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Microarrays of bladder cancer tissue are highly representative of proliferation index and histological grade
Author(s) -
Nocito Antonio,
Bubendorf Lukas,
Tinner Eva Maria,
Süess Katrin,
Wagner Urs,
Forster Thomas,
Kon Juha,
Fijan André,
Bruderer James,
Schmid Ulrico,
Ackermann Daniel,
Maurer Robert,
Alund Göran,
Knönagel Hartmut,
Rist Marcus,
Anabitarte Manuel,
Hering Franz,
Hardmeier Thomas,
Schoenenberger Andreas J.,
Flury Renata,
Jäger Peter,
Luc Fehr Jean,
Schraml Peter,
Moch Holger,
Mihatsch Michael J.,
Gasser Thomas,
Sauter Guido
Publication year - 2001
Publication title -
the journal of pathology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.964
H-Index - 184
eISSN - 1096-9896
pISSN - 0022-3417
DOI - 10.1002/1096-9896(200107)194:3<349::aid-path887>3.0.co;2-d
Subject(s) - tissue microarray , bladder cancer , proliferation index , pathology , dna microarray , cancer , medicine , index (typography) , biology , oncology , immunohistochemistry , gene expression , computer science , genetics , gene , world wide web
The number of genes suggested to play a role in cancer biology is rapidly increasing. To be able to test a large number of molecular parameters in sufficiently large series of primary tumours, a tissue microarray (TMA) approach has been developed where samples from up to 1000 tumours can be simultaneously analysed on one glass slide. Because of the small size of the individual arrayed tissue samples (diameter 0.6 mm), the question arises of whether these specimens are representative of their donor tumours. To investigate how representative are the results obtained on TMAs, a set of 2317 bladder tumours that had been previously analysed for histological grade and Ki67 labelling index (LI) was used to construct four replica TMAs from different areas of each tumour. Clinical follow‐up information was available from 1092 patients. The histological grade and the Ki67 LI were determined for every arrayed tumour sample (4×2317 analyses each). Despite discrepancies in individual cases, the grade and Ki67 information obtained on minute arrayed samples were highly similar to the data obtained on large sections ( p <0.0001). Most importantly, every individual association between grade or Ki67 LI and tumour stage or prognosis (recurrence, progression, tumour‐specific survival) that was observed in large section analysis could be fully reproduced on all four replica TMAs. These results show that intra‐tumour heterogeneity does not significantly affect the ability to detect clinico‐pathological correlations on TMAs, probably because of the large number of tumours that can be included in TMA studies. TMAs are a powerful tool for rapid identification of the biological or clinical significance of molecular alterations in bladder cancer and other tumour types. Copyright © 2001 John Wiley & Sons, Ltd.