Skip to main content
Top
Published in: Clinical & Experimental Metastasis 8/2018

Open Access 01-12-2018 | Original Paper

miR-21 expression analysis in budding colon cancer cells by confocal slide scanning microscopy

Authors: Kirsten Nguyen Knudsen, Jan Lindebjerg, Alexandra Kalmár, Béla Molnár, Flemming Brandt Sørensen, Torben Frøstrup Hansen, Boye Schnack Nielsen

Published in: Clinical & Experimental Metastasis | Issue 8/2018

Login to get access

Abstract

MicroRNA-21 (miR-21) expression in stromal fibroblastic cells in colorectal cancer is well-documented, whereas miR-21 expression in tumor budding cells (TBCs) is poorly described. TBCs are locally invasive carcinoma cells with increased metastatic properties and characteristics of epithelial to mesenchymal transition. This study was conducted to better characterize the expression of miR-21 in TBCs. First, chromogenic miR-21 in situ hybridization (ISH) staining was performed in 58 colon adenocarcinomas with evident TBCs. Then, to obtain unambiguous identification of miR-21 in the TBCs, twenty cases were selected for an additional multiplex fluorescence analysis combining miR-21 ISH with cytokeratin and laminin-5γ2 immunofluorescence. Employing confocal slide scanning microscopy, comprehensive digital images of the invasive front (10–40 mm2) were obtained from 16 of the 20 cases, and miR-21 expression was evaluated in cytokeratin-positive TBCs. The high resolution of the confocal digital slide images allowed a detailed examination of the confocal stacks of the multiplex-stained tissue sections. The cases with the highest fraction of miR-21 positive TBCs were all stage III cancers defined by the presence of regional lymph node metastasis. Some of the miR-21 positive TBCs were also laminin-5γ2 positive. The confocal image stacks also revealed that some TBCs were actually directly connected to malignant glands. In conclusion, miR-21 expression was unambiguously identified in TBCs by evaluation of digital slides obtained by confocal slide scanning microscopy. In addition, the digital confocal slides provided a more detailed understanding of local cancer cell invasion by allowing evaluation of the cell structures in three dimensions.
Appendix
Available only for authorised users
Literature
1.
go back to reference Kim VN (2005) MicroRNA biogenesis: coordinated cropping and dicing. Nat Rev Mol Cell Biol 6(5):376–385CrossRef Kim VN (2005) MicroRNA biogenesis: coordinated cropping and dicing. Nat Rev Mol Cell Biol 6(5):376–385CrossRef
3.
go back to reference Chan JA, Krichevsky AM, Kosik KS (2005) MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells. Cancer Res 65(14):6029–6033CrossRef Chan JA, Krichevsky AM, Kosik KS (2005) MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells. Cancer Res 65(14):6029–6033CrossRef
4.
go back to reference Slaby O et al (2007) Altered expression of miR-21, miR-31, miR-143 and miR-145 is related to clinicopathologic features of colorectal cancer. Oncology 72(5–6):397–402CrossRef Slaby O et al (2007) Altered expression of miR-21, miR-31, miR-143 and miR-145 is related to clinicopathologic features of colorectal cancer. Oncology 72(5–6):397–402CrossRef
5.
go back to reference Schetter AJ et al (2008) MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma. JAMA 299(4):425–436CrossRef Schetter AJ et al (2008) MicroRNA expression profiles associated with prognosis and therapeutic outcome in colon adenocarcinoma. JAMA 299(4):425–436CrossRef
6.
go back to reference Volinia S et al (2006) A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 103(7):2257–2261CrossRef Volinia S et al (2006) A microRNA expression signature of human solid tumors defines cancer gene targets. Proc Natl Acad Sci USA 103(7):2257–2261CrossRef
7.
go back to reference Krichevsky AM, Gabriely G (2009) miR-21: a small multi-faceted RNA. J Cell Mol Med 13(1):39–53CrossRef Krichevsky AM, Gabriely G (2009) miR-21: a small multi-faceted RNA. J Cell Mol Med 13(1):39–53CrossRef
8.
go back to reference Nielsen BS et al (2011) High levels of microRNA-21 in the stroma of colorectal cancers predict short disease-free survival in stage II colon cancer patients. Clin Exp Metastasis 28(1):27–38CrossRef Nielsen BS et al (2011) High levels of microRNA-21 in the stroma of colorectal cancers predict short disease-free survival in stage II colon cancer patients. Clin Exp Metastasis 28(1):27–38CrossRef
9.
go back to reference Kjaer-Frifeldt S et al (2012) The prognostic importance of miR-21 in stage II colon cancer: a population-based study. Br J Cancer 107(7):1169–1174CrossRef Kjaer-Frifeldt S et al (2012) The prognostic importance of miR-21 in stage II colon cancer: a population-based study. Br J Cancer 107(7):1169–1174CrossRef
10.
go back to reference Kang WK et al (2015) Stromal expression of miR-21 in T3-4a colorectal cancer is an independent predictor of early tumor relapse. BMC Gastroenterol 15:2CrossRef Kang WK et al (2015) Stromal expression of miR-21 in T3-4a colorectal cancer is an independent predictor of early tumor relapse. BMC Gastroenterol 15:2CrossRef
11.
go back to reference Bullock MD et al (2015) Stratifying risk of recurrence in stage II colorectal cancer using deregulated stromal and epithelial microRNAs. Oncotarget 6(9):7262–7279CrossRef Bullock MD et al (2015) Stratifying risk of recurrence in stage II colorectal cancer using deregulated stromal and epithelial microRNAs. Oncotarget 6(9):7262–7279CrossRef
12.
go back to reference Zlobec I, Lugli A (2010) Epithelial mesenchymal transition and tumor budding in aggressive colorectal cancer: tumor budding as oncotarget. Oncotarget 1(7):651–661PubMedPubMedCentral Zlobec I, Lugli A (2010) Epithelial mesenchymal transition and tumor budding in aggressive colorectal cancer: tumor budding as oncotarget. Oncotarget 1(7):651–661PubMedPubMedCentral
13.
go back to reference Dawson H, Lugli A (2015) Molecular and pathogenetic aspects of tumor budding in colorectal cancer. Front Med (Lausanne) 2:11 Dawson H, Lugli A (2015) Molecular and pathogenetic aspects of tumor budding in colorectal cancer. Front Med (Lausanne) 2:11
14.
go back to reference Brabletz T et al (2001) Variable beta-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment. Proc Natl Acad Sci USA 98(18):10356–10361CrossRef Brabletz T et al (2001) Variable beta-catenin expression in colorectal cancers indicates tumor progression driven by the tumor environment. Proc Natl Acad Sci USA 98(18):10356–10361CrossRef
15.
go back to reference Shinto E et al (2005) Prognostic implication of laminin-5 gamma 2 chain expression in the invasive front of colorectal cancers, disclosed by area-specific four-point tissue microarrays. Lab Investig 85(2):257–266CrossRef Shinto E et al (2005) Prognostic implication of laminin-5 gamma 2 chain expression in the invasive front of colorectal cancers, disclosed by area-specific four-point tissue microarrays. Lab Investig 85(2):257–266CrossRef
16.
go back to reference Kajiwara Y et al (2011) Expression of l1 cell adhesion molecule and morphologic features at the invasive front of colorectal cancer. Am J Clin Pathol 136(1):138–144CrossRef Kajiwara Y et al (2011) Expression of l1 cell adhesion molecule and morphologic features at the invasive front of colorectal cancer. Am J Clin Pathol 136(1):138–144CrossRef
17.
go back to reference Brabletz T et al (1998) Nuclear overexpression of the oncoprotein beta-catenin in colorectal cancer is localized predominantly at the invasion front. Pathol Res Pract 194(10):701–704CrossRef Brabletz T et al (1998) Nuclear overexpression of the oncoprotein beta-catenin in colorectal cancer is localized predominantly at the invasion front. Pathol Res Pract 194(10):701–704CrossRef
18.
go back to reference Ohtsuki K et al (2008) Prognostic value of immunohistochemical analysis of tumor budding in colorectal carcinoma. Anticancer Res 28(3B):1831–1836PubMed Ohtsuki K et al (2008) Prognostic value of immunohistochemical analysis of tumor budding in colorectal carcinoma. Anticancer Res 28(3B):1831–1836PubMed
19.
go back to reference Koelzer VH et al (2015) Tumor budding in colorectal cancer revisited: results of a multicenter interobserver study. Virchows Arch 466(5):485–493CrossRef Koelzer VH et al (2015) Tumor budding in colorectal cancer revisited: results of a multicenter interobserver study. Virchows Arch 466(5):485–493CrossRef
20.
go back to reference Hase K et al (1993) Prognostic value of tumor “budding” in patients with colorectal cancer. Dis Colon Rectum 36(7):627–635CrossRef Hase K et al (1993) Prognostic value of tumor “budding” in patients with colorectal cancer. Dis Colon Rectum 36(7):627–635CrossRef
21.
go back to reference Ueno H et al (2004) A new prognostic staging system for rectal cancer. Ann Surg 240(5):832–839CrossRef Ueno H et al (2004) A new prognostic staging system for rectal cancer. Ann Surg 240(5):832–839CrossRef
22.
go back to reference Wang LM et al (2009) Tumor budding is a strong and reproducible prognostic marker in T3N0 colorectal cancer. Am J Surg Pathol 33(1):134–141CrossRef Wang LM et al (2009) Tumor budding is a strong and reproducible prognostic marker in T3N0 colorectal cancer. Am J Surg Pathol 33(1):134–141CrossRef
23.
go back to reference Rogers AC et al (2016) Systematic review and meta-analysis of the impact of tumour budding in colorectal cancer. Br J Cancer 115(7):831–840CrossRef Rogers AC et al (2016) Systematic review and meta-analysis of the impact of tumour budding in colorectal cancer. Br J Cancer 115(7):831–840CrossRef
24.
go back to reference Mitrovic B et al (2012) Tumor budding in colorectal carcinoma: time to take notice. Mod Pathol 25(10):1315–1325CrossRef Mitrovic B et al (2012) Tumor budding in colorectal carcinoma: time to take notice. Mod Pathol 25(10):1315–1325CrossRef
25.
go back to reference Lugli A et al (2017) Recommendations for reporting tumor budding in colorectal cancer based on the International Tumor Budding Consensus Conference (ITBCC) 2016. Mod Pathol 30 9), pp 1299–1311CrossRef Lugli A et al (2017) Recommendations for reporting tumor budding in colorectal cancer based on the International Tumor Budding Consensus Conference (ITBCC) 2016. Mod Pathol 30 9), pp 1299–1311CrossRef
26.
go back to reference Jorgensen S et al (2010) Robust one-day in situ hybridization protocol for detection of microRNAs in paraffin samples using LNA probes. Methods 52(4):375–381CrossRef Jorgensen S et al (2010) Robust one-day in situ hybridization protocol for detection of microRNAs in paraffin samples using LNA probes. Methods 52(4):375–381CrossRef
27.
go back to reference Knudsen KN et al (2015) microRNA-17 Is the most up-regulated member of the miR-17-92 cluster during early colon cancer evolution. PLoS One 10(10):e0140503CrossRef Knudsen KN et al (2015) microRNA-17 Is the most up-regulated member of the miR-17-92 cluster during early colon cancer evolution. PLoS One 10(10):e0140503CrossRef
28.
go back to reference Sempere LF (2014) Tissue slide-based microRNA characterization of tumors: how detailed could diagnosis become for cancer medicine? Expert Rev Mol Diagn 14(7):853–869CrossRef Sempere LF (2014) Tissue slide-based microRNA characterization of tumors: how detailed could diagnosis become for cancer medicine? Expert Rev Mol Diagn 14(7):853–869CrossRef
29.
go back to reference Liu A et al (2009) MicroRNA expression profiling outperforms mRNA expression profiling in formalin-fixed paraffin-embedded tissues. Int J Clin Exp Pathol 2(6):519–527PubMedPubMedCentral Liu A et al (2009) MicroRNA expression profiling outperforms mRNA expression profiling in formalin-fixed paraffin-embedded tissues. Int J Clin Exp Pathol 2(6):519–527PubMedPubMedCentral
30.
go back to reference Siebolts U et al (2009) Tissues from routine pathology archives are suitable for microRNA analyses by quantitative PCR. J Clin Pathol 62(1):84–88CrossRef Siebolts U et al (2009) Tissues from routine pathology archives are suitable for microRNA analyses by quantitative PCR. J Clin Pathol 62(1):84–88CrossRef
31.
go back to reference Viegas MS et al (2007) An improved and cost-effective methodology for the reduction of autofluorescence in direct immunofluorescence studies on formalin-fixed paraffin-embedded tissues. Eur J Histochem 51(1):59–66PubMed Viegas MS et al (2007) An improved and cost-effective methodology for the reduction of autofluorescence in direct immunofluorescence studies on formalin-fixed paraffin-embedded tissues. Eur J Histochem 51(1):59–66PubMed
32.
go back to reference Langhorst MF, Schaffer J, Goetze B (2009) Structure brings clarity: structured illumination microscopy in cell biology. Biotechnol J 4(6):858–865CrossRef Langhorst MF, Schaffer J, Goetze B (2009) Structure brings clarity: structured illumination microscopy in cell biology. Biotechnol J 4(6):858–865CrossRef
33.
go back to reference Neil MA, Juskaitis R, Wilson T (1997) Method of obtaining optical sectioning by using structured light in a conventional microscope. Opt Lett 22(24):1905–1907CrossRef Neil MA, Juskaitis R, Wilson T (1997) Method of obtaining optical sectioning by using structured light in a conventional microscope. Opt Lett 22(24):1905–1907CrossRef
34.
go back to reference Knudsen KN et al (2017) MicroRNA-200b is downregulated in colon cancer budding cells. PLoS One 12(5):e0178564CrossRef Knudsen KN et al (2017) MicroRNA-200b is downregulated in colon cancer budding cells. PLoS One 12(5):e0178564CrossRef
35.
go back to reference Karamitopoulou E et al (2013) Proposal for a 10-high-power-fields scoring method for the assessment of tumor budding in colorectal cancer. Mod Pathol 26(2):295–301CrossRef Karamitopoulou E et al (2013) Proposal for a 10-high-power-fields scoring method for the assessment of tumor budding in colorectal cancer. Mod Pathol 26(2):295–301CrossRef
36.
go back to reference Nielsen BS, Holmstrom K (2013) Combined microRNA in situ hybridization and immunohistochemical detection of protein markers. Methods Mol Biol 986:353–365CrossRef Nielsen BS, Holmstrom K (2013) Combined microRNA in situ hybridization and immunohistochemical detection of protein markers. Methods Mol Biol 986:353–365CrossRef
37.
go back to reference Pirici D et al (2009) Antibody elution method for multiple immunohistochemistry on primary antibodies raised in the same species and of the same subtype. J Histochem Cytochem 57(6):567–575CrossRef Pirici D et al (2009) Antibody elution method for multiple immunohistochemistry on primary antibodies raised in the same species and of the same subtype. J Histochem Cytochem 57(6):567–575CrossRef
38.
go back to reference Baran B et al (2018) Difference between left-sided and right-sided colorectal cancer: a focused review of literature. Gastroenterol Res 11(4):264–273CrossRef Baran B et al (2018) Difference between left-sided and right-sided colorectal cancer: a focused review of literature. Gastroenterol Res 11(4):264–273CrossRef
39.
go back to reference Pyke C et al (1995) Laminin-5 is a marker of invading cancer cells in some human carcinomas and is coexpressed with the receptor for urokinase plasminogen activator in budding cancer cells in colon adenocarcinomas. Cancer Res 55(18):4132–4139PubMed Pyke C et al (1995) Laminin-5 is a marker of invading cancer cells in some human carcinomas and is coexpressed with the receptor for urokinase plasminogen activator in budding cancer cells in colon adenocarcinomas. Cancer Res 55(18):4132–4139PubMed
40.
go back to reference Sordat I et al (2000) Tumor cell budding and laminin-5 expression in colorectal carcinoma can be modulated by the tissue micro-environment. Int J Cancer 88(5):708–717CrossRef Sordat I et al (2000) Tumor cell budding and laminin-5 expression in colorectal carcinoma can be modulated by the tissue micro-environment. Int J Cancer 88(5):708–717CrossRef
41.
go back to reference Cottonham CL, Kaneko S, Xu L (2010) miR-21 and miR-31 converge on TIAM1 to regulate migration and invasion of colon carcinoma cells. J Biol Chem 285(46):35293–35302CrossRef Cottonham CL, Kaneko S, Xu L (2010) miR-21 and miR-31 converge on TIAM1 to regulate migration and invasion of colon carcinoma cells. J Biol Chem 285(46):35293–35302CrossRef
42.
go back to reference Zhang D, Xie L, Jin Y (2015) In situ detection of MicroRNAs: the art of MicroRNA research in human diseases. J Cytol Histol 1(Suppl 3):013 Zhang D, Xie L, Jin Y (2015) In situ detection of MicroRNAs: the art of MicroRNA research in human diseases. J Cytol Histol 1(Suppl 3):013
43.
go back to reference Stenvold H et al (2014) High tumor cell expression of microRNA-21 in node positive non-small cell lung cancer predicts a favorable clinical outcome. BMC Clin Pathol 14(1):9CrossRef Stenvold H et al (2014) High tumor cell expression of microRNA-21 in node positive non-small cell lung cancer predicts a favorable clinical outcome. BMC Clin Pathol 14(1):9CrossRef
44.
go back to reference Sempere LF et al (2010) Fluorescence-based codetection with protein markers reveals distinct cellular compartments for altered MicroRNA expression in solid tumors. Clin Cancer Res 16(16):4246–4255CrossRef Sempere LF et al (2010) Fluorescence-based codetection with protein markers reveals distinct cellular compartments for altered MicroRNA expression in solid tumors. Clin Cancer Res 16(16):4246–4255CrossRef
45.
go back to reference Nielsen BS et al (2014) miR-21 expression in cancer cells may not predict resistance to adjuvant trastuzumab in primary breast cancer. Front Oncol 4:207CrossRef Nielsen BS et al (2014) miR-21 expression in cancer cells may not predict resistance to adjuvant trastuzumab in primary breast cancer. Front Oncol 4:207CrossRef
46.
go back to reference Sempere LF et al (2007) Altered MicroRNA expression confined to specific epithelial cell subpopulations in breast cancer. Cancer Res 67(24):11612–11620CrossRef Sempere LF et al (2007) Altered MicroRNA expression confined to specific epithelial cell subpopulations in breast cancer. Cancer Res 67(24):11612–11620CrossRef
47.
go back to reference Koelzer VH, Zlobec I, Lugli A (2016) Tumor budding in colorectal cancer—ready for diagnostic practice? Hum Pathol 47(1):4–19CrossRef Koelzer VH, Zlobec I, Lugli A (2016) Tumor budding in colorectal cancer—ready for diagnostic practice? Hum Pathol 47(1):4–19CrossRef
48.
go back to reference Foldes-Papp Z, Demel U, Tilz GP (2003) Laser scanning confocal fluorescence microscopy: an overview. Int Immunopharmacol 3(13–14):1715–1729CrossRef Foldes-Papp Z, Demel U, Tilz GP (2003) Laser scanning confocal fluorescence microscopy: an overview. Int Immunopharmacol 3(13–14):1715–1729CrossRef
49.
go back to reference Bronsert P et al (2014) Cancer cell invasion and EMT marker expression: a three-dimensional study of the human cancer-host interface. J Pathol 234(3):410–422CrossRef Bronsert P et al (2014) Cancer cell invasion and EMT marker expression: a three-dimensional study of the human cancer-host interface. J Pathol 234(3):410–422CrossRef
50.
go back to reference Grigore AD et al (2016) Tumor budding: the name is EMT. Partial EMT. J Clin Med 5:5CrossRef Grigore AD et al (2016) Tumor budding: the name is EMT. Partial EMT. J Clin Med 5:5CrossRef
51.
go back to reference Han M et al (2012) Re-expression of miR-21 contributes to migration and invasion by inducing epithelial-mesenchymal transition consistent with cancer stem cell characteristics in MCF-7 cells. Mol Cell Biochem 363(1–2):427–436CrossRef Han M et al (2012) Re-expression of miR-21 contributes to migration and invasion by inducing epithelial-mesenchymal transition consistent with cancer stem cell characteristics in MCF-7 cells. Mol Cell Biochem 363(1–2):427–436CrossRef
52.
go back to reference Yue X et al (2016) Leukemia inhibitory factor promotes EMT through STAT3-dependent miR-21 induction. Oncotarget 7(4):3777–3790CrossRef Yue X et al (2016) Leukemia inhibitory factor promotes EMT through STAT3-dependent miR-21 induction. Oncotarget 7(4):3777–3790CrossRef
53.
go back to reference Ferraro A et al (2014) Epigenetic regulation of miR-21 in colorectal cancer: ITGB4 as a novel miR-21 target and a three-gene network (miR-21-ITGBeta4-PDCD4) as predictor of metastatic tumor potential. Epigenetics 9(1):129–141CrossRef Ferraro A et al (2014) Epigenetic regulation of miR-21 in colorectal cancer: ITGB4 as a novel miR-21 target and a three-gene network (miR-21-ITGBeta4-PDCD4) as predictor of metastatic tumor potential. Epigenetics 9(1):129–141CrossRef
54.
go back to reference Li C et al (2016) MicroRNA-21 promotes proliferation, migration, and invasion of colorectal cancer, and tumor growth associated with down-regulation of sec23a expression. BMC Cancer 16:605CrossRef Li C et al (2016) MicroRNA-21 promotes proliferation, migration, and invasion of colorectal cancer, and tumor growth associated with down-regulation of sec23a expression. BMC Cancer 16:605CrossRef
55.
go back to reference Nedaeinia R et al (2016) Locked nucleic acid anti-miR-21 inhibits cell growth and invasive behaviors of a colorectal adenocarcinoma cell line: LNA-anti-miR as a novel approach. Cancer Gene Ther 23(8):246–253CrossRef Nedaeinia R et al (2016) Locked nucleic acid anti-miR-21 inhibits cell growth and invasive behaviors of a colorectal adenocarcinoma cell line: LNA-anti-miR as a novel approach. Cancer Gene Ther 23(8):246–253CrossRef
56.
go back to reference Ortega FG et al (2015) miRNA in situ hybridization in circulating tumor cells-MishCTC. Sci Rep 5:9207CrossRef Ortega FG et al (2015) miRNA in situ hybridization in circulating tumor cells-MishCTC. Sci Rep 5:9207CrossRef
57.
go back to reference Leone E et al (2013) Targeting miR-21 inhibits in vitro and in vivo multiple myeloma cell growth. Clin Cancer Res 19(8):2096–2106CrossRef Leone E et al (2013) Targeting miR-21 inhibits in vitro and in vivo multiple myeloma cell growth. Clin Cancer Res 19(8):2096–2106CrossRef
58.
go back to reference Lee TJ et al (2017) RNA nanoparticle-based targeted therapy for glioblastoma through inhibition of oncogenic miR-21. Mol Ther 25(7):1544–1555CrossRef Lee TJ et al (2017) RNA nanoparticle-based targeted therapy for glioblastoma through inhibition of oncogenic miR-21. Mol Ther 25(7):1544–1555CrossRef
Metadata
Title
miR-21 expression analysis in budding colon cancer cells by confocal slide scanning microscopy
Authors
Kirsten Nguyen Knudsen
Jan Lindebjerg
Alexandra Kalmár
Béla Molnár
Flemming Brandt Sørensen
Torben Frøstrup Hansen
Boye Schnack Nielsen
Publication date
01-12-2018
Publisher
Springer Netherlands
Published in
Clinical & Experimental Metastasis / Issue 8/2018
Print ISSN: 0262-0898
Electronic ISSN: 1573-7276
DOI
https://doi.org/10.1007/s10585-018-9945-3

Other articles of this Issue 8/2018

Clinical & Experimental Metastasis 8/2018 Go to the issue
Webinar | 19-02-2024 | 17:30 (CET)

Keynote webinar | Spotlight on antibody–drug conjugates in cancer

Antibody–drug conjugates (ADCs) are novel agents that have shown promise across multiple tumor types. Explore the current landscape of ADCs in breast and lung cancer with our experts, and gain insights into the mechanism of action, key clinical trials data, existing challenges, and future directions.

Dr. Véronique Diéras
Prof. Fabrice Barlesi
Developed by: Springer Medicine