Cell, tissue and organ culture as in vitro models to study the biology of squamous cell carcinomas of the head and neck

被引:105
作者
Sacks, PG
机构
[1] Head and Neck Service, Department of Surgery, Mem. Sloan-Kettering Cancer Center, New York
[2] Mem. Sloan-Kettering Cancer Center, New York, NY 10021
关键词
epithelial cells; squamous cell carcinoma; premalignant; cell culture; in vitro;
D O I
10.1007/BF00049486
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In vitro models are currently being used to study head and neck squamous cell carcinoma (HNSCC). Several hundred HNSCC cell lines have been established by various investigators and used to study a broad spectrum of questions related to head and neck cancer. The head and neck model with respect to multistage carcinogenesis is now complete. Several techniques exist for the culture of normal epithelial cells from the upper aerodigestive tract (UADT). The biology of these UADT cells (oral cavity, oropharynx, hypopharynx and larynx) is being studied. Successful culture of premalignant lesions (dysplastic mucosa, leukoplakia, erythroplakia) has resulted in establishment of a limited number of premalignant cell lines and cell cultures. HPV infection of normal oral epithelial cells for immortalization (similar to premalignant cells) coupled with transformation with carcinogens (malignant cells) has established an experimental model for progression. Two in vivo models for oral carcinogenesis, the 7,12 dimethylbenz(a)anthracene-induced hamster cheek pouch model and the 4-nitroquinoline-N-oxide rat oral model, have been established in culture. Thus, multistage carcinogenesis models have been established from both human tissues and animal models and include cultures of normal, premalignant and malignant cells. Culture techniques for growing dissociated primary tumor cells for short term experimental analysis are being used. The culture of normal or tumor tissue as organ/explant cultures allows for the maintenance of normal cell-cell and cell-matrix interactions, but limits experimentation since these cultures cannot be propagated. Several three dimensional model systems are being used to obtain this histological complexity but allow for experimentation. The ability to culture normal, premalignant and malignant cells coupled with the use of a variety of culture techniques, should allow for the continued growth and experimentation in head and neck cancer research.
引用
收藏
页码:27 / 51
页数:25
相关论文
共 278 条
[1]   PROGRESSIVE DYSPLASIA AND ANEUPLOIDY ARE HALLMARKS OF MOUSE SKIN PAPILLOMAS - RELEVANCE TO MALIGNANCY [J].
ALDAZ, CM ;
CONTI, CJ ;
KLEINSZANTO, AJP ;
SLAGA, TJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (07) :2029-2032
[2]   HUMAN-EPIDERMIS RECONSTRUCTED BY CULTURE - IS IT NORMAL [J].
ASSELINEAU, D ;
BERNARD, BA ;
BAILLY, C ;
DARMON, M ;
PRUNIERAS, M .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1986, 86 (02) :181-186
[3]  
BAICI A, 1985, EXP CELL BIOL, V53, P213
[4]  
BAKER SR, 1985, LARYNGOSCOPE, V95, P43
[5]   STUDIES OF VARIATION IN INHERENT SENSITIVITIES TO RADIATION, 5-FLUOROURACIL AND METHOTREXATE IN A SERIES OF HUMAN AND MURINE TUMOR-CELL LINES INVITRO [J].
BELLAMY, AS ;
WHELAN, RDH ;
HILL, BT .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1984, 10 (01) :87-93
[6]  
BIJMAN JT, 1987, ANTICANCER RES, V7, P147
[7]   THE INTERACTION OF EPIDERMAL GROWTH-FACTOR AND RADIATION IN HUMAN HEAD AND NECK SQUAMOUS-CELL CARCINOMA CELL-LINES WITH VASTLY DIFFERENT RADIOSENSITIVITIES [J].
BONNER, JA ;
MAIHLE, NJ ;
FOLVEN, BR ;
CHRISTIANSON, TJH ;
SPAIN, K .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1994, 29 (02) :243-247
[8]  
BOUKAMP P, 1985, CANCER RES, V45, P5582
[9]   CALCIUM-REGULATED DIFFERENTIATION OF NORMAL HUMAN EPIDERMAL-KERATINOCYTES IN CHEMICALLY DEFINED CLONAL CULTURE AND SERUM-FREE SERIAL CULTURE [J].
BOYCE, ST ;
HAM, RG .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1983, 81 (01) :S33-S40
[10]   INVITRO ANTIPROLIFERATIVE AND METABOLIC-ACTIVITY OF 8 NOVEL 5-FLUORINATED URACIL NUCLEOSIDES [J].
BRAAKHUIS, BJM ;
VISSER, GWM ;
STRINGER, I ;
PETERS, GJ .
EUROPEAN JOURNAL OF CANCER, 1991, 27 (03) :250-253