InAADR

Protein Information

Protein Name: Apoptosis regulator Bcl-2 (P10415)
Gene Name: BCL2
Description: Apoptosis regulator Bcl-2
PDB ID: 1G5M
Protein Family:
Protein Category: Ion Channels

This panel provides drug-protein interaction and their ADRs along with references

Interacting Drugs Toxicity Mechanism Reference
Cisplatin Tumor Response Eleven (32%) and 14 (41%) advanced non-small-cell lung cancer (NSCLC) cases were found positive for DR5 and Bcl-2@ respectively@The response rate was significantly higher in patients with DR5 expression@therefore@Death receptor 5 and Bcl-2 protein expression is as predictors of tumor response [ ADR Type 2 ] Death receptor 5 and Bcl-2 protein expression as predictors of tumor response to gemcitabine and cisplatin in patients with advanced non-small-cell lung cancer
Docetaxel Cell Death Docetaxel is able to activate caspase-3@ induce Bcl-2 phosphorylation and apoptosis in cells that show a prolonged G2/M arrest@ but cells may also die by a caspase-3-independent cell death mechanism [ ADR Type 2 ] Variation in the kinetics of caspase-3 activation, Bcl-2 phosphorylation and apoptotic morphology in unselected human ovarian cancer cell lines as a response to docetaxel
Etoposide Cytotoxicity Bcl-2 modulates cytotoxicity of VP-16 between cleavable complex formation and subsequent induction of DNA recombination events [ ADR Type 3 ] Inhibition of etoposide (VP-16)-induced DNA recombination and mutant frequency by Bcl-2 protein overexpression
Gemcitabine Tumor Response Eleven (32%) and 14 (41%) advanced non-small-cell lung cancer (NSCLC) cases were found positive for DR5 and Bcl-2@ respectively@The response rate was significantly higher in patients with DR5 expression@therefore@Death receptor 5 and Bcl-2 protein expression is as predictors of tumor response. [ ADR Type 2 ] Death receptor 5 and Bcl-2 protein expression as predictors of tumor response to gemcitabine and cisplatin in patients with advanced non-small-cell lung cancer

This panel provides information on drug category

Toxicity Source

InAADR: Drug-Protein-ADRs database