Expression and potential role of Fas-associated phosphatase-1 in ovarian cancer

被引:60
作者
Meinhold-Heerlein, I
Stenner-Liewen, F
Liewen, H
Kitada, S
Krajewska, M
Krajewski, S
Zapata, JM
Monks, A
Scudiero, DA
Bauknecht, T
Reed, JC
机构
[1] Burnham Inst, Program Apoptosis & Cell Death Res, La Jolla, CA 92037 USA
[2] Natl Canc Inst, Dev Therapeut Program, Div Canc Treatment & Diagnost, Bethesda, MD USA
[3] Univ Bonn, Dept Gynecol & Obstet, Bonn, Germany
关键词
D O I
10.1016/S0002-9440(10)64084-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Fas-associated phosphatase-1 (FAP-1) is a protein-tyrosine phosphatase that binds the cytosolic tail of Fas (Apo1, CD95), presumably regulating Fas-induced apoptosis, Elevations of FAP-1 protein levels in some tumor cell lines have been correlated with resistance to Fas-induced apoptosis. To explore the expression of FAP-1 in ovarian cancer cell lines and archival tumor specimens, mouse monoclonal and rabbit polyclonal antibodies were generated against a FAP-1 peptide and recombinant FAP-1 protein. These antibodies were used for immunoblotting, Immunohistochemistry, and now-cytometry analysis of FAP-1 expression in the Fas-sensitive ovarian cancer lines HEY and BG-1, and In the Fas-resistant lines OVCAR-3 FR and SK-OV-3. All methods demonstrated high levels of FAP-1 in the resistant lines OVCAR-3 FR and SK-OV-3, but not in the Fas-sensitive lines HEY and BG-1. Furthermore, levels of FAP-1 protein also correlated with the amounts of FAP-1 mRNA, as determined by reverse transcriptase-polymerase chain reaction analysis. FAP-1 protein levels were Investigated by immunoblotting in the National Cancer Institute's panel of 60 human tumor cell lines. Although FAP-1 failed to correlate with Fas-resistance across the entire tumor panel, Fas-resistance correlated significantly with FAP-1 expression (P less than or equal to 0.05) and a low Fas/FAP-1 ratio (P less than or equal to 0.028) in ovarian cancer cell lines, FAP-1 expression was also evaluated in 95 archival ovarian cancer specimens using tissue-microarray technology, FAP-1 was expressed in neatly all tumors, regardless of histological type or grade, stage, patient age, response to chemotherapy, or patient survival We conclude that FAP-1 correlates significantly with Fas resistance in ovarian cancer cell lines and is commonly expressed in ovarian cancers.
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页码:1335 / 1344
页数:10
相关论文
共 42 条
[1]   Expression of FAP-1 (Fas-associated phosphatase) and resistance to Fas-mediated apoptosis in T cell lines derived from human T cell leukemia virus type 1-associated myelopathy/tropical spastic paraparesis patients [J].
Arai, M ;
Kannagi, M ;
Matsuoka, M ;
Sato, T ;
Yamamoto, N ;
Fujii, M .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1998, 14 (03) :261-267
[2]   No evidence for involvement of mouse protein-tyrosine phosphatase-BAS-like Fas-associated phosphatase-1 in Fas-mediated apoptosis [J].
Cuppen, E ;
Nagata, S ;
Wieringa, B ;
Hendriks, W .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (48) :30215-30220
[3]  
Disis ML, 1999, CLIN CANCER RES, V5, P1289
[4]   Comparison of apoptosis in wild-type and fas-resistant cells: Chemotherapy-induced apoptosis is not dependent on Fas/Fas ligand interactions [J].
Eischen, CM ;
Kottke, TJ ;
Martins, LM ;
Basi, GS ;
Tung, JS ;
Earnshaw, WC ;
Leibson, PJ ;
Kaufmann, SH .
BLOOD, 1997, 90 (03) :935-943
[5]  
GREVER MR, 1992, SEMIN ONCOL, V19, P622
[6]  
Hedlund TE, 1998, PROSTATE, V36, P92, DOI 10.1002/(SICI)1097-0045(19980701)36:2<92::AID-PROS4>3.0.CO
[7]  
2-G
[8]   Thymineless death in colon carcinoma cells is mediated via Fas signaling [J].
Houghton, JA ;
Harwood, FG ;
Tillman, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (15) :8144-8149
[9]   Functional interaction of Fas-associated phosphatase-1 (FAP-1) with p75NTR and their effect on NF-κB activation [J].
Irie, S ;
Hachiya, T ;
Rabizadeh, S ;
Maruyama, W ;
Mukai, J ;
Li, Y ;
Reed, JC ;
Bredesen, DE ;
Sato, TA .
FEBS LETTERS, 1999, 460 (02) :191-198
[10]   THE POLYPEPTIDE ENCODED BY THE CDNA FOR HUMAN CELL-SURFACE ANTIGEN FAS CAN MEDIATE APOPTOSIS [J].
ITOH, N ;
YONEHARA, S ;
ISHII, A ;
YONEHARA, M ;
MIZUSHIMA, S ;
SAMESHIMA, M ;
HASE, A ;
SETO, Y ;
NAGATA, S .
CELL, 1991, 66 (02) :233-243