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患有侵袭性肿瘤且存在基因多态性并伴有蛛网膜下腔出血的患者往往预后较差。

Patients with Invasive Tumors and Gene Polymorphisms with Subarachnoid Hemorrhage Tend to Have Poorer Prognosis.

作者信息

Siroya Hardik Lalit, Devi Bhagavatula Indira, Aripirala Prasanthi, Ramesh Shruthi Shimoga, Bhat Dhananjaya Ishwar, Shukla Dhaval Prem, Konar Subhash Kanti, Christopher Rita

机构信息

Department of Neurosurgery, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, India.

Department of Pediatrics, National Institute of Mental Health and Neuro Sciences (NIMHANS), Bengaluru, Karnataka, India.

出版信息

Asian J Neurosurg. 2022 Aug 24;17(2):199-208. doi: 10.1055/s-0042-1750784. eCollection 2022 Jun.

Abstract

Endothelial nitric oxide synthase ( gene polymorphisms are found to predict predisposition to aneurysmal rupture and development of vasospasm in a patient of subarachnoid hemorrhage (SAH). gene polymorphisms are also found to predict invasiveness of malignant cells. Studies are not available in literature to describe the effect of gene polymorphisms and correlation between aneurysm and carcinoma. This study aims to investigate whether positive cancer history influences clinical outcome following SAH and gene polymorphisms.  The gene polymorphisms were analyzed in seven consecutive patients (mean age, 52.28 ± 20 years) with a diagnosis of invasive systemic tumors from 2011 to 2017. The 4a/4b -786T> 894G > T polymorphisms of the gene were determined by polymerase chain reaction and restriction fragment length polymorphism.  Seven patients of aneurysmal SAH in association with malignancies were studied for polymorphisms expression and outcome. Three patients had carcinoma cervix: one patient of carcinoma breast and one each of transitional cell carcinoma of urinary bladder, spindle cell carcinoma of left kidney, and untreated patient of atypical pituitary (adenoma). A genotype study of gene polymorphisms in these patients shows common polymorphisms are involved in the determination of disease progression in malignancies and aneurysmal SAH.  Patients who expressed 4ab, -786T > TT/CC/TC, 894G > T GG/GT polymorphisms did better than patients who expressed only 4bb, though both were associated with poor prognosis.

摘要

内皮型一氧化氮合酶()基因多态性被发现可预测蛛网膜下腔出血(SAH)患者动脉瘤破裂的易感性和血管痉挛的发生。基因多态性也被发现可预测恶性细胞的侵袭性。文献中尚无研究描述基因多态性的影响以及动脉瘤与癌症之间的相关性。本研究旨在调查癌症病史阳性是否会影响SAH后的临床结局以及基因多态性。

对2011年至2017年连续7例诊断为侵袭性系统性肿瘤的患者(平均年龄52.28±20岁)进行了基因多态性分析。通过聚合酶链反应和限制性片段长度多态性测定基因的4a/4b -786T> 894G>T多态性。

对7例合并恶性肿瘤的动脉瘤性SAH患者进行了多态性表达和结局研究。3例患有宫颈癌:1例患有乳腺癌,1例患有膀胱移行细胞癌,1例患有左肾梭形细胞癌,1例患有未治疗的非典型垂体(腺瘤)。对这些患者进行的基因多态性基因型研究表明,常见的多态性参与了恶性肿瘤和动脉瘤性SAH疾病进展的确定。

表达4ab、-786T>TT/CC/TC、894G>T GG/GT多态性的患者比仅表达4bb的患者预后更好,尽管两者都与预后不良有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86f2/9473864/3cf158600fbd/10-1055-s-0042-1750784-i29021-1.jpg

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