Resveratrol induces p53-independent, X-linked inhibitor of apoptosis protein (XIAP)-mediated Bax protein oligomerization on mitochondria to initiate cytochrome c release and caspase activation. (Q35309349)

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English	Resveratrol induces p53-independent, X-linked inhibitor of apoptosis protein (XIAP)-mediated Bax protein oligomerization on mitochondria to initiate cytochrome c release and caspase activation.	scientific article

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6 February 2020

Resveratrol induces p53-independent, X-linked inhibitor of apoptosis protein (XIAP)-mediated Bax protein oligomerization on mitochondria to initiate cytochrome c release and caspase activation (English)

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6 February 2020

apoptotic process

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based on heuristic

inferred from title

1

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Varun Prabhu

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6 February 2020

Michael Amadori

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Rachael Scott

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Sana Hashmi

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28 June 2011

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6 February 2020

Journal of Biological Chemistry

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28749-28760

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6 February 2020

Autophagy in tumorigenesis and energy metabolism: friend by day, foe by night

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Resveratrol enhances antitumor activity of TRAIL in prostate cancer xenografts through activation of FOXO transcription factor

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Intracellular GSH depletion triggered mitochondrial Bax translocation to accomplish resveratrol-induced apoptosis in the U937 cell line

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Resveratrol-induced p53-independent apoptosis of human nasopharyngeal carcinoma cells is correlated with the downregulation of ΔNp63.

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Resveratrol induces apoptosis of human nasopharyngeal carcinoma cells via activation of multiple apoptotic pathways.

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Stepwise activation of BAX and BAK by tBID, BIM, and PUMA initiates mitochondrial apoptosis.

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Role for X-linked Inhibitor of apoptosis protein upstream of mitochondrial permeabilization

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Control of mitochondrial apoptosis by the Bcl-2 family

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Oligomerization of BAK by p53 utilizes conserved residues of the p53 DNA binding domain

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p53's mitochondrial translocation and MOMP action is independent of Puma and Bax and severely disrupts mitochondrial membrane integrity

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BCL-2 family proteins: critical checkpoints of apoptotic cell death

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Mitochondria, calcium, and calpain are key mediators of resveratrol-induced apoptosis in breast cancer

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Cytosolic accumulation of HSP60 during apoptosis with or without apparent mitochondrial release: evidence that its pro-apoptotic or pro-survival functions involve differential interactions with caspase-3

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Resveratrol inhibits tumor growth of human neuroblastoma and mediates apoptosis by directly targeting mitochondria

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Phase I dose escalation pharmacokinetic study in healthy volunteers of resveratrol, a potential cancer chemopreventive agent

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Intracellular nucleotides act as critical prosurvival factors by binding to cytochrome C and inhibiting apoptosome

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Resveratrol-caused apoptosis of human prostate carcinoma LNCaP cells is mediated via modulation of phosphatidylinositol 3'-kinase/Akt pathway and Bcl-2 family proteins

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Mechanisms of cytochrome c release from mitochondria

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Irradiation-induced translocation of p53 to mitochondria in the absence of apoptosis

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Clusterin inhibits apoptosis by interacting with activated Bax

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Bax-dependent regulation of Bak by voltage-dependent anion channel 2.

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Regulation of Bax activation and apoptotic response to microtubule-damaging agents by p53 transcription-dependent and -independent pathways

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Caspase activation: revisiting the induced proximity model

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Cytochrome C-mediated apoptosis

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Direct activation of Bax by p53 mediates mitochondrial membrane permeabilization and apoptosis

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Resveratrol induces extensive apoptosis by depolarizing mitochondrial membranes and activating caspase-9 in acute lymphoblastic leukemia cells.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190683

26 September 2018

Apoptosis induction by a novel anti-prostate cancer compound, BMD188 (a fatty acid-containing hydroxamic acid), requires the mitochondrial respiratory chain.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3190683

26 September 2018

Short-chain fatty acid-initiated cell cycle arrest and apoptosis of colonic epithelial cells is linked to mitochondrial function

1 reference

https://pubmed.ncbi.nlm.nih.gov/21712378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early steps in mitochondrial protein import: receptor functions can be substituted by the membrane insertion activity of apocytochrome c

1 reference

https://pubmed.ncbi.nlm.nih.gov/21712378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Resveratrol increases nitric oxide synthase, induces accumulation of p53 and p21(WAF1/CIP1), and suppresses cultured bovine pulmonary artery endothelial cell proliferation by perturbing progression through S and G2

1 reference

https://pubmed.ncbi.nlm.nih.gov/21712378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TNF-alpha signals apoptosis through a bid-dependent conformational change in Bax that is inhibited by E1B 19K

1 reference

https://pubmed.ncbi.nlm.nih.gov/21712378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structure of FADD and its mode of interaction with procaspase-8

1 reference

https://pubmed.ncbi.nlm.nih.gov/21712378

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1074/JBC.M110.202440

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712378%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712378%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21712378%20AND%20SRC:MED&resulttype=core&format=json

6 February 2020

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