Literature DB >> 11150435

The survivin:fas ratio in pediatric renal tumors.

S Takamizawa1, D Scott, J Wen, P Grundy, W Bishop, K Kimura, A Sandler.   

Abstract

BACKGROUND/
PURPOSE: Apoptosis factors inducing or preventing cell death may govern the behavior of certain tumors. Fas is a pro-apoptotic receptor that induces cell death when bound by its ligand and is expressed at greater levels in pediatric renal tumors of good prognosis. Survivin is a novel inhibitor of apoptosis that is expressed in a cell cycle-dependent manner and is abundantly expressed in several tumors of unfavorable histology. This study evaluates the expression of survivin, as well as the prognostic value of the survivin:fas ratio in various types and stages of pediatric renal tumors.
METHODS: Multiple apoptosis mRNA species were quantified by Rnase protection assay (RPA) in 32 pediatric renal tumors and adjacent normal kidney specimens before chemotherapy: Wilms' tumor (WT), n = 9; clear cell sarcoma (CCS), n = 4; rhabdoid tumor of the kidney (RTK), n = 5; mesoblastic nephroma (MN), n = 3 and normal kidney, n = 11. Western Blot and immunocytochemistry were used to confirm survivin protein expression in a selective specimen survey. Follow-up data were obtained on patient outcomes, and antiapoptotic to proapoptotic ratios were calculated and correlated with clinical recurrence of disease.
RESULTS: Pediatric renal tumors express greater levels of both pro- and antiapoptotic factors than normal kidney. Survivin and fas appeared to be expressed differentially in the tumor specimens sampled. Five of 10 (50%) tumors that went on to recur expressed survivin, whereas survivin was present in only 2 of 11 (18%) nonrecurrent tumors. Conversely, only 2 of 10 (20%) tumors that recurred were fas positive, whereas 5 of 11 (45%) tumors that did not recur expressed fas. The mean survivin:fas ratio was significantly greater in the 10 tumors that went on to recur after treatment (4 RTK, 3 CCS, 3 WT), than in tumors not recurring (2.16+/-1.4 v 1.0+/-1.07; P =.01, Kruskal-Wallis test). The positive predictive value of tumor recurrence was 85.7% (CI: 42.1%, 99.6%) and the negative predictive value was 71.4% (CI: 41.9%, 91.6%) when a cutoff ratio of 1.6 was considered.
CONCLUSIONS: The survivin:fas mRNA ratio is of prognostic value in its ability to predict recurrent disease in children undergoing treatment for pediatric renal tumors. In this series, a ratio of greater than 1.6 predicted recurrent disease with a high probability irrespective of clinical stage or pathologic type. Determining the survivin:fas ratio may guide treatment, follow-up and counseling of patients with pediatric renal tumors.

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Year:  2001        PMID: 11150435     DOI: 10.1053/jpsu.2001.20000

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  4 in total

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Journal:  Med Oncol       Date:  2006       Impact factor: 3.064

2.  Endogenous knockdown of survivin improves chemotherapeutic response in ALL models.

Authors:  D J Morrison; L E Hogan; G Condos; T Bhatla; N Germino; N P Moskowitz; L Lee; D Bhojwani; T M Horton; I Belitskaya-Levy; L M Greenberger; I D Horak; S A Grupp; D T Teachey; E A Raetz; W L Carroll
Journal:  Leukemia       Date:  2011-08-16       Impact factor: 11.528

3.  YM155 and chrysin cooperatively suppress survivin expression in SMARCB1/INI1-deficient tumor cells.

Authors:  Yuki Yoshino; Hiroaki Goto; Mieko Ito; Yoshinori Tsurusaki; Junko Takita; Yasuhide Hayashi; Masakatsu Yanagimachi
Journal:  Med Oncol       Date:  2022-09-29       Impact factor: 3.738

4.  Prognostic importance of survivin in breast cancer.

Authors:  S M Kennedy; L O'Driscoll; R Purcell; N Fitz-Simons; E W McDermott; A D Hill; N J O'Higgins; M Parkinson; R Linehan; M Clynes
Journal:  Br J Cancer       Date:  2003-04-07       Impact factor: 7.640

  4 in total

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