Genomic instability after allogeneic hematopoietic cell transplantation is frequent in oral mucosa, particularly in patients with a history of chronic graft-versus-host disease, and rare in nasal mucosa

被引:26
作者
Khan, Faisal M. [1 ,2 ]
Sy, Sarah [1 ]
Louie, Polly [1 ,2 ]
Ugarte-Torres, Alejandra [1 ]
Berka, Noureddine [1 ]
Sinclair, Gary D. [1 ]
Stewart, Douglas A. [1 ,2 ]
Russell, James A. [1 ,2 ]
Storek, Jan [1 ,2 ]
机构
[1] Univ Calgary, Calgary, AB, Canada
[2] Alberta Hlth Serv, Calgary, AB, Canada
基金
加拿大创新基金会;
关键词
BONE-MARROW-TRANSPLANTATION; MICROSATELLITE INSTABILITY; SOLID CANCERS; TETRANUCLEOTIDE REPEATS; DNA-DAMAGE; EXPRESSION; EPITHELIUM; MUTATIONS; NEOPLASIA;
D O I
10.1182/blood-2009-10-249201
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genomic instability (GI) of cells may lead to their malignant transformation. Carcinoma after hematopoietic cell transplantation (HCT) frequently involves some (eg, oral) but not other (eg, nasal) epithelia. We examined GI in oral and nasal mucosal specimens from 105 subjects, including short-term (7-98 days, n = 32) and long-term (4-22 yrs, n = 25) allogeneic HCT survivors. Controls included autologous HCT survivors (n = 11), patients treated with chemotherapy without HCT (n = 9) and healthy controls (n = 27). GI was detected in 60% oral versus only 4% nasal specimens in long-term allogeneic HCT survivors (P < .001). None of the controls showed GI. In oral specimens, GI was significantly associated with history of oral chronic graft-versus-host disease (cGVHD). We conclude that GI after HCT is frequent in some (oral) but rare in other (nasal) epithelia. This may explain why some epithelia (especially those involved with cGVHD) are prone to develop cancer. (Blood. 2010; 116(10):1803-1806)
引用
收藏
页码:1803 / 1806
页数:4
相关论文
共 20 条
[1]   Genome instability:: a mechanistic view of its causes and consequences [J].
Aguilera, Andres ;
Gomez-Gonzalez, Belen .
NATURE REVIEWS GENETICS, 2008, 9 (03) :204-217
[2]  
Ahrendt SA, 2000, CANCER RES, V60, P2488
[3]   Solid cancers after bone marrow transplantation [J].
Bhatia, S ;
Louie, AD ;
Bhatia, R ;
O'Donnell, MR ;
Fung, H ;
Kashyap, A ;
Krishnan, A ;
Molina, A ;
Nademanee, A ;
Niland, JC ;
Parker, PA ;
Snyder, DS ;
Spielberger, R ;
Stein, A ;
Forman, SJ .
JOURNAL OF CLINICAL ONCOLOGY, 2001, 19 (02) :464-471
[4]   Oxidative stress inactivates the human DNA mismatch repair system [J].
Chang, CL ;
Marra, G ;
Chauhan, DP ;
Ha, HT ;
Chang, DK ;
Ricciardiello, L ;
Randolph, A ;
Carethers, JM ;
Boland, CR .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2002, 283 (01) :C148-C154
[5]   Genomic instability and cancer [J].
Charames, GS ;
Bapat, B .
CURRENT MOLECULAR MEDICINE, 2003, 3 (07) :589-596
[6]  
Choi ICY, 2001, HAEMATOLOGICA, V86, P972
[7]   Impact of chronic GVHD therapy on the development of squamous-cell cancers after hematopoietic stem-cell transplantation:: an international case-control study [J].
Curtis, RE ;
Metayer, C ;
Rizzo, JD ;
Socié, G ;
Sobocinski, KA ;
Flowers, MED ;
Travis, WD ;
Travis, LB ;
Horowitz, MM ;
Deeg, HJ .
BLOOD, 2005, 105 (10) :3802-3811
[8]   Solid cancers after bone marrow transplantation [J].
Curtis, RE ;
Rowlings, PA ;
Deeg, HJ ;
Shriner, DA ;
Socie, G ;
Travis, LB ;
Horowitz, MM ;
Witherspoon, RP ;
Hoover, RN ;
Sobocinski, KA ;
Fraumeni, JF ;
Boice, JD .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (13) :897-904
[9]  
Dietmaier W, 1997, CANCER RES, V57, P4749
[10]   Frequent genomic alterations in epithelium measured by microsatellite instabihty following allogeneic hematopoietic cell transplantation in humans [J].
Faber, P ;
Fisch, P ;
Waterhouse, M ;
Schmitt-Graff, A ;
Bertz, H ;
Finke, J ;
Spyridonidis, A .
BLOOD, 2006, 107 (08) :3389-3396