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Sökning: onr:"swepub:oai:lup.lub.lu.se:52a30e29-7dd3-4716-93b3-37b841d53088" > A quantitative poly...

A quantitative polymerase chain reaction based method for molecular subtype classification of urinary bladder cancer—Stromal gene expressions show higher prognostic values than intrinsic tumor genes

Olah, Csilla (författare)
University of Duisburg-Essen
Hahnen, Christina (författare)
University of Duisburg-Essen
Nagy, Nikolett (författare)
Semmelweis University
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Musial, Joanna (författare)
University of Duisburg-Essen
Varadi, Melinda (författare)
Semmelweis University
Nyiro, Gabor (författare)
Semmelweis University
Gyorffy, Balazs (författare)
Semmelweis University
Hadaschik, Boris (författare)
University of Duisburg-Essen
Rawitzer, Josefine (författare)
University Hospital Essen
Ting, Saskia (författare)
University Hospital Essen
Sjödahl, Gottfrid (författare)
Lund University,Lunds universitet,Urologi - blåscancer, Malmö,Forskargrupper vid Lunds universitet,Genomiska analyser av urinblåscancer,LUCC: Lunds universitets cancercentrum,Övriga starka forskningsmiljöer,Urinblåsecancer,Sektion I,Institutionen för kliniska vetenskaper, Lund,Medicinska fakulteten,Urology - urothelial cancer, Malmö,Lund University Research Groups,Urothelial Cancer Genomics,LUCC: Lund University Cancer Centre,Other Strong Research Environments,Urothelial cancer,Section I,Department of Clinical Sciences, Lund,Faculty of Medicine,Skåne University Hospital
Hoffmann, Michéle J. (författare)
Heinrich Heine University Düsseldorf
Reis, Henning (författare)
Lund University,Skåne University Hospital
Szarvas, Tibor (författare)
University of Duisburg-Essen
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 (creator_code:org_t)
2021-10-02
2022
Engelska.
Ingår i: International Journal of Cancer. - : Wiley. - 0020-7136 .- 1097-0215. ; 150:5, s. 856-867
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Transcriptome-based molecular subtypes of muscle-invasive bladder cancer (MIBC) have been shown to be both prognostic and predictive, but are not used in routine clinical practice. We aimed to develop a feasible, reverse transcription quantitative polymerase chain reaction (RT-qPCR)-based method for molecular subtyping. First, we defined a 68-gene set covering tumor intrinsic (luminal, basal, squamous, neuronal, epithelial-to-mesenchymal, in situ carcinoma) and stromal (immune, extracellular matrix, p53-like) signatures. Then, classifier methods with this 68-gene panel were developed in silico and validated on public data sets with available subtype class information (MD Anderson [MDA], The Cancer Genome Atlas [TCGA], Lund, Consensus). Finally, expression of the selected 68 genes was determined in 104 frozen tissue samples of our MIBC cohort by RT-qPCR using the TaqMan Array Card platform and samples were classified by our newly developed classifiers. The prognostic value of each subtype classification system and molecular signature scores were assessed. We found that the reduced marker set combined with the developed classifiers were able to reproduce the TCGA II, MDA, Lund and Consensus subtype classification systems with an overlap of 79%, 76%, 69% and 64%, respectively. Importantly, we could successfully classify 96% (100/104) of our MIBC samples by using RT-qPCR. Neuronal and luminal subtypes and low stromal gene expressions were associated with poor survival. In conclusion, we developed a robust and feasible method for the molecular subtyping according to the TCGA II, MDA, Lund and Consensus classifications. Our results suggest that stromal signatures have a superior prognostic value compared to tumor intrinsic signatures and therefore underline the importance of tumor-stroma interaction during the progression of MIBC.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Nyckelord

bladder cancer
molecular subtype classification
neuronal signature
stroma

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