Skip to main content
Erschienen in: Journal of Cancer Research and Clinical Oncology 4/2019

02.01.2019 | Original Article – Cancer Research

A three-gene methylation marker panel for the nodal metastatic risk assessment of muscle-invasive bladder cancer

verfasst von: Beatrice Stubendorff, Kerstin Wilhelm, Kathleen Posselt, James Catto, Arndt Hartmann, Simone Bertz, Susanne Füssel, Vladimir Novotny, Marieta Toma, Mieczyslaw Gajda, Jan Lehmann, Heiko Wunderlich, Marc-Oliver Grimm, Michael Stöckle, Kerstin Junker

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 4/2019

Einloggen, um Zugang zu erhalten

Abstract

Purpose

In this study, we aimed to identify a DNA methylation pattern suitable for prognosis assessment of muscle-invasive bladder cancer and to investigate metastasis-associated processes regulated by DNA methylation.

Methods

Genome-wide methylation analysis was performed on 23 muscle-invasive bladder tumors by microarray analysis. Validation was performed by the qAMP technique in two different patient cohorts (n = 32 and n = 100). mRNA expression was analyzed in 12 samples. Protein expression was determined using tissue microarrays of 291 patients. Bladder cancer cell lines T24 and 253JB-V were used for functional analyses.

Results

Microarray analyses revealed KISS1R, SEPT9 and CSAD as putative biomarkers with hypermethylation in node-positive tumors. The combination of the three genes predicted the metastatic risk with sensitivity of 73% and specificity of 71% in cohort 1, and sensitivity of 82% and specificity of 54% in cohort 2. mRNA expression differences were detected for KISS1R (p = 0.04). Protein expression of KISS1R was significantly reduced (p < 0.001). Knockdown of SEPT9v3 resulted in increased cell migration by 28% (p = 0.04) and increased invasion by 22% (p = 0.004). KISS1R overexpression resulted in decreased cell migration (25%, p = 0.1).

Conclusions

We identified a methylation marker panel suitable to differentiate between patients with positive and negative lymph nodes at time of cystectomy. This enables a risk assessment for patients who potentially benefit from extended lymph node resection as well as from neoadjuvant chemotherapy and could improve the survival rates. Furthermore, we examined the impact of putative markers on tumor behavior. Hence, KISS1R and SEPT9 could represent a starting point for the development of novel therapy approaches.
Literatur
Zurück zum Zitat Dennis G Jr, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, Lempicki RA (2003) DAVID: database for annotation, visualization, and integrated discovery. Genome Biol 4(5):P3CrossRefPubMed Dennis G Jr, Sherman BT, Hosack DA, Yang J, Gao W, Lane HC, Lempicki RA (2003) DAVID: database for annotation, visualization, and integrated discovery. Genome Biol 4(5):P3CrossRefPubMed
Zurück zum Zitat Hope DB (1955) Pyridoxal phosphate as the coenzyme of the mammalian decarboxylase for l-cysteine sulphinic and l-cysteic acids. Biochem J 59(3):497–500CrossRefPubMedPubMedCentral Hope DB (1955) Pyridoxal phosphate as the coenzyme of the mammalian decarboxylase for l-cysteine sulphinic and l-cysteic acids. Biochem J 59(3):497–500CrossRefPubMedPubMedCentral
Zurück zum Zitat Muir AI, Chamberlain L, Elshourbagy NA, Michalovich D, Moore DJ, Calamari A, Szekeres PG, Sarau HM, Chambers JK, Murdock P, Steplewski K, Shabon U, Miller JE, Middleton SE, Darker JG, Larminie CGC, Wilson S, Bergsma DJ, Emson P, Faull R, Philpott KL, Harrison DC (2001) AXOR12, a novel human G protein-coupled receptor, activated by the peptide KiSS-1. J Biol Chem 276(31): 28969–28975. https://doi.org/10.1074/jbc.M102743200 CrossRefPubMed Muir AI, Chamberlain L, Elshourbagy NA, Michalovich D, Moore DJ, Calamari A, Szekeres PG, Sarau HM, Chambers JK, Murdock P, Steplewski K, Shabon U, Miller JE, Middleton SE, Darker JG, Larminie CGC, Wilson S, Bergsma DJ, Emson P, Faull R, Philpott KL, Harrison DC (2001) AXOR12, a novel human G protein-coupled receptor, activated by the peptide KiSS-1. J Biol Chem 276(31): 28969–28975. https://​doi.​org/​10.​1074/​jbc.​M102743200 CrossRefPubMed
Zurück zum Zitat Oakes CC, La Salle S, Robaire B, Trasler JM (2006) Evaluation of a quantitative DNA methylation analysis technique using methylation-sensitive/dependent restriction enzymes and real-time PCR. Epigenetics 1(3):146–152CrossRefPubMed Oakes CC, La Salle S, Robaire B, Trasler JM (2006) Evaluation of a quantitative DNA methylation analysis technique using methylation-sensitive/dependent restriction enzymes and real-time PCR. Epigenetics 1(3):146–152CrossRefPubMed
Zurück zum Zitat Schuller-Levis GB, Park E (2004) Taurine and its chloramine: modulators of immunity. Neurochem Res 29(1):117–126CrossRefPubMed Schuller-Levis GB, Park E (2004) Taurine and its chloramine: modulators of immunity. Neurochem Res 29(1):117–126CrossRefPubMed
Zurück zum Zitat Smith SC, Baras AS, Dancik G, Ru Y, Ding KF, Moskaluk CA, Fradet Y, Lehmann J, Stockle M, Hartmann A, Lee JK, Theodorescu D (2011) A 20-gene model for molecular nodal staging of bladder cancer: development and prospective assessment. Lancet Oncol 12(2):137–143CrossRefPubMedPubMedCentral Smith SC, Baras AS, Dancik G, Ru Y, Ding KF, Moskaluk CA, Fradet Y, Lehmann J, Stockle M, Hartmann A, Lee JK, Theodorescu D (2011) A 20-gene model for molecular nodal staging of bladder cancer: development and prospective assessment. Lancet Oncol 12(2):137–143CrossRefPubMedPubMedCentral
Zurück zum Zitat Sorensen AB, Warming S, Fuchtbauer EM, Pedersen FS (2002) Alternative splicing, expression, and gene structure of the septin-like putative proto-oncogene Sint1. Gene 285(1–2):79–89CrossRefPubMed Sorensen AB, Warming S, Fuchtbauer EM, Pedersen FS (2002) Alternative splicing, expression, and gene structure of the septin-like putative proto-oncogene Sint1. Gene 285(1–2):79–89CrossRefPubMed
Zurück zum Zitat Stathatos N, Bourdeau I, Espinosa AV, Saji M, Vasko VV, Burman KD, Stratakis CA, Ringel MD (2005) KiSS-1/G protein-coupled receptor 54 metastasis suppressor pathway increases myocyte-enriched calcineurin interacting protein 1 expression and chronically inhibits calcineurin activity. J Clin Endocrinol Metab 90(9):5432–5440. https://doi.org/10.1210/jc.2005-0963 CrossRefPubMed Stathatos N, Bourdeau I, Espinosa AV, Saji M, Vasko VV, Burman KD, Stratakis CA, Ringel MD (2005) KiSS-1/G protein-coupled receptor 54 metastasis suppressor pathway increases myocyte-enriched calcineurin interacting protein 1 expression and chronically inhibits calcineurin activity. J Clin Endocrinol Metab 90(9):5432–5440. https://​doi.​org/​10.​1210/​jc.​2005-0963 CrossRefPubMed
Metadaten
Titel
A three-gene methylation marker panel for the nodal metastatic risk assessment of muscle-invasive bladder cancer
verfasst von
Beatrice Stubendorff
Kerstin Wilhelm
Kathleen Posselt
James Catto
Arndt Hartmann
Simone Bertz
Susanne Füssel
Vladimir Novotny
Marieta Toma
Mieczyslaw Gajda
Jan Lehmann
Heiko Wunderlich
Marc-Oliver Grimm
Michael Stöckle
Kerstin Junker
Publikationsdatum
02.01.2019
Verlag
Springer Berlin Heidelberg
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 4/2019
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-018-02829-4

Weitere Artikel der Ausgabe 4/2019

Journal of Cancer Research and Clinical Oncology 4/2019 Zur Ausgabe

Erhöhtes Risiko fürs Herz unter Checkpointhemmer-Therapie

28.05.2024 Nebenwirkungen der Krebstherapie Nachrichten

Kardiotoxische Nebenwirkungen einer Therapie mit Immuncheckpointhemmern mögen selten sein – wenn sie aber auftreten, wird es für Patienten oft lebensgefährlich. Voruntersuchung und Monitoring sind daher obligat.

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Perioperative Checkpointhemmer-Therapie verbessert NSCLC-Prognose

28.05.2024 NSCLC Nachrichten

Eine perioperative Therapie mit Nivolumab reduziert das Risiko für Rezidive und Todesfälle bei operablem NSCLC im Vergleich zu einer alleinigen neoadjuvanten Chemotherapie um über 40%. Darauf deuten die Resultate der Phase-3-Studie CheckMate 77T.

Positiver FIT: Die Ursache liegt nicht immer im Dickdarm

27.05.2024 Blut im Stuhl Nachrichten

Immunchemischer Stuhltest positiv, Koloskopie negativ – in solchen Fällen kann die Blutungsquelle auch weiter proximal sitzen. Ein Forschungsteam hat nachgesehen, wie häufig und in welchen Lokalisationen das der Fall ist.

Update Onkologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.