ライフサイエンスコーパス: PTEN protein

1 prostate tumors correlates with loss of the PTEN protein.

2 of transcript and relatively high levels of PTEN protein.

3 KO phenotypes are caused by dysregulation of PTEN protein.

4 caused by the expression of inactive mutant PTEN protein.

5 nt in ATP show an increased level of nuclear PTEN protein.

6 PTEN protein analysis, from one deletion-positive and fi

7 This was confirmed by PTEN protein analysis.

8 Using PTEN protein and a 21-amino acid peptide based on the PT

9 the PTEN, which leads to down-regulation of PTEN protein and activation of Akt pathway.

10 ate event, although a dose-dependent loss of PTEN protein and function has been implicated in early s

11 ating agent sodium butyrate (NaBT) increased PTEN protein and mRNA expression and induced c-Jun NH2-t

12 ed AZD6244 treatment-induced upregulation of PTEN protein and mRNA expression.

13 ce of accurately assessing the expression of PTEN protein and not just its mutational status.

14 sely correlated with the endogenous level of PTEN protein and overexpression of PTEN-blocked Akt phos

15 egulation leads to a decreased expression of PTEN protein and stimulation of PI3K as well as phosphor

16 (DSF-Cu) led to the decreased expression of PTEN protein and the activation of AKT in a dose- and ti

17 stal axonal attenuation of miR-19a increased PTEN proteins and inactivated mTOR in the axons, but did

18 ster reduced phosphatase and tensin homolog (PTEN) proteins and elevated phosphorylated mammalian tar

19 nced nuclear-cytoplasmic localization of the Pten protein, and we developed the Pten(m3m4) model to s

20 and tensin homolog deleted in chromosome 10 (PTEN) protein, and PTEN phosphatase activity in cerebell

21 resulted in the transduction of a functional PTEN protein as evidenced by the upregulation of p27 and

22 nificantly blocked zinc-induced reduction of PTEN protein as well as the increase in Akt phosphorylat

23 sm involves truncation of the 403 amino acid PTEN protein at amino acid 68 by the Y68 frame shift, le

24 ria contain rare glands that fail to express PTEN protein because of mutation and/or deletion.

25 nd tissue-specific fashion with the TSC2 and PTEN proteins being coordinately regulated in those tiss

26 dent degradation and diminished abundance of PTEN protein but increased PTEN phosphatase activity.

27 hereas the tumor suppressive activity of the PTEN protein can be altered at multiple levels through a

28 Thus, a p73-PTEN protein complex is engaged to induce apoptosis inde

29 The PTEN protein consists of an amino-terminal phosphatase d

30 tivation and phosphatase and tensin homolog (PTEN) protein deactivation predicted axon growth across

31 nuclear mislocalization, resulting in rapid PTEN protein degradation, suppression of p53-mediated tr

32 , suggesting that BMP2 stimulation inhibited PTEN protein degradation.

33 Its action may be related to PTEN protein degradation.

34 TEN in the cell membrane is known to prevent PTEN protein degradation.

35 that F9 vinculin-null (vin(-/-)) cells lack PTEN protein despite normal PTEN mRNA levels.

36 rthermore, we also demonstrate that p73alpha/PTEN proteins directly bind one another.

37 and leukemias, the Jurkat T cell line lacks PTEN protein due to frame-shift mutations in both PTEN a

38 f urothelial carcinoma samples found loss of PTEN protein expression (36.4%, n = 11) and elevation of

39 ly with either decreased or complete loss of PTEN protein expression (P = 0.004).

40 t when fibroblasts are attached to collagen, PTEN protein expression and activity are inhibited due t

41 rmline PTEN promoter mutations have aberrant PTEN protein expression and an increased frequency of br

42 PTEN protein expression and BCR surface density may infl

43 e investigated the association between tumor PTEN protein expression and disease-free survival (DFS)

44 n and poor overall survival, whereas lack of PTEN protein expression associated with lower progressio

45 elated with PTEN mutation status; decreasing PTEN protein expression correlated with increasing CC sc

46 Overall, decreased PTEN protein expression correlated with PTEN mutation st

47 esized that phytoestrogen exposure regulates PTEN protein expression in the breast cancer cell line,

48 suggesting that the mechanism for increased PTEN protein expression is dependent upon transcription.

49 of eight melanoma samples with focal loss of PTEN protein expression to understand the features and m

50 Quantitative PTEN protein expression was found to be the key determin

51 Using immunohistochemistry, PTEN protein expression was lost or greatly reduced in 1

52 on between PIK3CA mutations and retention of PTEN protein expression was observed.

53 Their PTEN protein expression was restored by transfection wit

54 ritic arborization, and spine density, while PTEN protein expression was significantly increased in F

55 unexpected mechanism by which PD-1 decreases PTEN protein expression while increasing PTEN activity,

56 of p53 expression resulted in a decrease in PTEN protein expression, suggesting that p53 plays a cri

57 or PTENP1 depletion in DU145 cells decreased PTEN protein expression, which was similar to the origin

58 (18 cases), three showed down-regulation of PTEN protein expression.

59 opathological features were analyzed against PTEN protein expression.

60 targeted the 3'-UTR of PTEN mRNA to inhibit PTEN protein expression.

61 plicing as well as inhibition of full length PTEN protein expression.

62 inase-3beta (GSK-3beta) at Ser9, and reduced PTEN protein expression.

63 linical phenotypes and decreased full-length PTEN protein expression.

64 ion of protein translation and a decrease in PTEN protein expression.

65 y number increases of the gene and decreased PTEN protein function occurring through loss or haploins

66 The PTEN protein has a single catalytic domain possessing bo

67 The PTEN protein has at least two biochemical functions: it

68 Recently, PTEN protein has been shown to possess phosphatase activ

69 PTEN protein has lipid phosphatase and protein phosphata

70 Despite having reduced levels of PTEN protein, homozygous Pten(FV/FV) embryos have intact

71 elic mutated or PTEN wild-type patients lack PTEN protein, implying that additional PTEN inactivation

72 lted in a significant reduction in levels of PTEN protein in a dose- and time-dependent fashion in a

73 coexist with reduced or absent expression of PTEN protein in a variety of neoplasias.

74 region of PTEN, leading to the reduction of PTEN protein in bAMs.

75 in the correlation between loss of IPO11 and PTEN protein in human lung tumors.

76 Loss of PTEN protein in isolated glands was common in the initia

77 and the features associated with the loss of PTEN protein in this disease.

78 Herein, we show that PTEN protein induces a G1 block when reconstituted in PT

79 tructed different PTEN mutants that targeted PTEN protein into different subcellular compartments.

80 Thus, loss of PTEN protein is correlated with pathological markers of

81 We have found that PTEN protein is down-regulated under proteasome dysfunct

82 Here we show that the PTEN protein is enriched in cell bodies and axon termina

83 We have found that PTEN protein is overexpressed in laryngeal papillomas wh

84 The regulatory mechanism of PTEN protein is still not completely understood.

85 On the basis of experiments with two mutant PTEN proteins, it is shown that PI(4,5)P2 induces this c

86 transcripts and severely truncated unstable PTEN protein lacking its phosphatase domain.

87 In general, the inverse correlation between PTEN protein level and Akt phosphorylation was found in

88 The PTEN protein level in mammary epithelial cells was varia

89 zinc treatment results in a reduction of the PTEN protein level in parallel with increased NEDD4-1 ge

90 1 and PRL2 is negatively correlated with the PTEN protein level in the testis and PRL1(+/-)/PRL2(-/-)

91 PTEN and/or PTENP1 resulted in downregulated PTEN protein levels (Figure 2H), downregulation of both

92 hemia and 30-minute reperfusion (I-15/R-30), PTEN protein levels and activity were decreased, and lev

93 ns in MSI- CRCs lead to loss or reduction of PTEN protein levels and contribute to tumor progression.

94 ction-blocking antibodies reduces endogenous PTEN protein levels and inhibits its accumulation at cel

95 evidence that E-cadherin regulates both the PTEN protein levels and its recruitment to cell-cell jun

96 Remarkably, PTEN protein levels and phosphorylation of S380 were the

97 N-targeting miR-19a and miR-21 modulates the PTEN protein levels and the CS and CSL phenotypes, irres

98 These studies indicate that PTEN protein levels are dependent on the maintenance of

99 th high levels of pAKT and MKRN1 expression, PTEN protein levels are low and correlate with a low 5-y

100 Finally, we show that PTEN protein levels are sensitive to CMA and that PTEN a

101 ata indicate that BMP2 exposure can regulate PTEN protein levels by decreasing PTEN's association wit

102 xonal outgrowth and that local modulation of PTEN protein levels by miR-19a likely contributes to the

103 In general, PTEN protein levels correlated with mRNA levels, except

104 IP3R3 and PTEN protein levels directly correlate in human prostate

105 We show that ZEB2 modulates PTEN protein levels in a microRNA-dependent, protein cod

106 We found that exposure to BMP2 increased PTEN protein levels in a time- and dose-dependent manner

107 analogue ATPgammaS, did not reverse nuclear PTEN protein levels in all the cell types tested.

108 PTEN protein levels in BC PDX samples that were determin

109 N mRNA levels are the primary determinant of PTEN protein levels in BC.

110 to determine whether BMP2 stimulation alters PTEN protein levels in the breast cancer line, MCF-7.

111 to restore both nonsense and missense mutant PTEN protein levels in vitro.

112 ned increase in phospho-AKT expression, with PTEN protein levels reduced in both models.

113 sia with and without atypia exhibited higher PTEN protein levels than normal mammary epithelial cells

114 In PHT gastric mucosa 6 h after injury, PTEN protein levels were increased by 2.7-fold; unphosph

115 PTEN protein levels were low in SSc fibroblasts and corr

116 PTEN protein levels were restored in F9 vin(-/-) cells u

117 cells, ceRNA depletion resulted in decreased PTEN protein levels, a result similar to the findings re

118 overexpression in F9 vin(-/-) cells restored PTEN protein levels.

119 th MAGI-2 in F9 vin(-/-) cells also restored PTEN protein levels.

120 essential for DNA damage-induced increase of PTEN protein levels.

121 ion of missense mutations and showed reduced PTEN protein levels.

122 er(Ex5)) HCT116 cells, we observed increased PTEN protein levels.

123 and were inversely correlated with germline PTEN protein levels.

124 cetin or genistein, there was an increase in PTEN protein levels.

125 Phosphatase and tensin homologue (PTEN) protein levels are critical for tumor suppression.

126 vation identified tumors more likely to have PTEN protein loss (p = 4 x 10(-37)) and metabolically pe

127 PAX2 and PTEN protein loss occurs independently and accumulates w

128 revealed that Zn2+-induced ubiquitination of PTEN protein may mediate this process.

129 The PTEN protein negatively regulates cell migration and cel

130 o its lipid phosphatase activity, a role for PTEN protein phosphatase activity in cell cycle regulati

131 K1 autophosphorylation in its activation and PTEN protein phosphatase activity in governing glycolysi

132 the Y68 frame shift, leading to the loss of PTEN protein phosphatase and lipid phosphatase activitie

133 l characterized, the biological relevance of PTEN protein-phosphatase activity remains undefined.

134 or (GR) levels, which are rescued by loss of PTEN protein-phosphatase activity to restrain cell survi

135 ammary tumorigenesis, the additional loss of PTEN protein-phosphatase activity triggered an extensive

136 data suggest that the timing of the loss of PTEN protein plays a critical role in determining the di

137 The remaining C-terminal half of the PTEN protein plays a role in its stability and is mutate

138 The tumor suppressor function of the PTEN protein (PTEN) has been linked to its ability to de

139 ormalities mediated the relationship between PTEN protein reductions and reduced cognitive ability.

140 t evidence that p53 is able to down-regulate PTEN protein stability in stressed cells.

141 s some light on the mechanisms that regulate PTEN protein stability, which is important to fully eluc

142 mino acids play a role in the maintenance of PTEN protein stability.

143 this effect is not mediated through altered PTEN protein stability.

144 s not reduce PTEN message levels but affects PTEN protein stability.

145 activity with siRNA or by expressing active PTEN protein stimulated apoptotic signaling, which reduc

146 To define the minimal region in PTEN protein that is responsible for this anti-oncogenic

147 was transferred into melanoma cells lacking PTEN protein to express the protein at normal physiologi

148 urthermore, we demonstrate that reduction of PTEN protein to heterozygote levels in human MCF7 cells

149 with an E-cadherin blocking antibody reduced PTEN protein to undetectable levels in wild-type F9 cell

150 reveal that EIF5A2 is directly implicated in PTEN protein translation.

151 F9 vin(-/-) cells express PTEN protein upon transfection with a vinculin fragment

152 The presence of PTEN protein was determined by immunostaining, and the r

153 PTEN protein was examined in skin biopsy samples by immu

154 The increase in PTEN protein was rapid and was not due to an increase in

155 and tensin homolog deleted on chromosome 10 (PTEN) protein when compared with CD56(dim) NK cells.

156 t phosphorylation, we examined expression of PTEN protein, which acts as a negative regulator of the

157 , and 60% of these samples had low or absent PTEN protein, which could not be attributed to gene sile

158 ngly, some malignancies exhibit undetectable PTEN protein without mutations or loss of PTEN mRNA.