Pietruszewska Wioletta, Fendler Wojciech, Podwysocka Marta, Białas Adam J, Kuna Piotr, Kupryś-Lipińska Izabela, Borowiec Maciej
Department of Otolaryngology, Head and Neck Oncology, Medical University of Lodz, 90-419 Lodz, Poland.
Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.
Diagnostics (Basel). 2021 Jan 16;11(1):135. doi: 10.3390/diagnostics11010135.
To date, there has been no reliable test to identify unfavorable course of Chronic Rhinosinusitis with Nasal Polyps (CRSwNP), especially in aspirin intolerant patients. The research aimed to analyze the expression of transcript variants of and genes in the pathobiology of the disease. The study was performed on 409 adult patients: 206 CRSwNP patients including 44 (21.36%) aspirin intolerant patients and 203 healthy volunteers in the control group. Transcript variants of the and genes named as follows: COX1.1 for NM_000962, COX1.2 for NM_080591, COX1.3 for NM_001271165.1, COX1.4 for NM_001271368.1, COX1.5 for NM_001271166.1, COX2.1 for NM_000963.3, COX2.2 for AY_151286 and COX2.3 for BQ_722004 were confirmed using direct sequencing and quantified using targeted qPCR. The coexistence of all examined transcript variants in the study and the control group and significant differences between both were found. In aspirin sensitive patients, the levels of COX1.2, COX1.3, COX1.4 and COX1.5 isoforms were higher compared to aspirin-tolerant patients. The severity of symptoms was bigger in patients with higher expressions of variants: COX1.1 (R with dCt = -0.134; = 0.0490), COX1.3 (R = -0.1429; = 0.0400) and COX1.5 (Rs = -0.1499; = 0.032). The expression of COX1.1 (Rs = -0.098; = 0.049) and COX1.5 (Rs = -0.141; = 0.043) isoforms increased with polyposis advancement in endoscopy. With the CT extent of sinuses opacification, COX1.1 isoform also significantly increased (Rs = -0.163; = 0.020). The isoforms COX1.3, COX1.4, COX1.5 and COX2.1 may promote milder CRSwNP course. On the contrary, the variants COX1.1, COX1.2 and COX2.2 may be involved in a more aggressive disease.
迄今为止,尚无可靠的检测方法来识别伴鼻息肉的慢性鼻-鼻窦炎(CRSwNP)的不良病程,尤其是在阿司匹林不耐受的患者中。该研究旨在分析 和 基因转录变体在该疾病病理生物学中的表达。该研究对409名成年患者进行:206名CRSwNP患者,其中包括44名(21.36%)阿司匹林不耐受患者,以及203名作为对照组的健康志愿者。 和 基因的转录变体命名如下:NM_000962对应的COX1.1、NM_080591对应的COX1.2、NM_001271165.1对应的COX1.3、NM_001271368.1对应的COX1.4、NM_001271166.1对应的COX1.5、NM_000963.3对应的COX2.1、AY_151286对应的COX2.2以及BQ_722004对应的COX2.3,通过直接测序进行确认,并使用靶向定量聚合酶链反应(qPCR)进行定量。研究发现所有检测的转录变体在研究组和对照组中均共存,且两者之间存在显著差异。在阿司匹林敏感患者中,与阿司匹林耐受患者相比,COX1.2、COX1.3、COX1.4和COX1.5同工型的水平更高。变体表达较高的患者症状更严重:COX1.1(R与dCt = -0.134; = 0.0490)、COX1.3(R = -0.1429; = 0.0400)和COX1.5(Rs = -0.1499; = 0.032)。COX1.1(Rs = -0.098; = 0.049)和COX1.5(Rs = -0.141; = 0.043)同工型的表达随着鼻息肉在内镜检查中的进展而增加。随着鼻窦混浊的CT范围增加,COX1.1同工型也显著增加(Rs = -0.163; = 0.020)。COX1.3、COX1.4、COX1.5和COX2.1同工型可能促进CRSwNP病程较轻。相反,变体COX1.1、COX1.2和COX2.2可能与更具侵袭性的疾病有关。