Publications by authors named "Josipa Bilic"

Canadian goldenrod L.), an invasive plant in Europe, is known for its allelopathic activity and is rich in bioactive compounds like flavonoids and phenolic acids, with significant pharmacological potential. This study presents the LC-MS phenolic profiles of leaf and flower extracts from , an invasive alien plant in the Istria region (Croatia).

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  • - Rho GTPases, particularly RhoA, act as molecular switches that influence various cellular functions, and a study was conducted using a mouse model to explore RhoA's role in the intestinal lining.
  • - The study found that inhibiting RhoA did not visibly change the mice's appearance but led to increased levels of nuclear β-catenin and chronic activation of Wnt signaling in the intestinal epithelium, which affected cell differentiation but not proliferation.
  • - Older mice showed a notable rise in spontaneous intestinal tumors, suggesting that RhoA is vital for regulating the differentiation of intestinal epithelial cells and helps prevent tumor development through its influence on Wnt signaling.
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The use of probiotics in the diet of bivalves poses a great potential in aquaculture as an alternative to antibiotics. The aim of this study was to assess the effect of I on the phenolic content and antioxidant capacity (AC) of queen scallop extracts after one month of feeding. Total phenols (TP) ranged from 28.

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This study is based on assessing fecal indicator bacteria contamination along meteorological, hydrological and physical-chemical variables after high rainy events during the summer period. The study focused on four different coastal sites in the western and eastern Adriatic coast characterized by various geomorphological and hydrological features, levels of urbanization and anthropogenic pressures, with the aim of finding appropriate and effective solutions to ensure the safety and sustainability of tourism and public health. Detailed in-situ survey revealed a wide range of fecal indicator bacterial (FIB) across the different river mouths with concentrations of E.

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Black locust ( L.), an invasive tree in Europe, commonly known for its negative impact on biodiversity, is a rich source of phenolic compounds recognized in traditional medicine. Since the metabolite profile depends on the environment and climate, this study aimed to provide the first LC-MS phytochemical screening of the black locust from the Istria region (Croatia).

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The aim of this work was to assess the biopotential of the young inflorescence tissues of , and in order to evaluate the possibility of their application in the food industry, and to provide a polyphenolic fingerprint for their quality control. The contents of different bioactive compounds and their antioxidant capacities were spectrophotometrically measured, the main phenolic compounds were identified and quantified using LC-DAD-MS, the antidiabetic potential was determined using α-amylase and α-glucosidase inhibition assays, the anti-inflammatory potential was determined using a 5-lipoxygenase inhibition assay, and the cytotoxicity was determined by MTT assay. Using one-way ANOVA, principal component analysis, hierarchical clustering and Pearson's correlation coefficient, the relations between the samples, and between the samples and the measured parameters, were revealed.

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The aim of the present study was to map the painting materials, degradation processes, and biological features present on the mural painting in the church of St. Mary in Beram (Croatia) to study their possible interaction and produce information helping the preservation of this valuable painting. The research was conducted on micro samples of painting materials taken from different sites along the painting and the characterization of the present fungal species was carried out.

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  • - The study investigates how reduced RHOA signaling increases colorectal tumor growth and metastasis but hasn't clearly defined how RHOA signaling is inactivated in colon cancer cells.
  • - Using various colorectal cancer cell lines and primary tumors, the researchers found that RHOA mutations and promoter hypermethylation are not the main drivers for varying RHOA expression; however, RHOA copy number loss is present in 16% of tumors, leading to reduced expression.
  • - Additionally, miR-200a/b/429 inhibits RHOA expression, while TGF-β/SMAD4 enhances it; the findings reveal complex regulatory mechanisms affecting RHOA, including genetic, transcriptional, and post-transcriptional factors in
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  • The study investigates the role of EPHB6 in colorectal tumorigenesis, finding that its manipulation does not impact the growth or movement of colon cancer cells in various models.
  • Using EphB6 knockout mice, researchers determined that the inactivation of EPHB6 does not efficiently initiate intestinal tumors or affect survival and tumor characteristics.
  • However, introducing EPHB6 into colon cancer cells reduced lung metastasis, suggesting that the loss of EPHB6 is linked to increased metastatic spread in colorectal cancer.
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  • EPHA3 is frequently mutated in colorectal tumors, but its specific role in colorectal cancer has not been thoroughly studied.
  • Experiments showed that both wild type and mutant EPHA3 did not impact colon cancer cell growth, motility, or the development of tumors in mice.
  • The findings suggest that EPHA3 is not a key player in the process of colorectal tumor development, indicating that more research is needed on potential cancer driver genes identified in genomic studies.
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  • - Recent findings connect inherited MYO5B mutations to microvillus inclusion disease (MVID), a serious condition leading to severe diarrhea at birth, but research is limited due to the absence of animal models.
  • - This study introduces a new mouse model with a specific Myo5b gene deletion, which exhibits perinatal death, diarrhea, and misplacement of cell membrane proteins in gut cells, mirroring symptoms seen in MVID patients.
  • - The Myo5b knockout mice show structural defects in their intestines at just 20 days of gestation, suggesting these issues arise independently of external factors, making them a valuable tool for future research on MVID and testing new treatments.
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  • The study investigates the genetic characteristics of rapidly proliferating colorectal cancer cells to discover potential new treatment targets, focusing on the relationship between cell growth rates and gene expression.
  • Analysis of 52 colorectal cancer cell lines revealed that faster growth is linked to poor differentiation and specific genetic markers, with 1,290 genes correlated to growth rates, notably including GAPDH and PPOX.
  • Experimental inhibition of GAPDH and PPOX showed promise in slowing cancer cell growth, suggesting these genes could serve as innovative therapeutic targets in colorectal cancer management.
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  • Activation of the small GTPase RHOA is linked to cancer, but its role in colorectal cancer is not well understood.
  • Inactivation of RHOA promotes cancer progression and metastasis in colorectal cancer by enhancing Wnt/β-catenin signaling, leading to increased cell growth and invasive behavior.
  • The research reveals RHOA as a potential tumor suppressor in colorectal cancer, suggesting that it helps inhibit tumor growth and spread, challenging previous beliefs about RHO GTPases.
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Induced pluripotent stem cells (iPSCs) maintain during the first few culture passages a set of epigenetic marks and metabolites characteristic of their somatic cell of origin, a concept defined as epigenetic donor memory. These residual somatic features are lost over time after extensive culture passaging. Therefore, epigenetic donor memory may be responsible for the higher differentiation efficiency toward the tissue of origin observed in low passage iPSCs versus high passage iPSC or iPSCs derived from a different tissue source.

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Transcription-factor-induced reprogramming of somatic cells to pluripotency is a very inefficient process, probably due to the existence of important epigenetic barriers that are imposed during differentiation and that contribute to preserving cell identity. In an effort to decipher the molecular nature of these barriers, we followed a genome-wide approach, in which we identified macrohistone variants (macroH2A) as highly expressed in human somatic cells but downregulated after reprogramming to pluripotency, as well as strongly induced during differentiation. Knockdown of macrohistone variants in human keratinocytes increased the efficiency of reprogramming to pluripotency, whereas overexpression had opposite effects.

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Recent studies indicate that human-induced pluripotent stem cells contain genomic structural variations and point mutations in coding regions. However, these studies have focused on fibroblast-derived human induced pluripotent stem cells, and it is currently unknown whether the use of alternative somatic cell sources with varying reprogramming efficiencies would result in different levels of genetic alterations. Here we characterize the genomic integrity of eight human induced pluripotent stem cell lines derived from five different non-fibroblast somatic cell types.

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Generation of human induced pluripotent stem cells (hiPSCs) by the expression of specific transcription factors depends on successful epigenetic reprogramming to a pluripotent state. Although hiPSCs and human embryonic stem cells (hESCs) display a similar epigenome, recent reports demonstrated the persistence of specific epigenetic marks from the somatic cell type of origin and aberrant methylation patterns in hiPSCs. However, it remains unknown whether the use of different somatic cell sources, encompassing variable levels of selection pressure during reprogramming, influences the level of epigenetic aberrations in hiPSCs.

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The efficiency of somatic cell reprogramming to pluripotency using defined factors is dramatically affected by the cell type of origin. Here, we show that human keratinocytes, which can be reprogrammed at a higher efficiency than fibroblast [Nat Biotechnol 2008;26:1276-1284], share more genes hypermethylated at CpGs with human embryonic stem cells (ESCs) than other somatic cells frequently used for reprogramming. Moreover, pluripotent cells reprogrammed from keratinocytes (KiPS) are more similar to ESCs than those reprogrammed from fibroblasts (FiPS) in regard to DNA methylation levels, mostly due to the presence of genes that fail to acquire high levels of DNA methylation in FiPS cells.

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The state of a cell is defined by the genes it transcribes and the epigenetic landscape that regulates their expression. Pluripotent cells have markedly different epigenetic signatures when compared with differentiated cells. Permissive chromatin, high occurrence of bivalent domains, and low levels of heterochromatin allow pluripotent cells to react to distinctive stimuli and undergo changes of cell state by differentiating into various tissues.

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The utility of induced pluripotent stem (iPS) cells for investigating the molecular logic of pluripotency and for eventual clinical application is limited by the low efficiency of current methods for reprogramming. Here we show that reprogramming of juvenile human primary keratinocytes by retroviral transduction with OCT4, SOX2, KLF4 and c-MYC is at least 100-fold more efficient and twofold faster compared with reprogramming of human fibroblasts. Keratinocyte-derived iPS (KiPS) cells appear indistinguishable from human embryonic stem cells in colony morphology, growth properties, expression of pluripotency-associated transcription factors and surface markers, global gene expression profiles and differentiation potential in vitro and in vivo.

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Multiple signaling pathways, including Wnt signaling, participate in animal development, stem cell biology, and human cancer. Although many components of the Wnt pathway have been identified, unresolved questions remain as to the mechanism by which Wnt binding to its receptors Frizzled and Low-density lipoprotein receptor-related protein 6 (LRP6) triggers downstream signaling events. With live imaging of vertebrate cells, we show that Wnt treatment quickly induces plasma membrane-associated LRP6 aggregates.

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Signalling by Wnt proteins (Wingless in Drosophila) has diverse roles during embryonic development and in adults, and is implicated in human diseases, including cancer. LDL-receptor-related proteins 5 and 6 (LRP5 and LRP6; Arrow in Drosophila) are key receptors required for transmission of Wnt/beta-catenin signalling in metazoa. Although the role of these receptors in Wnt signalling is well established, their coupling with the cytoplasmic signalling apparatus remains poorly defined.

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