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Differencial proteome of clear-cell renal cell carcinoma (ccRCC) tissues
International Braz J Urol; Ribeiro, Ana Júlia Vieira de; Sandim, Vanessa; Ornellas, Antonio Augusto; Reis, Rodrigo Siqueira; Domont, Gilberto; Alves, Gilda.
  • Ribeiro, Ana Júlia Vieira de; National Institute of Cancer. Hematology Division. Applied Genetic Laboratory.
  • Sandim, Vanessa; National Institute of Cancer. Hematology Division. Applied Genetic Laboratory.
  • Ornellas, Antonio Augusto; National Institute of Cancer. Hematology Division. Applied Genetic Laboratory.
  • Reis, Rodrigo Siqueira; National Institute of Cancer. Hematology Division. Applied Genetic Laboratory.
  • Domont, Gilberto; National Institute of Cancer. Hematology Division. Applied Genetic Laboratory.
  • Alves, Gilda; National Institute of Cancer. Hematology Division. Applied Genetic Laboratory.
Int. braz. j. urol ; 39(1): 83-94, January-February/2013. tab, graf
Article in English | LILACS | ID: lil-670367
ABSTRACT
Purpose We attempted to detect, for the first time in a Brazilian cohort, differences in protein expression between clear-cell renal cell carcinoma (ccRCC) and their normal adjacent tissues, aiming to identify biomarkers and/or therapeutic target candidates for this disease. Material and Methods Twenty-four ccRCC and adjacent normal tissues were collected after surgery and their protein extracts were quantified, pooled and separated by two-dimensional polyacrylamide gel electrophoresis (2DE), followed by statistical analysis of the stained gels. Spots of interest were excised from the gels, digested with trypsin and identified by MALDI-TOF-TOF mass spectrometry. Results Twenty-six differential spots were detected between the two classes of tissues, among which twenty were identified by mass spectrometry and sixteen were found to be non-redundant. Eleven proteins were either underexpressed or undetected in the ccRCC extracts, such as prohibitin and peroxiredoxin-3, whereas five were found to be overexpressed or exclusively detected in the ccRCC extract, including αβ crystalin and heat shock protein 27. CONCLUSIONS Several proteins were detected at differential levels when compared to normal adjacent tissues, and, moreover, many have been previously described by their relationship with RCC. Therefore, this work corroborates previous reports on the search for biomarkers for ccRCC, as well as it points out new candidates that may be validated in future studies. .
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Full text: Available Index: LILACS (Americas) Main subject: Carcinoma, Renal Cell / Proteome / Kidney / Kidney Neoplasms Type of study: Prognostic study Limits: Adult / Aged / Aged80 / Female / Humans / Male Language: English Journal: Int. braz. j. urol Journal subject: Urology Year: 2013 Type: Article Affiliation country: Brazil

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Full text: Available Index: LILACS (Americas) Main subject: Carcinoma, Renal Cell / Proteome / Kidney / Kidney Neoplasms Type of study: Prognostic study Limits: Adult / Aged / Aged80 / Female / Humans / Male Language: English Journal: Int. braz. j. urol Journal subject: Urology Year: 2013 Type: Article Affiliation country: Brazil