Abstract | PURPOSE: Altered cyclin D1 (CD1), a cell cycle regulator, may play an important role in imparting aggressive nature to esophageal adenocarcinoma (EAC). CD1 gene single nucleotide polymorphism G/A870 results in two alternatively spliced transcripts, CD1a and CD1b. CD1b, preferentially encoded by the A870 allele, is putatively oncogenic. We hypothesized that CD1 A870 allele would be associated with higher CD1 protein expression, and increased genomic instability during EAC evolution, leading to more aggressive phenotype. PATIENTS AND METHODS: RESULTS: The A870 allele was associated with higher levels of CD1 protein expression in EAC (P = .032); in BE (P = .01) where it was associated with concomitant increased chromosome 9 polysomy (P = .002); and with a younger age at diagnosis (P < .001) and poor OS (P = .0003) of EAC patients. CONCLUSION: Our data suggest that CD1 A870 background may be imparting aggressive phenotype to EAC. It provides a molecular basis to explain the clinical biology associated with CD1 polymorphism whereas aberrant nuclear accumulation of CD1 protein enhances the acquisition of genomic instability (ie, clonal diversity), thus leading to early age of EAC diagnosis and poor OS. CD1 genotyping with other biomarkers may help create a biomarker-based prognostic model for EAC and CD1 may also serve as a therapeutic target.
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Authors | Julie G Izzo, Tsung-Teh Wu, Xifeng Wu, Joe Ensor, Rajyalakshmi Luthra, Jennifer Pan, Arlene Correa, Stephen G Swisher, Clifford K S Chao, Walter N Hittelman, Jaffer A Ajani |
Journal | Journal of clinical oncology : official journal of the American Society of Clinical Oncology
(J Clin Oncol)
Vol. 25
Issue 6
Pg. 698-707
(Feb 20 2007)
ISSN: 1527-7755 [Electronic] United States |
PMID | 17308274
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
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Chemical References |
- Biomarkers, Tumor
- Cyclin D1
- Guanine
- Adenine
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Topics |
- Adenine
(metabolism)
- Adenocarcinoma
(genetics, pathology, surgery)
- Adult
- Aged
- Biomarkers, Tumor
(genetics)
- Biopsy, Needle
- Cohort Studies
- Cyclin D1
(genetics, metabolism)
- Disease Progression
- Esophageal Neoplasms
(genetics, mortality, pathology, surgery)
- Esophagectomy
(methods)
- Esophagoscopy
- Female
- Gene Expression Regulation, Neoplastic
- Genomic Instability
- Guanine
(metabolism)
- Humans
- Immunohistochemistry
- Male
- Middle Aged
- Polymorphism, Genetic
- Probability
- Proportional Hazards Models
- Retrospective Studies
- Risk Assessment
- Sensitivity and Specificity
- Survival Analysis
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