2010
DOI: 10.1177/030089161009600504
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No Implication of Simian virus 40 in pathogenesis of Malignant Pleural Mesothelioma in Slovenia

Abstract: We found no evidence of SV40 presence in tissue samples from 103 Slovenian patients with malignant pleural mesothelioma. Asbestos exposure remains the main risk factor for malignant pleural mesothelioma in Slovenia.

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Cited by 9 publications
(9 citation statements)
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“…Tumor tissue specimens were routinely formalin-fixed and paraffin-embedded. Genomic DNA from formalin-fixed and paraffin-embedded tissue was extracted as previously described [40]. A Qiagen FlexiGene kit (Qiagen, Hilden, Germany) was used for extraction of genomic DNA from frozen wholeblood samples.…”
Section: Dna Extraction and Genotypingmentioning
confidence: 99%
“…Tumor tissue specimens were routinely formalin-fixed and paraffin-embedded. Genomic DNA from formalin-fixed and paraffin-embedded tissue was extracted as previously described [40]. A Qiagen FlexiGene kit (Qiagen, Hilden, Germany) was used for extraction of genomic DNA from frozen wholeblood samples.…”
Section: Dna Extraction and Genotypingmentioning
confidence: 99%
“…The other putative aetiological factor, Semian virus 40, was not implicated in pathogenesis of malignant pleural mesothelioma in Slovenia 23,24…”
Section: Discussionmentioning
confidence: 95%
“…NCI and non‐template control (NTC) were also included in each run. Additionally, amplification of the human glyceraldehyde‐3‐phosphate dehydrogenase (GADPH) gene with forward primer (G1) 5′‐TCCCTGAGCTGAACGGGAAG‐3′ and reverse primer (G2) 5′‐CGCCTGCTTCACCACCTTCT‐3′ (Hmeljak et al ., ) was used as a control of DNA isolation and PCR inhibition.…”
Section: Methodsmentioning
confidence: 99%
“…DNA extracted from Staphylococcus aureus NCI and non-template control (NTC) were also included in each run. Additionally, amplification of the human glyceraldehyde-3-phosphate dehydrogenase (GADPH) gene with forward primer (G1) 5′-TCCCTGAGCTGAACGG-GAAG-3′ and reverse primer (G2) 5′-CGCCTGCTTCAC-CACCTTCT-3′ (Hmeljak et al, 2010) was used as a control of DNA isolation and PCR inhibition. All PCR mixtures were conducted in a total volume of 15 lL and consisted of 1.5 lL of isolated DNA, 0.5 lM of each primer, 7.5 lL of QantiTect â SYBR â Green PCR Master Mix kit (Qiagen) and 5.25 lL of nuclease-free water (DEPC-treated).…”
Section: Detection Of Bacteriamentioning
confidence: 99%