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  • American Association for Cancer Research (AACR)  (6)
  • 1
    In: Molecular Cancer Research, American Association for Cancer Research (AACR), Vol. 3, No. 2 ( 2005-02-01), p. 71-77
    Abstract: Axillary lymph node status is the most important prognostic factor in predicting disease outcome in women with breast cancer. A number of chromosomal aberrations in primary breast tumors have been correlated with lymph node status and clinical outcome, but chromosomal changes particular to metastatic lymph node tumors have not been well studied. DNA samples isolated from laser-microdissected primary breast and metastatic axillary lymph node tumors from 25 women with invasive breast cancer were amplified using 52 microsatellite markers defining 26 chromosomal regions commonly deleted in breast cancer. Levels and patterns of allelic imbalance (AI) within and between breast and lymph node tumors were assessed to identify chromosomal alterations unique to primary or metastatic tumors and to examine the timing of metastatic potential. The overall frequency of AI in primary breast tumors (0.24) was significantly greater (P & lt; 0.001) than that in lymph node tumors (0.10), and congruent AI events were observed for & lt;20% of informative markers. AI at chromosomes 11q23.3 and 17p13.3 occurred significantly more frequently (P & lt; 0.05) in primary breast tumors alone; no chromosomal regions showed a significantly higher AI frequency in lymph nodes. Higher rates of AI in primary versus metastatic lymph node tumors suggest that acquisition of metastatic potential may be an early event in carcinogenesis, occurring before significant levels of AI accumulate in the primary tumor. In addition, patterns of AI were highly discordant between tumor types, suggesting that additional genetic alterations accumulated independently in the two cell populations.
    Type of Medium: Online Resource
    ISSN: 1541-7786 , 1557-3125
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2005
    detail.hit.zdb_id: 2097884-4
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  • 2
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2010
    In:  Cancer Research Vol. 70, No. 8_Supplement ( 2010-04-15), p. 2971-2971
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 70, No. 8_Supplement ( 2010-04-15), p. 2971-2971
    Abstract: Background: Research in the past decade has demonstrated the importance of the tumor microenvironment in breast cancer development and progression. Allelic imbalance evaluation of tumor and stromal components suggests a limited number of alterations in the tumor may lead to cellular transformation while tumor behavior may be driven by molecular changes in the surrounding stroma. Recent studies evaluating copy number changes in frozen stromal tissue, however, found no chromosomal alterations and suggested that earlier studies represent artifacts from the use of archive tissues. Methods: High-quality flash-frozen specimens were collected from breast quadrants from 14 patients undergoing mastectomy; patient characteristics ranged from prophylactic mastectomy to stage IV breast cancer. DNA was isolated (Gentra) from benign tissue sections and hybridized to GeneChip Human Mapping 250K arrays (Affymetrix). Genomic DNA from peripheral blood for each patient was genotyped to assess copy number variation (CNV) by paired analysis. CNVs were identified using Genome Console 3.0.2 (Affymetrix) with a minimum genomic size/fragment of 500 Kb and a minimum of 50 markers/segment. Results: Copy number changes ranging in size from 586-5061 kb were detected in 50% (7/14) patients in at least one quadrant, with a single patient having copy number changes present in each quadrant. 21% of quadrants (12/57) showed detectable copy number changes affecting 1 - 18 chromosomal arms. Copy number changes were detected not only in stroma from diseased breasts, but in prophylactic mastectomies, as well. Copy number changes were observed in all quadrants irrespective of tumor location. While copy number alterations on chromosomes 1q21, 2p21, 12p13, 14q12 and 18q12 were shared between patients, no patient had the same patterns of CNVs across all quadrants. Conclusions: Chromosomal alterations were detected in high-quality frozen breast stroma specimens utilizing genome-wide SNP array data, supporting earlier claims that breast stroma may be genetically unstable. Half of the patients in this study demonstrated copy number alterations in breast stroma distant from the tumor, suggesting that for a subgroup of breast cancer patients, widespread chromosomal instability may increase risk of recurrence. Note: This abstract was not presented at the AACR 101st Annual Meeting 2010 because the presenter was unable to attend. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 17-21; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2010;70(8 Suppl):Abstract nr 2971.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2010
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 3
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2008
    In:  Cancer Research Vol. 68, No. 9_Supplement ( 2008-05-15), p. 555-555
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 68, No. 9_Supplement ( 2008-05-15), p. 555-555
    Abstract: Background: Incidence of breast cancer varies across ethnic groups. Overall incidence is highest among Caucasian women (CW); however, incidence in women younger than 40 as well as mortality is highest among African American women (AAW). Although socioeconomic disparities are often blamed for these differences, AAW are more likely than CW to present with large, aggressive tumors with poor prognostic features such as estrogen receptor negativity, triple negative phenotype, and lymph node involvement, suggesting that molecular factors may also contribute to the younger age of onset and worse outcomes in AAW. In the present study, we have compared primary breast tumors from AAW and CW by gene expression profiling to identify differentially expressed genes that may explain why diagnosis at a young age, aggressive tumor biology and lower survival are more prevalent in AAW than CW with breast cancer. Materials and Methods: Breast tumor specimens were obtained from 26 pairs of age and stage-matched AAW and CW enrolled in the Clinical Breast Care Project (CBCP). Tumor cells were isolated by laser microdissection (Leica) and RNA isolated using the RNAqueous Micro kit (Ambion). RNA was amplified and labeled with biotin-11-UTP using two rounds of amplification with the MessageAmp II aRNA Amplification kit (Ambion). Fragmented aRNA was hybridized to the HG U133A 2.0 array (Affymetrix). A Mann-Whitney U test was used to identify differentially expressed genes (p ≤ 0.001). Results: Sixty-five genes were differentially expressed between AAW and CW. Twenty-eight genes were more highly expressed in AAW, including SOS1, TSPO, and PSPH, while 37genes had lower expression in AAW, including ZNF228, SCAMP4, and PSD3. Discussion: These results support a model in which molecular factors influence breast cancer onset, progression and prognosis in AAW. Genes with higher expression in tumors from AAW function in steroid, fatty acid, and serine biosynthesis, signal transduction, cell proliferation and adhesion, and cytoskeleton organization and biogenesis. Functions of genes with lower expression in AAW tumors include regulation of transcription, vesicular transport, iron metabolism, signal transduction, and extracellular matrix organization and biogenesis. These results suggest that breast tumors from AAW and CW differ at the gene expression level and that these differences may be responsible for the more aggressive clinical features of breast tumors in AAW compared to CW.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2008
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 4
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2015
    In:  Cancer Research Vol. 75, No. 1_Supplement ( 2015-01-01), p. B49-B49
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 75, No. 1_Supplement ( 2015-01-01), p. B49-B49
    Abstract: Background: Long thought to function only as an inert energy storage depot, the role of adipose tissue in breast tumorigenesis has been largely ignored. In light of increasing rates of obesity and use of breast conserving therapy and autologous fat grafting, improved understanding of the role of adipose in tumor etiology is crucial. Methods: Adipose adjacent to and distant from invasive breast tumors (n=20), or adjacent to non-malignant diagnoses (n=20) was laser microdissected from post-menopausal women. Gene expression data were generated using microarrays and data analyzed to identify significant patterns of differential expression between adipose groups, at the individual gene and molecular pathway level. Results: Pathway analysis revealed significant differences in immune response between non-malignant, distant and tumor adjacent adipose, with the highest response in tumor-adjacent and lowest in non-malignant adipose. Adipose from invasive breasts exhibits increased expression in anti-inflammatory genes, such as MARCO and VSIG4, while genes differentially expressed between tumor-adjacent and distant adipose such as SPP1, RRM2 and MMP9, are associated with increased cellular proliferation, invasion, and angiogenesis. Conclusions: Gene expression levels differ in breast adipose, depending on presence of or proximity to tumor cells. Heightened immunotolerance in adipose from invasive breasts provides a microenvironment favorable to tumorigenesis. In addition, tumor-adjacent adipose demonstrates expression of genes associated with tumor growth and progression. Together, these data suggest that adipose is not an inert component of the breast microenvironment but plays an active role in tumorigenesis. Citation Format: William C. Yarina, Lori A. Field, Brenda Deyarmin, Ryan van Laar, Jeffrey A. Hooke, Craig D. Shriver, Rachel E. Ellsworth. Molecular characterization of breast tumor-associated adipose. [abstract]. In: Abstracts: AACR Special Conference on Cellular Heterogeneity in the Tumor Microenvironment; 2014 Feb 26-Mar 1; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2015;75(1 Suppl):Abstract nr B49. doi:10.1158/1538-7445.CHTME14-B49
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2015
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 5
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2011
    In:  Cancer Research Vol. 71, No. 8_Supplement ( 2011-04-15), p. 3741-3741
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 71, No. 8_Supplement ( 2011-04-15), p. 3741-3741
    Abstract: Background: Breast tumors from African American women (AAW) have less favorable pathological characteristics and higher mortality rates than Caucasian women. While socioeconomic status may influence prognosis, biological factors are also likely to contribute to tumor behavior. Methods: Patients treated within an equal-access military medical center were matched by age, grade and ER status. Tumors were subjected to laser microdissection and RNA hybridized to HG U133A 2.0 microarrays. Data was analyzed using Partek Genomics Suite using a cutoff of P & lt;0.001, 1.5-fold change. Microarray results were validated by qRT-PCR. Results: Twenty-six pairs of matched tumor samples were identified. Clinico-pathological factors did not differ significantly for age at diagnosis, tumor size or stage, lymph node, hormone receptor, or HER2 status. Mortality was similar between the two groups. One putative and nineteen known genes were differentially expressed between populations with five genes expressed at higher and 15 genes at lower levels in tumors from AAW; hierarchical clustering classified 23/26 AAW and 26/26 CW correctly. Differential expression was validated (P & lt;0.001) for PSPHL (higher in AAW) and LTF and PSD3 (lower in AAW). Conclusions: Despite matching of tumors by pathological characteristics and provision of medical care in an equal-access health care system, a molecular signature differentiating AAW from CW tumors was detected, supporting a model in which aggressive tumor phenotypes are driven by molecular differences within the tumors. These differentially expressed genes are involved in immune response, cell cycle and metastasis and thus may contribute to the poor outcome in AAW. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2-6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2011;71(8 Suppl):Abstract nr 3741. doi:10.1158/1538-7445.AM2011-3741
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2011
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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  • 6
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2010
    In:  Cancer Research Vol. 70, No. 8_Supplement ( 2010-04-15), p. 2134-2134
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 70, No. 8_Supplement ( 2010-04-15), p. 2134-2134
    Abstract: Objective Histological grade classifies breast carcinomas into low-, intermediate- and high-grade. Developmental pathways for high-grade disease remain controversial; clinical data have been used to describe both linear models, in which high-grade tumors evolve from low-grade precursors, as well as models that depict low- and high-grade carcinomas as distinct molecular diseases. Genome-wide copy number alterations were examined in low- and high-grade breast tumors to identify genetic changes associated with the etiology of low- and high-grade breast carcinomas. Methods Tumors were diagnosed and characterized by a single, dedicated breast pathologist. DNA was isolated after laser microdissection from low- (n= 53) and high-grade (n=68) tumors. Genotype data were generated using Human Mapping 250K Sty arrays (Affymetrix). Copy number alterations and LOH were detected using GenomeConsole 3.0.2 (Affymetrix). Results The most common alterations in low-grade carcinomas were gain of chromosomes 1q (75%) and 16p (58%) and loss of chromosome 16q (86%). These alterations were frequently simple and included the entire chromosomal arm. In contrast, patterns of alterations were complex in high-grade tumors, frequently with alternating gains and losses on a single chromosomal arm. In high-grade tumors, the most frequent alterations included gain of chromosome 1q (85%), 8q (84%), and loss of chromosomes 8p (54%), 14q (57%) and 17p (69%). Loss of 16q (P & lt;0.0000005) and gain of 16p (P & lt;0.005) occurred significantly more frequently in low- compared to high-grade tumors, while gain of 8q24 (P & lt;0.000005) and 10p15-p14 (P & lt;0.00005) and loss of chromosome 17p13 (P & lt;0.00005) occurred significantly more frequently in high- compared to low-grade tumors. Only two samples, one low- and one high-grade, had a “flat” profile with no detectable chromosomal alterations. Conclusion Low- and high-grade breast tumors are genetically different. Gain of chromosome 1q is common in both low- and high-grade tumors, and may be an early event in tumorigenesis. Given the significantly different patterns of alterations, especially significantly higher loss of chromosome 16q in high- compared to low-grade tumors, high-grade disease may not arise from dedifferentiation of low-grade but rather represent a separate disease defined by unique genetic alterations. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 101st Annual Meeting of the American Association for Cancer Research; 2010 Apr 17-21; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2010;70(8 Suppl):Abstract nr 2134.
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2010
    detail.hit.zdb_id: 2036785-5
    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
    Location Call Number Limitation Availability
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