ARID1A Drug Discovery Landscape & Assay Solutions

TarMart Solution Ecosystem & Related Targets

Comprehensive reagent toolkit for ARID1A drug discovery and synthetic lethality screening. Select your modality below:

Component / Network Product Description Product Link
Antigen (WT) ARID1A ARID Domain Recombinant Protein (HEK293 expressed)
High purity (>95%), Endotoxin <1 EU/µg. Sequence Verified.
View ARID1A Products
Antigen (Mutant) ARID1A R1989* / Q1926* Truncation Mutants
Common cancer loss-of-function variants. Theoretical MW verified.
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Gene Delivery ARID1A sgRNA / Lentivirus KO Particles & Promise-ORF Lentivirus
For stable knockout/knockdown and rescue experiments.
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Benchmark Ab Anti-ARID1A Benchmark Antibody
Recombinant positive control for IHC/WB (sequence of clinical diagnostic clones).
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Validator ARID1A siRNA Set
For transient knockdown verification in synthetic lethal assays.
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Synthetic Lethality Partner A EZH2
Histone methyltransferase; PRC2 complex catalytic subunit. Primary synthetic lethality partner.
View EZH2 Products
Synthetic Lethality Partner B ARID1B
Critical paralog dependency in ARID1A-deficient cancers.
View ARID1B Products
Synthetic Lethality Partner C ATR
DNA damage response kinase; vulnerability target for ARID1A-mutant cancers.
View ATR Products
Pathway Associate SMARCB1 (INI1)
Core SWI/SNF complex subunit; frequently co-mutated.
View SMARCB1 Products
Critical Assay Challenge The TarMart Advantage (Technical Spec)
Generating robust ARID1A-deficient tumor models Sequence Verified Lentivirus for stable knockout/knockdown, essential for synthetic lethality screening.
Validating SWI/SNF complex PPI & domain mapping High Purity (>95%) recombinant ARID1A domain truncations (ARID, HSA, C-terminal) with Mass Spec confirmation.
Modeling loss-of-function mutations R1989* and Q1926* premature termination variants; High Purity for binding studies; Mutant vs WT selectivity panels.
Cross-species ortholog evaluation for tox Human / Mouse / Cyno ARID1A recombinant domain proteins available.
High background in target validation Validated ARID1A siRNA sets for orthogonal specificity checks in cell-based assays.

Live ARID1A R&D Tracker

Market data changes daily. Access the latest global pipeline status directly:

Global Clinical Landscape & Future Outlook

The therapeutic strategy for ARID1A-mutant cancers has shifted entirely from direct inhibition to synthetic lethality exploitation. As ARID1A is a tumor suppressor frequently lost in ovarian clear cell carcinoma, endometrial cancers, and gastric cancers, current R&D focuses on vulnerabilities in ARID1A-deficient tumors. Clinical-stage efforts target EZH2 (e.g., tazemetostat by Ipsen/Epizyme), ATR, and PARP inhibitors. The next wave of development includes targeted protein degradation (PROTACs) against ARID1B, molecular glues modulating SWI/SNF complex, and biomarker-driven patient stratification using ARID1A IHC loss-of-function detection.

Competitive Modality & Indication Snapshot

Modality Representative Players Key Indications Critical Assay Need
Synthetic Lethality (EZH2/ATR/PARP inhibitors) Epizyme (Ipsen), AstraZeneca, Merck KGaA, BMS Ovarian Clear Cell, Endometrial, Gastric Carcinoma Isogenic cell lines (ARID1A KO/mutant) for sensitivity screening
Targeted Protein Degrader (PROTAC) / Molecular Glue Foghorn Therapeutics, Prelude, Arvinas, Cullgen ARID1A-deficient Solid Tumors PPI assays using purified ARID1A domains; selectivity against ARID1B
Biomarker Diagnostic / IHC Roche Diagnostics, Agilent Pan-cancer screening (Gastric, Colorectal) Loss-of-function detection using high-specificity Anti-ARID1A benchmark Abs
Direct Epigenetic Regulator (Preclinical) Early-stage biotech / Academia Pan-tumor (ARID1A-mutant) DNA-binding assays (AT-rich motif) using high-purity ARID domain protein