Front-end genomics: using an alternative approach for the recovery of high-quality DNA from core needle biopsies
- PMID: 27777300
- DOI: 10.1136/jclinpath-2016-204061
Front-end genomics: using an alternative approach for the recovery of high-quality DNA from core needle biopsies
Abstract
Aims: Determine whether a simple prewash step will provide adequate amounts of high-quality DNA from core needle biopsies for molecular sequencing studies.
Methods: The quantitative and qualitative metrics of DNA recovered from core needle biopsies processed either by 1) formalin fixation and paraffin embedding (FFPE), 2) cells recovered after the core needle biopsy was washed, and 3) frozen sections of the core needle biopsy tissue were evaluated and compared to one another.
Results: Fairly equivalent amounts of DNA can be obtained from cells recovered from a prewash step relative to the FFPE and frozen section samples. The number of amplifiable DNA in the wash sample was greater than that from the FFPE samples. The average molecular size of DNA in the wash sample was greater than that of both the FFPE and frozen samples.
Conclusions: Although more starting material in terms of the number of cells was present in both the FFPE and frozen section samples than the wash samples, equivalent to better results were obtained from the latter with regard to quality. This approach may be a means to better aliquot the diminutive amounts of tissue associated with core needle biopsies, allowing dissociated cells to be dedicated for molecular studies while keeping the tissue intact for morphological studies.
Keywords: DNA; FIXATION; MOLECULAR GENETICS.
Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/.
Conflict of interest statement
Competing interests: None declared.
Similar articles
-
Core Needle Biopsy Wash Optimization: Enabling Specimen Integrity for both Cytological and Histological Evaluation.Anticancer Res. 2015 Nov;35(11):5905-13. Anticancer Res. 2015. PMID: 26504014
-
Core needle biopsy wash as a tool for acquiring additional diagnostic material for laboratory testing.J Clin Pathol. 2022 May;75(5):345-349. doi: 10.1136/jclinpath-2020-207318. Epub 2021 Mar 1. J Clin Pathol. 2022. PMID: 33649141
-
Prospective Evaluation of Unprocessed Core Needle Biopsy DNA and RNA Yield from Lung, Liver, and Kidney Tumors: Implications for Cancer Genomics.Anal Cell Pathol (Amst). 2018 Dec 10;2018:2898962. doi: 10.1155/2018/2898962. eCollection 2018. Anal Cell Pathol (Amst). 2018. PMID: 30652067 Free PMC article.
-
Establishing an accurate diagnosis of a parotid lump: evaluation of the current biopsy methods - fine needle aspiration cytology, ultrasound-guided core biopsy, and intraoperative frozen section.Br J Oral Maxillofac Surg. 2015 Sep;53(7):580-3. doi: 10.1016/j.bjoms.2015.03.015. Epub 2015 Apr 15. Br J Oral Maxillofac Surg. 2015. PMID: 25886878 Review.
-
Formalin fixation in the '-omics' era: a primer for the surgeon-scientist.ANZ J Surg. 2012 Jun;82(6):395-402. doi: 10.1111/j.1445-2197.2012.06092.x. Epub 2012 May 9. ANZ J Surg. 2012. PMID: 22571596 Review.
Cited by
-
Epigenetic biomarkers: Current strategies and future challenges for their use in the clinical laboratory.Crit Rev Clin Lab Sci. 2017 Nov-Dec;54(7-8):529-550. doi: 10.1080/10408363.2017.1410520. Epub 2017 Dec 11. Crit Rev Clin Lab Sci. 2017. PMID: 29226748 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources