Literature DB >> 27449741

Comparison of Picrosirius Red Staining With Second Harmonic Generation Imaging for the Quantification of Clinically Relevant Collagen Fiber Features in Histopathology Samples.

Cole R Drifka1,2,3, Agnes G Loeffler4,5, Kara Mathewson2, Guneet Mehta2, Adib Keikhosravi1,2, Yuming Liu2, Stephanie Lemancik6, William A Ricke6,7,5, Sharon M Weber8,5, W John Kao1,2,8,5, Kevin W Eliceiri1,2,5,3.   

Abstract

Stromal collagen alignment has been shown to have clinical significance in a variety of cancers and in other diseases accompanied by fibrosis. While much of the biological and clinical importance of collagen changes has been demonstrated using second harmonic generation (SHG) imaging in experimental settings, implementation into routine clinical pathology practice is currently prohibitive. To translate the assessment of collagen organization into routine pathology workflow, a surrogate visualization method needs to be examined. The objective of the present study was to quantitatively compare collagen metrics generated from SHG microscopy and commonly available picrosirius red stain with standard polarization microscopy (PSR-POL). Each technique was quantitatively compared with established image segmentation and fiber tracking algorithms using human pancreatic cancer as a model, which is characterized by a pronounced stroma with reorganized collagen fibers. Importantly, PSR-POL produced similar quantitative trends for most collagen metrics in benign and cancerous tissues as measured by SHG. We found it notable that PSR-POL detects higher fiber counts, alignment, length, straightness, and width compared with SHG imaging but still correlates well with SHG results. PSR-POL may provide sufficient and additional information in a conventional clinical pathology laboratory for certain types of collagen quantification.
© 2016 The Histochemical Society.

Entities:  

Keywords:  fibrillar collagen; histopathology; picrosirius red; polarized microscopy; second harmonic generation

Mesh:

Substances:

Year:  2016        PMID: 27449741      PMCID: PMC5006137          DOI: 10.1369/0022155416659249

Source DB:  PubMed          Journal:  J Histochem Cytochem        ISSN: 0022-1554            Impact factor:   2.479


  47 in total

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