Heterogeneous lack of expression of the tumour suppressor PTEN protein in human neoplastic tissues

被引:42
作者
Torres, J
Navarro, S
Roglá, I
Ripoll, F
Lluch, A
García-Conde, J
Llombart-Bosch, A
Cervera, J
Pulido, R
机构
[1] Inst Invest Citol, Valencia 46010, Spain
[2] Univ Valencia, Dept Patol, Valencia, Spain
[3] Univ Valencia, Hosp Clin Valencia, Serv Oncol & Hematol, Valencia, Spain
关键词
PTEN; tumour suppressor; cancer; protein phosphatases;
D O I
10.1016/S0959-8049(00)00366-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PTEN, a tumour suppressor gene located at chromosome 10q23 and commonly mutated or deleted in a variety of tumours, encodes a dual-specific/phosphatidylinositol-3,4,5-triphosphate (PIP3) phosphatase. We report the generation of an anti-PTEN monoclonal antibody (MAb) that recognises an epitope at the C-terminus of PTEN, and describe the heterogeneous lack of expression of the PTEN protein in human tumour tissues, as demonstrated by immunohistochemical methods. Our anti-PTEN MAb provides a useful tool for the study of PTEN protein expression in tumour samples, in the search for tumour prognostic molecular markers. (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:114 / 121
页数:8
相关论文
共 47 条
[1]   Mutational spectra of PTEN/MMAC1 gene: a tumor suppressor with lipid phosphatase activity [J].
Ali, IU ;
Schriml, LM ;
Dean, M .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (22) :1922-1932
[2]   New insights into tumor suppression: PTEN suppresses tumor formation by restraining the phosphoinositide 3-kinase AKT pathway [J].
Cantley, LC ;
Neel, BG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4240-4245
[3]   PTEN/MMAC1 mutations in primary glioblastomas and short-term cultures of malignant gliomas [J].
Chiariello, E ;
Roz, L ;
Albarosa, R ;
Magnani, I ;
Finocchiaro, G .
ONCOGENE, 1998, 16 (04) :541-545
[4]   PTEN is inversely correlated with the cell survival factor Akt/PKB and is inactivated via multiple mechanisms in haematological malignancies [J].
Dahia, PLM ;
Aguiar, RCT ;
Alberta, J ;
Kum, JB ;
Caron, S ;
Sill, H ;
Marsh, DJ ;
Ritz, J ;
Freedman, A ;
Stiles, C ;
Eng, C .
HUMAN MOLECULAR GENETICS, 1999, 8 (02) :185-193
[5]  
Davies MA, 1998, CANCER RES, V58, P5285
[6]   Impaired Fas response and autoimmunity in Pten+/- mice [J].
Di Cristofano, A ;
Kotsi, P ;
Peng, YF ;
Cordon-Cardo, C ;
Elkon, KB ;
Pandolfi, PP .
SCIENCE, 1999, 285 (5436) :2122-2125
[7]   Pten is essential for embryonic development and tumour suppression [J].
Di Cristofano, A ;
Pesce, B ;
Cordon-Cardo, C ;
Pandolfi, PP .
NATURE GENETICS, 1998, 19 (04) :348-355
[8]   Growth suppression of glioma cells by PTEN requires a functional phosphatase catalytic domain [J].
Furnari, FB ;
Lin, H ;
Huang, HJS ;
Cavenee, WK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (23) :12479-12484
[9]   The tumor-suppressor activity of PTEN is regulated by its carboxyl-terminal region [J].
Georgescu, MM ;
Kirsch, KH ;
Akagi, T ;
Shishido, T ;
Hanafusa, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (18) :10182-10187
[10]   Differential nuclear and cytoplasmic expression of PTEN in normal thyroid tissue, and benign and malignant epithelial thyroid tumors [J].
Gimm, O ;
Perren, A ;
Weng, LP ;
Marsh, DJ ;
Yeh, JJ ;
Ziebold, U ;
Gil, E ;
Hinze, R ;
Delbridge, L ;
Lees, JA ;
Mutter, GL ;
Robinson, BG ;
Komminoth, P ;
Dralle, H ;
Eng, C .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 156 (05) :1693-1700