Evidence map›Paper›PMID 39673649›Full record

ArticleMolecular biology reports2024

A simple and efficient "cell in situ collagen zymography" technique to evaluate cellular collagenase activities in thyroid cancer cell lines.

Ege Gokce Savas, Seniz Inanc Surer, Murat Sipahi, Didem Keles, Gulgun Oktay

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Article in Molecular biology reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1 citing paper in PubMed.

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5 · Who and what money

Authors and funding

5 authors.

Ege Gokce SavasDepartment of Chemistry, Faculty of Science, Dokuz Eylul University, Izmir, 35390, Türkiye.ORCID http://orcid.org/0000-0003-0188-7013
Seniz Inanc SurerDepartment of Medical Laboratory Techniques, Vocational School of Health Services, Izmir Tinaztepe University, Izmir, 35400, Türkiye.ORCID http://orcid.org/0000-0002-4985-9022
Murat SipahiDepartment of Medical Biochemistry, Institute of Health Sciences, Dokuz Eylul University, Izmir, 35340, Türkiye.ORCID http://orcid.org/0000-0003-1993-6741
Didem KelesDepartment of Medical Laboratory Techniques, Vocational School of Health Services, Izmir University of Economics, Izmir, 35330, Türkiye.ORCID http://orcid.org/0000-0001-7350-8049
Gulgun OktayDepartment of Medical Biochemistry, School of Medicine, Dokuz Eylul University, Izmir, 35340, Türkiye. gulgun.oktay@deu.edu.tr.ORCID http://orcid.org/0000-0002-0481-6029

Funding

Dokuz Eylul University Scientific Research Project Coordination Unit 2021.KB.SAĞ.036
6 · The paper itself

Abstract

backgroundCollagenases, a subgroup of matrix metalloproteinases (MMPs), play crucial roles in local invasion and metastasis in cancer. While substrate zymography and in situ zymography are commonly used to analyze the collagenases, traditional techniques have limitations in determining their local activities in vitro.

objectivesWe aimed to develop a new "cell in situ collagen zymography" technique to enhance the efficiency of studying local collagenase activities in vitro.

methodsWe utilized human thyroid cancer cell lines (8505 C, B-CPAP, FTC-133) and normal follicular thyroid cell line (Nhty-ori-3-1). We compared collagenase levels across these cell lines and selected 8505 C as a model due to its highest collagenase activity. We optimized factors including (i) fixation method (methanol, ethanol and zinc), (ii) dye-quenched (DQ) collagen concentration and (iii) collagen gel configuration. For gel configuration, cells were seeded under, on the top of, or between (sandwich) collagen gel layers. As controls, enzymatic activity was suppressed in the presence of EDTA, piroxicam and matrix metalloproteinase 8 inhibitor I. The optimized method was also applied to BCPAP, FTC-133, and Nthy-ori-3-1.

resultsOur optimization process revealed that that the best visualization of collagenase activity in 8505 C was provided by the "sandwich model" of gel, containing 25 µg/mL of DQ-collagen with 100% cold methanol fixation. We confirmed the optimized method's applicability in other thyroid cell lines. The use of inhibitors validated the specificity of the fluorescent signal to MMP activity.

conclusionThe innovative "cell in situ collagen zymography" technique offers an efficient, cost-effective, and rapid method for analyzing local collagenase activities in vitro.

Indexed as

CollagenCollagenasesThyroid NeoplasmsCell Line, TumorEnzyme AssaysHumansCollagenCollagenasesCollagenasesDQ-collagenGelatinasesIn situ zymographyMatrix metalloproteinasesThyroid cancer

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.