Cell cycle
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Chromosome human
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Clinical
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Up-regulation of p21WAF1 and Bax and
down-regulation of Bcl-2 may be the molecular mechanism through which
auristatin-PE inhibits cell growth and induces apoptosis. Li
Y, Singh B, AliN,SarkarFH.
-
pBax expression may be beneficial in predicting the effects of ACT on
patients with IDC. Nio
Y, Iguchi C, Yamasawa K, Sasaki S, Takamura M, Toga T, Dong M, Itakura
M, Tamura K.
|
DNA Structure
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The skipping of
exon 3 and the resultant splicing of exons 2 and 4 maintains the
original reading frame and predicts the existence of an interstitially
truncated form of the major Bax protein (Bax alpha), termed Bax delta.
Apte
SS, Mattei MG, Olsen BR.
|
Function
|
Gene frequency
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Frameshift mutations of hMSH3, hMLH3, BRCA-2, TGF-beta
type II receptor, and BAX genes were detected in MSI-H tumors.Yamamoto
H, Itoh F, Nakamura H, Fukushima H, Sasaki S, Perucho M,Imai K.
|
Homologue
-
Apoptosis
and occurrence of Bcl-2, Bak, Bax, Fas and FasL in the developing and
adult rat endocrine pancreas. Hanke
J.
|
Protein structure
|
Regulation
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In mutant K-ras pancreatic carcinoma cells,
programmed cell death correlates with expression and an increase,
respectively, in MDA-7 and BAX proteins and increases in the ratio of
BAX to BCL-2 proteins. Su
Z, Lebedeva IV, Gopalkrishnan RV, Goldstein NI, Stein CA, Reed JC,Dent
P,FisherPB.
|
- Combination of auristatin-PE and gemcitabine showed significantly
greater inhibition of cell growth and up-regulated expression of
p21WAF1 and Bax. Li
Y, Singh B, Ali N, Sarkar FH.
|
|
|
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Imbalance between antiapoptosis proteins (such as
Bcl-2, Bcl-XL, and Mcl-1) and proapoptotic proteins (such as Bax and
Bcl-Xs) is involved in the distinctive biologic features of
adenocarcinomas of the pancreas. Miyamoto
Y, Hosotani R, Wada M, Lee JU, Koshiba T, Fujimoto K, Tsuji S,
Nakajima S, Doi R, Kato M, Shimada Y, Imamura M.
|
-
Dynamic changes of the Bax/Bcl-2 ratio might be
important in determining point of apoptosis induction in pancreatic
cancer cells with p53 mutation. Wada
M, Hosotani R, Lee JU, Doi R, Koshiba T, Fujimoto K, Miyamoto Y, Tsuji
S, Nakajima S, Okuyama A, Imamura M.
|