GZMB, granzyme B, 3002

N. diseases: 290; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.340 Biomarker disease BEFREE Synergistic effect of granzyme B-azurin fusion protein on breast cancer cells. 30937652 2019
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.340 AlteredExpression disease BEFREE Granzyme B production by activated B cells derived from breast cancer-draining lymph nodes. 31357083 2019
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.340 Biomarker disease BEFREE Synergistic effect of granzyme B-azurin fusion protein on breast cancer cells. 30937652 2019
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.340 AlteredExpression disease BEFREE Granzyme B production by activated B cells derived from breast cancer-draining lymph nodes. 31357083 2019
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.340 AlteredExpression disease BEFREE Inhibition of the actin response by knocking down CDC42 or N-WASP led to a significant increase in granzyme B levels in target cells and was sufficient to convert resistant breast cancer cell lines into a highly susceptible phenotype. 30104240 2018
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.340 AlteredExpression disease BEFREE Inhibition of the actin response by knocking down CDC42 or N-WASP led to a significant increase in granzyme B levels in target cells and was sufficient to convert resistant breast cancer cell lines into a highly susceptible phenotype. 30104240 2018
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.340 Biomarker disease CTD_human Our data suggest that reduction in the proportion of gammadelta T cells and granzyme B gene polymorphism leads to defective immune function in breast cancer patients. 19446661 2009
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.340 GeneticVariation disease BEFREE Our data suggest that reduction in the proportion of gammadelta T cells and granzyme B gene polymorphism leads to defective immune function in breast cancer patients. 19446661 2009
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.340 GeneticVariation disease BEFREE Our data suggest that reduction in the proportion of gammadelta T cells and granzyme B gene polymorphism leads to defective immune function in breast cancer patients. 19446661 2009
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.340 Biomarker disease CTD_human Our data suggest that reduction in the proportion of gammadelta T cells and granzyme B gene polymorphism leads to defective immune function in breast cancer patients. 19446661 2009
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.330 AlteredExpression group BEFREE In immunocompetent mouse 4T1 breast tumor model, intratumoral delivery of rAd.sT inhibited both tumor growth and lung metastases. rAd.sT downregulated the expression of several transforming growth factor β (TGFβ) target genes involved in tumor growth and metastases, inhibited Th2 cytokine expression, and induced Th1 cytokines and chemokines, and granzyme B and perforin expression. rAd.sT treatment also increased the percentage of CD8<sup>+</sup> T lymphocytes, promoted the generation of CD4<sup>+</sup> T memory cells, reduced regulatory T lymphocytes (Tregs), and reduced bone marrow-derived suppressor cells. 31126191 2019
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.330 Biomarker group BEFREE Our findings underscore the need to investigate the function of GZMB<sup>+</sup> B cells in breast tumor immunity. 31357083 2019
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.330 Biomarker group BEFREE Administration (intravenous, tail vein) of GrB/4D5/26 to mice bearing BT474 M1 breast tumors resulted in significant tumor suppression. 23493312 2013
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.330 Biomarker group CTD_human Defective gammadelta T-cell function and granzyme B gene polymorphism in a cohort of newly diagnosed breast cancer patients. 19446661 2009
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0.300 Biomarker disease CTD_human Altered gene expression and function of peripheral blood natural killer cells in children with autism. 18762240 2009
CUI: C0013182
Disease: Drug Allergy
Drug Allergy
0.300 Biomarker group CTD_human Fulminant liver failure after vancomycin in a sulfasalazine-induced DRESS syndrome: fatal recurrence after liver transplantation. 19706026 2009
CUI: C0019158
Disease: Hepatitis
Hepatitis
0.300 Biomarker group CTD_human Fulminant liver failure after vancomycin in a sulfasalazine-induced DRESS syndrome: fatal recurrence after liver transplantation. 19706026 2009
CUI: C1257931
Disease: Mammary Neoplasms, Human
Mammary Neoplasms, Human
0.300 Biomarker disease CTD_human Defective gammadelta T-cell function and granzyme B gene polymorphism in a cohort of newly diagnosed breast cancer patients. 19446661 2009
CUI: C4704874
Disease: Mammary Carcinoma, Human
Mammary Carcinoma, Human
0.300 Biomarker disease CTD_human Defective gammadelta T-cell function and granzyme B gene polymorphism in a cohort of newly diagnosed breast cancer patients. 19446661 2009
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.120 GeneticVariation disease BEFREE Our positive results provide additional supportive evidence that GZMB gene is an important locus for vitiligo in Han Chinese population. 30158536 2018
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.120 Biomarker disease BEFREE The inflammatory cytotoxic markers such as Granzyme B and Perforin were also elevated in vitiligo and halo nevus, suggesting inflammatory responses in situ. 28385330 2017
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.120 GeneticVariation disease GWASCAT Genome-wide association studies of autoimmune vitiligo identify 23 new risk loci and highlight key pathways and regulatory variants. 27723757 2016
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.120 GeneticVariation disease GWASDB Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo. 22561518 2012
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.120 GeneticVariation disease GWASCAT Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501 2010
CUI: C0042900
Disease: Vitiligo
Vitiligo
0.120 GeneticVariation disease GWASDB Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo. 20410501 2010