m6A-centered Crosstalk Information
Mechanism of Crosstalk between m6A Modification and Epigenetic Regulation
| Crosstalk ID |
M6ACROT05634
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[1] | |||
m6A modification
hsa-miR-30d
hsa-miR-30d
YTHDC1
: m6A sites
Direct
Enhancement
Non-coding RNA
miR-30d
RUNX1
lncRNA miRNA circRNA
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| m6A Modification: | |||||
|---|---|---|---|---|---|
| m6A Regulator | YTH domain-containing protein 1 (YTHDC1) | READER | |||
| m6A Target | hsa-miR-30d | ||||
| Epigenetic Regulation that have Cross-talk with This m6A Modification: | |||||
| Epigenetic Regulation Type | Non-coding RNA (ncRNA) | ||||
| Epigenetic Regulator | hsa-miR-30d | microRNA | View Details | ||
| Regulated Target | Runt-related transcription factor 1 (RUNX1) | View Details | |||
| Crosstalk Relationship | m6A → ncRNA | Enhancement | |||
| Crosstalk Mechanism | m6A regulators directly modulate the functionality of ncRNAs through specific targeting ncRNA | ||||
| Crosstalk Summary | MiR-30d is a novel target for YTHDC1 through m6A modification, and hsa-miR-30d represses pancreatic ductal adenocarcinoma tumorigenesis via suppressing aerobic glycolysis. miR-30d inhibited aerobic glycolysis through regulating SLC2A1 and HK1 expression by directly targeting the transcription factor Runt-related transcription factor 1 (RUNX1), which bound to the promoters of the SLC2A1 and HK1 genes. | ||||
| Responsed Disease | Pancreatic ductal adenocarcinoma | ICD-11: 2C10.0 | |||
| Cell Process | Cell proliferation | ||||
| Cell metastasis | |||||
| Cell angiogenesis | |||||
In-vitro Model |
PANC-1 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0480 | |
| MIA PaCa-2 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0428 | ||
| Human Pancreatic Nestin-Expressing cells (Human Pancreatic Nestin-Expressing cells) | |||||
| AsPC-1 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0152 | ||
| BxPC-3 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0186 | ||
| Capan-1 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0237 | ||
| Capan-2 | Pancreatic ductal adenocarcinoma | Homo sapiens | CVCL_0026 | ||
| CFPAC-1 | Cystic fibrosis | Homo sapiens | CVCL_1119 | ||
| HPAC | Pancreatic adenocarcinoma | Homo sapiens | CVCL_3517 | ||
| SW1990 | Pancreatic adenocarcinoma | Homo sapiens | CVCL_1723 | ||
| In-vivo Model | To study the effect of miR-30d on liver metastasis of PDACs, 5 × 106 cells in 50 uL of PBS were injected into the spleens of nude mice (6 mice per group). Anesthetized mice were injected intraperitoneally with D-luciferin (150 mg/kg) every other week and imaged using an IVIS 100 imaging system (Xenogen, CA, USA) 10 min after the injection. The mice were sacrificed and their liver metastases were checked by standard histological examination 8-9 weeks after injection. | ||||
Full List of Potential Compound(s) Related to This m6A-centered Crosstalk
| 2C10: Pancreatic cancer | 182 Compound(s) Regulating the Disease | Click to Show/Hide the Full List | ||
| Atezolizumab | Approved | [2] | ||
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| Trimethadione | Approved | [3] | ||
| Synonyms |
Absentol; Absetil; Convenixa; Convexina; Edion; Epidione; Epidone; Epixal; Etydion; Minoaleuiatin; Minoaleviatin; Petidion; Petidon; Petilep; Petimalin; Pitmal; Ptimal; Tioxanona; Tredione; Tricione; Tridilona; Tridion; Tridione; Tridone; Trilidona; Trimedal; Trimedone; Trimetadiona; Trimetadione; Trimethadion; Trimethadionum; Trimethdione; Trimethin; Trimethinum; Trimetin; Trioksal; Trioxanona; Triozanona; Tromedone; Troxidone; Abbott Brand of Trimethadione; Trimetadione [DCIT]; A 2297; Mino-Aleviatin; Neo-Absentol; Tridione (TN); Trimetadiona [INN-Spanish]; Trimethadione [INN:JAN]; Trimethadionum [INN-Latin]; Trimethadione (JP15/INN); 3,3,5-Trimethyl-2,4-diketooxazolidine; 3,5,5,-Trimethyloxazolidine-2,4-dione; 3,5,5-TRIMETHYL-OXAZOLIDINE-2,4-DIONE; 3,5,5-Trimethyl-1,3-oxazolidine-2,4-dione; 3,5,5-Trimethyl-2,4-oxazolidinedione; 3,5,5-Trojmetylooksazolidyno-2,4-dion; 3,5,5-Trojmetylooksazolidyno-2,4-dion [Polish]
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| Motixafortide | Approved | [2] | ||
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| Uridine triacetate | Approved | [4] | ||
| Synonyms |
PN401
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| Bentiromide | Approved | [5] | ||
| Synonyms |
Bentiromide sodium; 41748-47-4; N-Benzoyl-L-tyrosyl-4-aminobenzoic acid sodium salt; NCGC00164607-01; EINECS 255-530-7; DSSTox_CID_26476; DSSTox_RID_81647; DSSTox_GSID_46476; DTXSID6046476; CHEMBL3188891; Tox21_112229; AKOS024373587; ACM41748474; Sodium (S)-4-((2-(benzoylamino)-3-(4-hydroxyphenyl)-1-oxopropyl)amino)benzoate; CAS-41748-47-4; FT-0771579; ST51012404; N-Benzoyl-L-tyrosine p-amidobenzoic acid sodium salt; sodium (S)-4-(2-benzamido-3-(4-hydroxyphenyl)propanamido)benzoate; N-Benzoyl-L-tyrosine p-amidobenzoic acid so
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| Olaparib | Approved | [2] | ||
| Synonyms |
AZD 2281; AZD2281; AZD-2281; Acylpiperazine analogue, 47; KU-0059436; KU-59436; Olaparib, KU-0059436, AZD2281,KU0059436, AZD2281; 4-[(3-{[4-Cyclopropylcarbonyl)piperazin-4-yl]carbonyl}-4-fluorophenyl)methyl]phtalazin-1(2H)-one; 4-[3-(4-Cyclopropanecarbonyl-piperazine-1-carbonyl)-4-fluoro-benzyl]-2H-phthalazin-1-one
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| Streptozocin | Approved | [6] | ||
| Synonyms |
Estreptozocina; STREPTOZOTOCIN; STRZ; Streptozocine; Streptozocinium; Streptozocinum; Streptozosin; Zanosar; Alkylating agent; Binds to DNA; Streptozocinium [Latin]; Streptozocine [INN-French]; Streptozocinum [INN-Latin]; Zanosar (TN); Streptozocin (USAN/INN); Streptozocin, Zanosar, STZ,Streptozotocin;N-(Methylnitrosocarbamoyl)-alpha-D-glucosamine; N-D-Glucosyl-(2)-N'-nitrosomethylharnstoff; N-D-Glucosyl-(2)-N'-nitrosomethylurea; D-Glucose, 2-deoxy-2-(((methylnitrosoamino)carbonyl)amino)-(9CI); 1-methyl-1-nitroso-3-[(2S,3R,4R,5S,6R)-2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]urea; 2-Deoxy-2-(((methylnitrosoamino)carbonyl)amino)-D-glucopyranose; 2-Deoxy-2-(3-methyl-3-nitrosoureido)-D-glucopyranose; 2-Deoxy-2[[(methylnitrosoamino)-carbonyl]amino]-D-glucopyranose; 2-deoxy-2-{[methyl(nitroso)carbamoyl]amino}-alpha-D-glucopyranose
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| Plazomicin | Phase 3 | [7] | ||
| Synonyms |
ACHN-490; UNII-LYO9XZ250J; 1154757-24-0; LYO9XZ250J; Plazomicin [USAN:INN]; Plazomicin (USAN); ZINC68150640; DB12615; D10151; D-Streptamine,
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| Taxol | Approved | [2] | ||
| Synonyms |
C47H51NO14; weekly paclitaxel; Micellar Paclitaxel; Paclitaxel [USAN:INN:BAN]; SCHEMBL15000506; Benzenepropanoic acid, beta-(benzoylamino)-alpha-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca(3,4)benz(1,2-b)oxet-9-yl ester, (2aR-(2aalpha,4beta,4abeta,6beta,9alpha(alphaR*,betaS*),11alpha,12alpha,12aalpha,12balpha))-
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| Ibrutinib | Phase 3 | [2] | ||
| Synonyms |
PCI-32765; Ibrutinib (BTK inhibitor)
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| Erlotinib | Approved | [8] | ||
| Synonyms |
Erlotinin; Tarceva; Erlotinib Base; OSI 744; R 1415; CP 358,774; CP-358774; Erlotinib(Tarceva); Tarceva (TN); CP-358,774; Erlotinib, OS-774; N-(3-ethynylphenyl)[6,7-bis(2-methoxyethoxy)quinazolin-4-yl]amine; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)-4-quinazolinamine; N-(3-Ethynylphenyl)-6,7-bis(2-methoxyethoxy)quinazolin-4-amine; [6,7-BIS(2-METHOXY-ETHOXY)QUINAZOLINE-4-YL]-(3-ETHYNYLPHENYL)AMINE; [6,7-Bis-(2-methoxy-ethoxy)-quinazolin-4-yl]-(3-ethynyl-phenyl)-amine; 4-[(3-Ethynylphenyl)amino]-6,7-bis(2-methoxyethoxy)quinazoline
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| Ruxolitinib | Approved | [9] | ||
| Synonyms |
Ruxolitinib (JAK inhibitor)
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| Nivolumab | Approved | [2] | ||
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| Coenzyme Q10 | Phase 2 | [2] | ||
| Synonyms |
CoQ10; Coenzyme Q10 (oral formulation); CoQ10 platform technology, Ryan (Receptagen); Coenzyme Q10 (oral formulation), Receptagen
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| Aglatimagene besadenovec | Phase 1/2 | [2] | ||
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| Zolbetuximab | Phase 3 | [10] | ||
| Synonyms |
IMAB362
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| AC-1204 | Phase 3 | [11] | ||
| Synonyms |
isoindoline hydrochloride; 32372-82-0; 2,3-Dihydroisoindole hydrochloride; 2,3-dihydro-1H-isoindole hydrochloride; 2,3-Dihydro-1H-isoindole HCl; Isoindoline HCl salt; 1H-Isoindole, 2,3-dihydro-, hydrochloride; Isoindoline hydrochloride, 97%; Isoindolinehydrochloride; Isoindoline, HCl; ISOINDOLINE HCL; AC1Q38WR; dihydroisoindole hydrochloride; KSC491I3F; AMBZ0192; SCHEMBL4702076; CTK3J1432; DTXSID50487241; MolPort-003-986-749; NOVIRODZMIZUPA-UHFFFAOYSA-N; BH168; CS-D1516; ACT08858; ACN-S003258; KS-000001RA
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| Radiosensitizer gene therapy | Phase 3 | [12] | ||
| Synonyms |
Radiosensitizer gene therapy (prostate cancer)
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| Glufosfomide | Phase 3 | [13] | ||
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| Yttrium (90Y) clivatuzumab tetraxetan | Phase 3 | [14] | ||
| Synonyms |
PAM4 mAb; Yttrium Y 90 clivatuzumab tetraxetan; Anti-MUC1 PAM4 monoclonal antibody; Clivatuzumab tetraxetan-[90Y]; HPAM4-Cide; IMMU-107; PAM-4; PAM4-Y-90; Yttrium-90-hPAM4; 90Y-clivatuzumab tetraxetan; 90Y-hPAM4
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| Y-90 Clivatuzumab | Phase 3 | [15] | ||
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| Civacir | Phase 3 | [16] | ||
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| GV1001 | Phase 3 | [17] | ||
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| Masitinib | Phase 3 | [2] | ||
| Synonyms |
790299-79-5; AB1010; Masatinib; Masitinib (AB1010); Masivet; AB-1010; AB 1010; UNII-M59NC4E26P; Masitinib [INN]; M59NC4E26P; 4-[(4-Methyl-1-piperazinyl)methyl]-N-[4-methyl-3-[[4-(3-pyridinyl)-2-thiazolyl]amino]phenyl]benzamide; CHEMBL1908391; CHEBI:63450; Masitinib (INN); N-(4-Methyl-3-((4-(pyridin-3-yl)thiazol-2-yl)amino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide; Q-201339; C28H30N6OS; N-(4-methyl-3-(4-(pyridin-3-yl)thiazol-2-ylamino)phenyl)-4-((4-methylpiperazin-1-yl)methyl)benzamide
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| Glufosfamide | Phase 3 | [2] | ||
| Synonyms |
Glucosylifostamide mustard; D 19575; D-19575; Glc-IPM; Glucosyl-ifosfamide mustard; Beta-D-Glucopyranose 1-(N,N'-bis(2-chloroethyl)phosphorodiamidate; Beta-D-Glucopyranose, 1-(N,N'-bis(2-chloroethyl)phosphorodiamidate); (2S,3R,4S,5S,6R)-2-bis(2-chloroethylamino)phosphoryloxy-6-(hydroxymethyl)oxane-3,4,5-triol
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| Sapacitabine | Phase 3 | [2] | ||
| Synonyms |
CYC682
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| Pelareorep | Phase 2 | [18] | ||
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| Pamrevlumab | Phase 3 | [19] | ||
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| GRASPA | Phase 1 | [20] | ||
| Synonyms |
L-asparaginase (erythrocyte-encapsulated, acute lymphoblastic leukemia/solid tumor), ERYtech
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| Pancreas algenpantucel-L | Phase 3 | [21] | ||
| Synonyms |
HyperAcute (TN)
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| CPI-613 | Phase 3 | [22] | ||
| Synonyms |
95809-78-2; 6,8-bis(benzylthio)octanoic acid; CPI 613; MLS006010202; SCHEMBL1062218; 6,8-Bis(benzylsulfanyl)octanoic acid; Octanoic acid, 6,8-bis((phenylmethyl)thio)-; Octanoic acid, 6,8-bis[(phenylMethyl)thio]-; 6,8-Bis[(phenylmethyl)thio]octanoic acid; CPI613; CHEMBL3186849; QCR-193; AOB1058; MolPort-023-219-128; HMS3656L06; C22H28O2S2; BCP04663; EX-A2043; s2776; AKOS025142095; BCP9000552; DB12109; RL06062; CS-0961; NCGC00344764-01; SMR004701300; AS-16613; BC261916; AK174899; HY-15453; BCP0726000030; KB-293127; AB0035874
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| Zarnestra | Phase 3 | [23] | ||
| Synonyms |
JAN; Tipifarnib; Tipifarnib [USAN]; R 115777; R115777; R-11577; R-115777; Tipifarnib (USAN/INN); Zarnestra, IND 58359, R115777, Tipifarnib; (R)-6-(Amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methyl-2(1H)-quinolinone; (R)-R115777; 2 (1H))-Quinolinone,6-(amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl)-4-(3-chlorophenyl)-1-methyl-, 2(1H)-quinolinone; 6-[(R)-amino(4-chlorophenyl)(1-methyl-1H-imidazol-5-yl)methyl]-4-(3-chlorophenyl)-1-methylquinolin-2(1H)-one; 6-[(R)-amino-(4-chlorophenyl)-(3-methylimidazol-4-yl)methyl]-4-(3-chlorophenyl)-1-methylquinolin-2-one; 6-[(S)-AMINO(4-CHLOROPHENYL)(1-METHYL-1H-IMIDAZOL-5-YL)METHYL]-4-(3-CHLOROPHENYL)-1-METHYLQUINOLIN-2(1H)-ONE
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| MM-398 | Phase 3 | [24] | ||
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| Marimastat | Phase 3 | [25] | ||
| Synonyms |
Marimastat [USAN]; BB 2516; BB-2516; Marimastat (USAN/INN); (2R,3S)-N-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N',3-dihydroxy-2-(2-methylpropyl)butanediamide; (2S,3R)-3-(((1S)-2,2-Dimethyl-1-(methylcarbamoxy)propyl)carboyl)-2-hydroxy-5-methylhexanohydroxamic acid; (2S,3R)-3-(((1S)-2,2-Dimethyl-1-(methylcarbamoyl)propyl)carbamoyl)-2-hydroxy-5-methylhexanohydroxamic acid; (2S,3R)-N(4)-[(2S)-3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl]-N(1),2-dihydroxy-3-(2-methylpropyl)butanediamide
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| AM0010 | Phase 3 | [26] | ||
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| ANX-510 | Phase 3 | [27] | ||
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| Napabucasin | Phase 3 | [2] | ||
| Synonyms |
83280-65-3; UNII-Z1HHM49K7O; 2-acetylnaphtho[2,3-b]furan-4,9-dione; Z1HHM49K7O; 2-Acetylnaphtho(2,3-b)furan-4,9-dione; 2-Acetyl-4H,9H-naphtho[2,3-b]furan-4,9-dione; Napabucasin [USAN:INN]; Napabucasin (BBI608); 2-Acetylfuranonaphthoquinone; CHEMBL64130; Napabucasin (JAN/USAN/INN); SCHEMBL1883845; Napabucasin - BBI 608/ FNQ; 2-Acetylfuro-1,4-naphthoquinone; DPHUWDIXHNQOSY-UHFFFAOYSA-N; MolPort-039-101-321; EX-A1314; ZINC13306865; s7977; AKOS027470201; DB12155; CS-1747; ACN-053294; HY-13919
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| Algenpantucel-L | Phase 3 | [28] | ||
| Synonyms |
HyperAcute pancreas (TN)
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| OT-101 | Phase 2/3 | [2] | ||
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| RP101 | Phase 2/3 | [29] | ||
| Synonyms |
SCHEMBL15589316; CHEMBL3703295; BDBM149820; US8975415,
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| NLG8189 | Phase 2/3 | [2] | ||
| Synonyms |
1-Methyl-D-tryptophan; Indoximod; 110117-83-4; D-Tryptophan, 1-methyl-; D-1MT; Indoximod (NLG-8189); D-1-methyltryptophan; UNII-TX5CYN1KMZ; D-(+)-1-Methyltryptophan; TX5CYN1KMZ; (R)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid; (2R)-2-amino-3-(1-methylindol-3-yl)propanoic acid; NSC-721782; (2R)-2-amino-3-(1-methyl-3-indolyl)propanoic acid; 1-MT; (2R)-2-azanyl-3-(1-methylindol-3-yl)propanoic acid; (2R)-2-amino-3-(1-methyl-1H-indol-3-yl)propanoic acid; D-l-Methyltryptophan; Indoximod [USAN:INN]; NLG-8189; NLG 8189
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| LY2157299 | Phase 2/3 | [2] | ||
| Synonyms |
Galunisertib; 700874-72-2; LY 2157299; LY-2157299; UNII-3OKH1W5LZE; 4-(2-(6-methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)quinoline-6-carboxamide; 3OKH1W5LZE; Galunisertib (LY2157299); AK-79916; 4-[5,6-Dihydro-2-(6-methyl-2-pyridinyl)-4H-pyrrolo[1,2-b]pyrazol-3-yl]-6-quinolinecarboxamide; 4-(2-(6-Methylpyridin-2-yl)-5,6-dihydro-4H-pyrrolo-[1,2-b]pyrazol-3-yl)quinoline-6-carboxamide; 4-[2-(6-methylpyridin-2-yl)-4H,5H,6H-pyrrolo[1,2-b]pyrazol-3-yl]quinoline-6-carboxamide
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| SM-88 | Phase 2/3 | [30] | ||
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| SiG12D-LODER | Phase 2 | [2] | ||
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| BNT141 | Phase 2 | [31] | ||
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| BNT321 | Phase 2 | [32] | ||
| Synonyms |
MVT-5873
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| BPM 31510 | Phase 2 | [33] | ||
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| GC4711 | Phase 2 | [34] | ||
| Synonyms |
UNII-FW5T90VM32; FW5T90VM32; GC-4419 dipropionate; Bis-propionato(gc4419); Avasopasem manganese dipropionate; GC-4711; 2248030-85-3; Manganese(II), bis-propionato((4aS,13aS,17aS,21aS)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-11,7-nitrilo-7H-dibenzo(b,H)(1,4,7,10)tetraaza-cycloheptadecine-kn5,kn13,kn18,kn21,kn22)-,
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| CYTO-401 | Phase 2 | [35] | ||
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| Zenocutuzumab | Phase 2 | [36] | ||
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| Cabiralizumab | Phase 2 | [2] | ||
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| VS-6063 | Phase 2 | [2] | ||
| Synonyms |
Defactinib hydrochloride; 1073160-26-5; Defactinib (hydrochloride); UNII-L2S469LM49; Defactinib hydrochloride [USAN]; L2S469LM49; Defactinib hydrochloride (USAN); Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsulfonyl)amino]-2-pyrazinyl]methyl]amino]-5-(trifluoromethyl)-2-pyrimidinyl]amino]-, hydrochloride; Defactinib HCl; Benzamide, N-methyl-4-((4-(((3-(methyl(methylsulfonyl)amino)-2-pyrazinyl)methyl)amino)-5-(trifluoromethyl)-2-pyrimidinyl)amino)-, hydrochloride (1:1); Benzamide, N-methyl-4-[[4-[[[3-[methyl(methylsu
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| MENK | Phase 2 | [13] | ||
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| CO-101 | Phase 2 | [37] | ||
| Synonyms |
methyl 2-(dimethylcarbamoyl)benzoate; 26593-43-1; Phthalamic acid, N,N-dimethyl-, methyl ester; CO 101; BRN 2504723; N,N-Dimethylphthalamic acid methyl ester; N,N-Dimethylphthalamic acid, methyl ester; AC1Q5ZAU; 2-09-00-00601 (Beilstein Handbook Reference); AC1L4V19; CTK4F8203; DTXSID50181156; 2-methoxycarbonyl-N,N-dimethylbenzamide; LS-109082; Benzoic acid,2-[(dimethylamino)carbonyl]-, methyl ester
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| MENK | Phase 2 | [2] | ||
| Synonyms |
IRT-101
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| TL-118 | Phase 2 | [38] | ||
| Synonyms |
Hamsa 1; TL-111; TL-112; Combination anti-angiogenic therapy (oral suspension, solid tumors), Tiltan Pharma
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| Antroquinonol | Phase 2 | [2] | ||
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Hocena; Fungal extract (cancer), Golden Biotechnology
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| NPC-1C | Phase 2 | [2] | ||
| Synonyms |
Ensituximab
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| Necuparanib | Phase 2 | [39] | ||
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| CCX872 | Phase 2 | [2] | ||
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| GC4419 | Phase 1/2 | [2] | ||
| Synonyms |
Avasopasem manganese; UNII-EY1WA413UL; EY1WA413UL; Avasopasem manganese [USAN]; SC-72325A; M-40419; 435327-40-5; Manganese, dichloro((4aS,13aS,17aS,21aS)-1,2,3,4,4a,5,6,12,13,13a,14,15,16,17,17a,18,19,20,21,21a-eicosahydro-7,11-nitrilo-7H-dibenzo(b,H)-5,13,18,21-tetraazacycloheptadecine-kappaN5,kappaN13,kappaN18,kappaN21,kappaN22)-, (pb-7-11-2344'3')-
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| External Link | ||||
| Istiratumab | Phase 2 | [18] | ||
| External Link | ||||
| GI-4000 | Phase 2 | [40] | ||
| External Link | ||||
| OCV-101 | Phase 2 | [41] | ||
| Synonyms |
OTS-11101
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| RX-3117 | Phase 2 | [2] | ||
| Synonyms |
Antimetabolite (cancer), Rexahn; Antimetabolite (cancer), Rexahn/ Teva
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| External Link | ||||
| Ensitiximab | Phase 2 | [13] | ||
| External Link | ||||
| GI-4000 + gemcitabine | Phase 2 | [42] | ||
| External Link | ||||
| BC-819 | Phase 2 | [43] | ||
| External Link | ||||
| IRT-102 | Phase 2 | [44] | ||
| External Link | ||||
| LE-DT | Phase 2 | [45] | ||
| Synonyms |
Liposomal docetaxel
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| TH-302 | Phase 2 | [2] | ||
| Synonyms |
evofosfamide; 918633-87-1; TH 302; TH302; UNII-8A9RZ3HN8W; Evofosfamide(TH 302); n,n'-bis(2-bromoethyl)phosphorodiamidic acid (1-methyl-2-nitro-1h-imidazol-5-yl)methyl ester; 8A9RZ3HN8W; compound 3b; Evofosfamide;HAP-302; Phosphorodiamidic acid, N,N'-bis(2-bromoethyl)-, (1-methyl-2-nitro-1H-imidazol-5-yl)methyl ester; 2-bromo-N-[(2-bromoethylamino)-[(3-methyl-2-nitroimidazol-4-yl)methoxy]phosphoryl]ethanamine; Evofosfamide [USAN:INN]; Evofosfamide(TH-302); C9H16Br2N5O4P; CHEMBL260046; SCHEMBL2357174
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| External Link | ||||
| Demcizumab | Phase 2 | [13] | ||
| External Link | ||||
| Anti-PSCA mab | Phase 2 | [46] | ||
| External Link | ||||
| ALT-803 | Phase 2 | [18] | ||
| Synonyms |
IL-15 agonist/ IL-15R alpha-Fc fusion complex (cancer), Altor BioScience
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| External Link | ||||
| ARQ 761 | Phase 2 | [2] | ||
| External Link | ||||
| Reolysinpelareorep | Phase 2 | [2] | ||
| External Link | ||||
| PBI-05204 | Phase 2 | [2] | ||
| External Link | ||||
| PCI-27483 | Phase 2 | [47] | ||
| External Link | ||||
| RX-0201 | Phase 2 | [13] | ||
| External Link | ||||
| CP-613 | Phase 2 | [48] | ||
| External Link | ||||
| CART 19 | Preclinical | [49] | ||
| External Link | ||||
| VT-122 | Phase 1 | [13] | ||
| External Link | ||||
| PEGPH20 | Phase 2 | [50] | ||
| External Link | ||||
| Ficlatuzumab | Phase 2 | [2] | ||
| Synonyms |
AV-299
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| Tigatuzumab | Phase 2 | [51] | ||
| External Link | ||||
| CRS-207 | Phase 2 | [52] | ||
| External Link | ||||
| CAP1-6D | Phase 2 | [53] | ||
| Synonyms |
Modified CEA peptide (pancreatic cancer), University of Chicago
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| SGT-53 | Phase 2 | [2] | ||
| Synonyms |
P53 gene stimulator (solid tumor), Synergene Therapeutics
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| Tarextumab | Phase 2 | [54] | ||
| External Link | ||||
| BVD-523 | Phase 2 | [2] | ||
| External Link | ||||
| Ocaperidone | Phase 2 | [18] | ||
| Synonyms |
Ocaperidona; 129029-23-8; UNII-26HUS7139V; 3-(2-(4-(6-Fluoro-1,2-benzisoxazol-3-yl)piperidino)ethyl)-2,9-dimethyl-4H-pyrido(1,2-a)pyrimidin-4-one; 26HUS7139V; Ocaperidonum; Ocaperidonum [INN-Latin]; Ocaperidona [INN-Spanish]; 4H-Pyrido[1,2-a]pyrimidin-4-one,3-[2-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]ethyl]-2,9-dimethyl-; Ocaperidone (USAN); Ocaperidone [USAN:INN:BAN]; 3-[2-[4-(6-Fluorobenzo[d]isoxazol-3-yl)piperidin-1-yl]ethyl]-2,9-dimethyl-4H-pyrido[1,2-a]pyrimidin-4-one; 3-[2-[4-(6-fluoro-1,2-benzoxazol-3-yl)piperidin-1-yl]ethyl]-2,9-dimethylpyrido[1,2-a]pyrimidin-4-one; 8-[2-[4-(6-fluorobenzo[d]isoxazol-3-yl)-1-piperidyl]ethyl]-2,9-dimethyl-6,10-diazabicyclo[440]deca-2,4,8,10-tetraen-7-one; FG-3019
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| Encapsulated live cells converting ifosfamide | Phase 2 | [2] | ||
| External Link | ||||
| LY2603618 | Phase 2 | [55] | ||
| Synonyms |
Rabusertib; 911222-45-2; LY 2603618; LY-2603618; UNII-3S9L1NU6U7; 3S9L1NU6U7; IC-83; ly2603618 IC-83; (S)-1-(5-bromo-4-methyl-2-(morpholin-2-ylmethoxy)phenyl)-3-(5-methylpyrazin-2-yl)urea; n-(5-bromo-4-methyl-2-((2s)-2-morpholinylmethoxy)phenyl)-n'-(5-methyl-2-pyrazinyl)urea; LY2603618 (IC-83); Rabusertib [USAN:INN]; 3-(5-Bromo-4-methyl-2-[(2s)-morpholin-2-ylmethoxy]phenyl)-1-(5-methylpyrazin-2-yl)urea; N-[5-Bromo-4-methyl-2-[(2S)-2-morpholinylmethoxy)phenyl]-N'-(5-methyl-2-pyrazinyl)urea
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| Salirasib | Discontinued in Phase 1/2 | [56] | ||
| Synonyms |
162520-00-5; Farnesylthiosalicylic acid; S-Farnesylthiosalicylic acid; UNII-MZH0OM550M; MZH0OM550M; CHEMBL23293; AK186909; Farnesyl Thiosalicylic Acid; 2-[[(2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrien-1-yl]thio]benzoic Acid; 2-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]sulfanylbenzoic acid; 2-((2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienylthio)benzoic acid; 2-(((2E,6E)-3,7,11-Trimethyl-2,6,10-dodecatrienyl)sulfanyl)benzoic acid; Benzoic acid, 2-(((2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrienyl)thio)-; FTS; Farnesylthiosalicyclic acid; FTS, Thyreos; Ras antagonists, Thyreos; S-trans; Th-101; Trans-farnesylthiosalicylicacid; FTS (oral, cancer), Concordia; Farnesylthiosalicyclic acid (oral, cancer), Concordia; Ras-inhibitors (cancer), Concordia; FTS (oral, cancer), Concordia/Ono; KD032
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| MM-141 | Phase 2 | [2] | ||
| External Link | ||||
| GB1275 | Phase 1/2 | [57] | ||
| External Link | ||||
| ABTL0812 | Phase 1/2 | [58] | ||
| Synonyms |
(9Z,12Z)-2-Hydroxy-9,12-octadecadienoic acid; (9Z,12Z)-2-hydroxyoctadeca-9,12-dienoic acid; (9Z,12Z)-2-hydroxyoctadecadienoic acid; (alpha)-Hydroxylinoleic acid; .ALPHA.-HYDROXYLINOLEIC ACID; 0DE74TJ7EZ; 2-hydroxy-9Z,12Z-Octadecadienoic acid; 2-hydroxylinoleic acid; 57818-44-7; 9,12-Octadecadienoic acid, 2-hydroxy-, (9Z,12Z)-; 9,12-Octadecadienoic acid, 2-hydroxy-, (Z,Z)-; ABTL0812; ABTL-0812; a-Hydroxylinoleic acid; AKOS040740632; alpha-Hydroxylinoleic acid; CHEBI:136927; CS-7178; DTXSID301258077; hydroxylinoleic acid; HY-U00141; LMFA02000290; MS-24253; s9611; SCHEMBL320069; UNII-0DE74TJ7EZ
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| GP-2250 | Phase 1/2 | [59] | ||
| External Link | ||||
| Delolimogene mupadenorepvec | Phase 1/2 | [60] | ||
| Synonyms |
LOAd703
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| GSK3145095 | Phase 1/2 | [61] | ||
| Synonyms |
1622849-43-7; CHEMBL4452233; (S)-5-benzyl-N-(7,9-difluoro-2-oxo-2,3,4,5-tetrahydro-1H-benzo[b]azepin-3-yl)-4H-1,2,4-triazole-3-carboxamide; UNII-B4D3WPS7JY; B4D3WPS7JY; SCHEMBL17312826; BCP31015; EX-A3069; BDBM50502339; s8845; GSK-3145095; HY-111946; CS-0094287; GSK 3145095; FC1=CC2=C(NC(=O)[C@H](CC2)NC(=O)C2=NN=C(CC3=CC=CC=C3)N2)C(F)=C1; (S)-5-Benzyl-N-(7,9-difluoro-2-oxo-2,3,4,5-tetrahydro-1hbenzo(b)azepin-3-yl)-1H-1,2,4-triazole-3-carboxamide (7,7-dimethyl-2- oxobicyclo(2.2.1)heptan-1-yl)
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| Encapsulated cell therapy | Phase 1/2 | [62] | ||
| External Link | ||||
| ETBX-011 cancer vaccine | Phase 1/2 | [40] | ||
| External Link | ||||
| BPX-601 | Phase 1/2 | [63] | ||
| External Link | ||||
| NANT | Phase 1/2 | [2] | ||
| External Link | ||||
| BrevaRex | Phase 1/2 | [64] | ||
| Synonyms |
BrevaRex MAb; monoclonal antibody
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| DCVax-Pancreas | Phase 1/2 | [65] | ||
| Synonyms |
Dendritic cell-based immunotherapy (pancreatic cancer), Northwest Biotherapeutics
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| PEGylated hyaluronidase (human recombinant) | Phase 1/2 | [66] | ||
| Synonyms |
PEGylated hyaluronidase; PEGylated hyaluronidase (human recombinant) (intravenous, stroke/cancer), Halozyme
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| CAR-T cells targeting mesothelin | Phase 1/2 | [67] | ||
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| MALP-2S | Phase 1/2 | [68] | ||
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| Anti-Mesothelin CAR-T cells | Phase 1/2 | [69] | ||
| External Link | ||||
| Anti-MUC1 CAR T Cells | Phase 1/2 | [70] | ||
| External Link | ||||
| Anti-HER2 CAR-T | Phase 1/2 | [71] | ||
| External Link | ||||
| CAR-T Cells targeting EpCAM | Phase 1/2 | [72] | ||
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| Anti-MUC1 AR20.5 | Phase 1/2 | [18] | ||
| External Link | ||||
| AR20.5 | Phase 1/2 | [2] | ||
| External Link | ||||
| G0-203-2c | Phase 1/2 | [73] | ||
| External Link | ||||
| LOAd703 | Phase 1/2 | [2] | ||
| External Link | ||||
| Anti-mesothelin CAR transduced PBL | Phase 1/2 | [74] | ||
| External Link | ||||
| M9241 | Phase 1 | [75] | ||
| Synonyms |
NHS-IL12
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| NBF-006 | Phase 1 | [76] | ||
| External Link | ||||
| AB680 | Phase 1 | [77] | ||
| Synonyms |
AB-680; UNII-J6K8WSV73A; J6K8WSV73A; CHEMBL4471306; 2105904-82-1; (((((2R,3S,4R,5R)-5-(6-chloro-4-(((S)-1-(2-fluorophenyl)ethyl)amino)-1H-pyrazolo[3,4-b]pyridin-1-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methoxy)(hydroxy)phosphoryl)methyl)phosphonic acid; [[(2~{R},3~{S},4~{R},5~{R})-5-[6-chloranyl-4-[[(1~{S})-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl]methylphosphonic acid; SCHEMBL19100484; GTPL10707; BDBM50527134; HY-125286; CS-0090231; [[(2R,3S,4R,5R)-5-[6-chloro-4-[[(1S)-1-(2-fluorophenyl)ethyl]amino]pyrazolo[3,4-b]pyridin-1-yl]-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl]methylphosphonic acid; QDH
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| STAT400 | Phase 1 | [78] | ||
| External Link | ||||
| CEND-1 | Phase 1 | [79] | ||
| Synonyms |
iRGD; UNII-Z8MXU5GH4Q; Z8MXU5GH4Q; iRGD-peptide; 1392278-76-0; Internalized-arginylglycylaspartic acid cyclic peptide; Q48988348; L-Cysteine, L-cysteinyl-L-arginylglycyl-L-alpha-aspartyl-L-lysylglycyl-L-prolyl-L-alpha-aspartyl-, cyclic (1->9)-disulfide
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| CAR-T Cells targeting EGFRvIII | Phase 1 | [80] | ||
| External Link | ||||
| HuCART-meso cells | Phase 1 | [81] | ||
| External Link | ||||
| OCV-105 | Phase 1 | [82] | ||
| Synonyms |
Cancer vaccine (pancreas), Otsuka/OncoTherapy
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| SBP-101 | Phase 1 | [13] | ||
| Synonyms |
diethyl dihydroxyhomospermine
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| RG7882 | Phase 1 | [18] | ||
| External Link | ||||
| CART-meso-19 T cells | Phase 1 | [83] | ||
| External Link | ||||
| MOv19-BBz CAR T cells | Phase 1 | [84] | ||
| External Link | ||||
| Anti-MUC1 AR20.5 mab | Phase 1 | [85] | ||
| External Link | ||||
| Anti-CEA-CAR T | Phase 1 | [86] | ||
| External Link | ||||
| MVT-5873 | Phase 1 | [18] | ||
| External Link | ||||
| CART-meso cells | Phase 1 | [87] | ||
| External Link | ||||
| CAR-20/19-T Cells | Phase 1 | [88] | ||
| External Link | ||||
| CARTmeso/19 | Phase 1 | [89] | ||
| External Link | ||||
| CAR-T Cells targeting Mesothelin | Phase 1 | [80] | ||
| External Link | ||||
| CAR-T Cells targeting CEA | Phase 1 | [80] | ||
| External Link | ||||
| HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine | Phase 1 | [90] | ||
| Synonyms |
HLA-A*2402-restricted KIF20A and VEGFR-1 epitope peptide vaccine (pancreatic cancer, subcutaneous)
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| Anti-hCD70 CAR transduced PBL | Phase 1 | [91] | ||
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| MORAb-066 | Phase 1 | [92] | ||
| Synonyms |
Anti-tissue factor monoclonal antibody (pancreatic tumor), Morphotek
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| Anti-MUC1 mab | Phase 1 | [93] | ||
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| Anti-meso-CAR vector transduced T cells | Phase 1 | [94] | ||
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| CRS-207 + GVAX | Phase 2 | [13] | ||
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| Autologous T cells transfected with chimeric anti-mesothelin immunoreceptor SS1 | Phase 1 | [95] | ||
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| Meso-CART | Phase 1 | [96] | ||
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| ASG-5ME | Phase 1 | [97] | ||
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| Anti-CD133-CAR vector-transduced T cells | Phase 1 | [98] | ||
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| IRX4204 | Phase 1 | [2] | ||
| Synonyms |
220619-73-8; CHEMBL75133; UNII-877M97Z38Y; VTP-194204; 877M97Z38Y; KB-145960; SCHEMBL3437269; MolPort-042-665-869; ZINC1550770; IRX-4204; 3-Methyl-5-[2-methyl-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-cyclopropyl]-penta-2,4-dienoic acid; BDBM50101445; DB11806; VTP 194204; (+)-VTP-194204; AGN 4204; (2E,4E)-3-Methyl-5-[(1S,2S)-2-methyl-2-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalen-2-yl)-cyclopropyl]-penta-2,4-dienoic acid
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| AbGn-107 | Phase 1 | [2] | ||
| External Link | ||||
| LMB-100 | Phase 1/2 | [2] | ||
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| PLX7486 | Phase 1 | [99] | ||
| External Link | ||||
| CAR-T Cells targeting HER2 | Phase 1 | [80] | ||
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| CAR-T Cells targeting MUCI | Phase 1 | [80] | ||
| External Link | ||||
| SEL-403 | Phase 1 | [2] | ||
| External Link | ||||
| CAR-T Cells targeting PSCA | Phase 1 | [80] | ||
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| Anti-CEA CAR-T cells | Phase 1 | [100] | ||
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| MVT-1075 | Phase 1 | [2] | ||
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| CAR-CLD18 T cell | Clinical trial | [101] | ||
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| CART-meso cells | Clinical trial | [102] | ||
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| PMID28460551-Compound-1 | Patented | [103] | ||
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| Tanomastat | Discontinued in Phase 3 | [104] | ||
| Synonyms |
Tanomastat (USAN/INN); (2S)-4-[4-(4-chlorophenyl)phenyl]-4-oxo-2-(phenylsulfanylmethyl)butanoic acid
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| Larotaxel | Discontinued in Phase 3 | [105] | ||
| Synonyms |
Benzenepropanoic acid; PNU 100940; XRP 9881; XRP9881
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| Apricoxib | Discontinued in Phase 2 | [106] | ||
| Synonyms |
TG01
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| Lintitript | Discontinued in Phase 2 | [107] | ||
| Synonyms |
SR 27897; SR 27897B; SR27897; SR-27897; SR-27897B; 1-((2-(4-(2-Chlorophenyl)thiazol-2-yl)aminocarbonyl)indolyl)acetic acid; 2-((4-(o-Chlorophenyl)-2-thiazolyl)carbamoyl)indole-1-acetic acid; 2-[2-[[4-(2-chlorophenyl)-1,3-thiazol-2-yl]carbamoyl]indol-1-yl]acetic acid
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| Merbarone | Discontinued in Phase 2 | [108] | ||
| Synonyms |
NSC-336628
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| LY293111 | Discontinued in Phase 2 | [109] | ||
| Synonyms |
Etalocib; 161172-51-6; UNII-THY6RIW44R; LY 293111; THY6RIW44R; CHEMBL329123; LY-193111; 2-[3-[3-[2-ethyl-4-(4-fluorophenyl)-5-hydroxyphenoxy]propoxy]-2-propylphenoxy]benzoic acid; VML295; Etalocib [USAN:INN]; Etalocib (USAN); GTPL2948; SCHEMBL1649516; CTK8E7596; C33H33FO6; VML 295; DTXSID70167073; YFIZRWPXUYFCSN-UHFFFAOYSA-N; MolPort-009-019-411; ZINC3930629; AC1L4328; PDSP2_001221; BDBM50029450; PDSP1_001237; 1758AH; DB12850; RT-013626; D04074; L001468; J-009797; Benzoic acid, 2-(3-(3-((5-ethyl-4'-fluoro-2-hydroxy(1,1'-bipheny
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| HMN-214 | Discontinued in Phase 1 | [110] | ||
| Synonyms |
N-(4-methoxyphenyl)sulfonyl-N-[2-[(E)-2-(1-oxidopyridin-4-yl)ethenyl]phenyl]acetamide; (E)-4-(2-(2-(N-Acetyl-N-((p-methoxyphenyl)sulfonyl)amino)phenyl)ethenyl)pyridine 1-oxide
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| RG7600 | Discontinued in Phase 1 | [111] | ||
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| IC261 | Preclinical | [112] | ||
| Synonyms |
IC-261; IC 261
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| ANAVEX 1007 | Preclinical | [113] | ||
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| IPH-4201 | Terminated | [114] | ||
| Synonyms |
MAb-16D10; MAb-J28; FAPP-targeting mAb (pancreatic cancer), Innate Pharma; FAPP-targeting mAb (pancreatic cancer), Universite de la Mediterranee/ INSERM; Feto-acinar pancreatic protein-targeting monoclonal antibodies (pancreatic cancer), Innate Pharma; Feto-acinar pancreatic protein-targeting monoclonal antibodies (pancreatic cancer), Universite de la Mediterranee/ INSERM
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| MesoTarg | Investigative | [115] | ||
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| PAT-PM-1 | Investigative | [115] | ||
| Synonyms |
PM-1; Human monoclonal antibody (pancreatic cancer), Patrys; Human MAb (pancreas cancer), OncoMab/ Acceptys; Human monoclonal antibody (pancreatic cancer), OncoMab/ Acceptys; PM-1 antibody, OncoMab/ Acceptys
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| OP-04 | Investigative | [115] | ||
| Synonyms |
OP-04 program (prodrug, pancreatic cancer); OP-04 program (prodrug, pancreatic cancer), Onco-Pharmakon
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| VLI-27 | Investigative | [116] | ||
| Synonyms |
AKT inhibitor (pancreatic cancer), NovaLead Pharma
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| GS-326 | Investigative | [115] | ||
| Synonyms |
GS-326C
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| PX-12 | Phase 2 | [117] | ||
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| Prodigiosin | Investigative | [115] | ||
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| Pbi-shPDX-1 LP | Investigative | [115] | ||
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| Gastrin 17C diphtheria toxoid conjugate | Investigative | [115] | ||
| Synonyms |
Gastrin 17C diphtheria toxoid conjugate (pancreatic cancer)
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| HS-P1 | Investigative | [115] | ||
| Synonyms |
HS-310; Endoplasmin modulator (pancreas tumor, HeatShock/fusion protein/antigen), Heat Biologics; Gp-96-Ig + unspecified tumor antigen secreting live cell vaccine (pancreas tumor, HeatShock), Heat Biologics
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References
: m6A sites