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NASA Scientific and Technical Aerospace Reports

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20040111695 Dartmouth Coll., Hanover, NH<br />

Improving Symptoms Control QOL <strong>and</strong> Quality of Care for Women with Breast Cancer: Developing a Research<br />

Program on Neurological Effects via Doctoral Education<br />

Bakitas, Marie; Ahles, Tim A.; May 2004; 30 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-03-1-0298<br />

Report No.(s): AD-A425848; No Copyright; Avail: CASI; A03, Hardcopy<br />

The purpose of this traineeship is to develop the academic, clinical, <strong>and</strong> research skills of an expert advanced practice<br />

nurse within the context of a mentor’s (Tim A. Ahles, Ph.D.) funded program of research of the (central nervous system CNS)<br />

cognitive Effects of Chemotherapy. The scope of the program is to support Ms. Bakitas’ doctoral education with an ultimate<br />

career goal of becoming a Clinical Breast Cancer Research Scientist. In conjunction with the doctoral program, through a<br />

mentored research experience Ms. Bakitas is exp<strong>and</strong>ing an established research program on CNS effects of breast cancer<br />

treatment by developing a parallel focus on the peripheral nervous system effects of chemotherapy, (Chemotherapy-Induced<br />

Peripheral Neuropathy CIPN), on quality of life. The major achievements of the trainee at the midterm, are successful<br />

accomplishment of the planned training%activities/tasks originally outlined for the first year, with an additional achievement<br />

of developing (as a co- investigator), a funded grant on chemotherapy induced peripheral -neuropathy. The significance of<br />

these achievements is that the training is providing the initial foundation for developing a clinical nurse expert towards a<br />

program of breast cancer researcher.<br />

DTIC<br />

Cancer; Education; Females; Mammary Gl<strong>and</strong>s; Medical Science; Neurology; Peripheral Nervous System; Signs <strong>and</strong><br />

Symptoms<br />

20040111696 Burnham Inst., La Jolla, CA<br />

Investigation of Novel Human CED-4 Homolog NAC-X in Apoptosis Regulation of Breast Cancer<br />

Damiano, Jason S.; May 2004; 8 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-01-1-0166<br />

Report No.(s): AD-A425851; No Copyright; Avail: CASI; A02, Hardcopy<br />

Proteins containing a Caspase-Associated Recruitment Domain (CARD) have previously been shown to-serve as key<br />

regulators of tumor cell survival as well as regulators of other- cellular processes, such as cytokine production. Interleukin-l<br />

beta (IL-1B) is a cytokine which has been found to be expressed in breast cancer cells <strong>and</strong> may be associated with more<br />

aggressive <strong>and</strong> invasive breast tumors. Here we report the cloning <strong>and</strong> functional characterization of NAC-X or CLAN<br />

(CARD, LRR, And NACHT-containing protein). CLAN was found to be expressed in several breast cancer cell lines as well<br />

as in monocytes by RT-PCR. Co-immunoprecipitation studies revealed that CLAN associated several other proteins including<br />

caspase-l, Nod2, <strong>and</strong> NAC. When assayed using an IL-1B ELISA, CLAN was found to induce the activation of caspase-l in<br />

response to bacterial infection or LPS, implying a role for this protein in the innate immune response. CLAN also was found<br />

to enhance cell death following bacterial infection independently of caspase-l. Through its interactions with other<br />

CARD-containing proteins, CLAN may regulate the survival of breast cancer cells <strong>and</strong> Could be utilized as a novel anti- tumor<br />

target or diagnostic/prognostic biomarker.<br />

DTIC<br />

Apoptosis; Bacterial Diseases; Cancer; Cells (Biology); Mammary Gl<strong>and</strong>s<br />

20040111697 Wake Forest Univ., Winston-Salem, NC<br />

Sequence Variants in Estrogen Receptors <strong>and</strong> Risk for Prostate Cancer<br />

Chang, Bao-Li; Mar. 2004; 28 pp.; In English<br />

Contract(s)/Grant(s): DAMD17-03-1-0046<br />

Report No.(s): AD-A425852; No Copyright; Avail: CASI; A03, Hardcopy<br />

This post doctoral research training aims to prepare the trainee for further prostate cancer research through a genetic<br />

epidemiology study of the role of estrogen receptors (ERs) in prostate cancer etiology. Two goals were proposed in this<br />

postdoctoral training project: 1) to further the trainee’s ability to be an efficient researcher of prostate cancer genetics by<br />

enhancing the trainee’s ability to use bioinformatics tools for genetic data analyses. 2) to comprehensively evaluate multiple<br />

genetic variants in ER genes using both family-based <strong>and</strong> case-control study designs, thus providing the trainee with realworld<br />

experience in genetic <strong>and</strong> bioinformatics analyses. Consistent with those%%goals, major accomplishments in the first<br />

half of the training period include: 1) attending statistic <strong>and</strong> bioinformatics courses, conferences, <strong>and</strong> workshops. 2) complete<br />

sequencing of all 14 exons, <strong>and</strong> the -2kb promoter region of the ESR2 gene in 96 subjects for the identification of mutations<br />

<strong>and</strong> sequence variants. 3) application of the statistics <strong>and</strong> bioinformatics skills gained in various courses <strong>and</strong> workshops for<br />

208

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