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  • metastasis  (2)
  • EXP; Experiment; Madeira; Madeira_S  (1)
  • GnRH  (1)
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  • 1
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    PANGAEA
    In:  Supplement to: Ramalhosa, Patricio; Debus, Sarah-Lena; Kaufmann, Manfred; Lenz, Mark (2016): A non-native macroalga is less attractive for herbivores but more susceptible to light limitation and grazing stress than a comparable native species. Helgoland Marine Research, 70(1), https://doi.org/10.1186/s10152-016-0478-3
    Publication Date: 2023-01-13
    Description: Experiments were conducted from 4 June to September 2007 inside laboratory facilities at the south coast of Madeira (32°38'N, 16°54'W). The organisms used for this study were the sea urchin Paracentrotus lividus collected at Doca do Cavacas (32° 38'06 N; 16° 56'52 W), the red seaweed Grateloupia imbricata collected from the marina of Funchal (32° 38'41 N; 16° 54'46 W) at 0.5 m water depth, and the brown seaweed Stypopodium zonale collected from boulders at Reis Magos, Caniço (32° 83'45 N; 16° 49'25 W) in water depths of 3-7 m. The study consisted of three sequential stages: (i) assessing algal light compensation points, (ii) inducing light limitation and grazing, (iii) assessing grazer consumption rates in no-choice feeding assays after light limitation and grazer impact. For the latter we used the algal material from stage (ii) (see additional file 1). Pilot studies were carried out in June 2007 to identify the Light Compensation Point (LCP) for both algal species, i.e. the light intensity at which the rate of photosynthesis (measured as oxygen production) equals respiration. For this, we reduced the amount of incoming light by placing various layers of black plastic gauze material with a mesh size of 1 mm on top of each aquarium. For both macroalgae, we had a total of 12 aquaria (3.5 L each) of with each was loaded with 30 - 40 g wet weight of seaweed material. We randomly assigned two aquaria to each of six different light regimes. The number of gauze layers used was 0, 1, 2, 3, 4 and 5. After we recorded the concentration of dissolved oxygen with an oxymeter (Oxi 197, WTW Wissenschaftlich-Technische Werkstätten GmbH, Weilheim, Germany) twice a day (9am and 5pm) for the following 4 days (see additional file 2). Experiments were carried out in July 2007 for G. imbricata, and in September 2007 for S. zonale. We conducted a two-factorial experiment for each of the species in which we crossed two levels of grazing ("grazed" and "non-grazed") with six levels of light intensities (0-5 layers of gauze material) and each treatment combination was replicated eight times (n=8). Consequently, we had 6 x 8 = 48 aquaria of which each contained one sea urchin, while another 48 aquaria had no sea urchins. The latter were used to determine total algal growth rates under the different light regimes in the absence of grazers and to provide non-grazed algal material for the feeding assays. In total we had 96 aquaria for each of the two seaweed species in the study and the respective treatments, i.e. light limitation and grazing, were imposed simultaneously for 21 days. We tested for possible effects of the previously applied light limitation and grazing (see stage (ii)) on grazer consumption rates in no-choice feeding assays that lasted for 24 h. Hence, the number of replicates for the assays at stage (iii) was the same as at stage (ii). Grazer consumption rates of algal material were determined as the grazers' total consumption, which was calculated using the equation suggested by Cronin and Hay (1996-a): [Ai x (Cf / Ci) - Af ] where Ai and Af were the initial and final weight of the algae portions used in the feeding assays; Ci and Cf are the equivalent weights of the growth control algal pieces before and after the assays (Sotka et al., 2002). Finally, consumption rates were standardised for grazer wet biomass (g alga/g grazer). Negative consumption was recorded in case algal growth rates during the assays exceeded consumption rates (see additional file 3 raw data).
    Keywords: EXP; Experiment; Madeira; Madeira_S
    Type: Dataset
    Format: application/zip, 211.5 kBytes
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  • 2
    ISSN: 1573-7276
    Keywords: metastasis ; microvessel density ; ovarian carcinoma ; proto-oncogenes ; resistance-related proteins
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Relationships between the incidence of metastatic spread and microvessel density, expression of proto-oncogene products, or expression of resistance-related proteins were investigated in human ovarian carcinomas by immunohistochemistry. Ovarian carcinomas with a high microvessel density showed a significantly increased formation of metastases (P=0.005). Tumors with positive immunoreactivity of c-jun and c-myc products had a higher metastatic spread; however, these results were not statistically significant. A marginally significant correlation existed between the expression of erbB1 (EGFR) and metastatic spread (P=0.05). No significant relationship was found between the expression of the resistance-related proteins P-glycoprotein or glutathione S-transferase-π and the incidence of metastases. Furthermore, no correlation was detected between expression of the heat shock protein 70 and the occurrence of metastases.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-7217
    Keywords: breast cancer ; CD44 variants ; metastasis ; tumor progression marker
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Splice variants of CD44 expressed in a metastasizing cell line derived from a rat pancreatic adenocarcinoma have been shown recently to confer metastatic potential onto non-metastasizing rat pancreatic carcinoma and sarcoma cell lines. Homologues of these variants have also been detected in a variety of human malignancies. Using antibodies raised against a bacterially expressed fusion protein containing variant CD44 sequences, we have explored the expression of variant CD44 glycoproteins on tumors of the female breast. The material examined included normal tissue, hyperplastic lesions, 103 primary invasive mammary carcinomas, 10in situ carcinomas, 12 local recurrences and 18 lymph node metastases. Using a polyclonal serum directed against several variant CD44 epitopes, normal mammary epithelia as well as ductal hyperplasias were negative for these splice variants, while the variant CD44 epitopes were detectable in all but six of the primary invasive carcinomas. From the reaction with various monoclonal antibodies and polyclonal sera specific for individual epitopes it is obvious that the tumors predominantly express CD44 variants encoded by exons v5 to v7. Interestingly, all investigated lymph node metastases reacted positively with the variant-specific antibodies, in contrast to primary tumors which reacted in 54% to 86% of the cases, depending on the antibody used. Statistical analysis revealed a significant correlation between expression of variant exons v3/v4 and v6 and increased tumor grade (p = 0.001 and p 〈 0.05, respectively; Fisher's exact test). Exon v6 is carried by the variants which confer metastatic capability in the rat. These results indicate that the expression of the CD44 variants is upregulated in mammary carcinomas and is closely linked to tumor anaplasia.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-7217
    Keywords: breast cancer ; gonadotropin-releasing hormone-analog ; GnRH ; receptor
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Gonadotropin-releasing hormone analogs (GnRH-A) have been added to the armentarium in the therapy of hormone-dependent breast cancer in premenopausal women. The effect of chronic GnRH-A-treatment in premenopausal women is based on the suppression of the hypothalamus-pituitary-ovarian axis and the reduction of sex-steroid serum levels. In addition, a number of experimental and clinical data have been accumulated indicating a direct action of GnRH-A on breast cancer cells and tissue. In this study we analyzed 235 human breast cancer biopsies for specific GnRH-A-binding. We demonstrate high affinity GnRH-A binding sites in human breast cancer tissues. The evaluation of clinical data showed no correlation of the level of GnRH-A-binding with classical tumor parameters.
    Type of Medium: Electronic Resource
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