Constitutive activation of Stat3 signaling confers resistance to apoptosis in human U266 myeloma cells

被引:1449
作者
Catlett-Falcone, R
Landowski, TH
Oshiro, MM
Turkson, J
Levitzki, A
Savino, R
Ciliberto, G
Moscinski, L
Fernández-Luna, JL
Nuñez, G
Dalton, WS [1 ]
Jove, R
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Mol Oncol Program, Tampa, FL 33612 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Clin Invest Program, Tampa, FL 33612 USA
[3] Univ S Florida, Coll Med, Dept Pathol, Tampa, FL 33612 USA
[4] Univ S Florida, Coll Med, Dept Biochem & Mol Biol, Tampa, FL 33612 USA
[5] Univ S Florida, Coll Med, Dept Internal Med, Tampa, FL 33612 USA
[6] Hebrew Univ Jerusalem, Inst Life Sci, IL-91904 Jerusalem, Israel
[7] Ist Rec Biol Mol P Angeletti, I-00040 Pomezia, Italy
[8] Hosp Univ Marques Valdecilla, Santander 39008, Spain
[9] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[10] Univ Michigan, Sch Med, Comprehens Canc Ctr, Ann Arbor, MI 48109 USA
关键词
D O I
10.1016/S1074-7613(00)80011-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Interleukin 6 (IL-6) is the major survival factor for myeloma tumor cells and induces signaling through the STAT proteins. We report that one STAT family member, Stat3 is constitutively activated in bone marrow mononuclear cells from patients with multiple myeloma and in the IL-6-dependent human myeloma cell line U266, Moreover, U266 cells are inherently resistant to Fas-mediated apoptosis and express high levels of the antiapoptotic protein Bcl-x(L). Blocking IL-6 receptor signaling from Janus kinases to the Stat3 protein inhibits Bcl-x(L) expression and induces apoptosis, demonstrating that Stat3 signaling is essential for the survival of myeloma tumor cells. These findings provide evidence that constitutively activated Stat3 signaling contributes to the pathogenesis of multiple myeloma by preventing apoptosis.
引用
收藏
页码:105 / 115
页数:11
相关论文
共 56 条
[1]   MOLECULAR-CLONING OF APRF, A NOVEL IFN-STIMULATED GENE FACTOR-3 P91-RELATED TRANSCRIPTION FACTOR INVOLVED IN THE GP130-MEDIATED SIGNALING PATHWAY [J].
AKIRA, S ;
NISHIO, Y ;
INOUE, M ;
WANG, XJ ;
WEI, S ;
MATSUSAKA, T ;
YOSHIDA, K ;
SUDO, T ;
NARUTO, M ;
KISHIMOTO, T .
CELL, 1994, 77 (01) :63-71
[2]   Bcl-x(L) can inhibit apoptosis in cells that have undergone Fas-induced protease activation [J].
Boise, LH ;
Thompson, CB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (08) :3759-3764
[3]   BCL-X, A BCL-2-RELATED GENE THAT FUNCTIONS AS A DOMINANT REGULATOR OF APOPTOTIC CELL-DEATH [J].
BOISE, LH ;
GONZALEZGARCIA, M ;
POSTEMA, CE ;
DING, LY ;
LINDSTEN, T ;
TURKA, LA ;
MAO, XH ;
NUNEZ, G ;
THOMPSON, CB .
CELL, 1993, 74 (04) :597-608
[4]   Stat3 activation is required for cellular transformation by v-src [J].
Bromberg, JF ;
Horvath, CM ;
Besser, D ;
Lathem, WW ;
Darnell, JE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (05) :2553-2558
[5]   STAT3 beta, a splice variant of transcription factor STAT3, is a dominant negative regulator of transcription [J].
Caldenhoven, E ;
vanDijk, TB ;
Solari, R ;
Armstrong, J ;
Raaijmakers, JAM ;
Lammers, JWJ ;
Koenderman, L ;
deGroot, RP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (22) :13221-13227
[6]  
Cao XM, 1996, MOL CELL BIOL, V16, P1595
[7]  
Chai SK, 1997, J IMMUNOL, V159, P4720
[8]   BCL-X(L) AND BCL-2 REPRESS A COMMON PATHWAY OF CELL-DEATH [J].
CHAO, DT ;
LINETTE, GP ;
BOISE, LH ;
WHITE, LS ;
THOMPSON, CB ;
KORSMEYER, SJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 182 (03) :821-828
[9]   Abrogation of interleukin-3 dependence of myeloid cells by the v-src oncogene requires SH2 and SH3 domains which specify activation of STATs [J].
Chaturvedi, P ;
Sharma, S ;
Reddy, EP .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (06) :3295-3304
[10]   Interleukin-6 inhibits Fas-induced apoptosis and stress-activated protein kinase activation in multiple myeloma cells [J].
Chauhan, D ;
Kharbanda, S ;
Ogata, A ;
Urashima, M ;
Teoh, G ;
Robertson, M ;
Kufe, DW ;
Anderson, KC .
BLOOD, 1997, 89 (01) :227-234