Development of highly specific and sensitive PNA-clamp PCR assay for the detection of common mutations (BRAF V600E and NRAS) in CRC using FFPE tissue sample
Joint Authors
Mikaeel, Reger R.
Pringle, James Howard
Source
Issue
Vol. 21, Issue 2 العلوم الصرفة و الهندسية (31 Dec. 2018), pp.99-129, 31 p.
Publisher
Publication Date
2018-12-31
Country of Publication
Iraq
No. of Pages
31
Main Subjects
Abstract EN
Background : Colorectal cancer (CRC) is a frequent and widespread malignancy.
Commonly mutated KRAS, BRAF and NRAS genes lead to constant activation of the MAPK pathway; consequently transforming basal stem cells into adenocarcinoma.
Selective inhibitors of the MAPK pathway, such as Cetuximab and Panitumumab, have been implemented in clinical practice since 2004.
Sanger sequencing and pyro sequencing have been commonly used for detection of BRAF and NRAS mutation in the UK.
Nevertheless, sometimes the analytical sensitivity of these methods is not high enough to detect a low percentage of cells containing the mutation.
Methods: a highly sensitive and specific Peptide nucelic acide (PNA)-clamp PCR was developed and validated firstly on cell lines that were known to harbour the mutations in BRAFV600E or NRAS codons 12 and 13.
The wild type and mutant DNA was serially diluted to test the sensitivity of the assay.
Total DNA was extracted from 84 formalin fixed paraffin embedded (FFPE) tissues including adenomas, carcinoma and hyperplastic polyps; and screened for BRAFV600E or NRAS mutations.
Results: the highly sensitive PNA-clamp QUASAqPCR assay significantly detected 1:2000 ratio of mutant to wild type background (P < 0.01).
The assay on FFPE tissue showed 15.47 % (13 / 84) BRAFV600E and 8.33% (7 / 84) NRAS mutants, of which NRAS c.38G > A (G13D) was the most common.
BRAFV600E mutation was significantly associated to right side tumour (P< 0.014), but was not related to any other clinical features.
However, there was no significant association between NRAS mutation and any clinicopathological features.
Conclusion: this study demonstrates the sensitivity, specificity and utility of PNA-clamp PCR assay in detecting the common point mutations in CRC in a low percentage of cells containing the mutation, providing an attractive tool for future research and therapeutic applications.
American Psychological Association (APA)
Mikaeel, Reger R.& Pringle, James Howard. 2018. Development of highly specific and sensitive PNA-clamp PCR assay for the detection of common mutations (BRAF V600E and NRAS) in CRC using FFPE tissue sample. Journal of Dohuk University،Vol. 21, no. 2 العلوم الصرفة و الهندسية, pp.99-129.
https://search.emarefa.net/detail/BIM-898410
Modern Language Association (MLA)
Mikaeel, Reger R.& Pringle, James Howard. Development of highly specific and sensitive PNA-clamp PCR assay for the detection of common mutations (BRAF V600E and NRAS) in CRC using FFPE tissue sample. Journal of Dohuk University Vol. 21, no. 2 Pure and Engineering Sciences (2018), pp.99-129.
https://search.emarefa.net/detail/BIM-898410
American Medical Association (AMA)
Mikaeel, Reger R.& Pringle, James Howard. Development of highly specific and sensitive PNA-clamp PCR assay for the detection of common mutations (BRAF V600E and NRAS) in CRC using FFPE tissue sample. Journal of Dohuk University. 2018. Vol. 21, no. 2 العلوم الصرفة و الهندسية, pp.99-129.
https://search.emarefa.net/detail/BIM-898410
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 128-129
Record ID
BIM-898410