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Int J Mol Sci ; 15(10): 17344-65, 2014 Sep 29.
Article in English | MEDLINE | ID: mdl-25268611

ABSTRACT

Gender-related differences in colorectal cancer (CRC) are not fully understood. Recent studies have shown that CRC arising in females are significantly associated with CpG island methylator phenotype (CIMP-high). Using array comparative genomic hybridization, we analyzed a cohort of 116 CRCs (57 males, 59 females) for chromosomal copy number aberrations (CNA) and found that CRC in females had significantly higher numbers of gains involving chromosome arms 1q21.2-q21.3, 4q13.2, 6p21.1 and 16p11.2 and copy number losses of chromosome arm 11q25 compared to males. Interestingly, a subset of male CRCs (46%) exhibited a "feminization" phenomenon in the form of gains of X chromosomes (or an arm of X) and/or losses of the Y chromosome. Feminization of cancer cells was significantly associated with microsatellite-stable CRCs (p-value 0.003) and wild-type BRAF gene status (p-value 0.009). No significant association with other clinicopathological parameters was identified including disease-free survival. In summary, our data show that some CNAs in CRC may be gender specific and that male cancers characterized by feminization may constitute a specific subset of CRCs that warrants further investigation.


Subject(s)
Colorectal Neoplasms/genetics , Genome, Human , Adult , Aged , Aged, 80 and over , Chromosomes, Human, X , Chromosomes, Human, Y , Colorectal Neoplasms/mortality , Colorectal Neoplasms/pathology , Comparative Genomic Hybridization , DNA Copy Number Variations , Demography , Disease-Free Survival , Female , Feminization , Humans , In Situ Hybridization, Fluorescence , Male , Microsatellite Instability , Middle Aged , Proto-Oncogene Proteins B-raf/genetics , Sex Factors
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