Emerging evidence on the pathobiology of mucositis

被引:105
作者
Al-Dasooqi, Noor [1 ]
Sonis, Stephen T. [2 ]
Bowen, Joanne M. [3 ]
Bateman, Emma [1 ]
Blijlevens, Nicole [4 ]
Gibson, Rachel J. [5 ]
Logan, Richard M. [6 ]
Nair, Raj G. [7 ,8 ]
Stringer, Andrea M. [9 ]
Yazbeck, Roger [9 ]
Elad, Sharon [10 ]
Lalla, Rajesh V. [11 ,12 ]
机构
[1] Univ Adelaide, Discipline Med, Adelaide, SA 5000, Australia
[2] Brigham & Womens Hosp, Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Univ Adelaide, Discipline Physiol, Adelaide, SA 5000, Australia
[4] Univ Med Ctr Nijmegen, Dept Haematol, NL-6500 HB Nijmegen, Netherlands
[5] Univ Adelaide, Discipline Anat & Pathol, Adelaide, SA 5000, Australia
[6] Univ Adelaide, Sch Dent, Adelaide, SA 5005, Australia
[7] Griffith Univ, Discipline Oral Med, Gold Coast, Qld, Australia
[8] Queensland Hlth, Dept Haematol & Oncol, Gold Coast, Qld, Australia
[9] Univ S Australia, Sch Pharm & Med Sci, Adelaide, SA 5001, Australia
[10] Univ Rochester, Med Ctr, Div Oral Med, Eastman Inst Oral Hlth, Rochester, NY 14642 USA
[11] Univ Connecticut, Ctr Hlth, Sect Oral Med, Farmington, CT 06030 USA
[12] Univ Connecticut, Ctr Hlth, Neag Comprehens Canc Ctr, Farmington, CT 06030 USA
关键词
Mucosal injury; Cancer therapy; Targeted drugs; Toxicity; Alimentary tract; Pharmacogenetics; NF-KAPPA-B; ALIMENTARY-TRACT MUCOSITIS; CYCLOOXYGENASE-2; COX-2; EXPRESSION; TIGHT JUNCTION PERMEABILITY; METASTATIC BREAST-CANCER; PRO-INFLAMMATORY CYTOKINES; STEM-CELL TRANSPLANTATION; INDUCED ORAL MUCOSITIS; DARK AGOUTI RAT; MUCOSAL INJURY;
D O I
10.1007/s00520-013-1900-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Background Considerable progress has been made in our understanding of the biological basis for cancer therapy-induced mucosal barrier injury (mucositis). The last formal review of the subject by MASCC/ISOO was published in 2007; consequently, an update is timely. Methods Panel members reviewed the biomedical literature on mucositis pathobiology published between January 2005 and December 2011. Results Recent research has provided data on the contribution of tissue structure changes, inflammation and microbiome changes to the development of mucositis. Additional research has focused on targeted therapy-induced toxicity, toxicity clustering and the investigation of genetic polymorphisms in toxicity prediction. This review paper summarizes the recent evidence on these aspects of mucositis pathobiology. Conclusion The ultimate goal of mucositis researchers is to identify the most appropriate targets for therapeutic interventions and to be able to predict toxicity risk and personalize interventions to genetically suitable patients. Continuing research efforts are needed to further our understanding of mucositis pathobiology and the pharmacogenomics of toxicity.
引用
收藏
页码:3233 / 3241
页数:9
相关论文
共 107 条
[1]
Afshar S, 2002, INT ASS DENT RES M
[2]
Irinotecan-induced alterations in intestinal cell kinetics and extracellular matrix component expression in the dark agouti rat [J].
Al-Dasooqi, Noor ;
Bowen, Joanne M. ;
Gibson, Rachel J. ;
Logan, Richard M. ;
Stringer, Andrea M. ;
Keefe, Dorothy M. .
INTERNATIONAL JOURNAL OF EXPERIMENTAL PATHOLOGY, 2011, 92 (05) :357-365
[3]
Matrix metalloproteinases are possible mediators for the development of alimentary tract mucositis in the dark agouti rat [J].
Al-Dasooqi, Noor ;
Gibson, Rachel J. ;
Bowen, Joanne M. ;
Logan, Richard M. ;
Stringer, Andrea M. ;
Keefe, Dorothy M. .
EXPERIMENTAL BIOLOGY AND MEDICINE, 2010, 235 (10) :1244-1256
[4]
Trastuzumab induces gastrointestinal side effects in HER2-overexpressing breast cancer patients [J].
Al-Dasooqi, Noor ;
Bowen, Joanne M. ;
Gibson, Rachel J. ;
Sullivan, Thomas ;
Lees, Jude ;
Keefe, Dorothy M. .
INVESTIGATIONAL NEW DRUGS, 2009, 27 (02) :173-178
[5]
Mechanism of IL-1β-induced increase in intestinal epithelial tight junction permeability [J].
Al-Sadi, Rana ;
Ye, Dongmei ;
Dokladny, Karol ;
Ma, Thomas Y. .
JOURNAL OF IMMUNOLOGY, 2008, 180 (08) :5653-5661
[6]
IL-1β-Induced Increase in Intestinal Epithelial Tight Junction Permeability Is Mediated by MEKK-1 Activation of Canonical NF-κB Pathway [J].
Al-Sadi, Rana ;
Ye, Dongmei ;
Said, Hamid M. ;
Ma, Thomas Y. .
AMERICAN JOURNAL OF PATHOLOGY, 2010, 177 (05) :2310-2322
[7]
Personalized medicine for mucositis: Bayesian networks identify unique gene clusters which predict the response to gamma-D-glutamyl-L-tryptophan (SCV-07) for the attenuation of chemoradiation-induced oral mucositis [J].
Alterovitz, Gil ;
Tuthill, Cynthia ;
Rios, Israel ;
Modelska, Katharina ;
Sonis, Stephen .
ORAL ONCOLOGY, 2011, 47 (10) :951-955
[8]
New thoughts on the pathobiology of regimen-related mucosal injury [J].
Anthony, Lowell ;
Bowen, Joanne ;
Garden, Adam ;
Hewson, Ian ;
Sonis, Stephen .
SUPPORTIVE CARE IN CANCER, 2006, 14 (06) :516-518
[9]
A phase I/II double-blind, placebo-controlled study of recombinant human interleukin-11 for mucositis and acute GVHD prevention in allogeneic stem cell transplantation [J].
Antin, JH ;
Lee, SJ ;
Neuberg, D ;
Alyea, E ;
Soiffer, RJ ;
Sonis, S ;
Ferrara, JLM .
BONE MARROW TRANSPLANTATION, 2002, 29 (05) :373-377
[10]
Application of distance matrices to define associations between acute toxicities in colorectal cancer patients receiving chemotherapy [J].
Aprile, Giuseppe ;
Ramoni, Marco ;
Keefe, Dorothy ;
Sonis, Stephen .
CANCER, 2008, 112 (02) :284-292