BCL2, BCL2 apoptosis regulator, 596

N. diseases: 1456; N. variants: 27
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
0.060 AlteredExpression disease BEFREE SIGNIFICANCE: In the first clinical study to evaluate venetoclax in a solid tumor, we demonstrate that combining venetoclax with endocrine therapy has a tolerable safety profile and elicits notable activity in ER and BCL2-positive metastatic breast cancer. 30518523 2019
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
0.060 Biomarker disease BEFREE In this Review, we discuss how a pro-apoptotic subgroup of the BCL2 protein family, known as the BH3-only proteins, controls apoptosis and anoikis during mammary gland homeostasis and to what extent their inhibition confers tumor suppressive functions in metastatic breast cancer. 30139926 2018
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
0.060 Biomarker disease BEFREE p53, cathepsin D, Bcl-2 are joint prognostic indicators of breast cancer metastatic spreading. 27538498 2016
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
0.060 AlteredExpression disease BEFREE Resistance to chemotherapy via Stat3-dependent overexpression of Bcl-2 in metastatic breast cancer cells. 12400004 2002
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
0.060 AlteredExpression disease BEFREE In this study, we determined the plasma levels of bcl-2 and nitric oxide in 45 patients with metastatic breast cancer using an ELISA technique and correlated them with clinical and biological factors that may affect the outcome of disease.The results were as follows. 11917941 2001
CUI: C0278488
Disease: Carcinoma breast stage IV
Carcinoma breast stage IV
0.060 AlteredExpression disease BEFREE In conclusion, we found that in metastatic breast cancer, there is no significant association between tumor Bcl-2 expression and response to paclitaxel, median time to progression, or survival, suggesting that the main mechanism of paclitaxelinduced cytotoxicity in breast tumors is independent of Bcl-2 expression. 11051254 2000