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Commentary: Next-Generation Sequence Analysis of Parathyroid Carcinoma.

作者信息

Costa-Guda Jessica

机构信息

Center for Regenerative Medicine and Skeletal Development, Department of Reconstructive Sciences, University of Connecticut School of Dental Medicine, Farmington, Connecticut.

Center for Molecular Oncology, Carole and Ray Neag Comprehensive Cancer Center, University of Connecticut School of Medicine, Farmington, Connecticut.

出版信息

J Endocr Soc. 2018 Oct 22;3(3):560-562. doi: 10.1210/js.2018-00315. eCollection 2019 Mar 1.

DOI:10.1210/js.2018-00315
PMID:30793092
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6378759/
Abstract
摘要

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本文引用的文献

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Comprehensive Genomic Characterization of Parathyroid Cancer Identifies Novel Candidate Driver Mutations and Core Pathways.甲状旁腺癌的综合基因组特征分析确定了新的候选驱动突变和核心通路。
J Endocr Soc. 2018 Sep 3;3(3):544-559. doi: 10.1210/js.2018-00043. eCollection 2019 Mar 1.
2
Molecular genetic insights into sporadic primary hyperparathyroidism.散发性原发性甲状旁腺功能亢进症的分子遗传学研究进展。
Endocr Relat Cancer. 2019 Feb 1;26(2):R53-R72. doi: 10.1530/ERC-18-0304.
3
Parathyroid Carcinoma Causing Mild Hyperparathyroidism in Neurofibromatosis Type 1: A Case Report and Systematic Review.1型神经纤维瘤病中导致轻度甲状旁腺功能亢进的甲状旁腺癌：一例报告及系统评价
Endocr Metab Immune Disord Drug Targets. 2019;19(3):382-388. doi: 10.2174/1871530318666180910123316.
4
Parathyroid carcinoma in multiple endocrine neoplasm type 1 syndrome: case report and systematic literature review.多发性内分泌腺瘤病 1 型综合征中的甲状旁腺癌：病例报告及系统文献复习。
Clin Exp Med. 2018 Nov;18(4):585-593. doi: 10.1007/s10238-018-0512-7. Epub 2018 Jun 20.
5
Molecular genetics of syndromic and non-syndromic forms of parathyroid carcinoma.甲状旁腺癌的综合征型和非综合征型的分子遗传学。
Hum Mutat. 2017 Dec;38(12):1621-1648. doi: 10.1002/humu.23337. Epub 2017 Sep 25.
6
Genomic profiling reveals mutational landscape in parathyroid carcinomas.基因组分析揭示甲状旁腺癌的突变特征。
JCI Insight. 2017 Mar 23;2(6):e92061. doi: 10.1172/jci.insight.92061.
7
Sequence artifacts in DNA from formalin-fixed tissues: causes and strategies for minimization.福尔马林固定组织中 DNA 的序列人为假象：原因与最小化策略。
Clin Chem. 2015 Jan;61(1):64-71. doi: 10.1373/clinchem.2014.223040. Epub 2014 Nov 24.
8
Whole-exome sequencing studies of parathyroid carcinomas reveal novel PRUNE2 mutations, distinctive mutational spectra related to APOBEC-catalyzed DNA mutagenesis and mutational enrichment in kinases associated with cell migration and invasion.甲状旁腺癌的全外显子组测序研究揭示了新的PRUNE2突变、与载脂蛋白B编辑复合体催化的DNA诱变相关的独特突变谱以及与细胞迁移和侵袭相关激酶中的突变富集。
J Clin Endocrinol Metab. 2015 Feb;100(2):E360-4. doi: 10.1210/jc.2014-3238. Epub 2014 Nov 11.
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