Liu Rong-Zong, Godbout Roseline
Department of Oncology, Cross Cancer Institute, University of Alberta, Edmonton, AB T6G 1Z2, Canada.
Cancers (Basel). 2020 Dec 18;12(12):3823. doi: 10.3390/cancers12123823.
Treatment for early stage and localized prostate cancer (PCa) is highly effective. Patient survival, however, drops dramatically upon metastasis due to drug resistance and cancer recurrence. The molecular mechanisms underlying PCa metastasis are complex and remain unclear. It is therefore crucial to decipher the key genetic alterations and relevant molecular pathways driving PCa metastatic progression so that predictive biomarkers and precise therapeutic targets can be developed. Through PCa cohort analysis, we found that a fatty acid-binding protein (FABP) gene cluster (containing five FABP family members) is preferentially amplified and overexpressed in metastatic PCa. All five FABP genes reside on chromosome 8 at 8q21.13, a chromosomal region frequently amplified in PCa. There is emerging evidence that these FABPs promote metastasis through distinct biological actions and molecular pathways. In this review, we discuss how these FABPs may serve as drivers/promoters for PCa metastatic transformation using patient cohort analysis combined with a review of the literature.
早期局限性前列腺癌(PCa)的治疗效果显著。然而,由于耐药性和癌症复发,一旦发生转移,患者生存率会急剧下降。PCa转移的分子机制复杂,尚不清楚。因此,至关重要的是要破译驱动PCa转移进展的关键基因改变和相关分子途径,以便开发预测性生物标志物和精确的治疗靶点。通过PCa队列分析,我们发现一个脂肪酸结合蛋白(FABP)基因簇(包含五个FABP家族成员)在转移性PCa中优先扩增并过表达。所有五个FABP基因都位于8号染色体的8q21.13上,这是PCa中经常扩增的染色体区域。越来越多的证据表明,这些FABP通过不同的生物学作用和分子途径促进转移。在这篇综述中,我们结合文献综述,利用患者队列分析讨论这些FABP如何可能作为PCa转移转化的驱动因素/促进因素。