School of Medicine, Institute of Clinical Medicine, Pathology and Forensic Medicine, and Translational Cancer Research Area, University of Eastern Finland, Kuopio, Finland.
School of Medicine, Institute of Clinical Medicine, University of Eastern Finland, Kuopio, Finland.
Cancer Med. 2021 Jun;10(11):3593-3603. doi: 10.1002/cam4.3915. Epub 2021 May 7.
Numerous factors influence breast cancer (BC) prognosis, thus complicating the prediction of outcome. By identifying biomarkers that would distinguish the cases with poorer response to therapy already at the time of diagnosis, the rate of survival could be improved. Lately, Piwi-interacting RNAs (piRNAs) have been introduced as potential cancer biomarkers, however, due to the recently raised challenges in piRNA annotations, further evaluation of piRNAs' involvement in cancer is required. We performed small RNA sequencing in 227 fresh-frozen breast tissue samples from the Eastern Finnish Kuopio Breast Cancer Project material to study the presence of piRNAs in BC and their associations with the clinicopathological features and outcome of BC patients. We observed the presence of three small RNAs annotated as piRNA database entries (DQ596932, DQ570994, and DQ571955) in our samples. The actual species of these RNAs however remain uncertain. All three small RNAs were upregulated in grade III tumors and DQ596932 additionally in estrogen receptor negative tumors. Furthermore, patients with estrogen receptor positive BC and higher DQ571955 had shorter relapse-free survival and poorer BC-specific survival, thus indicating DQ571955 as a candidate predictive marker for radiotherapy response in estrogen receptor positive BC. DQ596932 showed possible prognostic value in BC, whereas DQ570994 was identified as a candidate predictive marker for tamoxifen and chemotherapy response. These three small RNAs appear as candidate biomarkers for BC, which could after further investigation provide novel approaches for the treatment of therapy resistant BC. Overall, our results indicate that the prevalence of piRNAs in cancer is most likely not as comprehensive as has been previously thought.
许多因素影响乳腺癌(BC)的预后,从而使结局预测变得复杂。通过鉴定在诊断时就能区分对治疗反应较差的病例的生物标志物,可以提高生存率。最近,Piwi 相互作用 RNA(piRNA)已被引入作为潜在的癌症生物标志物,然而,由于 piRNA 注释最近提出的挑战,需要进一步评估 piRNA 参与癌症的情况。我们对来自东芬兰库奥皮奥乳腺癌项目的 227 个新鲜冷冻的乳腺组织样本进行了小 RNA 测序,以研究 piRNA 在 BC 中的存在及其与 BC 患者的临床病理特征和结局的关系。我们观察到在我们的样本中存在三种被注释为 piRNA 数据库条目的小 RNA(DQ596932、DQ570994 和 DQ571955)。然而,这些 RNA 的实际种类仍不确定。这三种小 RNA 在 3 级肿瘤中上调,DQ596932 还在雌激素受体阴性肿瘤中上调。此外,雌激素受体阳性 BC 患者中 DQ571955 较高者的无复发生存率和 BC 特异性生存率更差,表明 DQ571955 是雌激素受体阳性 BC 放疗反应的候选预测标志物。DQ596932 在 BC 中显示出可能的预后价值,而 DQ570994 被鉴定为他莫昔芬和化疗反应的候选预测标志物。这三种小 RNA 似乎是 BC 的候选生物标志物,经过进一步研究可能为治疗耐药性 BC 提供新的方法。总的来说,我们的研究结果表明,piRNA 在癌症中的普遍程度可能并不像之前认为的那么广泛。