Chromosome breakpoint distribution in nonmelanoma skin cancers


Autoria(s): Pavarino, E. C.; Rossit, ARB; Tajara, E. H.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/11/1997

Resumo

We have identified chromosome regions that may be sites of genes activated as a result of chromosomal rearrangements observed in 61 of the 86 skin tumors referenced in the literature. The data showed that most of the breakpoints were distributed throughout the genome and some tended to cluster. Highest frequencies of breakpoints were observed in chromosomes with high relative length, except chromosomes 14 and 15 that were more often affected in malignant tumors, despite their size. Our work provides a starting point for more detailed studies that may allow identification of these genes as important keys in the development and progression of skin cancers. (C) Elsevier B.V., 1997.

Formato

81-84

Identificador

http://dx.doi.org/10.1016/S0165-4608(96)00433-5

Cancer Genetics and Cytogenetics. New York: Elsevier B.V., v. 99, n. 1, p. 81-84, 1997.

0165-4608

http://hdl.handle.net/11449/36805

10.1016/S0165-4608(96)00433-5

WOS:A1997YC66200014

Idioma(s)

eng

Publicador

Elsevier B.V.

Relação

Cancer Genetics and Cytogenetics

Direitos

closedAccess

Tipo

info:eu-repo/semantics/article