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Prognostic role of FUT8 expression in relation to p53 status in stage II and III colorectal cancer

机译:FUT8表达与II期和III期大肠癌中p53状态的预后关系

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摘要

The expression of fucosyltransferase 8, an enzyme responsible for core fucosylation encoded by FUT8, influences tumor biology and correlates with patient prognosis in several solid cancers. We hypothesized that p53 alteration modifies prognostic associations of FUT8 expression in colorectal cancer (CRC), since FUT8 has recently been identified as a direct transcriptional target of wild-type p53. Utilizing multiple datasets of microarray and RNA sequence of CRC, FUT8 mRNA was found to be highly expressed in wild-type p53 tumors (n = 382) compared to those of mutant p53 (n = 437). Prognostic values of FUT8 expression in conjunction with the p53 status for disease-free survival (DFS) were analyzed using two independent cohorts of stage II and III CRC after curative surgery, including the immunohistochemistry (IHC) cohort (n = 123) and the microarray cohort (n = 357). In both cohorts, neither FUT8 expression nor the p53 status was associated with DFS. Strikingly, positive expression of FUT8 protein was significantly associated with better DFS only in tumors with negative p53, while it had no prognostic impact in tumors with positive p53 in the IHC cohort. Although not statistically significant, a similar prognostic trend was observed in the microarray cohort when patients were stratified by the p53 status. Our results suggest that the prognostic values of FUT8 expression on DFS may be modified by the p53 status, and the expression of FUT8 protein can be a prognostic biomarker for patients with stage II and III CRC.
机译:岩藻糖基转移酶8(一种由FUT8编码的核心岩藻糖基化酶)的表达影响肿瘤生物学,并与几种实体癌的患者预后相关。我们假设p53改变会改变结直肠癌(CRC)中FUT8表达的预后关联,因为FUT8最近已被确定为野生型p53的直接转录靶标。与突变p53(n = 437)相比,利用多个微阵列数据集和CRC的RNA序列,发现FUT8 mRNA在野生型p53肿瘤(n = 382)中高表达。使用治愈性手术后的两个独立的II期和III期CRC队列分析了FUT8表达与p53状态的无病生存期(DFS)的预后价值,包括免疫组化(IHC)队列(n = 123)和微阵列同类群组(n = 357)。在这两个队列中,FUT8表达和p53状态均与DFS无关。令人惊讶的是,仅在p53阴性的肿瘤中,FUT8蛋白的阳性表达与更好的DFS显着相关,而在IHC队列中,对p53阳性的肿瘤没有预后影响。尽管在统计学上不显着,但当按p53状态对患者进行分层时,在微阵列队列中观察到了相似的预后趋势。我们的结果表明,DUT上FUT8表达的预后价值可能会因p53状态而改变,FUT8蛋白的表达可能成为II期和III期CRC患者的预后生物标志物。

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