全基因组微RNA分析发现,胰腺癌组织中miR-210-3p的过度表达可预测其局部侵袭性

IF 1.6 4区 医学 Q4 ONCOLOGY Anticancer research Pub Date : 2024-11-01 DOI:10.21873/anticanres.17297
Tomohisa Otsu, Masamichi Hayashi, Keizo Fujita, Daigo Kobayashi, Nobuhiko Nakagawa, Keisuke Kurimoto, Hideki Takami, Koki Nakanishi, Shinichi Umeda, Dai Shimizu, Norifumi Hattori, Mitsuro Kanda, Chie Tanaka, Goro Nakayama, Yasuhiro Kodera
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引用次数: 0

摘要

背景/目的:胰腺导管腺癌(PDAC)的严重恶性程度主要在于频繁的局部浸润和远处转移。关于局部浸润性,我们曾报道在切除的 PDAC 标本表面检测到的癌症特异性分子改变,即所谓的分子手术切缘(MSM)阳性,与术后局部复发和远处转移显著相关。然而,由于解剖学上的限制,在胰腺癌切除术中实现适当的手术切缘往往具有挑战性。因此,根据原发肿瘤的基因图谱预测局部侵袭性对于避免阳性 MSM 至关重要:研究了全基因组 miRNA 表达谱,并对 MSM 阳性和阴性病例进行了比较。在另一个验证队列中对候选 miRNA 进行评估,并检查其临床病理特征。将候选miRNA的模拟物或抑制物构建体转染至PDAC细胞系,以评估miRNA在胰腺癌细胞系中的功能并检测下游靶标:结果:在通过miRNA表达阵列检测的MSM阳性候选miRNA中,miR-210-3p高表达组的无复发生存期(RFS)明显较短(p=0.015)。miR-210-3p高表达与肿瘤直径大(p=0.001)、前侵阳性(p=0.010)和淋巴结转移阳性(pConclusion)明显相关:原发性PDAC组织中高表达的低氧诱导型miR-210-3p通过抑制ISCU的表达,导致线粒体功能障碍,从而诱导局部侵袭性特征,这可能导致术后RFS结果不佳。
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Genome-wide microRNA Analysis Identified miR-210-3p Over-expression in Pancreatic Cancer Tissues as a Predictor of their Local Invasiveness.

Background/aim: The severe malignancy of pancreatic ductal adenocarcinoma (PDAC) is mainly due to frequent local invasiveness and distant metastasis. As for local invasiveness, we previously reported that cancer-specific molecular alterations detected on resected PDAC specimen surfaces, so-called molecular surgical margin (MSM) positiveness, were significantly associated with postoperative locoregional recurrence and distant metastasis. However, due to anatomical limitations, achieving adequate surgical margins during pancreatic cancer resection is often challenging. Therefore, predicting local invasiveness based on the primary tumor's gene profile is crucial to avoid positive MSM.

Materials and methods: Genome-wide miRNA expression profiles were examined and compared between MSM-positive and negative cases. Candidate miRNAs were evaluated in another validation cohort, and their clinicopathological characteristics were examined. Mimic or inhibitor constructs of the candidate miRNA were transfected to PDAC cell lines to evaluate the miRNA function in the pancreatic cancer cell lines and detect the downstream targets.

Results: Among some candidates with highly expressed miRNAs in MSM-positive cases by miRNA expression array, recurrence-free survival (RFS) was significantly shorter in the miR-210-3p high expression group (p=0.015). High miR-210-3p was significantly associated with large tumor diameter (p=0.001), anterior invasion positive (p=0.010), and positive lymph node metastasis (p<0.001). miR-210-3p inhibition in PDAC cell lines resulted in decreased proliferation and invasiveness. The iron-sulfur cluster assembly enzyme (ISCU) gene was identified as a target of miR-210-3p. ISCU reduction was significantly observed in PDAC primary tumors with high levels of miR-210-3p, leading to mitochondrial dysfunction in miR-210-3p-overexpressing PDAC cell lines, as demonstrated by glycolysis stress tests.

Conclusion: Highly expressed hypoxia-inducible miR-210-3p in primary PDAC tissues induces locally invasive characteristics through mitochondrial dysfunction by suppressing ISCU expression, which may result in poor postoperative RFS outcomes.

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来源期刊
Anticancer research
Anticancer research 医学-肿瘤学
CiteScore
3.70
自引率
10.00%
发文量
566
审稿时长
2 months
期刊介绍: ANTICANCER RESEARCH is an independent international peer-reviewed journal devoted to the rapid publication of high quality original articles and reviews on all aspects of experimental and clinical oncology. Prompt evaluation of all submitted articles in confidence and rapid publication within 1-2 months of acceptance are guaranteed. ANTICANCER RESEARCH was established in 1981 and is published monthly (bimonthly until the end of 2008). Each annual volume contains twelve issues and index. Each issue may be divided into three parts (A: Reviews, B: Experimental studies, and C: Clinical and Epidemiological studies). Special issues, presenting the proceedings of meetings or groups of papers on topics of significant progress, will also be included in each volume. There is no limitation to the number of pages per issue.
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