Multiphoton Microscopic Study of the Renal Cell Carcinoma Pseudocapsule: Implications for Tumour Enucleation
To utilize Multiphoton Microscopy (MPM) as a novel imaging technique to characterize and quantify collagen at the Renal Cell Carcinoma Pseudocapsule, to assess for both intra-tumoral and inter-tumoral variation of collagen characteristics. MPM combines Second Harmonic Generation and Two Photon Excit...
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Published in | Urology (Ridgewood, N.J.) Vol. 144; pp. 249 - 254 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Elsevier Inc
01.10.2020
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Abstract | To utilize Multiphoton Microscopy (MPM) as a novel imaging technique to characterize and quantify collagen at the Renal Cell Carcinoma Pseudocapsule, to assess for both intra-tumoral and inter-tumoral variation of collagen characteristics. MPM combines Second Harmonic Generation and Two Photon Excitation Fluorescence to image extracellular matrix architecture.
Twenty partial nephrectomy specimen tissues were retrieved, cut into 5-micron sections, mounted on slides and deparaffinized. The pseudocapsules (PCs) were imaged with 2X and 20X objective at selected Regions of Interest. Corresponding clinical information was retrieved. PC thickness was determined. Collagen parameters measured included quantification by the Collagen Area Ratio, and qualitative measurements by the Collagen Fiber Density and Collagen Reticulation Index.
The boundaries between tumor, PC and normal renal parenchyma were distinguished by MPM without need for staining. In the thickest areas of the PC, collagen content and density were quantitatively higher compared to the thinnest areas. Median Collagen Area Ratio was higher in the thickest compared to the thinnest areas of the PC (P = .01). Clear Cell RCC specimens had a consistently higher Collagen Fiber Density in both the thickest and thinnest areas compared to non-Clear Cell RCC specimens (P = .02).
We demonstrated the ability of MPM to quantify collagen characteristics of PCs without fluorescent labeling. Tumor enucleation for Renal Cell Carcinoma along its PC remains debatable with regards to oncological safety. Even with a complete and intact PC, the PC is not a homogenous structure, and varies in its thickness and its collagen characteristics within, and between tumors. |
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AbstractList | To utilize Multiphoton Microscopy (MPM) as a novel imaging technique to characterize and quantify collagen at the Renal Cell Carcinoma Pseudocapsule, to assess for both intra-tumoral and inter-tumoral variation of collagen characteristics. MPM combines Second Harmonic Generation and Two Photon Excitation Fluorescence to image extracellular matrix architecture.
Twenty partial nephrectomy specimen tissues were retrieved, cut into 5-micron sections, mounted on slides and deparaffinized. The pseudocapsules (PCs) were imaged with 2X and 20X objective at selected Regions of Interest. Corresponding clinical information was retrieved. PC thickness was determined. Collagen parameters measured included quantification by the Collagen Area Ratio, and qualitative measurements by the Collagen Fiber Density and Collagen Reticulation Index.
The boundaries between tumor, PC and normal renal parenchyma were distinguished by MPM without need for staining. In the thickest areas of the PC, collagen content and density were quantitatively higher compared to the thinnest areas. Median Collagen Area Ratio was higher in the thickest compared to the thinnest areas of the PC (P = .01). Clear Cell RCC specimens had a consistently higher Collagen Fiber Density in both the thickest and thinnest areas compared to non-Clear Cell RCC specimens (P = .02).
We demonstrated the ability of MPM to quantify collagen characteristics of PCs without fluorescent labeling. Tumor enucleation for Renal Cell Carcinoma along its PC remains debatable with regards to oncological safety. Even with a complete and intact PC, the PC is not a homogenous structure, and varies in its thickness and its collagen characteristics within, and between tumors. OBJECTIVETo utilize Multiphoton Microscopy (MPM) as a novel imaging technique to characterize and quantify collagen at the Renal Cell Carcinoma Pseudocapsule, to assess for both intra-tumoral and inter-tumoral variation of collagen characteristics. MPM combines Second Harmonic Generation and Two Photon Excitation Fluorescence to image extracellular matrix architecture. METHODSTwenty partial nephrectomy specimen tissues were retrieved, cut into 5-micron sections, mounted on slides and deparaffinized. The pseudocapsules (PCs) were imaged with 2X and 20X objective at selected Regions of Interest. Corresponding clinical information was retrieved. PC thickness was determined. Collagen parameters measured included quantification by the Collagen Area Ratio, and qualitative measurements by the Collagen Fiber Density and Collagen Reticulation Index. RESULTSThe boundaries between tumor, PC and normal renal parenchyma were distinguished by MPM without need for staining. In the thickest areas of the PC, collagen content and density were quantitatively higher compared to the thinnest areas. Median Collagen Area Ratio was higher in the thickest compared to the thinnest areas of the PC (P = .01). Clear Cell RCC specimens had a consistently higher Collagen Fiber Density in both the thickest and thinnest areas compared to non-Clear Cell RCC specimens (P = .02). CONCLUSIONSWe demonstrated the ability of MPM to quantify collagen characteristics of PCs without fluorescent labeling. Tumor enucleation for Renal Cell Carcinoma along its PC remains debatable with regards to oncological safety. Even with a complete and intact PC, the PC is not a homogenous structure, and varies in its thickness and its collagen characteristics within, and between tumors. |
Author | Tiong, Ho Yee Tay, Wy Keat Tan, Yi Quan Thamboo, Thomas Paulraj Ooi, Li Yin |
Author_xml | – sequence: 1 givenname: Yi Quan surname: Tan fullname: Tan, Yi Quan email: yi_quan_tan@nuhs.edu.sg organization: Department of Urology, National University Hospital, National University Health System, Singapore – sequence: 2 givenname: Wy Keat surname: Tay fullname: Tay, Wy Keat organization: Department of Urology, National University Hospital, National University Health System, Singapore – sequence: 3 givenname: Li Yin surname: Ooi fullname: Ooi, Li Yin organization: Department of Pathology, National University Hospital, National University Health System, Singapore – sequence: 4 givenname: Thomas Paulraj surname: Thamboo fullname: Thamboo, Thomas Paulraj organization: Department of Pathology, National University Hospital, National University Health System, Singapore – sequence: 5 givenname: Ho Yee surname: Tiong fullname: Tiong, Ho Yee organization: Department of Urology, National University Hospital, National University Health System, Singapore |
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contributor: fullname: Jacob – volume: 11 start-page: 3785 year: 2016 ident: 10.1016/j.urology.2020.06.064_bib0014 article-title: Visualization of basement membranes in normal breast and breast cancer tissues using multiphoton microscopy publication-title: Oncol Lett doi: 10.3892/ol.2016.4472 contributor: fullname: Wu – volume: 118 start-page: 118 year: 2016 ident: 10.1016/j.urology.2020.06.064_bib0020 article-title: Multiphoton microscopy for rapid histopathological evaluation of kidney tumours publication-title: BJU Int doi: 10.1111/bju.13377 contributor: fullname: Jain – volume: 6 start-page: 655 year: 1982 ident: 10.1016/j.urology.2020.06.064_bib0009 article-title: Prognostic significance of morphologic parameters in renal cell carcinoma publication-title: Am J Surg Pathol doi: 10.1097/00000478-198210000-00007 contributor: fullname: Fuhrman – volume: 19 start-page: 490 year: 2019 ident: 10.1016/j.urology.2020.06.064_bib0019 article-title: Collagen organization of renal cell carcinoma differs between low and high grade tumours publication-title: BMC Cancer doi: 10.1186/s12885-019-5708-z contributor: fullname: Best – volume: 2 start-page: 64 year: 2015 ident: 10.1016/j.urology.2020.06.064_bib0006 article-title: Tumour enucleation for renal cell carcinoma publication-title: J Kidney Cancer VHL doi: 10.15586/jkcvhl.2015.27 contributor: fullname: Smith – volume: 26 start-page: 38 year: 2006 ident: 10.1016/j.urology.2020.06.064_bib0023 article-title: Collagen reorganization at the tumour-stromal interface facilitates local invasion publication-title: BMC Med doi: 10.1186/1741-7015-4-38 contributor: fullname: Provenzano – volume: 1 start-page: 11323 year: 2015 ident: 10.1016/j.urology.2020.06.064_bib0022 article-title: Differences in peritumoral pseudocapsule characteristics according to clinicopathological factors in clinical T1a renal tumours publication-title: Int J Clin Exp Pathol contributor: fullname: Kim – volume: 6 start-page: 129 year: 2013 ident: 10.1016/j.urology.2020.06.064_bib0005 article-title: From molecular structure to tissue architecture: collagen organization probed by SHG microscopy publication-title: J Biophotonics doi: 10.1002/jbio.201200092 contributor: fullname: Cicchi – volume: 7 start-page: 82609 year: 2016 ident: 10.1016/j.urology.2020.06.064_bib0018 article-title: Positive association of collagen type I with non-muscle invasive bladder cancer progression publication-title: Oncotarget doi: 10.18632/oncotarget.12089 contributor: fullname: Brooks |
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Snippet | To utilize Multiphoton Microscopy (MPM) as a novel imaging technique to characterize and quantify collagen at the Renal Cell Carcinoma Pseudocapsule, to assess... OBJECTIVETo utilize Multiphoton Microscopy (MPM) as a novel imaging technique to characterize and quantify collagen at the Renal Cell Carcinoma Pseudocapsule,... |
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SubjectTerms | Aged Carcinoma, Renal Cell - diagnostic imaging Carcinoma, Renal Cell - surgery Female Humans Kidney Neoplasms - diagnostic imaging Kidney Neoplasms - surgery Male Microscopy, Fluorescence, Multiphoton Middle Aged Nephrectomy - methods Retrospective Studies |
Title | Multiphoton Microscopic Study of the Renal Cell Carcinoma Pseudocapsule: Implications for Tumour Enucleation |
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