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BIOMARKER:

MTAP deletion

i
Other names: MTAP, Methylthioadenosine Phosphorylase, S-Methyl-5'-Thioadenosine Phosphorylase, MSAP, 5’-Methylthioadenosine Phosphorylase, MTA Phosphorylase, MTAPase, C86fus, Epididymis Secretory Sperm Binding Protein, Epididymis Luminal Protein 249, MeSAdo Phosphorylase, HEL-249, DMSMFH, DMSFH, LGMBF, BDMF
Entrez ID:
Related biomarkers:
11d
Real-World Prevalence and Structural Validation of the Canonical 9p21 MTAP-CDKN2A/B Deletion in Non-NSCLC Solid Tumors. (PubMed, Cancers (Basel))
Our findings demonstrate that MTAP deletion is an infrequent but genomically coherent event in solid tumors, characterized by a canonical 9p21 co-deletion pattern. This real-world analysis underscores the importance of comprehensive genomic profiling to identify patients who may benefit from emerging MTAP-directed therapies.
Journal • Real-world evidence • Tumor mutational burden
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TMB (Tumor Mutational Burden) • CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • MTAP (Methylthioadenosine Phosphorylase) • CDKN2B (Cyclin Dependent Kinase Inhibitor 2B) • MAT2A (Methionine Adenosyltransferase 2A)
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TMB-L • CDKN2A deletion • MTAP deletion
14d
Systemic Therapy for Advanced Pancreatic Cancer in 2025: Current Standard-of-Care and Emerging Therapeutic Strategies. (PubMed, J Gastroenterol Hepatol)
Emerging immunotherapies targeting Claudin18.2 and CXCR4 offer hope to overcome tumor resistance. Together, these strategies underscore the promise of molecular stratification, synthetic lethality, and novel targets to improve pancreatic cancer survival.
Review • Journal • IO biomarker
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KRAS (KRAS proto-oncogene GTPase) • BRAF (B-raf proto-oncogene) • HRD (Homologous Recombination Deficiency) • CLDN18 (Claudin 18) • NRG1 (Neuregulin 1) • MTAP (Methylthioadenosine Phosphorylase) • CXCR4 (Chemokine (C-X-C motif) receptor 4)
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HRD • KRAS wild-type • MTAP deletion • RAS wild-type • NRG1 fusion
23d
MTAP Loss Is Frequent in Oncogene-Driven NSCLC and May Confer Sensitivity to Combined PRMT5 Inhibitors and Targeted Therapies. (PubMed, Ann Oncol)
MTAP loss is frequent in oncogene-driven NSCLC, particularly in ALK-, RET-, and EGFR-altered subtypes. MTA-cooperative PRMT5 inhibition demonstrates broad activity in MTAP-deleted, oncogene-driven models and, and may enhance targeted therapy efficacy in selected settings.
Journal
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EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase) • CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • MTAP (Methylthioadenosine Phosphorylase)
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EGFR mutation • ALK rearrangement • CDKN2A deletion • MTAP deletion
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Xalkori (crizotinib) • Tagrisso (osimertinib) • Alecensa (alectinib) • navlimetostat (BMS‐986504)
25d
Coupled-Enzyme Assay for MTAP Activity in Biological Samples. (PubMed, Anal Biochem)
MTAP activity was also measured across a panel of cancer cell lines to determine intracellular MTAP levels and to complement whole-blood measurements. This approach enables real-time evaluation of MTAP function and drug response in μL volumes of lysate, providing a direct biological or clinical platform for tracking targeted MTAP therapies.
Journal
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CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • MTAP (Methylthioadenosine Phosphorylase) • CDKN2B (Cyclin Dependent Kinase Inhibitor 2B) • MAT2A (Methionine Adenosyltransferase 2A)
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MTAP deletion
30d
Association of CDKN2A/B and MTAP deletions in adult-type diffuse gliomas. (PubMed, J Neuropathol Exp Neurol)
Discordant CDKN2A/B and MTAP tumors affect the association between MTAP IHC and copy number status of MTAP and CDKN2A/B. These findings suggest that adult-type diffuse gliomas, regardless of IDH status, follow a stereotypic pathway involving concurrent CDKN2A/B and MTAP heterozygous deletion but may diverge for CDKN2A/B and MTAP homozygous deletion.
Journal
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CDKN2A (Cyclin Dependent Kinase Inhibitor 2A) • MTAP (Methylthioadenosine Phosphorylase) • CDKN2B (Cyclin Dependent Kinase Inhibitor 2B)
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CDKN2A deletion • MTAP deletion
1m
A Phase II Study Evaluating BMS-986504 in MTAP-deleted Pancreatic Cancer (clinicaltrials.gov)
P2, N=60, Suspended, M.D. Anderson Cancer Center | Not yet recruiting --> Suspended
Trial suspension
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MTAP (Methylthioadenosine Phosphorylase)
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MTAP deletion
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gemcitabine • albumin-bound paclitaxel • oxaliplatin • irinotecan • navlimetostat (BMS‐986504)
1m
Phase 1b Trial of BMS-986504 in Combination With Olaparib in Patients With MTAP Loss (clinicaltrials.gov)
P1, N=36, Recruiting, M.D. Anderson Cancer Center | Not yet recruiting --> Recruiting | Initiation date: Jun 2026 --> Feb 2026
Enrollment open • Trial initiation date
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MTAP (Methylthioadenosine Phosphorylase)
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MTAP deletion
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Lynparza (olaparib) • navlimetostat (BMS‐986504)
1m
Journey of Methionine Adenosyltransferase 2A Inhibitors: From Bench to Advanced Clinical Trials. (PubMed, J Med Chem)
Here, we trace the evolution of MAT2A inhibitors from early substrate-competitive molecules to allosteric inhibitors now in clinical evaluation. We discuss the design of next-generation inhibitors with improved potency, selectivity, and pharmacokinetic properties, including central nervous system penetration.
Review • Journal
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MTAP (Methylthioadenosine Phosphorylase) • MAT2A (Methionine Adenosyltransferase 2A)
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MTAP deletion
2ms
New P1/2 trial
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MTAP (Methylthioadenosine Phosphorylase)
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MTAP deletion • IDH wild-type
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vopimetostat (TNG462)
2ms
New P2/3 trial
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MTAP (Methylthioadenosine Phosphorylase)
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MTAP deletion
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Keytruda (pembrolizumab) • cisplatin • carboplatin • paclitaxel • albumin-bound paclitaxel • pemetrexed • navlimetostat (BMS‐986504)
2ms
New P1/2 trial • First-in-human
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MTAP (Methylthioadenosine Phosphorylase)
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MTAP deletion
2ms
New P2/3 trial
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MTAP (Methylthioadenosine Phosphorylase)
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MTAP deletion
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gemcitabine • albumin-bound paclitaxel • navlimetostat (BMS‐986504)