Gene Expression Profiling Identifies WNT7A As a Possible Candidate Gene for Decreased Cancer Risk in Fragile X Syndrome Patients

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• 作者：Mó ; nica Alej ; ra Rosales-Reynoso ; Alej ; ra Berenice Ochoa-Herná ; ndez ; Adriana Aguilar-Lemarroy ; Luis Felipe Jave-Suá ; rez ; Rogelio Troyo-Sanromá ; n ; Patricio Barros-Nú ; ñ ; ez
• 关键词：Fragile X syndrome ; Tumor suppressor genes ; Oncogenes ; WNT7A ; Cancer risk
• 刊名：Archives of Medical Research
• 出版年：2010
• 出版时间：February 2010
• 年：2010
• 卷：41
• 期：2
• 页码：110-118.e2
• 全文大小：472 K

文摘

Background and Aims

Although sporadic cases of cancer in patients with fragile X syndrome (FXS) have been reported, extensive studies carried out in Denmark and Finland concluded that cancer incidence in these patients is lower than in the general population. On the other hand, the FMR1 protein, which is involved in the translation process, is absent in FXS patients. Hence, it is reasonable to assume that these patients exhibit an abnormal expression of some proteins involved in regulating tumor suppressor genes and/or oncogenes, thus explaining its decreased cancer frequency. We undertook this study to analyze the expression of oncogenes and tumor suppressor genes in fragile X syndrome patients.

Methods

Molecular analysis of the FMR1 gene was achieved in 10 male patients and controls. Total RNA from peripheral blood was used to evaluate expression of oncogenes and tumor suppressor genes included in a 10,000 gene microarray library. Quantitative real-time PCR was utilized to confirm genes with differential expression.

Results

Among 27 genes showing increased expression in FXS patients, only eight genes exhibited upregulation in at least 50 % of them. Among these, ARMCX2 and PPP2R5C genes are tumor suppressor related. Likewise, 23/65 genes showed decreased expression in >50 % of patients. Among them, WNT7A gene is a ligand of the β-catenin pathway, which is widely related to oncogenic processes. Decreased expression of WNT7A was confirmed by quantitative RT-PCR. Expression of c-Myc, c-Jun, cyclin-D and PPARδ genes, as target of the β-catenin pathway, was moderately reduced in FXS patients.

Conclusions

Results suggest that this diminished expression of the WNT7A gene may be related to a supposed protection of FXS patients to develop cancer.