35 research outputs found

    Analysis of K-ras gene codon 12 mutation in pancreatic tissue of patients with pancreatic cancer

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    Ovo istraživanje je imalo za cilj da se analizira prisustvo mutacije u kodonu 12 gena K-ras u pankreasnom tkivu pacijenata sa karcinomom pankreasa i da se proceni da li ova mutacija predstavlja potencijalni molekularni marker za karcinom pankreasa u srpskoj populaciji. Istraživanje je obuhvatilo analizu 40 uzoraka tkiva pankreasa pacijenata sa kliničkom dijagnozom karcinoma pankreasa. Prisustvo mutacije u kodonu 12 gena K-ras analizirano je metodom PCR-RFLP (polymerase chain reaction - restriction fragment length poly­morphism). Rezultati istraživanja ukazuju da je mutacija u kodonu 12 gena K-ras u tkivu pankreasa prisutna sa visokom učestalošću (66 %) kod pacijenata sa karcinomom pankreasa.The aim of this study was to analyze K-ras codon 12 mutation in the pancreatic tissue of Serbian patients with pancreatic cancer and assess whether the given mutation can be used as a molecular marker for this disease. The study was performed on pancreatic tissue samples obtained from 40 patients with clinical diagnosis of pancreatic cancer. The presence of K-ras codon 12 mutation was analyzed by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Our study showed that K-ras mutation is present with a high frequency (66%) in the pancreatic tissue of patients with pancretic cancer

    The utility of Tc-99m-EDDA/HYNIC-TOC scintigraphy for assessment of lung lesions in patients with neuroendocrine tumors

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    Our aim was to assess clinical utility of Tc-99m-EDDA/HYNIC-TOC scintigraphy for evaluation of lung lesions in patients with neuroendocrine tumors (NETs). Single photon emission computed tomography (SPECT) of the thorax and whole body scintigraphy were performed in 34 patients using Tc-99m-EDDA/HYNIC-TOC. Visual assessment was complemented by semiquantitative evaluation based on tumor to non-tumor (TINT) ratio. Clinical, laboratory, and histological findings served as the standard for comparison. Enhanced tracer uptake was observed on both SPECT and whole body scintigraphy in 29 of 34 patients (88% sensitivity). TINT ratios were significantly higher on SPECT than whole body images (2.96 +/- 1.07 vs. 1.70 +/- 0.43, p LT 0.01) and did not correlate with NET proliferation index Ki-67 (r= - 0.36, p=0.27). Conclusion: Tc-99m-EDDA/HYNIC-TOC scintigraphy is useful for evaluation of NET tissue in the lungs. SPECT provides better visualization of lung lesions than whole body scintigraphy. The intensity of tracer uptake, however, does not relate to the proliferation rate of NETs. Tc-99m-EDDA/HYNIC-TOC scintigraphy may be helpful for selecting and monitoring treatment options, particularly when radiolabeled somatostatin analogue therapy becomes available

    Effect of Lithium on Disturbed Severely Mentally Retarded Patients

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    dignostic and

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    Endoscopic removal of pedunculated leiomyoma of the sigmoid colon (case report and literature review o

    Analysis of K-ras gene codon 12 mutation in pancreatic tissue of patients with pancreatic cancer

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    Ovo istraživanje je imalo za cilj da se analizira prisustvo mutacije u kodonu 12 gena K-ras u pankreasnom tkivu pacijenata sa karcinomom pankreasa i da se proceni da li ova mutacija predstavlja potencijalni molekularni marker za karcinom pankreasa u srpskoj populaciji. Istraživanje je obuhvatilo analizu 40 uzoraka tkiva pankreasa pacijenata sa kliničkom dijagnozom karcinoma pankreasa. Prisustvo mutacije u kodonu 12 gena K-ras analizirano je metodom PCR-RFLP (polymerase chain reaction - restriction fragment length poly­morphism). Rezultati istraživanja ukazuju da je mutacija u kodonu 12 gena K-ras u tkivu pankreasa prisutna sa visokom učestalošću (66 %) kod pacijenata sa karcinomom pankreasa.The aim of this study was to analyze K-ras codon 12 mutation in the pancreatic tissue of Serbian patients with pancreatic cancer and assess whether the given mutation can be used as a molecular marker for this disease. The study was performed on pancreatic tissue samples obtained from 40 patients with clinical diagnosis of pancreatic cancer. The presence of K-ras codon 12 mutation was analyzed by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Our study showed that K-ras mutation is present with a high frequency (66%) in the pancreatic tissue of patients with pancretic cancer

    ANALYSIS OF K-RAS GENE CODON 12 MUTATION IN PANCREATIC TISSUE OF PATIENTS WITH PANCREATIC CANCER

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    Abstract — The aim of this study was to analyze K-ras codon 12 mutation in the pancreatic tissue of Serbian patients with pancreatic cancer and assess whether the given mutation can be used as a molecular marker for this disease. The study was performed on pancreatic tissue samples obtained from 40 patients with clinical diagnosis of pancreatic cancer. The presence of K-ras codon 12 mutation was analyzed by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Our study showed that K-ras mutation is present with a high frequency (66%) in the pancreatic tissue of patients with pancretic cancer
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