A. Hoos et C. Cordon-cardo, Tissue microarray profiling of cancer specimens and cell lines: Opportunities and limitations, LAB INV, 81(10), 2001, pp. 1331-1338
The implementations of high-throughput genetic technologies, such as oligon
ucleotide microarrays, generate myriad points of data. The identified poten
tial candidate genes need to be further characterized and selected using a
large number of well-characterized tumors and stringent criteria. Tissue mi
croarrays allow for such high-throughput expression profiling of tumor samp
les, providing, in addition, information at the microanatomical level. Diff
erent techniques could be applied for identification of specific phenotypic
(immunohistochemistry and in situ hybridization) or genotypic (fluorescenc
e in situ hybridization) alterations, holding strong potential for translat
ional research. Tissue microarrays consisting of 0.6-mm biopsies of paraffi
n-embedded tissues are well validated and have been used for various clinic
opathological studies. This review discusses the technical considerations f
or construction of such arrays from paraffin-embedded tissues and cell line
s and outlines their potential for clinical research applications. The use
of paraffin-embedded tissues has some limitations with regard to analysis o
f RNA or certain proteins, To overcome such limitations, we have developed
a cryoarray strategy allowing for the processing of multiple frozen tissue
specimens and/or cell lines on a single tissue block. These approaches offe
r the opportunity to conduct pilot and validation studies of potential targ
ets using clinical samples linked to clinicopathological databases.