Modified screen-printed carbon electrodes application for protein tumor markers determination

Screen-printed carbon electrodes were modified with gold nanoparticles bound with DNA-aptamers by two different methods. Aptamers can selectively bind protein tumor markers from the blood plasma. The electrodes were tested. Signals obtained via squire-wavy voltammetry from modified electrodes covered with blood plasma of the healthy donors and donors with lung cancer can be distinguished

Expression of inhibitor of apoptosis protein Livin in renal cell carcinoma and non-tumorous adult kidney

The antiapoptotic Livin/ML-IAP gene has recently gained much attention as a potential new target for cancer therapy. Reports indicating that livin is expressed almost exclusively in tumours, but not in the corresponding normal tissue, suggested that the targeted inhibition of livin may present a novel tumour-specific therapeutic strategy. Here, we compared the expression of livin in renal cell carcinoma and in non-tumorous adult kidney tissue by quantitative real-time reverse transcription-PCR, immunoblotting, and immunohistochemistry. We found that livin expression was significantly increased in tumours (P=0.0077), but was also clearly detectable in non-tumorous adult kidney. Transcripts encoding Livin isoforms α and β were found in both renal cell carcinoma and normal tissue, without obvious qualitative differences. Livin protein in renal cell carcinoma samples exhibited cytoplasmic and/or nuclear staining. In non-tumorous kidney tissue, Livin protein expression was only detectable in specific cell types and restricted to the cytoplasm. Thus, whereas the relative overexpression of livin in renal cell carcinoma indicates that it may still represent a therapeutic target to increase the apoptotic sensitivity of kidney cancer cells, this strategy is likely to be not tumour-specific

Tumor perfusion assessed by dynamic contrast-enhanced MRI correlates to the grading of renal cell carcinoma: Initial results

In this study, we investigated whether assessment of the tumor perfusion by dynamic contrast-enhanced magnetic resonance imaging (DCE MRI) enables to estimate the morphologic grading of renal cell carcinomas. A total of 21 patients with suspected renal cell cancer were examined using a Gadobutrol-enhanced, dynamic saturation-recovery, turbo-fast, low-angle shot sequence. Tumor perfusion and the tissue-blood ratio within the entire tumor and the most highly vascularized part of the tumor were calculated according to the model of Miles. Immediately after examination, patients underwent surgery, and the results from imaging were compared with the morphological analysis of the histologic grading. Fourteen patients had G2 tumors, and seven patients had G3 tumors. Significantly higher perfusion values (p < 0.05) were obtained in G3 tumors than in G2 tumors when the entire tumor area was considered (1.59 ± 0.44 (ml/g/min) vs. 1.08 ± 0.38 (ml/g/min)) or its most highly vascularized part (2.14 ± 0.89 (ml/g/min) vs. 1.40 ± 0.49 (ml/g/min)). By contrast, the tissue-blood ratios did not differ significantly between the two groups. In conclusion, unlike tissue-blood ratio, surrogate parameters of the tumor perfusion determined by DCE MRI seem to allow an estimation of the grading of renal cell carcinoma. However, further studies with high case numbers and including patients with G1 tumors are required to evaluate the full potential and clinical impact

ETHIBLOC_Reloaded: First in-vivo results of the re-designed zein-based fluid embolic agent

Purpose: To describe angiographic, computed-tomography (CT) and pathologic features of ETHIBLOC_Reloaded as a re-designed zein-based fluid embolic agent. Materials and methods: In eight pigs, both kidneys underwent selective transarterial embolization (with complete embolization as embolization endpoint). Each group consisted of two pigs with four embolized kidneys: I-pure ETHIBLOC_Reloaded, II-ETHIBLOC_Reloaded/iodized oil mixture (1:1), III-ETHIBLOC_Reloaded/ethanol-60% mixture (8:2) and IV-Histoacryl/iodized oil mixture (1:3). One hour after embolization, CT imaging, sacrifice and kidney harvest followed. Angiographic (visibility and vascular occlusion pattern), CT (visibility) and pathologic (vascular occlusion pattern) features were compared. Results: The embolization endpoint was reached in all animals. Applying Angiography, embolic agents were definitely visible during embolization in all study groups. Vascular occlusion occurred from distal (arcuate and interlobar arteries) to proximal (renal artery), whereby the most distal levels were reached in II and III. Applying CT imaging, embolic agents were definitely visible in hilar and intraparenchymal arteries in all groups. Pathology proved occlusion of segmental, interlobar and arcuate arteries in all groups, and additionally occlusion of interlobular arteries, pre-glomerular arterioles and glomerular capillaries in I, II and III. Conclusion: ETHIBLOC_Reloaded is a promising re-designed zein-based embolic agent that can be used safely and effectively for transarterial embolization of the pig kidney