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声带白斑中遗传多态性和蛋白水平:系统评价。

Genetic polymorphisms and protein levels in vocal fold leukoplakia: a systematic review.

机构信息

Programa Associado de Pós-Graduação em Fonoaudiologia, Universidade Federal da Paraíba, João Pessoa, PB, Brasil.

Laboratório de Biologia Molecular, Centro de Oncohematologia Pediátrica, Hospital Universitário Oswaldo Cruz, Universidade de Pernambuco, Recife, PE, Brasil.

出版信息

Braz J Med Biol Res. 2022 Mar 11;55:e11920. doi: 10.1590/1414-431X2022e11920. eCollection 2022.

Abstract

Vocal fold leukoplakia (VFL) has a risk of malignant transformation. Therefore, patients can have symptoms such as dysphonia, vocal strain, difficulty breathing, and dysphagia. Additionally, there is a genetic predisposition that can be associated with genetic polymorphisms. We aimed to evaluate the influence of genetic polymorphisms and protein levels in the etiology of VFL. Our study followed the PRISMA checklist and was registered on PROSPERO database. The questions were: "Are genetic polymorphisms involved in the etiology of VFL? Are protein levels altered in patients with VFL?". Eligibility criteria were case control studies that compared the presence of polymorphisms or/and protein levels of subjects diagnosed with VFL and healthy controls. Of the 905 articles retrieved, five articles with a total of 1038 participants were included in this study. The C allele of the single nucleotide polymorphisms (SNP)-819 T/C IL-10, A allele of the SNP -592 A/C IL-10, CT genotype of the SNP rs11886868 C/T BCL11A, GG genotype of the SNP rs4671393 A/G BCL11A, LL genotype, and L allele of (GT)n repeat polymorphisms of the HO-1 were risk factors for VFL development. Nevertheless, there was a lack of association between VFL and the -1082 A/G IL-10, rs14024 CK-1, and -309 T/G Mdm2 SNPs. The concentrations of the MDM2, BCL11A, and HO-1 proteins were modified, while IL-10 levels were normally expressed in these subjects. In conclusion, most markers evaluated in this review could be potential indicators to develop effective therapies, avoiding a malignant transformation of the lesion.

摘要

声带白斑(VFL)有恶变的风险。因此,患者可能会出现声音嘶哑、发声困难、呼吸困难和吞咽困难等症状。此外,还有遗传易感性,可能与遗传多态性有关。我们旨在评估遗传多态性和蛋白质水平对 VFL 病因的影响。我们的研究遵循 PRISMA 清单,并在 PROSPERO 数据库中注册。问题是:“遗传多态性是否参与 VFL 的病因?VFL 患者的蛋白质水平是否改变?”。纳入标准为病例对照研究,比较诊断为 VFL 的患者和健康对照者的多态性或/和蛋白质水平。从 905 篇文章中检索到 5 篇文章,共纳入 1038 名参与者。白细胞介素-10 单核苷酸多态性(SNP)-819T/C 的 C 等位基因、白细胞介素-10 SNP-592A/C 的 A 等位基因、BCL11A 单核苷酸多态性 rs11886868C/T 的 CT 基因型、BCL11A 单核苷酸多态性 rs4671393A/G 的 GG 基因型、HO-1 的(GT)n 重复多态性的 LL 基因型和 L 等位基因是 VFL 发展的危险因素。然而,VFL 与白细胞介素-10 -1082A/G、CK-1 rs14024 和 Mdm2 -309T/G 单核苷酸多态性之间没有关联。这些患者的 MDM2、BCL11A 和 HO-1 蛋白浓度发生改变,而白细胞介素-10 水平正常表达。总之,本研究评价的大多数标志物可能是开发有效治疗方法的潜在指标,避免病变发生恶性转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/695e/8922550/fdf4e18ba96a/1414-431X-bjmbr-55-e11920-gf001.jpg

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