83 research outputs found
How activists and target organizations collaborate in the face of emerging contingencies:setbacks and inaction: constraining or enablers of change?
In this paper, we attempt to examine the sources of agency of target organizations when engaged in collective change processes organized by activists concerned with environmental issues and sustainable development in the eastern part of the Netherlands. In combining social movement and institutional entrepreneurship literature, we examine why and how target organizations engage in collective action, change their practices, and adopt new ones in the pursuit of solving a common issue with the help of activists. We found that motivations and intentions to contribute to collective action were instrumental in the beginning of their participation. However, as the project evolves, intentions changed through a reorientation of existing practices and positions in the collective change process of target organizations. This shift was caused by inaction and other setbacks where target organizations and activists were exposed. These changes in turn, set in new practice development and organizational forms necessary to continue collective change. With these findings, we contribute to an understanding of network mobilization by showing the emergent and dynamic character of collective change and especially indicate setbacks and inaction as both constraining and necessary condition for change
Mobilizing Resources for Collective Action and Sustainable Development: Mobilizing Interests or Shared Values?
BCAR1/p130Cas protein and primary breast cancer: prognosis and response to tamoxifen treatment
BCAR1/p130Cas protein and primary breast cancer: prognosis and response to tamoxifen treatment
Bcar1/p130Cas protein and primary breast cancer: prognosis and response to tamoxifen treatment
BACKGROUND: The product of the Bcar1/p130Cas (breast cancer
resistance/p130Crk-associated substrate) gene causes resistance to
antiestrogen drugs in human breast cancer cells in vitro. To investigate
its role in clinical breast cancer, we determined the levels of
Bcar1/p130Cas protein in a large series of primary breast carcinomas.
METHODS: We measured Bcar1/p130Cas protein in cytosol extracts from 937
primary breast carcinomas by western blot analysis. The levels of
Bcar1/p130Cas protein were tested for associations and trends against
clinicopathologic and patient characteristics, the lengths of relapse-free
survival and overall survival (n = 775), and the efficacy of first-line
treatment with tamoxifen for recurrent or metastatic disease (n = 268).
RESULTS: Bcar1/p130Cas levels in primary tumors were associated with
age/menopausal status and the levels of estrogen receptor and progesterone
receptor. In univariate survival analysis, higher Bcar1/p130Cas levels
were associated with poor relapse-free survival and overall survival (both
two-sided P =.04; log-rank test for trend). In multivariate analysis, a
high level of Bcar1/p130Cas was independently associated with poor
relapse-free survival and overall survival. The response to tamoxifen
therapy in patients with recurrent disease was reduced in patients with
primary tumors that expressed high levels of Bcar1/p130Cas. In
multivariate analysis for response, Bcar1/p130Cas was independent of
classical predictive factors, such as estrogen receptor status,
age/menopausal status, disease-free interval, and dominant site of
relapse. CONCLUSION: Patients with primary breast tumors expressing a high
level of Bcar1/p130Cas protein appear to experience more rapid disease
recurrence and have a greater risk of (intrinsic) resistance to tamoxifen
therapy. Thus, measurement of Bcar1/p130Cas may provide useful prognostic
information for patients with primary or metastatic breast cancer
Prenatal Exposure to Organohalogens, Including Brominated Flame Retardants, Influences Motor, Cognitive, and Behavioral Performance at School Age
BACKGROUND: Organohalogen compounds (OHCs) are known to have neurotoxic effects on the developing brain. OBJECTIVE: We investigated the influence of prenatal exposure to OHCs, including brominated flame retardants, on motor, cognitive, and behavioral outcome in healthy children of school age. METHODS: This study was part of the prospective Groningen infant COMPARE (Comparison of Exposure-Effect Pathways to Improve the Assessment of Human Health Risks of Complex Environmental Mixtures of Organohalogens) study. It included 62 children in whose mothers the following compounds had been determined in the 35th week of pregnancy: 2,2'-bis-(4 chlorophenyl)1,1'-dichloroethene, pentachlorophenol (PCP), polychlorinated biphenyl congener 153 (PCB-153), 4-hydroxy-2,3,3',4',5-pentachlorobiphenyl (4OH-CB-107),4OH-CB-146,4OH-CB-187,2,2',4,4'-tetrabromodipheryl ether (BDE-47), BDE-99, BDE-100, BDE-153, BDE-154, and hexabromocy-clododecane. Thyroid hormones were determined in umbilical cord blood. When the children were 5-6 years of age, we assessed their neuropsychological functioning: motor performance (coordination, fine motor skills), cognition (intelligence, visual perception, visuomotor integration, inhibitory control, verbal memory, and attention), and behavior. RESULTS: Brominated flame retardants correlated with worse fine manipulative abilities, worse attention, better coordination, better visual perception, and better behavior. Chlorinated OHCs correlated with less choreiform, dyskinesia. Hydroxylated polychlorinated biphenyls correlated with worse fine manipulative abilities, better attention, and better visual perception. The wood protective agent (PCP) correlated with worse coordination, less sensory integrity, worse attention, and worse visuomotor integration. CONCLUSIONS: Our results demonstrate for the first time that transplacental transfer of polybrominated flame retardants is associated with the development of children at school age. Because of the widespread use of these compounds, especially in the United States, where concentrations in the environment are four times higher than in Europe, these results cause serious concern
Performance of gastrointestinal pathologists within a national digital review panel for Barrett's oesophagus in the Netherlands:results of 80 prospective biopsy reviews
Aims: The histopathological diagnosis of low-grade dysplasia (LGD) in Barrett's oesophagus (BO) is associated with poor interobserver agreement and guidelines dictate expert review. To facilitate nationwide expert review in the Netherlands, a web-based digital review panel has been set up, which currently consists of eight 'core' pathologists. The aim of this study was to evaluate if other pathologists from the Dutch BO expert centres qualify for the expert panel by assessing their performance in 80 consecutive LGD reviews submitted to the panel. Methods: Pathologists independently assessed digital slides in two phases. Both phases consisted of 40 cases, with a group discussion after phase I. For all cases, a previous consensus diagnosis made by five core pathologists was available, which was used as reference. The following criteria were used: (1) percentage of 'indefinite for dysplasia' diagnoses, (2) percentage agreement with consensus diagnosis and (3) proportion of cases with a consensus diagnosis of dysplasia underdiagnosed as non-dysplastic. Benchmarks were based on scores of the core pathologists. Results: After phase I, 1/7 pathologists met the benchmark score for all quality criteria, yet three pathologists only marginally failed the agreement with consensus diagnosis (score 68.3%, benchmark 69%). After a group discussion and phase II, 5/6 remaining aspirant panel members qualified with all scores within the benchmark range. Conclusions: The Dutch BO review panel now consists of 14 pathologists, who - after structured assessments and group discussions - can be considered homogeneous in their review of biopsies with LGD
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