MANDAVILLI 2 Fondation Ipsen is placed under the auspices of Fondation de France MOLECULAR MARKERS 3 4 Foreword by Inder M. Verma 7 Part I: Molecular markers 9 J. Michael Bishop Senescence and metastasis in mouse models of breast cancer 15 Joan Massagué Metastasis genes and functions 21 Zena Werb Transcriptional regulation of the metastatic program 25 Inder M. Verma BRCA1 maintains constitutive heterochromatin formation: a unifying hypothesis of its function 29 Tak Wah Mak The role of RhoC in development and metastasis 35 Part II: Motility and invasiveness 37 Robert Weinberg Mechanisms of malignant progression 43 Daniel Louvard Fascin, a novel target of b-catenin-Tcf signaling, is expressed at the invasive front of human colon cancer 49 Gerhard Christofori Distinct mechanisms of tumor cell invasion and metastasis 55 Douglas Hanahan Multiple parameters influence acquisition by solid tumors CONTENTS of a capability for invasive growth 59 Part III : Mechanisms of metastasis 61 Richard Hynes Cellular mechanisms contributing to metastasis 67 Ann Chambers Novel imaging approaches for studying tumor metastasis 73 Jeffrey Pollard Macrophages are a cellular toolbox that tumors sequester to promote their progression to malignancy 79 Wolf-Hervé Fridman T effector/memory cells, the ultimate control of metastasis in humans 85 Kari Alitalo Inhibition of lymphangiogenesis and metastasis 91 Shahin Rafii Contribution of CXCR4+VEGFR1+ pro-angiogenic hematopoietic cells to tumor oncogenesis 97 Part IV : Cancer stem cells 99 Paolo Comoglio Invasive growth : a MET-driven genetic program for cancer and stem cells 105 Hans Clevers Wnt and Notch cooperate to maintain proliferative compartments in crypts and intestinal neoplasia 111 Owen N. -
Conference Program
Conference Program Note: All Scientific Sessions will be held in the Omni Hotel at 675 L Street. Poster Sessions will be held at the Hard Rock Hotel at the corner of 5th Avenue & L Street. Sunday, January 20 7:00 p.m.-7:10 p.m. Welcoming Remarks 7:10 p.m.-8:00 p.m. Keynote Address Omni Hotel San Diego, Grand Ballroom Metastasis and diversity in breast cancer Kornelia Polyak, Dana-Farber Cancer Institute, Boston, MA 8:00 p.m.-9:30 p.m. Opening Reception Monday, January 21 7:00 a.m.-8:00 a.m. Continental Breakfast Omni Hotel San Diego, Art Gallery 8:00 a.m.-10:00 a.m. Session 1: The Soil Session Chairperson: Zena Werb, Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA Omni Hotel San Diego, Grand Ballroom Microenvironmental control of bone metastasis Sylvain Provot, INSERM, Paris, France The role of the microenvironment protein cathelicidin LL-37 in pancreatic ductal adenocarcinoma* Christopher Heeschen, Spanish National Cancer Research Centre (CNIO), Madrid, Spain Normalizing tumor cell metabolism in breast cancer metastasis: A novel therapeutic approach Brunhilde Felding-Habermann, Scripps Research Institute, La Jolla, CA Identification of luminal breast cancers that establish a tumor supportive macroenvironment defined by proangiogenic platelets and bone marrow derived cells* Timothy Marsh, Brigham and Women’s Hospital, Boston, MA The extracellular matrix is fertile soil Richard Hynes, Massachusetts Institute of Technology, Cambridge, MA *Short talks from proffered papers Program and Proceedings • January 20-23, 2013 • San Diego, CA 7 Program 10:00 a.m.-10:30 a.m. -
Meeting Report
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Elsevier - Publisher Connector Cell Stem Cell Meeting Report Cancer and Stem Cell Biology: How Tightly Intertwined? Carla F. Kim1,2,3,* and Peter B. Dirks4,* 1Stem Cell Program, Children’s Hospital Boston, Boston, MA 02115, USA 2Department of Genetics, Harvard Medical School, Boston, MA 02115, USA 3Harvard Stem Cell Institute, Cambridge, MA 02138, USA 4Developmental and Stem Cell Biology Program, Department of Surgery, Arthur and Sonia Labatt Brain Tumor Research Center, Hospital for Sick Children, University of Toronto, 555 University Avenue, Toronto, Ontario M5G1X8, Canada *Correspondence: [email protected] (C.F.K.), [email protected] (P.B.D.) DOI 10.1016/j.stem.2008.07.012 Ever since the discovery of cancer stem cells in leukemia and, more recently, in solid tumors, enormous attention has been paid to the apparent stem cell nature of cancer. These concepts were the focus of the ‘‘Stem Cells and Cancer’’ symposium held recently at the University of California, San Francisco, and the inspiration for this overview of current research and important questions emerging in this area. This year’s annual UCSF Helen Diller Family Comprehensive confer these properties accumulate. When these additional Cancer Center Symposium focused on stem cells and cancer. events occur in progenitor cell populations derived from mutant This symposium provided a representation of all facets of stem HSC clones, cancer progression occurs. Thus, the phenotype of cell biology: from the role of stem and progenitor cells in devel- the cancer stem cell may be more similar to the normal progen- opment to adult tissues, normal stem cells versus cancer stem itor population than to the HSC itself. -
SILENT WINGS MUSEUM: Newsletter the Legacy of the World War II Glider Pilots Vol
SILENT WINGS MUSEUM: Newsletter The Legacy of the World War II Glider Pilots Vol. 19 No. 3 Spring 2020 General Information 6202 N. I- 27 Lubbock, Texas 79403 - 9710 Direct Line 806.775.3049 Information 806.775.3796 Fax 806.775.3337 Web www.silentwingsmuseum.com Directions Driving: North Lubbock, I-27 at Exit 9. The museum is located in the historic old airport terminal building just two blocks east of I-27. Look for the silver “G” wings on the tower above the entrance. Flying: The museum is accessible by taxi or rental car from the airport terminal. The museum is adjacent to and within easy walking distance of Lubbock Aero, FBO at Lubbock Remembering Operation Varsity 75th Anniversary Preston Smith International Aiport. GPS March 24, 1945 Coordinates for the museum are: N 33” 39.467’ IN THIS ISSUE W101”49.911’ Around the Museum 2 Upcoming Changes Admission Fees Combat Training for Glider Pilots 3 General Admission $8.00 Welcoming Dorothy Svgdik 4 Senior Citizens (60+) $6.00 Children (ages 7-17) $5.00 National WWII Glider Pilots Association 5 Students (w/ college id) $5.00 Children (6 & under w/ family) Free Research & News Museum Members Free The Leon B. Spencer Research Team 7 The Rhine Crossing Active Duty Military Free The Flying Pipeline 12 In Memoriam 20 Museum Hours New Membership Program 21 Tuesday - Saturday 10 AM - 5 PM Upcoming Exhibits 22 Sunday 1 PM - 5 PM Call For Holiday Hours 1 2 AROUND THE MUSEUM Museum Staff Directory Director of the Municipal Museums Jacqueline Bober Assistant Municipal Museums Manager Museum Curator Eddy Grigsby Sebastian Forbush Museum Curator Museums Store Manager Sharon McCullar David Seitz Marketing and Special Events Coordinator Education and Volunteer Coordintor Jacqueline Marchildon Dorothy Svgdik UPCOMING CHANGES: Going Digital Silent Wings Museum Newsletter is Going Digital! SILENT WINGS Help bring the Silent Wings Museum newsletter into the digital MUSEUM: Newsletter age! We are preparing to transition to a digital newsletter by the The Legacy of the World War II Glider Pilots Vol. -
Iman Aftab Khan
MOLECULAR MECHANISMS OF ERBB2-DRIVEN THREE-DIMENSIONAL BREAST TUMOUR GROWTH. By Iman Aftab Khan Submitted in partial fulfilment of the requirements for the degree of Doctor of Philosophy At Dalhousie University Halifax, Nova Scotia August 2018 © Copyright by Iman Aftab Khan, 2018 Dedicated to my parents Late Dr. Aftab Ahmad Khan and Mrs. Fatima Bisquerra Khan For their unconditional love, patience and struggle to support my decisions that helped me realize my dreams. ii Table of Contents LIST OF TABLES ........................................................................................................... ix LIST OF FIGURES .......................................................................................................... x ABSTRACT .................................................................................................................... xiii LIST OF ABBREVIATIONS USED ............................................................................ xiv ACKNOWLEDGEMENTS ......................................................................................... xxv CHAPTER 1. INTRODUCTION .................................................................................... 1 Resistance to detachment-induced cell death as a critical feature of ErbB2- driven breast cancer: an overview of project goals. ...................................................... 1 1.1 The role of the cell-ECM interactions in the mammary gland development and functions.................................................................................. -
Stromelysin-1 Regulates Adipogenesis During Mammary Gland Involution Caroline M
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by PubMed Central Stromelysin-1 Regulates Adipogenesis during Mammary Gland Involution Caroline M. Alexander,* Sushma Selvarajan,‡ John Mudgett,ʈ and Zena Werb§ *McArdle Laboratory for Cancer Research, University of Wisconsin Medical School, Madison, Wisconsin 53706-1599; ‡Department of Pharmaceutical Chemistry and §Department of Anatomy, University of California San Francisco, San Francisco, California 94143-0452; and ʈDepartment of Immunology, Merck Research Laboratory, Rahway, New Jersey 07065 Abstract. The matrix metalloproteinase MMP-3/stro- lial cell death after weaning, but instead alter the stro- melysin-1 (Str1) is highly expressed during mammary mal microenvironment. We used adipogenic 3T3-L1 gland involution induced by weaning. During involu- cells as a cell culture model to test the function of tion, programmed cell death of the secretory epithe- MMPs during adipocyte differentiation. Fibroblastic lium takes place concomitant with the repopulation of 3T3-L1 progenitor cells expressed very low levels of the mammary fat pad with adipocytes. In this study, we MMPs or TIMPs. The transcription of a number of have used a genetic approach to determine the role of MMP and TIMP mRNAs [Str1, MT1-MMP, (MMP-14) Str1 during mammary involution. Although Str1 has collagenase-3 (MMP-13), gelatinase A (MMP-2), and been shown to induce unscheduled apoptosis when ex- TIMP-1, -2 and -3] was induced in committed preadipo- pressed ectopically during late pregnancy (Alexander, cytes, but only differentiated adipocytes expressed an C.M., E.W. Howard, M.J. Bissell, and Z. Werb. 1996. J. activated MMP, gelatinase A.