A Dynamic Oral Cancer Field Unraveling the Underlying Biology and Its Clinical Implication

被引:24
作者
Tsui, Ivy F. L. [3 ,4 ]
Garnis, Cathie [2 ,4 ]
Poh, Catherine F. [1 ,3 ]
机构
[1] Univ British Columbia, Dept Oral Biol & Med Sci, Vancouver, BC V6T 1Z3, Canada
[2] Univ British Columbia, Dept Surg, Vancouver, BC V6T 1Z3, Canada
[3] Univ British Columbia, Dept Pathol & Lab Med, Vancouver, BC V6T 1Z3, Canada
[4] Univ British Columbia, Dept Canc Genet & Dev Biol, British Columbia Canc Res Ctr, Vancouver, BC V6T 1Z3, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
oral cancer; direct fluorescence visualization; field cancerization; clonality; SQUAMOUS-CELL CARCINOMA; COMMON CLONAL ORIGIN; NECK-CANCER; FLUORESCENCE VISUALIZATION; EPITHELIAL DYSPLASIA; PREMALIGNANT LESIONS; ARRAY CGH; HEAD; TUMORS; RISK;
D O I
10.1097/PAS.0b013e3181b669c2
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Oral cancer is a complex disease that is characterized by histologic and genetic heterogeneity. The evolution and progression of this disease is thought to result from the accumulation of alterations in molecular pathways. Although the oral cavity is accessible for routine screening of suspicious lesions, gene alterations are known to accrue in histologically normal tissues. Therefore, some cancer forerunners may remain undetected clinically or histologically. Recently emerging optical and molecular technologies have provided a powerful means for redefining the extent of the field of alteration. Often this means expanding upon regions detectable with standard white light approaches. In this report, we used a newly developed optical technique, direct fluorescence visualization, to define a contiguous field that extended beyond the margins of a clinically visible oral squamous cell carcinoma. Multiple biopsies were taken within this contiguous optically altered field. Genome alterations detected for each specimen were compared to define whether each lesion arose independently or as a consequence of a shared progenitor cell. Our results indicate that the field effect of oral cancer is extremely dynamic, with different genetic alterations present in different biopsies within a field. This case study also demonstrated that 2 genetically unrelated squamous cell carcinoma could be developed within 10 mm at the right lateral tongue of this patient. These findings provide evidence for the importance to implement optical technologies in defining surgical margins and support the use of whole genome technologies in the diagnosis of clonal versus independent lesions of the oral cavity, which may have implications on treatment strategies.
引用
收藏
页码:1732 / 1738
页数:7
相关论文
共 42 条
[1]   Oral white lesions with special reference to precancerous and tobacco related lesions: Conclusions of an international symposium held in Uppsala, Sweden, May 18-21 1994 [J].
Axell, T ;
Pindborg, JJ ;
Smith, CJ ;
vanderWaal, I .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1996, 25 (02) :49-54
[2]   Multiple microalterations detected at high frequency in oral cancer [J].
Baldwin, C ;
Garnis, C ;
Zhang, LW ;
Rosin, MP ;
Lam, WL .
CANCER RESEARCH, 2005, 65 (17) :7561-7567
[3]   Proliferative verrucous leukoplakia and its related lesions [J].
Batsakis, JG ;
Suarez, P ;
El-Naggar, AK .
ORAL ONCOLOGY, 1999, 35 (04) :354-359
[4]  
Bedi GC, 1996, CANCER RES, V56, P2484
[5]   Expanding fields of genetically altered cells in head and neck squamous carcinogenesis [J].
Braakhuis, BJM ;
Leemans, CR ;
Brakenhoff, RH .
SEMINARS IN CANCER BIOLOGY, 2005, 15 (02) :113-120
[6]  
Braakhuis BJM, 2003, CANCER RES, V63, P1727
[7]   Second field tumors: A new opportunity for cancer prevention? [J].
Braakhuis, BJM ;
Brakenhoff, RH ;
Leemans, CR .
ONCOLOGIST, 2005, 10 (07) :493-500
[8]   MOLECULAR ASSESSMENT OF HISTOPATHOLOGICAL STAGING IN SQUAMOUS-CELL CARCINOMA OF THE HEAD AND NECK [J].
BRENNAN, JA ;
MAO, L ;
HRUBAN, RH ;
BOYLE, JO ;
EBY, YJ ;
KOCH, WM ;
GOODMAN, SN ;
SIDRANSKY, D .
NEW ENGLAND JOURNAL OF MEDICINE, 1995, 332 (07) :429-435
[9]   Defining Genomic Alteration Boundaries for a Combined Small Cell and Non-small Cell Lung Carcinoma [J].
Buys, Timon P. H. ;
Aviel-Ronen, Sarit ;
Waddell, Thomas K. ;
Lam, Wan L. ;
Tsao, Ming-Sound .
JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (02) :227-239
[10]  
Califano J, 1996, CANCER RES, V56, P2488