Impact ofIGF-IandCYP19Gene Polymorphisms on the Survival of Patients With Metastatic Prostate Cancer
Aged, 80 and over
Male
0301 basic medicine
Polymorphism, Genetic
Prostatic Neoplasms
Middle Aged
Prognosis
3. Good health
03 medical and health sciences
Aromatase
Humans
Insulin-Like Growth Factor I
Neoplasm Metastasis
Aged
Repetitive Sequences, Nucleic Acid
DOI:
10.1200/jco.2005.02.9439
Publication Date:
2006-04-28T22:28:22Z
AUTHORS (13)
ABSTRACT
PurposeThe prognosis of metastatic prostate cancer significantly differs among individuals. While various clinical and biochemical prognostic factors for survival have been suggested, the progression and response to treatment of those patients may also be defined by host genetic factors. In this study, we evaluated genetic polymorphisms as prognostic predictors of metastatic prostate cancer.Patients and MethodsOne hundred eleven prostate cancer patients with bone metastasis at the diagnosis were enrolled in this study. Thirteen genetic polymorphisms were genotyped using polymerase chain reaction-restriction fragment length polymorphism or an automated sequencer with a genotyping software.ResultsAmong the polymorphisms, the long allele (over 18 [CA] repeats) of insulin-like growth factor-I (IGF-I) and the long allele (over seven [TTTA] repeats) of cytochrome P450 (CYP) 19 were significantly associated with a worse cancer-specific survival (P = .016 and .025 by logrank test, respectively). The presence of the long allele of either the IGF-I or CYP19 polymorphisms was an independent risk factor for death (P = .019 or .026, respectively). Furthermore, the presence of the long allele of both the IGF-I and CYP19 polymorphisms was a stronger predictor for survival (P = .001).ConclusionThe prognosis of metastatic prostate cancer patients is suggested to be influenced by intrinsic genetic factors. The IGF-I (CA) repeat and CYP19 (TTTA) repeat polymorphisms may be novel predictors in prostate cancer patients with bone metastasis at the diagnosis.
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