Ultraviolet and ionizing radiation enhance the growth of BCCs and trichoblastomas in patched heterozygous knockout mice

被引:311
作者
Aszterbaum, M
Epstein, J
Oro, A
Douglas, V
LeBoit, PE
Scott, MP
Epstein, EH
机构
[1] Univ Calif San Francisco, Dept Dermatol, San Francisco, CA 94110 USA
[2] Stanford Univ, Dept Dermatol, Stanford, CA 94305 USA
[3] Univ Calif San Francisco, Dept Dermatol & Pathol, San Francisco, CA 94115 USA
[4] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[6] Stanford Univ, Sch Med, Howard Hughes Med Inst, Stanford, CA 94305 USA
关键词
D O I
10.1038/15242
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Basal cell carcinomas, the commonest human skin cancers, consistently have abnormalities of the hedgehog signaling pathway and often have PTCH gene mutations. We report here that Ptch(+/-) mice develop primordial follicular neoplasms resembling human trichoblastomas, and that exposure to ultraviolet radiation or ionizing radiation results in an increase in the number and size of these tumors and a shift in their histologic features so that they more closely resemble human basal cell carcinoma. The mouse basal cell carcinomas and trichoblastoma-like tumors resemble human basal cell carcinomas in their loss of normal hemidesmosomal components, presence of p53 mutations, frequent loss of the normal remaining Ptch allele, and activation of hedgehog target gene transcription. The Ptch mutant mice provide the first mouse model, to our knowledge, of ultraviolet and ionizing radiation-induced basal cell carcinoma-like tumors, and also demonstrate that Ptch inactivation and hedgehog target gene activation are essential for basal cell carcinoma tumorigenesis.
引用
收藏
页码:1285 / 1291
页数:7
相关论文
共 39 条
[1]   DEVELOPMENTAL EXPRESSION OF NICEIN ADHESION PROTEIN (LAMININ-5) SUBUNITS SUGGESTS MULTIPLE MORPHOGENIC ROLES [J].
ABERDAM, D ;
AGUZZI, A ;
BAUDOIN, C ;
GALLIANO, MF ;
ORTONNE, JP ;
MENEGUZZI, G .
CELL ADHESION AND COMMUNICATION, 1994, 2 (02) :115-129
[2]   Altered expression of the hemidesmosome-anchoring filament complex proteins in basal cell carcinoma: Possible role in the origin of peritumoral lacunae [J].
Bahadoran, P ;
Perrin, C ;
Aberdam, D ;
SpadaforaPisani, A ;
Meneguzzi, G ;
Ortonne, JP .
BRITISH JOURNAL OF DERMATOLOGY, 1997, 136 (01) :35-42
[3]  
BOGOVSKI P, 1994, TUMOURS MOUSE PATHOL, V2, P11
[4]   PARENTAL ORIGIN OF CHROMOSOME 9Q22.3-Q31 LOST IN BASAL-CELL CARCINOMAS FROM BASAL-CELL NEVUS SYNDROME PATIENTS [J].
BONIFAS, JM ;
BARE, JW ;
KERSCHMANN, RL ;
MASTER, SP ;
EPSTEIN, EH .
HUMAN MOLECULAR GENETICS, 1994, 3 (03) :447-448
[5]   Activation of the transcription factor Gli1 and the Sonic hedgehog signalling pathway in skin tumours [J].
Dahmane, N ;
Lee, J ;
Robins, P ;
Heller, P ;
Altaba, ARI .
NATURE, 1997, 389 (6653) :876-881
[6]  
DELLAPORTA G, 1960, J NATL CANCER I, V25, P573
[7]  
Epstein J.H., 1985, MODELS DERMATOLOGY, V2, P303
[8]  
EPSTEIN JH, 1965, J NATL CANCER I, V34, P741
[9]   EXPRESSION PATTERN OF THE BULLOUS PEMPHIGOID-180 ANTIGEN IN NORMAL AND NEOPLASTIC EPITHELIA [J].
FAIRLEY, JA ;
HEINTZ, PW ;
NEUBURG, M ;
DIAZ, LA ;
GIUDICE, GJ .
BRITISH JOURNAL OF DERMATOLOGY, 1995, 133 (03) :385-391
[10]   Relationship between sunlight exposure and a key genetic alteration in basal cell carcinoma [J].
Gailani, MR ;
Leffell, DJ ;
Ziegler, A ;
Gross, EG ;
Brash, DE ;
Bale, AE .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (06) :349-354