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Biochemical and molecular markers in renal cell carcinoma: an update and future prospects 

Authors: M. K. Kashyap a;  A. Kumar b;  N. Emelianenko c;  A. Kashyap d;  R. Kaushik e;  R. Huang f;  M. Khullar g;  S. K. Sharma h;  S. K. Singh h;  A. K. Bhargave d; S. K. Upadhyaya d
Affiliations:   a Department of Veterinary Biosciences, University of Illinois, Urbana-Champaign, USA
b Department of Microbiology and Immunology, Institute of Pathology, Safdarjung Campus, New Delhi, India
c International University of Nature, Society and Man 'Dubna', Moscow, Russia
d Department of Botany, M. S. College, SRE (C. C. S. University), Meerut, UP, India
e Department of Applied Chemistry, M. D. S. University, Ajmer, RJ, India
f Veterinary Pathobiology, University of Illinois, Urbana-Champaign, USA
g Department of Experimental Medicine and Biotechnology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
h Department of Urology, Postgraduate Institute of Medical Education and Research, Chandigarh, India
DOI: 10.1080/13547500500218534
Publication Frequency: 6 issues per year
Published in: journal Biomarkers, Volume 10, Issue 4 July 2005 , pages 258 - 294
Subject: Biomarkers;
Formats available: HTML (English) : PDF (English)
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Abstract

Cancer is a big problem in the developed world as well as in developing countries. Renal cell carcinoma (RCC) accounts for approximately 3% of adult malignancies and 90-95% of neoplasms arising from the kidney. RCC is more common in men than in women (2:1), and it most often occurs in patients between the ages of 50-70 years. In all cancers the cancerous cells release particular kind of proteins (called tumour markers) and blood tests are used to detect the presence of these markers. These tumour markers nowadays are an area of interest for oncologists who search for a possible solution in the detection and treatment of RCC. Different kinds of biochemical and molecular markers such as ferritin, MN/CA9, apoptotic index, p53, IL-2, gamma-enolase, CD44, CD95, chromosome instability and loss of heterozygosity have been tested in RCC, but so far no marker fulfils one or the other criteria to be considered as an ideal marker for RCC. This review gives basic and updated information about the different kinds of biomarkers studied in RCC and about the role implementation of genomics and proteomics in RCC.
Keywords: Renal cell carcinoma; ferritin; prognostic marker; MN/CA9; kidney; prognostic value; p75; iNOS; reverse transcription polymerase chain reaction (RT-PCR); microsatellite markers
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