Disease

Malignant Mesothelioma

About the Disease
Mesothelioma, Malignant, also known as malignant mesothelioma, is related to malignant pleural mesothelioma and peritoneal mesothelioma, and has symptoms including chest pain, dyspnea and fatigue. An important gene associated with Mesothelioma, Malignant is BCL10 (BCL10 Immune Signaling Adaptor), and among its related pathways/superpathways is Cytoskeletal Signaling. The drugs Dexamethasone acetate and Dexamethasone have been mentioned in the context of this disorder. Affiliated tissues include lung, testis and t cells, and related phenotypes are pleural effusion and cough

Common Targets
HCK | NCOR1 | RNF2 | LINGO2 | SLX4 | GTF2B | PARP3 | FGR | RECQL4 | SMARCC1 | NF2 | FLCN | FOLR2 | CSK | BTK | SMO | ERCC1 | LRRK2 | SLC22A1 | ST14 | MELTF | FGFR2 | GLI2 | LILRB4 | PATZ1 | SMARCA2 | G5133 | KIF7 | KIT | NRAS | CDK6 | ELANE | NAE1 | Protein Kinase B (PKB/Akt) (nonspecified subtype) | RRM1 | CDCA4 | AXL | SUFU | Phosphatidylinositol 3-kinase (PI3K) (nonspecified subtype) | CD3 Complex (T Cell Receptor Complex) | CSF1R | G29126 | CSPG4 | Ephrin Receptor (nonspecified subtype) | LAG3 | LCK | CDK4 | LOC102724428 | G7295 | G673 | mTOR complex 1 | RASGRF2 | GLI3 | DDR2 | REV1 | PIK3CB | STK36 | BCR | HHIP | DCK | ARID2 | PAK5 | DNA Topoisomerase II (nonspecified subtype) | FGFR3 | DLC1 | SUPT6H | NFATC2 | G1029 | SLC22A6 | PIK3CD | SLC46A1 | EIF4E | GART | PDGFRB | NR0B2 | G142 | LGALS9 | PDPN | REV3L | TPBG | BRD1 | USP6 | MSLN | FOXM1 | PTCH2 | RBM6 | SLC22A8 | PTCH1 | G2475 | DPP4 | HLA-A | FLT4 | PRF1 | CRTAM | G7157 | IHH | PTK2B | SLC22A2 | SMARCA4 | RAD50 | GSTT1 | NEDD8-activating enzyme E1 | G3480 | DAPK1 | MTHFD1 | G5747 | FLT1 | DICER1 | WWTR1 | NCL | EPHB6 | TNFAIP3 | ERCC2 | mTOR complex 2 | SETD2 | FGFR1 | RARB | Tubulin | FRK | SMARCE1 | RAF1 | BLK | TEK | TGFB2 | FGFR4 | ZIC1 | DDR1 | SIK2 | SAV1 | Transcriptional Enhancer Factor (TEAD) (nonspecified subype) | FOLR1 | MLLT1 | LYN | CTLA4 | PIK3CA | G4233 | PRLR | PBRM1 | FLT3 | Focal Adhesion Kinases (FAK) (nonspecified subtype) | SIK1 | WT1 | PARP2 | G3082 | NF1 | G672 | TYMS | SDK1 | VDAC1 | CMKLR1 | RET | PDGFRA | BRIP1 | TNFRSF8 | GNAS | FYN | G3146 | KMT2D | MGMT | PRDX3 | CREBBP | TOP2A | MTHFR | GSTM1 | VHL | BAP1 | DDX3X | ATR | Histone deacetylase (nonspecified subtype) | DHFR | ARID1A | KDR | VSIR | G2146 | GSTP1 | G1956 | PAX7 | CD19 | THBD | ROBO2 | CYP19A1 | APC | CHEK2 | G3845 | GLI1 | RASSF1 | TGFBR2 | PIK3CG | TNFRSF9 | DCC | ARID3C | G10413 | SBDS | ABL1 | AURKA | G6714 | MLH1 | YES1 | LATS2 | DNA Methyltransferase (DNMT) (nonspecified subtype) | CUBN

疾病靶点研报
Malignant Mesothelioma

Note: If you'd like to get a target analysis report for Malignant Mesothelioma, or if you are interested to learn how our AI-powered BDE-Chem can design therapeutic molecules to interact with the target(s) above against the disease of Malignant Mesothelioma at a cost 90% lower than traditional approaches, please feel free to contact us at BD@silexon.ai.

Other Diseases

Bronchitis, Chronic | Lymphangioma | Nephritis, Interstitial | Myelomeningocele | Leishmaniasis, Visceral | Astrocytoma | Large Granular Lymphocytic Leukemia | Gangliosidosis, GM1 | Hypertension, Pulmonary | Hepatoblastoma | Autoimmune Interstitial Lung, Joint, And Kidney Disease | Retinopathy, Diabetic | Sarcoidosis | Ophthalmia, Sympathetic | Tatton-Brown-Rahman Syndrome | Withdrawal Syndrome | Argininosuccinic Aciduria | Best Macular Dystrophy | Stroke, Ischemic | Dystonia Musculorum Deformans | Cardiospondylocarpofacial Syndrome | Spinocerebellar Ataxia Type 15 | Coronary Heart Disease | Peritonitis | Pompe Disease | Phosphoglycerate Dehydrogenase Deficiency | Senior-Loken Syndrome | Arthritis, Reactive | Carpenter Syndrome | Autoimmune Disease | Chondroma | IgA Nephropathy | Achromatopsia | Mitochondrial Disease | Wagner Disease | Diabetes Insipidus | Rhabdoid Tumor | Pontocerebellar Hypoplasia Type 7 | Roberts Syndrome | Choroiditis | Blomstrand Osteochondrodysplasia | Seizures-scoliosis-macrocephaly Syndrome | LEOPARD Syndrome | Pseudomyxoma Peritonei | Neuroectodermal Tumors, Primitive | Sialidosis | Usher Syndrome Type III | Liver Failure | Polycystic Ovary Syndrome | Acute Anterior Uveitis | Achondrogenesis | Optic Neuropathy, Anterior Ischemic | Hepatitis, Autoimmune | Bruck Syndrome | Colitis | Renal Hypomagnesemia 3 | Congenital Muscular Dystrophy | Cancer, Prostate | Trichorhinophalangeal Syndrome | Hypertrophy | Aneurysm, Abdominal Aortic | Familial Pheochromocytoma-paraganglioma | Chiari Malformation Type I | Gastrointestinal Disorders | Cerebrovascular Disorders | Corneal Ulcer | Hemangioendothelioma | Diarrhea | Craniolenticulosutural Dysplasia | Chediak-Higashi Syndrome | Atelosteogenesis Type 2 | Primary Erythromelalgia | Myofibromatosis | T-cell Prolymphocytic Leukemia | Dowling-Degos Disease | Smith-Magenis Syndrome | Thyroid Hormone Resistance | Pigment Dispersion Syndrome | Walker-Warburg Syndrome | Eiken Syndrome | Epithelioid Hemangioma | L-2-Hydroxyglutaric Aciduria | Focal Cortical Dysplasia Type 2 | Cleidocranial Dysplasia | Spinocerebellar Ataxia | Fabry's Disease | Hashimoto Thyroiditis | Chondrodysplasia Punctata 1, X-linked Recessive | Purpura, Thrombotic Thrombocytopenic | Blepharophimosis Syndrome | Blue Rubber Bleb Nevus Syndrome | Megalencephaly | Tenosynovial Giant Cell Tumor | Filariasis | Hepatic Steatosis | Williams Syndrome | Congenital Afibrinogenemia | Phosphoenolpyruvate Carboxykinase Deficiency, Cytosolic | Glomerulonephritis | Epidermodysplasia Verruciformis | Gastritis, Atrophic | Trigonocephaly | Nephroblastoma | PHARC Syndrome | Bullous Pemphigoid | Eclampsia | Hypertension | Pierson Syndrome | Vogt-Koyanagi-Harada Syndrome | Mandibuloacral Dysplasia With Type A Lipodystrophy | Perivascular Epithelioid Cell Tumor | Pericarditis | Stuve-Wiedemann Syndrome | Osteosarcoma | Leukoplakia, Oral | Ectodermal Dysplasia | Motor Neuron Diseases | Fontaine Progeroid Syndrome | Gitelman Syndrome | Chondrosarcoma | Learning Disability | Thin Basement Membrane Disease | Stargardt Disease | Epithelial-myoepithelial Carcinoma | Hermansky-Pudlak Syndrome | Cryoglobulinemia | Hyperacusis | Mumps | Lymphoma, Mantle Cell | Nasodigitoacoustic Syndrome | Angelman Syndrome | Osmotic Demyelination Syndrome | Feingold Syndrome | Trimethylaminuria | Alazami Syndrome | Osteomalacia | Ellis-Van Creveld Syndrome | Pernicious Anemia | Charcot-Marie-Tooth Disease Type 4B1 | Episodic Ataxia Type 1 | Amyotrophic Lateral Sclerosis-parkinsonism-dementia Complex | Hyperekplexia | Carcinoma, Signet Ring Cell | Torticollis | Leigh Syndrome | Exfoliative Dermatitis | Pterygium | Conn Syndrome | Carcinoid Syndrome | Hemorrhoids | Allergic Contact Dermatitis | Plasma Cell Leukemia | Wolman Disease | COACH Syndrome | Gangliosidosis | Niemann-Pick Disease | Renal-hepatic-pancreatic Dysplasia | Epidermolytic Ichthyosis, Annular | Amelogenesis Imperfecta | Acromicric Dysplasia | Colitis, Microscopic | Cholesteryl Ester Storage Disease | Primary Hyperoxaluria | Niemann-Pick Disease, Type B | Ocular Surface Squamous Neoplasia | Epidermal Nevus Syndrome | Persistent Fetal Circulation | Tetraplegia | Muscular Dystrophy | Peutz-Jeghers Syndrome | Scapuloperoneal Myopathy, X-linked Dominant | Spitzoid Melanoma | Thyroid Dysgenesis | Harlequin Ichthyosis | Spinocerebellar Ataxia Type 6 | Leukocyte Adhesion Deficiency | Small Lymphocytic Lymphoma | Osteopathia Striata With Cranial Sclerosis | Amyotrophic Lateral Sclerosis | Crigler-Najjar Syndrome | Tardive Dyskinesia | Limb Girdle Muscular Dystrophy | Acrodysostosis | Thrombosis | Mitochondrial DNA Depletion Syndrome | Marfan Syndrome | Hyperuricemia | Trismus-pseudocamptodactyly Syndrome | High Molecular Weight Kininogen Deficiency | 3-methylglutaconic Aciduria Type IV | Hypertension, Portal | Congenital Hereditary Endothelial Dystrophy Type I | Oculocutaneous Albinism | Abetalipoproteinemia | Miyoshi Myopathy | Pseudohypoparathyroidism Type 2 | Familial Episodic Pain Syndrome | Molybdenum Cofactor Deficiency | Intellectual Disability, Autosomal Dominant 5 | Neurodevelopmental Disorders | Placenta Previa | Thymoma, Malignant | Cohen Syndrome | Atelosteogenesis Type 1 | Polyarteritis Nodosa | Hyperparathyroidism | Kabuki Syndrome 2 | Vitiligo | Renal Tubular Dysgenesis | Pain | Strabismus | Vertebrobasilar Insufficiency | Pemphigus Foliaceus | Irritable Bowel Syndrome | Centronuclear Myopathy | Dwarfism | Takenouchi-Kosaki Syndrome | Urofacial Syndrome | Cantu Syndrome | Lupus Erythematosus | Cervical Dystonia | ACTH-independent Macronodular Adrenal Hyperplasia | Brachial Plexus Neuropathy | Glaucoma | Angioimmunoblastic T-cell Lymphoma | Shwachman-Bodian-Diamond Syndrome | Nager Acrofacial Dysostosis | Pneumonia, Mycoplasma | Anal Fissure | Pitt-Hopkins Syndrome | Choreoathetosis, Hypothyroidism, And Neonatal Respiratory Distress | Hypokalemic Periodic Paralysis | Autonomic Neuropathy | Lipodystrophy | Glaucomatocyclitic Crisis | Anterior Segment Dysgenesis | Communication Disorders | Fundus Albipunctatus | Syphilis | Neovascular Glaucoma | Sialidosis Type I | Leukodystrophies | Rolandic Epilepsy | Oligospermia | Craniofrontonasal Syndrome | Imerslund-Grasbeck Syndrome | Scleroderma, Diffuse | Combined Deficiency Of Factor V And Factor VIII | Cocaine-Related Disorders | Nemaline Myopathy 10 | Carey-Fineman-Ziter Syndrome | Hyperbilirubinemia, Neonatal | Prader-Willi Syndrome | Tendinopathy | Diffuse Palmoplantar Keratoderma | Lymphoma, Primary Cutaneous Anaplastic Large Cell | Intracranial Hypertension | Familial Hemiplegic Migraine | Crohn's Disease | Benign Familial Neonatal Convulsions | Mitochondrial DNA Depletion Syndrome 13 | Scleroderma | Ganglioglioma | Knobloch Syndrome | Congenital Heart Block | Duane Retraction Syndrome | Kashin-Beck Disease | Giant Axonal Neuropathy | Sponastrime Dysplasia | CDKL5 Deficiency Disorder | Hernia, Inguinal | Prolidase Deficiency | Costello Syndrome | Cerebellofaciodental Syndrome | Hydrolethalus Syndrome | Snyder-Robinson Syndrome | Gerodermia Osteodysplastica | Hypogammaglobulinemia | Leukocyte Adhesion Deficiency Type 1 | Bainbridge-Ropers Syndrome | Acrodermatitis Enteropathica | Acromesomelic Dysplasia | Papulopustular Rosacea | Agranulocytosis | Leukoplakia | Mesial Temporal Lobe Epilepsy With Hippocampal Sclerosis | Pseudo-pseudohypoparathyroidism | Menkes Disease | Heart Block | Genitopatellar Syndrome | Pulverulent Zonular Cataract | Sclerocornea | Macrodactyly | Kleine-Levin Syndrome | B-cell Chronic Lymphocytic Leukemia | Membranous Nephropathy | Galactosialidosis | Vici Syndrome | Uveitis, Anterior | Osteitis | Non-proliferative Diabetic Retinopathy | Periventricular Nodular Heterotopia | Coenzyme Q10 Deficiency | Cardiomyopathy, Peripartum | Pregnancy, Ectopic | Alopecia Areata | Pneumonia, Viral | Incontinentia Pigmenti | Waardenburg Syndrome Type 1 | GLUT1 Deficiency Syndrome | Cranioectodermal Dysplasia | Primary Torsion Dystonia | Bethlem Myopathy | Eosinophilia | Odonto-onycho-dermal Dysplasia | Oculocutaneous Albinism Type 1 | Endometritis | Agammaglobulinemia | Raine Syndrome | Pancreatitis | Chylothorax, Congenital | Papillon-Lefevre Syndrome | Uremia | Episodic Ataxia Type 2 | Progressive Familial Intrahepatic Cholestasis | Headache | Carney Triad | Huntington's Disease-like 2 | Acute Chest Syndrome | Chronic Kidney Disease | Hemochromatosis Type 2 | Norrie Disease | Fibrosis | Renal Tubular Acidosis | Waardenburg Syndrome Type 4A | Peters-plus Syndrome | Usher Syndrome Type I | Pierpont Syndrome | Urethritis | Danon Disease | Bleeding Disorder Due To CalDAG-GEFI Deficiency | Multiple Sclerosis, Primary Progressive | Syncope | Asthma, Exercise-induced | Oculocutaneous Albinism Type 2 | Neurodegeneration Due To Cerebral Folate Transport Deficiency | Mixed Connective Tissue Disease | 6-pyruvoyl-tetrahydropterin Synthase Deficiency | Chorioretinitis | N-acetylglutamate Synthase Deficiency | Osteomyelitis | Lyme Disease | Dystrophy, Cone-rod | NGLY1 Deficiency | Alpers Syndrome | Methylmalonic Aciduria And Homocystinuria, CblC Type | Maternally Inherited Diabetes And Deafness | Bartter Syndrome | Leber Congenital Amaurosis | Sclerosteosis 2 | LMNA-related Congenital Muscular Dystrophy | 3-hydroxy-3-methylglutaric Aciduria | Granular Corneal Dystrophy Type 1 | Adrenoleukodystrophy, X-linked | Neurofibrosarcoma | Chromosome 5q Deletion Syndrome | Martsolf Syndrome | Pouchitis | Parapsoriasis | Goldenhar Syndrome | Cyclic Vomiting Syndrome | Brooke-Spiegler Syndrome | Muir-Torre Syndrome | Tendinitis | Hypersomnia | Neuromyelitis Optica | 3-methylglutaconic Aciduria | Epicondylitis | Amelanotic Melanoma | Leprosy | Takotsubo Cardiomyopathy | Optic Nerve Hypoplasia, Bilateral | Riboflavin Transporter Deficiency Neuronopathy | Galloway-Mowat Syndrome | Mosaic Variegated Aneuploidy Syndrome 2 | Meningococcal Infections | ADNP Syndrome | Pulmonary Vein Stenosis | Paronychia | Cervicitis | Retinitis | Enterocolitis, Necrotizing | Diabetic Neuropathy | Chromosome 8q21.11 Deletion Syndrome | Klinefelter Syndrome | Subcortical Band Heterotopia | McCune-Albright Syndrome | Anti-NMDA Receptor Encephalitis | Atrial Septal Defect | Pathological Gambling