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      Kindlin-2 expression in arsenite- and cadmium-transformed bladder cancer cell lines and in archival specimens of human bladder cancer.

      Biology
      Animals, Arsenic, pharmacology, Cadmium, Cell Line, Tumor, Cytoskeletal Proteins, biosynthesis, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Humans, Immunohistochemistry, methods, Membrane Proteins, Mice, Muscle Proteins, Neoplasm Invasiveness, Neoplasm Proteins, Oligonucleotide Array Sequence Analysis, Prognosis, Tumor Markers, Biological, metabolism, Urinary Bladder, Urinary Bladder Neoplasms

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          Abstract

          To confirm a microarray study that suggested that Kindlin-2 might play a role in the development and progression of bladder cancer. There has been no previous examination of Kindlin-2 expression in human bladder cancer. A combination of real-time polymerase chain reaction, Western analysis, and immunohistochemistry was used to characterize Kindlin-2 expression in arsenite (As(+3))- and cadmium (Cd(+2))-transformed human cell lines, their tumor transplants in immunocompromised mice, and in archival specimens of human bladder and bladder cancer. The results show that the Kindlin-2 expression patterns in the cell lines were not duplicated in the tumor tissues. However, it was shown that Kindlin-2 was expressed in the stromal element of all the transplanted tumors and archival specimens of human bladder cancer. It was also shown that a small number of high-grade invasive urothelial cancers have focal expression of Kindlin-2 in the tumor cells. Kindlin-2 is expressed in the stromal component of most, if not all, human bladder cancers. Kindlin-2 is not expressed in normal urothelium. Kindlin-2 is expressed in a small subset of high-grade invasive bladder cancers and may have potential as a prognostic marker for tumor progression. Copyright © 2011 Elsevier Inc. All rights reserved.

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