Genetics and Genomics of Chronic Pancreatitis with a Focus on Disease Biology and Molecular Pathogenesis

被引:3
作者
Khan, Erum [1 ]
Chakrabarty, Soura [2 ]
Shariff, Sanobar [3 ]
Bardhan, Mainak [4 ,5 ]
机构
[1] Univ Alabama Birmingham, Alzheimers Dis Res Ctr, Dept Neurol, Birmingham, AL USA
[2] Univ Cambridge, Dept Pathol, Cambridge, England
[3] Yerevan State Med Univ, Yerevan, Armenia
[4] Baptist Hlth South Florida, Miami Canc Inst, Dept Med Oncol, Miami, FL USA
[5] Baptist Hlth South Florida, Miami Canc Inst, Dept Med Oncol, Miami, FL 33176 USA
来源
GLOBAL MEDICAL GENETICS | 2023年 / 10卷 / 04期
关键词
pancreatitis; chronic pancreatitis; genetics; genomics; CATIONIC TRYPSINOGEN GENE; CLEAVAGE SITE MUTATION; NECROSIS-FACTOR-ALPHA; TNF-ALPHA; ALCOHOL-DEHYDROGENASE; OXIDATIVE STRESS; CYSTIC-FIBROSIS; RISK; POLYMORPHISMS; VARIANTS;
D O I
10.1055/s-0043-1776981
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chronic pancreatitis is a long-term fibroinflammatory condition of the pancreas with varying incidences across countries. The recent increase in its occurrence implies the involvement of genetic, hereditary, and unconventional risk factors. However, there is a lack of updated literature on recent advances in genetic polymorphisms of chronic pancreatitis. Therefore, this review aims to present recent findings on the genetic implications of chronic pancreatitis based on individual gene mechanisms and to discuss epigenetics and epistasis involved in the disease. Four mechanisms have been implicated in the pathogenesis of chronic pancreatitis, including premature activation of proteases, endoplasmic reticulum stress, ductal pathway dysfunction, and inflammatory pathway dysfunction. These mechanisms involve genes such as PRSS1, PRSS2, SPINK, CEL, PNLIP, PNLIPRP2, CFTR, CaSR, CLDN2, Alpha 1 antitrypsin, and GGT1 . Studying genetic polymorphisms on the basis of altered genes and their products may aid clinicians in identifying predispositions in patients with and without common risk factors. Further research may also identify associations between genetic predispositions and disease staging or prognosis, leading to personalized treatment protocols and precision medicine.
引用
收藏
页码:324 / 334
页数:11
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