Telomere biology disorders

被引:52
作者
Kam, Michelle L. W. [1 ]
Nguyen, Trang T. T. [2 ]
Ngeow, Joanne Y. Y. [2 ,3 ]
机构
[1] Singapore Gen Hosp, Dept Resp & Crit Care Med, Singapore, Singapore
[2] Nanyang Technol Univ, Lee Kong Chian Sch Med, Singapore, Singapore
[3] Natl Canc Ctr, Canc Genet Serv, Div Med Oncol, Singapore, Singapore
关键词
IDIOPATHIC PULMONARY-FIBROSIS; RECESSIVE DYSKERATOSIS-CONGENITA; GRANULOCYTE-STIMULATING FACTOR; BONE-MARROW-TRANSPLANTATION; SEVERE APLASTIC-ANEMIA; LIVER-TRANSPLANTATION; REVERSE-TRANSCRIPTASE; HEPATOPULMONARY SYNDROME; INHIBITOR IMETELSTAT; LUNG TRANSPLANTATION;
D O I
10.1038/s41525-021-00198-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Telomere biology disorders (TBD) are a heterogeneous group of diseases arising from germline mutations affecting genes involved in telomere maintenance. Telomeres are DNA-protein structures at chromosome ends that maintain chromosome stability; their length affects cell replicative potential and senescence. A constellation of bone marrow failure, pulmonary fibrosis, liver cirrhosis and premature greying is suggestive, however incomplete penetrance results in highly variable manifestations, with idiopathic pulmonary fibrosis as the most common presentation. Currently, the true extent of TBD burden is unknown as there is no established diagnostic criteria and the disorder often is unrecognised and underdiagnosed. There is no gold standard for measuring telomere length and not all TBD-related mutations have been identified. There is no specific cure and the only treatment is organ transplantation, which has poor outcomes. This review summarises the current literature and discusses gaps in understanding and areas of need in managing TBD.
引用
收藏
页数:13
相关论文
共 100 条
[1]   Exome Sequencing Identifies Mutant TINF2 in a Family With Pulmonary Fibrosis [J].
Alder, Jonathan K. ;
Stanley, Susan E. ;
Wagner, Christa L. ;
Hamilton, Makenzie ;
Hanumanthu, Vidya Sagar ;
Armanios, Mary .
CHEST, 2015, 147 (05) :1361-1368
[2]  
Allen RJ, 2017, LANCET RESP MED, V5, P869, DOI [10.1016/S2213-2600(17)30387-9, 10.1016/s2213-2600(17)30387-9]
[3]   Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita [J].
Alter, Blanche P. ;
Baerlocher, Gabriela M. ;
Savage, Sharon A. ;
Chanock, Stephen J. ;
Weksler, Babette B. ;
Willner, Judith P. ;
Peters, June A. ;
Giri, Neelarn ;
Lansdorp, Peter M. .
BLOOD, 2007, 110 (05) :1439-1447
[4]   Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up [J].
Alter, Blanche P. ;
Giri, Neelam ;
Savage, Sharon A. ;
Rosenberg, Philip S. .
HAEMATOLOGICA, 2018, 103 (01) :30-39
[5]   Telomerase mutations in families with idiopathic pulmonary fibrosis [J].
Armanios, Mary Y. ;
Chen, Julian J. -L. ;
Cogan, Joy D. ;
Alder, Jonathan K. ;
Ingersoll, Roxann G. ;
Markin, Cheryl ;
Lawson, William E. ;
Xie, Mingyi ;
Vulto, Irma ;
Phillips, John A., III ;
Lansdorp, Peter M. ;
Greider, Carol W. ;
Loyd, James E. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (13) :1317-1326
[6]   Therapeutic effect of androgen therapy in a mouse model of aplastic anemia produced by short telomeres [J].
Baer, Christian ;
Huber, Nicolas ;
Beier, Fabian ;
Blasco, Maria A. .
HAEMATOLOGICA, 2015, 100 (10) :1267-1274
[7]   Extensive allelic variation and ultrashort telomeres in senescent human cells [J].
Baird, DM ;
Rowson, J ;
Wynford-Thomas, D ;
Kipling, D .
NATURE GENETICS, 2003, 33 (02) :203-207
[8]   Telomerase gene therapy rescues telomere length, bone marrow aplasia, and survival in mice with aplastic anemia [J].
Bar, Christian ;
Manuel Povedano, Juan ;
Serrano, Rosa ;
Benitez-Buelga, Carlos ;
Popkes, Miriam ;
Formentini, Ivan ;
Bobadilla, Maria ;
Bosch, Fatima ;
Blasco, Maria A. .
BLOOD, 2016, 127 (14) :1770-1779
[9]   Pirfenidone Therapy for Familial Pulmonary Fibrosis: A Real-Life Study [J].
Bennett, David ;
Refini, Rosa Metella ;
Valentini, Maria Lucia ;
Fui, Annalisa ;
Fossi, Antonella ;
Pieroni, Maria ;
Mazzei, Maria Antonietta ;
Rottoli, Paola .
LUNG, 2019, 197 (02) :147-153
[10]   The molecular genetics of the telomere biology disorders [J].
Bertuch, Alison A. .
RNA BIOLOGY, 2016, 13 (08) :696-706