ASXL3 gene mutations inhibit cell proliferation and promote cell apoptosis in mouse cardiomyocytes by upregulating lncRNA NONMMUT063967.2

Biochemistry and Biophysics Reports - Tập 35 - Trang 101505 - 2023
Zequn Liu1, Yanmin Jiang2, Fu Fang1, Ru Li1, Jin Han1, Xin Yang1, Qiong Deng1, Lu-Shan Li1, Ting-ying Lei1, Dong-Zhi Li1, Can Liao1
1Department of Prenatal Diagnostic Center, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, Guangdong, China
2Institute of Obstetrics and Gynecology, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, Guangzhou, 510623, Guangdong, China

Tài liệu tham khảo

van der Linde, 2011, Birth prevalence of congenital heart disease worldwide: a systematic review and meta-analysis, J. Am. Coll. Cardiol., 58, 2241, 10.1016/j.jacc.2011.08.025 Brida, 2022, Heart failure in adults with congenital heart disease, Int. J. Cardiol., 357, 39, 10.1016/j.ijcard.2022.03.018 Lu, 2022, Heart failure and patient-reported outcomes in adults with congenital heart disease from 15 countries, J. Am. Heart Assoc., 11, 10.1161/JAHA.121.024993 Farr, 2022, Adult survivors of moderate and great complexity congenital heart disease undergoing general surgery procedures: how do they fare?, Am. J. Surg., 223, 841, 10.1016/j.amjsurg.2021.08.021 Parikh, 2019, Incidence of ESKD and mortality among children with congenital heart disease after cardiac surgery, Clin. J. Am. Soc. Nephrol., 14, 1450, 10.2215/CJN.00690119 Brock, 2019, Atrial fibrillation in adults with congenital heart disease following cardiac surgery in a single center: analysis of incidence and risk factors, Congenit. Heart Dis., 14, 924, 10.1111/chd.12857 Giri, 2017, Novel compound heterozygous ASXL3 mutation causing Bainbridge-ropers like syndrome and primary IGF1 deficiency, Int. J. Pediatr. Endocrinol., 2017, 8, 10.1186/s13633-017-0047-9 Duployez, 2016, Unlike ASXL1 and ASXL2 mutations, ASXL3 mutations are rare events in acute myeloid leukemia with t(8;21, Leuk. Lymphoma, 57, 199, 10.3109/10428194.2015.1037754 Wayhelova, 2019, Novel de novo frameshift variant in the ASXL3 gene in a child with microcephaly and global developmental delay, Mol. Med. Rep., 20, 505 Zhang, 2021, Alteration of long non-coding RNAs and mRNAs expression profiles by compound heterozygous ASXL3 mutations in the mouse brain, Bioengineered, 12, 6935, 10.1080/21655979.2021.1974811 Fu, 2021, Compound heterozygous mutation of the ASXL3 gene causes autosomal recessive congenital heart disease, Hum. Genet., 140, 333, 10.1007/s00439-020-02200-z Xu, 2022, Emerging role of LncRNAs in autoimmune, Lupus, Inflammation., 45, 937, 10.1007/s10753-021-01607-8 Kichi, 2022, The emerging role of EMT-related lncRNAs in therapy resistance and their applications as biomarkers, Curr. Med. Chem., 29, 4574, 10.2174/0929867329666220329203032 Nociti, 2021, What do we know about the role of lncRNAs in multiple sclerosis?, Neural Regen Res, 16, 1715, 10.4103/1673-5374.306061 Okuyan, 2022, LncRNAs in osteoarthritis, Clin. Chim. Acta, 532, 145, 10.1016/j.cca.2022.05.030 Ye, 2021, Potential therapeutic targeting of lncRNAs in cholesterol homeostasis, Front Cardiovasc Med, 8, 10.3389/fcvm.2021.688546 Shefler, 2022, Skin-expressing lncRNAs in inflammatory responses, Front. Genet., 13, 10.3389/fgene.2022.835740 Marguerie, 2006, Congenital heart defects in Fgfr2-IIIb and Fgf10 mutant mice, Cardiovasc. Res., 71, 50, 10.1016/j.cardiores.2006.03.021 Huang, 2022, MicroRNA-338-3p as a therapeutic target in cardiac fibrosis through FGFR2 suppression, J. Clin. Lab. Anal., 36, 10.1002/jcla.24584 Mundhofir, 2013, p.Ser252Trp and p.Pro253Arg mutations in FGFR2 gene causing Apert syndrome: the first clinical and molecular report of Indonesian patients, Singap. Med. J., 54, e72, 10.11622/smedj.2013055 Ali, 2020, Beyond the RNA-dependent function of LncRNA genes, Elife, 9, 10.7554/eLife.60583 Panni, 2020, Non-coding RNA regulatory networks, Biochim Biophys Acta Gene Regul Mech, 1863, 10.1016/j.bbagrm.2019.194417 Toni, 2020, Dysregulated micro-RNAs and long noncoding RNAs in cardiac development and pediatric heart failure, Am. J. Physiol. Heart Circ. Physiol., 318, H1308, 10.1152/ajpheart.00511.2019 Touma, 2016, Decoding the long noncoding RNA during cardiac maturation: a roadmap for functional discovery, Circ Cardiovasc Genet, 9, 395, 10.1161/CIRCGENETICS.115.001363 Kim, 2021, Spatiotemporal expression of long noncoding RNA Moshe modulates heart cell lineage commitment, RNA Biol., 18, 640, 10.1080/15476286.2021.1976549 Ma, 2021, Long non-coding RNA SAP30-2:1 is downregulated in congenital heart disease and regulates cell proliferation by targeting HAND2, Front. Med., 15, 91, 10.1007/s11684-020-0778-5 Lu, 2021, Knockdown of long noncoding RNA SNHG14 protects H9c2 cells against hypoxia-induced injury by modulating miR-25-3p/KLF4 Axis in vitro, J. Cardiovasc. Pharmacol., 77, 334, 10.1097/FJC.0000000000000965 Zhu, 2018, Long noncoding RNA TUG1 promotes cardiac fibroblast transformation to myofibroblasts via miR-29c in chronic hypoxia, Mol. Med. Rep., 18, 3451