State Key Laboratory of Oncology in Southern China, Cancer Center, Sun Yat-sen University, Guangzhou, People's Republic of China.
PLoS One. 2012;7(3):e33762. doi: 10.1371/journal.pone.0033762. Epub 2012 Mar 16.
Small cell carcinoma of the cervix (SCCC) is very rare, and due to the long time period required to recruit sufficient numbers of patients, there is a paucity of information regarding the prognostic factors associated with survival. MicroRNAs (miRNAs) have been used as cancer-related biomarkers in a variety of tumor types, and the objective of this study was to determine whether microRNA expression profiles can predict clinical outcome in SCCC.
METHODOLOGY/PRINCIPAL FINDINGS: Forty-four patients with SCCC who underwent radical hysterectomy between January 2000 and October 2009 were enrolled. Using the GeneCopoeia All-in-One™ Customized Human qPCR Primer Array, the expression profiles of 30 miRNAs associated with tumor metastasis was obtained from the formalin-fixed paraffin embedded samples of all 44 patients. Seven miRNAs, has-let-7c, has-miR-10b, has-miR-100, has-miR-125b, has-miR-143, has-miR-145 and has-miR-199a-5p were significantly down-regulated in advanced stage SCCC patients (FIGO IB2-IV) compared to early stage SCCC patients (FIGOIB1). Among, downregulation of six miRNAs, has-let-7c, has-miR-100, has-miR-125b, has-miR-143, has-miR-145 and has-miR-199a-5p were significantly associated with lymph node metastasis and reduced survival in SCCC. Kaplan-Meier survival analyses revealed that SCCC patients with low expression of has-miR-100 (P = 0.019) and has-miR-125b (P = 0.020) projected a significant tendency towards poorer prognosis.
CONCLUSIONS/SIGNIFICANCE: This study demonstrates that downregulation of 7 miRNA associated with advanced stage, 6 miRNAs with metastasis and 2 with poor prognosis in SCCC. Functional analysis of these miRNAs may enhance our understanding of SCCC, as altered expression of specific miRNAs may regulate the metastatic pathway and provide novel targets for therapy.
宫颈小细胞癌(SCCC)非常罕见,由于需要很长时间才能招募到足够数量的患者,因此有关与生存相关的预后因素的信息很少。 microRNAs(miRNAs)已被用作多种肿瘤类型的癌症相关生物标志物,本研究的目的是确定 miRNA 表达谱是否可以预测 SCCC 的临床结果。
方法/主要发现:2000 年 1 月至 2009 年 10 月期间,我们招募了 44 例接受根治性子宫切除术的 SCCC 患者。使用 GeneCopoeia All-in-One™Customized Human qPCR Primer Array,从所有 44 例患者的福尔马林固定石蜡包埋样本中获得了与肿瘤转移相关的 30 个 miRNA 的表达谱。在晚期 SCCC 患者(FIGO IB2-IV)中,有 7 个 miRNA,包括 has-let-7c、has-miR-10b、has-miR-100、has-miR-125b、has-miR-143、has-miR-145 和 has-miR-199a-5p 的表达明显低于早期 SCCC 患者(FIGO IB1)。其中,has-let-7c、has-miR-100、has-miR-125b、has-miR-143、has-miR-145 和 has-miR-199a-5p 的下调与 SCCC 的淋巴结转移和生存率降低显著相关。Kaplan-Meier 生存分析显示,miR-100(P=0.019)和 miR-125b(P=0.020)低表达的 SCCC 患者预后明显较差。
结论/意义:本研究表明,与晚期、6 个与转移相关和 2 个与预后不良相关的 SCCC 相关的 7 个 miRNA 下调。对这些 miRNA 的功能分析可以增强我们对 SCCC 的理解,因为特定 miRNA 的表达改变可能会调节转移途径,并为治疗提供新的靶点。