Update on familial cancer syndromes and the skin

被引:53
作者
Tsao, H [1 ]
机构
[1] Massachusetts Gen Hosp, Dept Dermatol, Boston, MA 02114 USA
关键词
D O I
10.1016/S0190-9622(00)90285-8
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Familial cancer syndromes reflect an inherited predisposition to develop benign and malignant tumors. Clinically the cancers occur at an earlier age and involve multiple foci of tumor formation at multiple sites. In the past 10 years, the molecular basis of many of these cancer syndromes have been unraveled with the advent of powerful genetic technologies. Entities which were hypothesized to be related on the basis of clinical features have now been shown to be linked or disparate through genetic analysis. This article reviews some of the recent advances in the clinical and molecular aspects of familial cancer syndromes that involve the skin.
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收藏
页码:939 / 969
页数:31
相关论文
共 308 条
[1]   MAMMALIAN DNA NUCLEOTIDE EXCISION-REPAIR RECONSTITUTED WITH PURIFIED PROTEIN-COMPONENTS [J].
ABOUSSEKHRA, A ;
BIGGERSTAFF, M ;
SHIVJI, MKK ;
VILPO, JA ;
MONCOLLIN, V ;
PODUST, VN ;
PROTIC, M ;
HUBSCHER, U ;
EGLY, JM ;
WOOD, RD .
CELL, 1995, 80 (06) :859-868
[2]   Germline mutations of the MEN1 gene in familial multiple endocrine neoplasia type 1 and related states [J].
Agarwal, SK ;
Kester, MB ;
Debelenko, LV ;
Heppner, C ;
EmmertBuck, MR ;
Skarulis, MC ;
Doppman, JL ;
Kim, YS ;
Lubensky, IA ;
Zhuang, ZP ;
Green, JS ;
Guru, SC ;
Manickam, P ;
Olufemi, SE ;
Liotta, LA ;
Chandrasekharappa, SC ;
Collins, FS ;
Spiegel, AM ;
Burns, AL ;
Marx, SJ .
HUMAN MOLECULAR GENETICS, 1997, 6 (07) :1169-1175
[3]  
Al-Saleem T, 1998, CANCER-AM CANCER SOC, V83, P2208, DOI 10.1002/(SICI)1097-0142(19981115)83:10<2208::AID-CNCR21>3.0.CO
[4]  
2-K
[5]   Mutations in the TSC1 gene account for a minority of patients with tuberous sclerosis [J].
Ali, JBM ;
Sepp, T ;
Ward, S ;
Green, AJ ;
Yates, JRW .
JOURNAL OF MEDICAL GENETICS, 1998, 35 (12) :969-972
[6]   Growth rate characteristics of acoustic neuromas associated with neurofibromatosis type 2 [J].
Abaza, MM ;
Makariou, E ;
Armstrong, M ;
Lalwani, AK .
LARYNGOSCOPE, 1996, 106 (06) :694-699
[7]  
ARGENYI ZB, 1994, J CUTAN PATHOL, V21, P549
[8]   Identification of mutations in the human PATCHED gene in sporadic basal cell carcinomas and in patients with the basal cell nevus syndrome [J].
Aszterbaum, M ;
Rothman, A ;
Johnson, RL ;
Fisher, M ;
Xie, JW ;
Bonifas, JM ;
Zhang, XL ;
Scott, MP ;
Epstein, EH .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1998, 110 (06) :885-888
[9]   A SYNDROME OF VARIOUS CUTANEOUS PIGMENTED LESIONS, MYXOID NEUROFIBROMATA AND ATRIAL-MYXOMA - THE NAME SYNDROME [J].
ATHERTON, DJ ;
PITCHER, DW ;
WELLS, RS ;
MACDONALD, DM .
BRITISH JOURNAL OF DERMATOLOGY, 1980, 103 (04) :421-429
[10]   Point mutations causing Bloom's syndrome abolish ATPase and DNA helicase activities of the BLM protein [J].
Bahr, A ;
De Graeve, F ;
Kedinger, C ;
Chatton, B .
ONCOGENE, 1998, 17 (20) :2565-2571