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miR-125a-5p 的调控增加了 FAK 的磷酸化,这有助于胃肠道间质瘤对伊马替尼的耐药性。

miR-125a-5p regulation increases phosphorylation of FAK that contributes to imatinib resistance in gastrointestinal stromal tumors.

机构信息

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Clinical Pathology/Cytology, Cancer Center Karolinska, Karolinska University Hospital, SE-17176 Stockholm, Sweden; Division of Hematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, Taiwan.

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden; Clinical Pathology/Cytology, Cancer Center Karolinska, Karolinska University Hospital, SE-17176 Stockholm, Sweden.

出版信息

Exp Cell Res. 2018 Oct 1;371(1):287-296. doi: 10.1016/j.yexcr.2018.08.028. Epub 2018 Aug 24.

Abstract

The use of imatinib mesylate has greatly improved the clinical outcome for gastrointestinal stromal tumor (GIST) patients. However, imatinib resistance is still a major clinical challenge, and the molecular mechanisms are not fully understood. We have previously shown that miR-125a-5p and its mRNA target PTPN18 modulate imatinib response in GIST cells. Herein, we evaluated phosphorylated FAK (pFAK) as a candidate downstream target of PTPN18 and the possible association of this regulation with imatinib resistance in GIST. FAK and pFAK expressions were evaluated in GIST882 cells transfected with short hairpin RNA or short interfering RNA targeting PTPN18 or miR-125a-5p mimic, imatinib-resistant GIST882R subclones and clinical samples using Western blot analyses. FAK phosphorylation was blocked using the FAK inhibitor 14 (FAKi) and the effects on cell viability and apoptosis were evaluated using WST-1 assay and cleaved PARP expression. Clinical associations of FAK and pFAK expression with imatinib resistance, KIT mutation and patient outcome were assessed by Fisher's exact test or log-rank test. Over-expression of miR-125a-5p and silencing of PTPN18 increased pFAK, but not FAK, expression in GIST cells. Higher pFAK expression was observed in the GIST882R subclones with acquired imatinib resistance compared to their imatinib-sensitive parental cells. Treatment with FAKi in imatinib-resistant GIST882R cells reduced cell viability and increased apoptosis upon imatinib treatment. Additionally, FAKi could rescue the imatinib resistance effect mediated by miR-125a-5p over-expression. In clinical samples, high FAK and pFAK expressions were associated with KIT mutation status, and high FAK expression was also associated with metastasis in GIST. Higher pFAK was found in cases with shorter overall survival. Our findings highlight an important role for miR-125a-5p regulation and its downstream target pFAK for imatinib resistance in GIST. pFAK and FAK may have prognostic values in GIST.

摘要

甲磺酸伊马替尼的应用极大地改善了胃肠道间质瘤(GIST)患者的临床预后。然而,伊马替尼耐药仍然是一个主要的临床挑战,其分子机制尚未完全阐明。我们之前已经表明,miR-125a-5p及其 mRNA 靶标 PTPN18 可调节 GIST 细胞对伊马替尼的反应。在此,我们评估了磷酸化 FAK(pFAK)作为 PTPN18 的候选下游靶标,并研究了这种调控与 GIST 伊马替尼耐药之间的可能关联。使用 Western blot 分析评估了转染 PTPN18 短发夹 RNA 或短发夹 RNA 或 miR-125a-5p 模拟物、伊马替尼耐药 GIST882R 亚克隆和临床样本的 GIST882 细胞中的 FAK 和 pFAK 表达。使用 FAK 抑制剂 14(FAKi)阻断 FAK 磷酸化,并使用 WST-1 测定和 cleaved PARP 表达评估对细胞活力和凋亡的影响。使用 Fisher 精确检验或对数秩检验评估 FAK 和 pFAK 表达与伊马替尼耐药、KIT 突变和患者预后的临床关联。miR-125a-5p 的过表达和 PTPN18 的沉默增加了 GIST 细胞中的 pFAK,但不增加 FAK 的表达。与对伊马替尼敏感的亲本细胞相比,获得性伊马替尼耐药的 GIST882R 亚克隆中观察到更高的 pFAK 表达。在伊马替尼耐药的 GIST882R 细胞中用 FAKi 治疗可降低细胞活力并增加伊马替尼治疗时的凋亡。此外,FAKi 可以挽救 miR-125a-5p 过表达介导的伊马替尼耐药作用。在临床样本中,高 FAK 和 pFAK 表达与 KIT 突变状态相关,高 FAK 表达也与 GIST 中的转移相关。在总生存期较短的病例中发现 pFAK 较高。我们的研究结果强调了 miR-125a-5p 调节及其下游靶标 pFAK 在 GIST 中对伊马替尼耐药的重要作用。pFAK 和 FAK 在 GIST 中可能具有预后价值。

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