共 67 条
The 14-3-3 proteins: integrators of diverse signaling cues that impact cell fate and cancer development
被引:498
作者:

Morrison, Deborah K.
论文数: 0 引用数: 0
h-index: 0
机构:
NCI Frederick, Lab Cell & Dev Signaling, Frederick, MD 21702 USA NCI Frederick, Lab Cell & Dev Signaling, Frederick, MD 21702 USA
机构:
[1] NCI Frederick, Lab Cell & Dev Signaling, Frederick, MD 21702 USA
关键词:
ORGAN SIZE CONTROL;
HIPPO PATHWAY;
JNK PHOSPHORYLATION;
CONTACT INHIBITION;
GROWTH-CONTROL;
GENE-PRODUCT;
DNA-DAMAGE;
B-RAF;
MTOR;
TSC2;
D O I:
10.1016/j.tcb.2008.10.003
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The highly conserved 14-3-3 protein family has risen to a position of importance in cell biology owing to its involvement in vital cellular processes, such as metabolism, protein trafficking, signal transduction, apoptosis and cell-cycle regulation. The 14-3-3 proteins are phosphoserine/phospho-threonine binding proteins that interact with a diverse array of binding partners. Because many 14-3-3 interactions are phosphorylation-dependent, 14-3-3 has been tightly integrated into the core phosphoregulatory pathways that are crucial for normal growth and development and that often become dysregulated in human disease states such as cancer. This review examines the recent advances that further elucidate the role of 14-3-3 proteins as integrators of diverse signaling cues that influence cell fate decisions and tumorigenesis.
引用
收藏
页码:16 / 23
页数:8
相关论文
共 67 条
[1]
14-3-3 proteins: A historic overview
[J].
Aitken, Alastair
.
SEMINARS IN CANCER BIOLOGY,
2006, 16 (03)
:162-172

Aitken, Alastair
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Edinburgh, Sch Biol Sci, Edinburgh EH9 3JR, Midlothian, Scotland Univ Edinburgh, Sch Biol Sci, Edinburgh EH9 3JR, Midlothian, Scotland
[2]
BRCA1 is a selective co-activator of 14-3-3σ gene transcription in mouse embryonic stem cells
[J].
Aprelikova, O
;
Pace, AJ
;
Fang, B
;
Koller, BH
;
Liu, ET
.
JOURNAL OF BIOLOGICAL CHEMISTRY,
2001, 276 (28)
:25647-25650

Aprelikova, O
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Div Clin Sci, Sect Mol Signaling & Oncogenesis, NIH, Bethesda, MD 20892 USA

Pace, AJ
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Div Clin Sci, Sect Mol Signaling & Oncogenesis, NIH, Bethesda, MD 20892 USA

Fang, B
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Div Clin Sci, Sect Mol Signaling & Oncogenesis, NIH, Bethesda, MD 20892 USA

Koller, BH
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Div Clin Sci, Sect Mol Signaling & Oncogenesis, NIH, Bethesda, MD 20892 USA

Liu, ET
论文数: 0 引用数: 0
h-index: 0
机构: NCI, Div Clin Sci, Sect Mol Signaling & Oncogenesis, NIH, Bethesda, MD 20892 USA
[3]
Identification of differentially expressed genes in oral squamous cell carcinoma
[J].
Arora, S
;
Matta, A
;
Shukla, NK
;
Deo, SVS
;
Ralhan, R
.
MOLECULAR CARCINOGENESIS,
2005, 42 (02)
:97-108

Arora, S
论文数: 0 引用数: 0
h-index: 0
机构: All India Inst Med Sci, Dept Biochem, New Delhi 110029, India

Matta, A
论文数: 0 引用数: 0
h-index: 0
机构: All India Inst Med Sci, Dept Biochem, New Delhi 110029, India

Shukla, NK
论文数: 0 引用数: 0
h-index: 0
机构: All India Inst Med Sci, Dept Biochem, New Delhi 110029, India

Deo, SVS
论文数: 0 引用数: 0
h-index: 0
机构: All India Inst Med Sci, Dept Biochem, New Delhi 110029, India

Ralhan, R
论文数: 0 引用数: 0
h-index: 0
机构:
All India Inst Med Sci, Dept Biochem, New Delhi 110029, India All India Inst Med Sci, Dept Biochem, New Delhi 110029, India
[4]
The two TORCs and Akt
[J].
Bhaskar, Prashanth T.
;
Hay, Nissim
.
DEVELOPMENTAL CELL,
2007, 12 (04)
:487-502

Bhaskar, Prashanth T.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA

Hay, Nissim
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA Univ Illinois, Coll Med, Dept Biochem & Mol Genet, Chicago, IL 60607 USA
[5]
Regulation of mTOR function in response to hypoxia by REDD1 and the TSC1/TSC2 tumor suppressor complex
[J].
Brugarolas, J
;
Lei, K
;
Hurley, RL
;
Manning, BD
;
Reiling, JH
;
Hafen, E
;
Witter, LA
;
Ellisen, LW
;
Kaelin, WG
.
GENES & DEVELOPMENT,
2004, 18 (23)
:2893-2904

Brugarolas, J
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Lei, K
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Hurley, RL
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Manning, BD
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Reiling, JH
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Hafen, E
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Witter, LA
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Ellisen, LW
论文数: 0 引用数: 0
h-index: 0
机构: Dana Farber Canc Inst, Boston, MA 02115 USA

Kaelin, WG
论文数: 0 引用数: 0
h-index: 0
机构:
Dana Farber Canc Inst, Boston, MA 02115 USA Dana Farber Canc Inst, Boston, MA 02115 USA
[6]
Activity of TSC2 is inhibited by AKT-mediated phosphorylation and membrane partitioning
[J].
Cai, SL
;
Tee, AR
;
Short, JD
;
Bergeron, JM
;
Kim, J
;
Shen, JJ
;
Guo, RF
;
Johnson, CL
;
Kiguchi, K
;
Walker, CL
.
JOURNAL OF CELL BIOLOGY,
2006, 173 (02)
:279-289

Cai, SL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Tee, AR
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Short, JD
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Bergeron, JM
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Kim, J
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Shen, JJ
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Guo, RF
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Johnson, CL
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Kiguchi, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA

Walker, CL
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA Univ Texas, MD Anderson Canc Ctr, Dept Carcinogenesis, Smithville, TX 78957 USA
[7]
YAP1 increases organ size and expands undifferentiated progenitor cells
[J].
Camargo, Fernando D.
;
Gokhale, Sumita
;
Johnnidis, Jonathan B.
;
Fu, Dongdong
;
Bell, George W.
;
Jaenisch, Rudolf
;
Brummelkamp, Thijn R.
.
CURRENT BIOLOGY,
2007, 17 (23)
:2054-2060

Camargo, Fernando D.
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

Gokhale, Sumita
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

Johnnidis, Jonathan B.
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

Fu, Dongdong
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

Bell, George W.
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

Jaenisch, Rudolf
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA

Brummelkamp, Thijn R.
论文数: 0 引用数: 0
h-index: 0
机构:
Whitehead Inst Biomed Res, Cambridge, MA 02142 USA Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[8]
14-3-3σ is required to prevent mitotic catastrophe after DNA damage
[J].
Chan, TA
;
Hermeking, H
;
Lengauer, C
;
Kinzler, KW
;
Vogelstein, B
.
NATURE,
1999, 401 (6753)
:616-620

Chan, TA
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Program Human Genet, Baltimore, MD 21231 USA

Hermeking, H
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Program Human Genet, Baltimore, MD 21231 USA

Lengauer, C
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Program Human Genet, Baltimore, MD 21231 USA

Kinzler, KW
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Program Human Genet, Baltimore, MD 21231 USA

Vogelstein, B
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Johns Hopkins Oncol Ctr, Program Human Genet, Baltimore, MD 21231 USA
[9]
Wnt/β-catenin signaling in development and disease
[J].
Clevers, Hans
.
CELL,
2006, 127 (03)
:469-480

论文数: 引用数:
h-index:
机构:
[10]
The stress-inducted proteins RTP801 and RTP801L are negative regulators of the mammalian target of rapamycin pathway
[J].
Corradetti, MN
;
Inoki, K
;
Guan, KL
.
JOURNAL OF BIOLOGICAL CHEMISTRY,
2005, 280 (11)
:9769-9772

Corradetti, MN
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Inst Life Sci, Dept Biol Chem, Ann Arbor, MI 48109 USA

Inoki, K
论文数: 0 引用数: 0
h-index: 0
机构: Univ Michigan, Inst Life Sci, Dept Biol Chem, Ann Arbor, MI 48109 USA

Guan, KL
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Michigan, Inst Life Sci, Dept Biol Chem, Ann Arbor, MI 48109 USA Univ Michigan, Inst Life Sci, Dept Biol Chem, Ann Arbor, MI 48109 USA