CD38, CD38 molecule, 952

N. diseases: 473; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
0.500 Biomarker disease CTD_human Systems level analysis and identification of pathways and networks associated with liver fibrosis. 25380136 2014
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
0.500 Biomarker disease RGD Altered CD38 expression in thioacetamide-induced rat model of liver cirrhosis. 16343077 2005
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.500 Biomarker disease CTD_human Cardioplegia prevents ischemia-induced transcriptional alterations of cytoprotective genes in rat hearts: a DNA microarray study. 16214533 2005
CUI: C0151744
Disease: Myocardial Ischemia
Myocardial Ischemia
0.500 Biomarker disease RGD Myocardial ischemia and reperfusion reduce the levels of cyclic ADP-ribose in rat myocardium. 12111041 2002
CUI: C0001925
Disease: Albuminuria
Albuminuria
0.300 Biomarker phenotype CTD_human This enhanced glomerular injury in CD38(-/-) or CD38-shRNA mice was accompanied by increased albuminuria and proteinuria. 21992601 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.240 Biomarker disease BEFREE The clinical phenotype of anti-CD38-positive Type 2 diabetes differs from the LADA (latent autoimmune diabetes of adults) phenotype. 15505998 2005
Diabetes Mellitus, Non-Insulin-Dependent
0.240 Biomarker disease BEFREE Autoimmunity to CD38 and GAD in Type I and Type II diabetes: CD38 and HLA genotypes and clinical phenotypes. 12242463 2002
Diabetes Mellitus, Non-Insulin-Dependent
0.240 GeneticVariation disease BEFREE Autoantibody response to CD38 in Caucasian patients with type 1 and type 2 diabetes: immunological and genetic characterization. 11289039 2001
Diabetes Mellitus, Non-Insulin-Dependent
0.240 GeneticVariation disease BEFREE The Arg140Trp mutation on CD38 thus appears to contribute to the development of Type II diabetes mellitus via the impairment of glucose-induced insulin secretion in the presence of other genetic defects. 9754820 1998
Diabetes Mellitus, Non-Insulin-Dependent
0.240 Biomarker disease RGD Expression of CD38 gene, but not of mitochondrial glycerol-3-phosphate dehydrogenase gene, is impaired in pancreatic islets of GK rats. 7669044 1995
Diabetes Mellitus, Insulin-Dependent
0.220 AlteredExpression disease BEFREE We utilized surface expression of CD38 on newly activated CD4 memory T cells as a strategy to identify type 1 diabetes associated autoreactive T cells activated by influenza vaccination in healthy subjects. 30619245 2018
Diabetes Mellitus, Insulin-Dependent
0.220 Biomarker disease MGD Targeted disruption of CD38 accelerates autoimmune diabetes in NOD/Lt mice by enhancing autoimmunity in an ADP-ribosyltransferase 2-dependent fashion. 16585549 2006
Diabetes Mellitus, Insulin-Dependent
0.220 Biomarker disease BEFREE Recently, the presence of CD38 autoantibodies has been found in a significant number (9-15%) of patients with Type 2 or long-standing Type 1 diabetes. 15505998 2005
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy
0.200 Biomarker disease RGD Role of kidney ADP-ribosyl cyclase in diabetic nephropathy. 19073639 2009
CUI: C0018800
Disease: Cardiomegaly
Cardiomegaly
0.200 Biomarker phenotype RGD Inhibition of ADP-ribosyl cyclase attenuates angiotensin II-induced cardiac hypertrophy. 18719074 2009
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.100 Biomarker disease BEFREE In conclusion, Daratumumab is a human IgG1κ monoclonal antibody targeting CD38 and is used to treat multiple myeloma. 31693245 2020
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.100 Biomarker disease BEFREE VS38 is a viable alternative to bright CD38 to identify plasma cells and particularly helpful in myeloma cases with dim CD38 and after daratumumab. 31679012 2020
CUI: C0026764
Disease: Multiple Myeloma
Multiple Myeloma
0.100 Biomarker disease BEFREE The model is validated with clinical data from the anti-FcRn antibody M281 and is used to conduct a scenario test to quantify the interaction among M-protein, the characteristic paraprotein of multiple myeloma (MM), and the anti-CD38 antibody daratumumab indicated for MM treatment. 31449666 2020
CUI: C4551538
Disease: refractory multiple myeloma
refractory multiple myeloma
0.100 Biomarker disease BEFREE Daratumumab (DARA) is a humanized Immunoglobulin G(IgG)1-kappa monoclonal antibody against CD38 antigen that is shown to improve outcomes in relapsed/refractory plasma cell myeloma (PCM) patients. 31313879 2020
CUI: C4551538
Disease: refractory multiple myeloma
refractory multiple myeloma
0.100 Biomarker disease BEFREE The anti-CD38 antibody daratumumab is approved for treatment of refractory multiple myeloma and acts by depletion of plasma cells and modification of various T-cell functions. 31630242 2020
CUI: C4551538
Disease: refractory multiple myeloma
refractory multiple myeloma
0.100 Biomarker disease BEFREE Pretreatment CD38-positive regulatory T-cells affect the durable response to daratumumab in relapsed/refractory multiple myeloma patients. 31004032 2020
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.100 Biomarker group BEFREE Anti-CD38 mAbs-mediated PC depletion in autoimmunity and organ transplants is currently under investigation. 31783629 2019
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.100 Biomarker group BEFREE In conclusion, these data indicate that depletion of CD38-expressing cells could be a therapeutic mechanism for treating autoimmune diseases. 31085699 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE Based on the high activity and favorable toxicity profile of daratumumab, other CD38 antibodies, such as isatuximab, MOR202, and TAK-079, are being evaluated in MM and other malignancies. 30826127 2019
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.100 Biomarker group BEFREE Anti-CD38/CD3 XmAb T-cell-recruiting antibodies with different affinities for CD38 and CD3 were assessed <i>in vitro</i> and <i>in vivo</i> for their redirected T-cell lysis activity against cancer cell lines, their lower levels of cytokine release, and their potency in the presence of high levels of soluble CD38. 30918018 2019