78 research outputs found

    Podróż do kresu mapy. Destrukcja kartografii jako dekonstrukcja – perspektywa pragmatyczna

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    Artykuł dotyczy funkcjonowania map i ich wyobrażeń w warunkach wojennych na przykładzie polskiego materiału dotyczącego II wojny światowej. Punktem wyjścia jest relacja Mirona Biało- szewskiego zawarta w opowiadaniu Rajza dotycząca ucieczki jego rodziny we wrześniu 1939 roku w stronę granicy wschodniej. Opowiadanie wprowadza wątki, które są obecne w innych tek- stach okołowojennych i powojennych autora Pamiętnika z powstania warszawskiego, i które są interpretowane w kontekście innych źródeł (przede wszystkim literackich). Mapy używane podczas wojny miały wymiar propagandowy, dezorientowały zarówno swoich, jak i obcych użyt- kowników (czytelników). Okres wojenny oznacza ciągłe zapotrzebowanie na mapy oraz ujaw- nia deficyt przestawień kartograficznych, a jednocześnie ciągle zmieniająca się rzeczywistość obnaża ich bezużyteczność, w skrajnych przypadkach sprowadzając je do surowca wtórnego. Wojna jest stanem wyjątkowym, w którym proces dekonstrukcji kartografii zostaje przyśpie- szony. Jest to więc moment, w którym postulaty nurtu krytycznego w historii i teorii kartografii zostają spełnione, a pragmatyka dowartościowana. To użytkownik w konkretnej sytuacji dokonuje demaskacji racjonalnego umysłu stojącego za kartografią

    Wound fluids collected from patients after IORT treatment activates extrinsic apoptotic pathway in MCF7 breast cancer cell line

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    Objectives: Intraoperative radiotherapy (IORT) relates to irradiation of diseased tissue during the surgery within the tumor bed. The reason for this process is based on the fact that the increase in the radiation dose increases local tumor control. It was shown that postoperative fluids obtained from patients after breast cancer conserving surgery, stimulated motility and invasiveness of tumor cells in vitro. The results obtained from TARGIT clinical trial demonstrated that IORT significantly inhibits the stimulatory effect of wound fluids on tumor cells in vitro. We therefore speculated that wound fluids collected from patients after IORT treatment may induce the apoptosis in breast cancer cell lines and it may be a reason for their lower proliferation rate and potential to metastasis. Material and methods: Breast cancer MCF7 cell line was incubated with wound fluids collected from patients after conserving breast cancer surgery or surgery followed by IORT for 4 days. Then the expression of markers associated with extrinsic or intrinsic apoptosis pathway was established. Results: Our results clearly indicate activation of extrinsic apoptosis pathway by wound fluids collected from patients after IORT treatment. No changes in apoptotic markers were seen in cells treated with wound fluids collected from patients after the surgery alone. Conclusions: Thus we confirmed that wound fluids collected from patients after IORT treatment may induce the apoptosis in breast cancer cell lines and it may be a reason for their lower proliferation rate and invasiveness of tumor cells in vitro

    Dynamic interactions in the tumor niche: how the cross-talk between CAFs and the tumor microenvironment impacts resistance to therapy

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    The tumor microenvironment (TME) is a complex ecosystem of cells, signaling molecules, and extracellular matrix components that profoundly influence cancer progression. Among the key players in the TME, cancer-associated fibroblasts (CAFs) have gained increasing attention for their diverse and influential roles. CAFs are activated fibroblasts found abundantly within the TME of various cancer types. CAFs contribute significantly to tumor progression by promoting angiogenesis, remodeling the extracellular matrix, and modulating immune cell infiltration. In order to influence the microenvironment, CAFs engage in cross-talk with immune cells, cancer cells, and other stromal components through paracrine signaling and direct cell-cell interactions. This cross-talk can result in immunosuppression, tumor cell proliferation, and epithelial-mesenchymal transition, contributing to disease progression. Emerging evidence suggests that CAFs play a crucial role in therapy resistance, including resistance to chemotherapy and radiotherapy. CAFs can modulate the tumor response to treatment by secreting factors that promote drug efflux, enhance DNA repair mechanisms, and suppress apoptosis pathways. This paper aims to understand the multifaceted functions of CAFs within the TME, discusses cross-talk between CAFs with other TME cells, and sheds light on the contibution of CAFs to therapy resistance. Targeting CAFs or disrupting their cross-talk with other cells holds promise for overcoming drug resistance and improving the treatment efficacy of various cancer types

    Primary cancer-associated fibroblasts exhibit high heterogeneity among breast cancer subtypes

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    Background: Cancer-associated fibroblasts (CAFs) are a diverse subset of cells, that is recently gaining in popularity and have the potential to become a new target for breast cancer therapy; however, broader research is required to understand their mechanisms and interactions with breast cancer cells. The goal of the study was to isolate CAFs from breast cancer tumour and characterise isolated cell lines. We concentrated on numerous CAF biomarkers that would enable their differentiation.  Materials and methods: Flow cytometry, immunofluorescence, and reverse transcription quantitative real-time polymerase chain reaction (RT-qPCR) were used to phenotype the primary CAFs. Conclusions: According to our findings, there was no significant pattern in the classification of cancer-associated fibroblasts. The results of biomarkers expression were heterogeneous, thus no specific subtypes were identified. Furthermore, a comparison of cancer-associated fibroblasts derived from different BC subtypes (luminal A and B, triple-negative, HER2 positive) did not  reveal any clear trend of expression

    MiRNAs from serum-derived extracellular vesicles as biomarkers for uveal melanoma progression

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    Uveal melanoma (UM) is a rare type of malignancy that originates from melanocytes located in the choroid, iris and the ciliary body of the eye. UM has a very high mortality upon metastatic spread to the liver, the prime target organ for UM metastasis. The lack of effective therapies for advanced stages of the disease aggravate the prognosis further. Moreover, biomarkers for early detection and progression of UM, especially the molecular traits governing the development of metastasis, are still not available in clinical practice. One extensively studied components of liquid biopsies are exosomes, a subtype of extracellular vesicle. Due to their unique molecular cargo, they could be used as carriers of early markers of cancer development and progression. For characterisation of the miRNA profiles present in circulating serum-derived exosomes of patients with diagnosed primary and metastatic UM, we have analysed the miRNA cargos using next-generation sequencing followed by RT-qPCR validation in a cohort of patients (control n=20; primary n=9; metastatic n=11). Nine miRNAs clearly differentiating these patient groups have been established. We show that hsa-miR-223 and hsa-miR-203a are the most promising biomarker candidates, allowing categorization of patients into local and advanced UM. Additionally, the comparison of miRNA expression levels in exosomes derived from UM patients with those derived from healthy donors, revealed that hsa-miR-144 has the potential to be used as an early marker for presence of UM. Taken together, this pilot study reveals that miRNAs extracted from circulating exosomes could be exploited as potential biomarkers in UM diagnosis and, more importantly, for indicating metastatic spread

    Coupled changes in western South Atlantic carbon sequestration and particle reactive element cycling during millennial-scale Holocene climate variability.

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    Funder: Alexander von Humboldt FoundationFunder: Petrobras/CENPES Geochemistry NetworkFunder: National Petroleum Agency of BrazilABSTRACT: Continental shelves have the potential to remove atmospheric carbon dioxide via the biological pump, burying it in seafloor sediments. The efficiency of marine carbon sequestration changes rapidly due to variations in biological productivity, organic carbon oxidation, and burial rate. Here we present a high temporal resolution record of marine carbon sequestration changes from a western South Atlantic shelf site sensitive to Brazil Current-driven upwelling. The comparison of biological records to rare earth element (REE) patterns from authigenic oxides shows a strong relationship between higher biological productivity and stronger particle reactive element cycling (i.e. REE cycling) during rapid climate change events. This is the first evidence that authigenic oxides archive past changes in upper ocean REE cycling by the exported organic carbon. In addition, our data suggest that Brazil Current-driven upwelling varies on millennial-scales and in time with continental precipitation anomalies as registered in Brazilian speleothems during the Holocene. This indicates an ocean-atmosphere control on the biological pump, most probably related to South American monsoon system variability

    The Mych Gene Is Required for Neural Crest Survival during Zebrafish Development

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    Background: Amomg Myc family genes, c-Myc is known to have a role in neural crest specification in Xenopus and in craniofacial development in the mouse. There is no information on the function of other Myc genes in neural crest development, or about any developmental role: of zebrafish Myc genes. Principal Findings: We isolated the zebrafish mych (myc homologue) gene. Knockdown of mych leads to sever defects in craniofacial development and in certain other tissues including the eye. These phenotypes appear to be caused by cell death in the neural crest and in the eye field in the anterior brain. Significance: Mych is a novel factor required for neural crest cell survival in zebrafish

    Lacunarity, lexicography and beyond: integration of the introduction of a linguo-cultural concept and the development of L2 learners’ dictionary skills

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    The paper discusses the integration of presenting theoretical linguocultural knowledge and developing dictionary skills in advanced students of a foreign language. The proposed approach allows showing students the interdisciplinary character of various issues, one of which is cross-linguistic lacunarity. It is given as an example of a phenomenon, whose introduction can be combined with the development of students’ dictionary use abilities. Lacunarity consists in the lack of some source language elements in the target language. Two main kinds of lacunae are distinguished: linguistic and referential ones. The focal issue of the paper is how the information on the lacunary character of words can be presented to advanced students of English as a foreign language, in this paper Polish learners, so that they could consider the phenomenon in terms of bilingual lexicography: first, becoming aware of the specifics of their description; second, practising their dictionary skills by analysing entries for selected lacunary lexical and phraseological units; third, combining the information and skills in doing creative tasks, related to lacunarity and its bilingual lexicographic descriptions. Furthermore, additional activities are proposed for revising the acquired knowledge on lacunarity and advancing dictionary use. Offering students tasks, which require them to adopt a different perspective, aims to increase their involvement in the learning process and to foster their autonomy as learners. Encouraging learners to reflect on lacunae and their lexicographic description is expected to familiarize them with the phenomenon and simultaneously to develop their dictionary skills by doing especially designed [email protected] University of Bialystok101-11

    Warszawa tyłem do powodzi, czyli pod nami choćby potop — rekonesans

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