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NASA Scientific and Technical Aerospace Reports

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strengthens our central hypothesis that BCCIP regulates cell cycle control. In the next funding year, we will strive to<br />

accomplish the objectives of tasks 5-6.<br />

DTIC<br />

Cancer; Mammary Gl<strong>and</strong>s; Proteins; Ribonucleic Acids<br />

20040111598 New Mexico Univ., Albuquerque, NM<br />

University of New Mexico Undergraduate Breast Cancer Training Program: Pathway to Research Careers<br />

Griffith, Jeffrey K.; Apr. 2004; 15 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-02-1-0513<br />

Report No.(s): AD-A425668; No Copyright; Avail: CASI; A03, Hardcopy<br />

We have established a three-phase training program to motivate talented undergraduate students, especially students from<br />

under-represented Southwestern minorIties, to pursue careers in breast cancer research. Phase I provides a well-rounded<br />

introduction to the theory <strong>and</strong> practice of breast cancer research. This phase includes inquiry-based tutorials that integrate key<br />

concepts in normal <strong>and</strong> cancer breast biology; visits to specialized laboratories that utilize state- of-the-art technologies for<br />

breast cancer research; structured interactions with surgeons, medical oncologists <strong>and</strong> their patients, radiologists <strong>and</strong><br />

pathologists in settings that introduce the clinical realities of breast cancer diagnosis <strong>and</strong> treatment; seminars presented by the<br />

Program’s research mentors; a weekly, journal club that introduces current issues in breast cancer research while developing<br />

presentation <strong>and</strong> critical reading skills <strong>and</strong> a research project supervised by one of the program’s mentors. During phases II<br />

<strong>and</strong> III, trainees have opportunities to continue their research projects throughout their senior years, <strong>and</strong> then in graduate<br />

school, respectively. The success of the program wIll be evaluated in the short term by the satisfaction of the trainees <strong>and</strong><br />

mentors, <strong>and</strong> in the longer term by the number of trainees that goes on to graduate studies in breast cancer- related programs.<br />

DTIC<br />

Cancer; Education; Mammary Gl<strong>and</strong>s; Medical Science; Occupation; Students<br />

20040111599 University of Central Florida, Orl<strong>and</strong>o, FL<br />

Role of Schwannomin <strong>and</strong> Paxillin in Cell Growth Control<br />

Fern<strong>and</strong>ez-Valle, Cristina; May 2004; 7 pp.; In English; Original contains color illustrations<br />

Contract(s)/Grant(s): DAMD17-03-1-0211<br />

Report No.(s): AD-A425669; No Copyright; Avail: CASI; A02, Hardcopy<br />

Preliminary results indicate that phosphorylation of serine 518 is not required for localization of schwannomin to the<br />

plasma membrane <strong>and</strong> filopodia <strong>and</strong> lameliapodia. This indicates that schwannomin binding to paxillin does not require<br />

phosphorylation of serine 518 by Pak, a racactivated serine/threonine kinase. It suggests that schwannomin firsts binds paxillin<br />

<strong>and</strong> targets to the membrane where local activation of p21 activated kinase by cdc42 or rac stimulates phosphorylation of<br />

serine 518 on schwannomin <strong>and</strong> the ensuing change in morphology.<br />

DTIC<br />

Cell Division; Cells (Biology)<br />

20040111600 Beth Israel Deaconess Medical Center, Boston, MA<br />

Effects of CSK Homologous Kinase Overexpression on HER2/Neu-Mediated Signal Transduction Pathways in Breast<br />

Cancer Cells<br />

Zagozdzon, Radoslaw; Avraham, Hava; Apr. 2004; 11 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-02-1-0302<br />

Report No.(s): AD-A425671; No Copyright; Avail: CASI; A03, Hardcopy<br />

Our proposal aims to investigate in details the potential function of CHK in breast cancer as a signal transducer in the<br />

signaling pathway from HER2/Neu receptor. The studies conducted in the period reported included: 1) studies on the effects<br />

of CHK on the HER2/Neu-induced tumorigenesis in vivo, <strong>and</strong> 2) generation of CHK-derivatives. Our major findings are as<br />

follows: Task 2: We created transgenic mice to study the effects of CHK on ErbB2-mediated signaling in vivo as well as on<br />

ErbB2-induced mammary tumor formation in vivo. Task 3: We used an alternative approach to successfully generate CHK<br />

derivatives which can be used in experimental CHK-based protein therapy of mammary tumors.<br />

DTIC<br />

Cancer; Genetics; Mammary Gl<strong>and</strong>s; Transferring<br />

183

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