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Abstract A55: Regional differences in breast cancer biomarkers in American Indian and Alaska Native women A55:美洲印第安人和阿拉斯加原住民女性乳腺癌生物标志物的地区差异
Pub Date : 2010-10-01 DOI: 10.1158/1055-9965.DISP-10-A55
J. Kaur, R. Vierkant, S. Myers
Introduction: Breast cancer is a major cause of cancer mortality in American Indian and Alaska Native (AIAN) women. However regional differences are striking with lowers rates in Arizona and highest in Alaska with almost a three-fold difference in incidence and mortality between the two states. These differences may be due in part to varying levels of biologic tumor aggressiveness. To evaluate this, we compared a panel of biomarkers on consecutively diagnosed AIAN breast cancer cases from AZ (N=53) and AK (N=42). Methods: Retrospective analysis of tissue blocks measured expression levels for the following panel of biomarkers: ER and PR (ordinally coded as positive vs. negative); her2, BCL-2, and EGFR (coded 0.1.2. and 3+) and P53, MIB-1 and cyclin D (continuous percent of cells stained). Distributions of biomarker values were compared across state of residence using t-tests for continuous and ordinally scaled markers and chi-square tests of significance for binary markers. Age adjusted analyses were also carried out using linear and logistic regression models as appropriate to account for possible differences in age at diagnosis across states. Chart reviews recorded demographics and treatment characteristics. Results: The following demographics were observed with 95 cases of AIAN women with breast cancer analyzed. Average age at diagnosis was similar in the two states (mean, 58.4 for AZ vs. 56.1 for AK, t-test p value=0.45). 74% presented with a palpable mass. 32% had lumpectomy and axillary node dissection. 28% were premenopausal. 8% had a first-degree relative with breast cancer. 46% received adjuvant chemotherapy. 54% received adjuvant hormonal therapy. Cases from AK had higher levels of p53 staining (40.3 vs. 18.5, p=0.004) and lower levels of both EGFR (mean ordinal scaling 0.15 vs. 0.53, p=0.02) and Her2 (mean ordinal scaling 0.81 vs. 1.32, p=0.02) tan those from AZ. No differences in distribution were observed for MIB-1, Cyclin D, BCL-2, ER or PR. When examined together, the triple negative combination of ER/PR/Her2 also did not differ across states (12% for AK vs.13%forAZ, p=0.85). Conclusions: Our findings indicate that regional differences in biomarker expression levels of P53, EGFR and Her2 may exist in AIAN women. Further research is needed to confirm our results and determine to what extent these differences may explain the observed differences in mortality. Genetic testing for BRCA1,2 or other genetic associations with breast cancer have not been done in these populations and may also be useful to examine the reasons for differences in incidence and mortality. In addition, AIAN women are more likely to present with palpable masses representing higher risk stages of breast cancer. Outreach activities in this population continue to be highly important to change mortality. Supported in part by NCI U01 114609 Spirit of Eagles Community Network Program Citation Information: Cancer Epidemiol Biomarkers Prev 2010;19(10 Suppl):A55.
简介:乳腺癌是美国印第安人和阿拉斯加原住民(AIAN)妇女癌症死亡的主要原因。然而,地区差异是惊人的,亚利桑那州的发病率较低,阿拉斯加州的发病率最高,两个州的发病率和死亡率几乎相差三倍。这些差异可能部分是由于不同程度的生物肿瘤侵袭性。为了评估这一点,我们比较了AZ (N=53)和AK (N=42)连续诊断的AIAN乳腺癌病例的一组生物标志物。方法:回顾性分析组织块测量以下生物标志物的表达水平:ER和PR(通常编码为阳性和阴性);her2、BCL-2和EGFR(编码0.1.2)。和3+)和P53, MIB-1和cyclin D(连续百分比的细胞染色)。使用t检验对连续和有序刻度标记进行比较,使用卡方检验对二元标记进行显著性检验。年龄调整分析也酌情使用线性和逻辑回归模型进行,以解释各州诊断年龄可能存在的差异。图表回顾了记录的人口统计学和治疗特征。结果:对95例亚洲女性乳腺癌患者进行了以下统计分析。两州的平均诊断年龄相似(AZ为58.4岁,AK为56.1岁,t检验p值=0.45)。74%表现为可触及的肿块。32%行乳房肿瘤切除术和腋窝淋巴结清扫。28%为绝经前。8%的人有一级亲属患有乳腺癌。46%接受了辅助化疗。54%接受了辅助激素治疗。与AZ患者相比,AK患者的p53染色水平较高(40.3比18.5,p=0.004), EGFR(平均顺序标度0.15比0.53,p=0.02)和Her2(平均顺序标度0.81比1.32,p=0.02)水平较低。在mb -1、Cyclin D、BCL-2、ER或PR的分布上没有差异。当一起检查时,ER/PR/Her2的三阴性组合在各州之间也没有差异(AK为12%,AZ为13%,p=0.85)。结论:我们的研究结果表明,在亚洲女性中,P53、EGFR和Her2的生物标志物表达水平可能存在区域差异。需要进一步的研究来证实我们的结果,并确定这些差异在多大程度上可以解释观察到的死亡率差异。在这些人群中还没有进行BRCA1、2或其他与乳腺癌相关的基因检测,也可能有助于检查发病率和死亡率差异的原因。此外,亚洲妇女更有可能出现可触及的肿块,这代表了乳腺癌的高风险阶段。在这一人群中开展外联活动对改变死亡率仍然非常重要。部分由NCI U01 114609老鹰精神社区网络项目支持。引文信息:癌症流行病学生物标志物pre 2010;19(10增刊):A55。
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引用次数: 0
Social capital as a framework for community based participatory research in cancer prevention and control 社会资本作为基于社区的癌症预防和控制参与性研究的框架
Pub Date : 2007-11-01 DOI: 10.1037/e520982012-008
Donna Kenerson, M. Hargreaves, Kushal A. Patel, C. Larson, J. Drake, Venita Bush
B41 Purpose: The aim of this research was to explore whether key dimensions of social capital might inform the community based participatory research (CBPR) approach to cancer prevention and control interventions that target low-income African American communities.
 Methodology: Focus groups were conducted at community health centers located in Nashville, Chattanooga, and Memphis. African American men and women, representing low-income urban communities, participated in 54 focus groups. The focus groups used semi-structured questions integrating multiple health-related constructs of social capital with community perceptions centering on the facilitators and barriers to cancer control and prevention. These constructs included community groups, neighborhoods, networks, collective action, communication, and leadership.
 Results:
 Participants characterized community as going beyond physical boundaries to interactions among neighbors. Varied beliefs were expressed about the decline in neighborhood cohesion that included changes in racial or ethnic composition and gentrification. Church pastors and politicians were considered leaders of the community; however, church leaders were perceived as more active in the health-related needs of their communities. The poor health of communities was attributed to a lack of motivation by community members to change lifestyles and behaviors. Perceptions surrounding cancer included the belief that cancer was a death sentence and people generally did not want to know if they had cancer. On the other hand, some believed that an early diagnosis of cancer might improve one’s survival, and that there needed to be greater communication of this fact. Major barriers to cancer-related screening included the fear of cancer screening outcomes and the general lack of knowledge related to health screening guidelines.
 Conclusion: Findings suggest the need for greater awareness of the social processes affecting the health of communities. This heightened awareness can improve the understanding of health and health inequalities affected by social capital. The assessment of social capital, as a health-related construct, may enhance community based participatory research focusing on cancer disparities by creating opportunities for individual and group interactions that facilitate effective and sustainable community health action.
 Funded by NIH 5P20 MD 000516 (EXPORT), NCI U01 CA114641 (Community Networks Program)
目的:本研究的目的是探讨社会资本的关键维度是否可以为针对低收入非洲裔美国人社区的基于社区的参与式研究(CBPR)方法提供信息,以进行癌症预防和控制干预。
方法:焦点小组在纳什维尔、查塔努加和孟菲斯的社区卫生中心进行。代表低收入城市社区的非裔美国人男女参加了54个焦点小组。焦点小组采用半结构化问题,将社会资本的多种健康相关结构与社区观念结合起来,以癌症控制和预防的促进因素和障碍为中心。这些结构包括社区团体、邻里、网络、集体行动、沟通和领导。
结果:
参与者将社区描述为超越物理边界的邻居之间的互动。人们对社区凝聚力的下降表达了不同的看法,包括种族或民族构成的变化和士绅化。教会牧师和政治家被认为是社区的领袖;然而,教会领袖被认为更积极地满足其社区的健康相关需求。社区健康状况不佳的原因是社区成员缺乏改变生活方式和行为的动力。人们对癌症的认知包括认为癌症是一种死刑判决,人们通常不想知道自己是否患有癌症。另一方面,一些人认为癌症的早期诊断可能会提高一个人的存活率,并且需要对这一事实进行更多的交流。癌症相关筛查的主要障碍包括对癌症筛查结果的恐惧以及普遍缺乏与健康筛查指南相关的知识。
结论:研究结果表明,需要提高对影响社区健康的社会进程的认识。提高认识可以增进对受社会资本影响的健康和健康不平等现象的理解。社会资本评估作为一种与健康有关的结构,可以通过为促进有效和可持续的社区卫生行动的个人和团体互动创造机会,加强以社区为基础的关注癌症差异的参与性研究。
由NIH 5P20 MD 000516 (EXPORT), NCI U01 CA114641(社区网络计划)资助
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引用次数: 0
Sexual health inventory in men screened for prostate cancer 前列腺癌筛查男性的性健康调查
Pub Date : 2007-04-01 DOI: 10.1016/S0022-5347(18)31948-7
F. Bianco, B. McHone, K. Wagner, J. Burgess, T. Jarrett, S. Patierno
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引用次数: 0
Stage III colon cancer prognosis prediction by gene expression profiling. 基因表达谱预测III期结肠癌预后。
Pub Date : 2006-12-01 DOI: 10.1200/jco.2007.25.18_suppl.10590
A. Barrier, P. Böelle, D. Brault, A. Flahault, S. Dudoit, A. Lemoine
B20 Purpose. This study aimed to assess the possibility to build a microarray-based prognosis predictor (PP) for stage III colon cancer that could be used to guide postoperative chemotherapy. Material and methods. Thirty-six patients, operated on for a stage III colon cancer, were included in this study. Eighteen patients have subsequently developed a liver metastasis, while the other 18 have remained disease-free for at least 5 years. Tumor mRNA samples were profiled using the Affymetrix HGU133A GeneChip. Patients were repeatedly and randomly divided into 10,000 training (TS) and validation sets (VS) of 10 different sizes. For each TS/VS split, a 30-gene prognosis predictor (PP), identified on the TS by selecting the 30 most differentially expressed genes and applying diagonal linear discriminant analysis, was used to predict the prognoses of VS patients. Results. The 10,000 30-gene PP yielded the following average prognosis prediction performance measures: 72.9% accuracy, 72.2% sensitivity, 73.6% specificity. Improvements in prognosis prediction were observed with increasing TS size (76.1% accuracy, 75.2% sensitivity, and 77.1% specificity for TS of size 32). The 30-gene PP were found to be highly-variable in composition across TS/VS splits. A total of 7,096 genes were included in the 10,000 PP; the higher number of selections for a gene was 5,896. Conclusions. Microarray gene expression profiling is able to predict the prognosis of stage III colon cancer patients and, thus, might be used to guide adjuvant chemotherapy.
B20的目的。本研究旨在评估构建基于微阵列的III期结肠癌预后预测器(PP)的可能性,该预测器可用于指导术后化疗。材料和方法。36名III期结肠癌手术患者参与了这项研究。18名患者随后发生肝转移,而其他18名患者至少5年没有发病。使用Affymetrix HGU133A基因芯片分析肿瘤mRNA样本。将患者反复随机分为10个不同大小的10000个训练集(TS)和验证集(VS)。对于每次TS/VS分裂,通过选择30个差异表达最多的基因并应用对角线性判别分析,在TS上确定一个30基因预后预测因子(PP),用于预测VS患者的预后。结果。1万个30个基因的PP产生了以下平均预后预测指标:准确率72.9%,敏感性72.2%,特异性73.6%。随着TS大小的增加,预后预测有所改善(对于32大小的TS,准确率为76.1%,灵敏度为75.2%,特异性为77.1%)。发现30个基因的PP在TS/VS分裂中组成高度可变。10000个PP中共包含7096个基因;一个基因的较高选择数为5896。结论。微阵列基因表达谱能够预测III期结肠癌患者的预后,因此可能用于指导辅助化疗。
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引用次数: 0
Genetic Susceptibility to Lung Cancer 肺癌的遗传易感性
Pub Date : 2003-08-01 DOI: 10.1016/B978-0-323-52357-8.00006-8
M. Spitz, Q. Wei, Q. Dong, C. Amos, Xifeng Wu
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引用次数: 5
期刊
Cancer Epidemiology and Prevention Biomarkers
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